Trial Outcomes & Findings for Comparative Analysis of Outcomes Among Patients Treated With Xeljanz vs Biologics (NCT NCT03964649)
NCT ID: NCT03964649
Last Updated: 2021-06-02
Results Overview
In this outcome measure number of participants who were on combination therapy with index medication and who were on monotherapy during 12 months pre-index date were reported. Participants with a use of at least 1 of 4 specific csDMARDs (methotrexate, sulfasalazine, hydroxychloroquine, leflunomide) within 90 days on or after the index date were considered as being treated with combination therapy. Participants who did not take any csDMARDs along with index medication were considered being treated with monotherapy.
COMPLETED
7308 participants
Within 90 days after index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
2021-06-02
Participant Flow
Participants with rheumatoid arthritis (RA), who newly initiated tofacitinib or biologic disease-modifying antirheumatic drug (bDMARDs), between 01 February 2016 and 31 July 2019 (identification period), were identified using Truven Health MarketScan Research database. Data for eligible participants from database were evaluated in this retrospective observational study. Index date = date of first claim for index medication (bDMARDs or tofacitinib) during identification period of 3.5 years.
Baseline characteristics- age, sex, region of enrollment were evaluated at index date. Other study specific characteristics were observed over 12 months before index date (12 months pre-index baseline period) and/or over variable-length pre-index baseline period. Variable-length pre-index baseline period was minimum of 1 year and could have been maximum up to 5.68 years before index date.
Participant milestones
| Measure |
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Overall Study
STARTED
|
349
|
304
|
2728
|
192
|
1948
|
349
|
376
|
325
|
204
|
533
|
|
Overall Study
COMPLETED
|
349
|
304
|
2728
|
192
|
1948
|
349
|
376
|
325
|
204
|
533
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
0
|
0
|
0
|
0
|
0
|
0
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Race and Ethnicity were not collected from any participant.
Baseline characteristics by cohort
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
Total
n=7308 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|---|---|---|---|---|---|
|
Age, Continuous
|
55.48 years
STANDARD_DEVIATION 11.04 • n=349 Participants
|
55.93 years
STANDARD_DEVIATION 11.26 • n=304 Participants
|
51.42 years
STANDARD_DEVIATION 10.35 • n=2728 Participants
|
56.70 years
STANDARD_DEVIATION 14.90 • n=192 Participants
|
51.85 years
STANDARD_DEVIATION 10.89 • n=1948 Participants
|
55.85 years
STANDARD_DEVIATION 12.33 • n=349 Participants
|
55.63 years
STANDARD_DEVIATION 12.55 • n=376 Participants
|
56.13 years
STANDARD_DEVIATION 11.90 • n=325 Participants
|
55.99 years
STANDARD_DEVIATION 11.65 • n=204 Participants
|
55.88 years
STANDARD_DEVIATION 11.45 • n=533 Participants
|
53.14 years
STANDARD_DEVIATION 11.30 • n=7308 Participants
|
|
Sex: Female, Male
Female
|
282 Participants
n=349 Participants
|
250 Participants
n=304 Participants
|
2124 Participants
n=2728 Participants
|
156 Participants
n=192 Participants
|
1523 Participants
n=1948 Participants
|
279 Participants
n=349 Participants
|
302 Participants
n=376 Participants
|
257 Participants
n=325 Participants
|
158 Participants
n=204 Participants
|
448 Participants
n=533 Participants
|
5779 Participants
n=7308 Participants
|
|
Sex: Female, Male
Male
|
67 Participants
n=349 Participants
|
54 Participants
n=304 Participants
|
604 Participants
n=2728 Participants
|
36 Participants
n=192 Participants
|
425 Participants
n=1948 Participants
|
70 Participants
n=349 Participants
|
74 Participants
n=376 Participants
|
68 Participants
n=325 Participants
|
46 Participants
n=204 Participants
|
85 Participants
n=533 Participants
|
1529 Participants
n=7308 Participants
|
|
Race and Ethnicity Not Collected
|
—
|
—
|
—
|
—
|
—
|
—
|
—
|
—
|
—
|
—
|
0 Participants
Race and Ethnicity were not collected from any participant.
|
|
Region of Enrollment
United States · Northeast Region
|
96 Participants
n=349 Participants
|
69 Participants
n=304 Participants
|
422 Participants
n=2728 Participants
|
45 Participants
n=192 Participants
|
331 Participants
n=1948 Participants
|
51 Participants
n=349 Participants
|
55 Participants
n=376 Participants
|
57 Participants
n=325 Participants
|
41 Participants
n=204 Participants
|
114 Participants
n=533 Participants
|
1281 Participants
n=7308 Participants
|
|
Region of Enrollment
United States · North Central Region
|
62 Participants
n=349 Participants
|
58 Participants
n=304 Participants
|
605 Participants
n=2728 Participants
|
21 Participants
n=192 Participants
|
390 Participants
n=1948 Participants
|
74 Participants
n=349 Participants
|
46 Participants
n=376 Participants
|
77 Participants
n=325 Participants
|
37 Participants
n=204 Participants
|
93 Participants
n=533 Participants
|
1463 Participants
n=7308 Participants
|
|
Region of Enrollment
United States · South Region
|
143 Participants
n=349 Participants
|
137 Participants
n=304 Participants
|
1349 Participants
n=2728 Participants
|
104 Participants
n=192 Participants
|
952 Participants
n=1948 Participants
|
178 Participants
n=349 Participants
|
235 Participants
n=376 Participants
|
120 Participants
n=325 Participants
|
97 Participants
n=204 Participants
|
256 Participants
n=533 Participants
|
3571 Participants
n=7308 Participants
|
|
Region of Enrollment
United States · West Region
|
45 Participants
n=349 Participants
|
40 Participants
n=304 Participants
|
348 Participants
n=2728 Participants
|
22 Participants
n=192 Participants
|
274 Participants
n=1948 Participants
|
46 Participants
n=349 Participants
|
37 Participants
n=376 Participants
|
71 Participants
n=325 Participants
|
29 Participants
n=204 Participants
|
70 Participants
n=533 Participants
|
982 Participants
n=7308 Participants
|
|
Region of Enrollment
United States · Unknown Region
|
3 Participants
n=349 Participants
|
0 Participants
n=304 Participants
|
4 Participants
n=2728 Participants
|
0 Participants
n=192 Participants
|
1 Participants
n=1948 Participants
|
0 Participants
n=349 Participants
|
3 Participants
n=376 Participants
|
0 Participants
n=325 Participants
|
0 Participants
n=204 Participants
|
0 Participants
n=533 Participants
|
11 Participants
n=7308 Participants
|
|
Mean Number of bDMARDs Received During 12 Months Pre-Index Baseline Period
|
1.11 number of bDMARDs
STANDARD_DEVIATION 0.32 • n=349 Participants
|
1.40 number of bDMARDs
STANDARD_DEVIATION 0.59 • n=304 Participants
|
1.11 number of bDMARDs
STANDARD_DEVIATION 0.31 • n=2728 Participants
|
1.31 number of bDMARDs
STANDARD_DEVIATION 0.80 • n=192 Participants
|
1.06 number of bDMARDs
STANDARD_DEVIATION 0.24 • n=1948 Participants
|
1.41 number of bDMARDs
STANDARD_DEVIATION 0.56 • n=349 Participants
|
1.19 number of bDMARDs
STANDARD_DEVIATION 0.45 • n=376 Participants
|
1.31 number of bDMARDs
STANDARD_DEVIATION 0.62 • n=325 Participants
|
1.20 number of bDMARDs
STANDARD_DEVIATION 0.45 • n=204 Participants
|
1.22 number of bDMARDs
STANDARD_DEVIATION 0.42 • n=533 Participants
|
1.23 number of bDMARDs
STANDARD_DEVIATION 0.49 • n=7308 Participants
|
|
Mean Number of bDMARDs Received During Variable Length Pre-Index Baseline Period
|
1.46 number of bDMARDs
STANDARD_DEVIATION 0.73 • n=349 Participants
|
1.61 number of bDMARDs
STANDARD_DEVIATION 0.81 • n=304 Participants
|
1.24 number of bDMARDs
STANDARD_DEVIATION 0.55 • n=2728 Participants
|
1.88 number of bDMARDs
STANDARD_DEVIATION 1.12 • n=192 Participants
|
1.23 number of bDMARDs
STANDARD_DEVIATION 0.65 • n=1948 Participants
|
1.83 number of bDMARDs
STANDARD_DEVIATION 1.09 • n=349 Participants
|
1.58 number of bDMARDs
STANDARD_DEVIATION 0.91 • n=376 Participants
|
1.78 number of bDMARDs
STANDARD_DEVIATION 1.14 • n=325 Participants
|
1.79 number of bDMARDs
STANDARD_DEVIATION 0.95 • n=204 Participants
|
1.58 number of bDMARDs
STANDARD_DEVIATION 0.78 • n=533 Participants
|
1.55 number of bDMARDs
STANDARD_DEVIATION 0.87 • n=7308 Participants
|
|
Mean Number of csDMARDs Received During 12 Months Pre-Index Baseline Period
|
1.58 csDMARDs
STANDARD_DEVIATION 0.66 • n=349 Participants
|
1.48 csDMARDs
STANDARD_DEVIATION 0.66 • n=304 Participants
|
1.56 csDMARDs
STANDARD_DEVIATION 0.69 • n=2728 Participants
|
1.39 csDMARDs
STANDARD_DEVIATION 0.59 • n=192 Participants
|
1.61 csDMARDs
STANDARD_DEVIATION 0.72 • n=1948 Participants
|
1.56 csDMARDs
STANDARD_DEVIATION 0.72 • n=349 Participants
|
1.50 csDMARDs
STANDARD_DEVIATION 0.67 • n=376 Participants
|
1.56 csDMARDs
STANDARD_DEVIATION 0.68 • n=325 Participants
|
1.49 csDMARDs
STANDARD_DEVIATION 0.69 • n=204 Participants
|
1.63 csDMARDs
STANDARD_DEVIATION 0.73 • n=533 Participants
|
1.57 csDMARDs
STANDARD_DEVIATION 0.70 • n=7308 Participants
|
|
Mean Number of csDMARDs Received During Variable Length Pre-Index Baseline Period
|
1.91 csDMARDs
STANDARD_DEVIATION 0.89 • n=349 Participants
|
1.88 csDMARDs
STANDARD_DEVIATION 0.87 • n=304 Participants
|
1.76 csDMARDs
STANDARD_DEVIATION 0.82 • n=2728 Participants
|
1.66 csDMARDs
STANDARD_DEVIATION 0.80 • n=192 Participants
|
1.82 csDMARDs
STANDARD_DEVIATION 0.85 • n=1948 Participants
|
1.76 csDMARDs
STANDARD_DEVIATION 0.86 • n=349 Participants
|
1.73 csDMARDs
STANDARD_DEVIATION 0.82 • n=376 Participants
|
1.93 csDMARDs
STANDARD_DEVIATION 0.91 • n=325 Participants
|
1.71 csDMARDs
STANDARD_DEVIATION 0.88 • n=204 Participants
|
2.02 csDMARDs
STANDARD_DEVIATION 0.92 • n=533 Participants
|
1.81 csDMARDs
STANDARD_DEVIATION 7,308 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 11
|
792.87 dollars
STANDARD_DEVIATION 3,620.60 • n=349 Participants
|
1,742.02 dollars
STANDARD_DEVIATION 9,856.48 • n=304 Participants
|
369.35 dollars
STANDARD_DEVIATION 3,438.00 • n=2728 Participants
|
635.71 dollars
STANDARD_DEVIATION 1,873.22 • n=192 Participants
|
321.38 dollars
STANDARD_DEVIATION 1,966.71 • n=1948 Participants
|
732.68 dollars
STANDARD_DEVIATION 3,025.76 • n=349 Participants
|
663.43 dollars
STANDARD_DEVIATION 2,707.95 • n=376 Participants
|
999.43 dollars
STANDARD_DEVIATION 3,233.47 • n=325 Participants
|
1,078.26 dollars
STANDARD_DEVIATION 2,531.66 • n=204 Participants
|
1,129.36 dollars
STANDARD_DEVIATION 3,563.67 • n=533 Participants
|
576.61 dollars
STANDARD_DEVIATION 3,563.16 • n=7308 Participants
|
|
Quan-Charlson Comorbidity Score During 12 Months Pre-Index Baseline Period
|
1.77 units on a scale
STANDARD_DEVIATION 1.14 • n=349 Participants
|
1.89 units on a scale
STANDARD_DEVIATION 1.32 • n=304 Participants
|
1.63 units on a scale
STANDARD_DEVIATION 1.04 • n=2728 Participants
|
1.95 units on a scale
STANDARD_DEVIATION 1.46 • n=192 Participants
|
1.70 units on a scale
STANDARD_DEVIATION 1.13 • n=1948 Participants
|
1.94 units on a scale
STANDARD_DEVIATION 1.43 • n=349 Participants
|
1.72 units on a scale
STANDARD_DEVIATION 1.22 • n=376 Participants
|
2.54 units on a scale
STANDARD_DEVIATION 1.81 • n=325 Participants
|
2.01 units on a scale
STANDARD_DEVIATION 1.52 • n=204 Participants
|
2.10 units on a scale
STANDARD_DEVIATION 1.46 • n=533 Participants
|
1.78 units on a scale
STANDARD_DEVIATION 1.23 • n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Methotrexate Sodium
|
279 Participants
n=349 Participants
|
220 Participants
n=304 Participants
|
2440 Participants
n=2728 Participants
|
155 Participants
n=192 Participants
|
1,732 Participants
n=1948 Participants
|
306 Participants
n=349 Participants
|
313 Participants
n=376 Participants
|
253 Participants
n=325 Participants
|
152 Participants
n=204 Participants
|
396 Participants
n=533 Participants
|
6246 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Folic Acid
|
226 Participants
n=349 Participants
|
177 Participants
n=304 Participants
|
2,024 Participants
n=2728 Participants
|
126 Participants
n=192 Participants
|
1,435 Participants
n=1948 Participants
|
230 Participants
n=349 Participants
|
272 Participants
n=376 Participants
|
197 Participants
n=325 Participants
|
122 Participants
n=204 Participants
|
329 Participants
n=533 Participants
|
5138 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Prednisone
|
219 Participants
n=349 Participants
|
203 Participants
n=304 Participants
|
1,930 Participants
n=2728 Participants
|
123 Participants
n=192 Participants
|
1,379 Participants
n=1948 Participants
|
250 Participants
n=349 Participants
|
251 Participants
n=376 Participants
|
232 Participants
n=325 Participants
|
157 Participants
n=204 Participants
|
368 Participants
n=533 Participants
|
5112 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Hydroxychloroquine Sulfate
|
106 Participants
n=349 Participants
|
98 Participants
n=304 Participants
|
919 Participants
n=2728 Participants
|
43 Participants
n=192 Participants
|
711 Participants
n=1948 Participants
|
102 Participants
n=349 Participants
|
109 Participants
n=376 Participants
|
112 Participants
n=325 Participants
|
59 Participants
n=204 Participants
|
211 Participants
n=533 Participants
|
2470 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Acetaminophen/Hydrocodone Bitartrate
|
82 Participants
n=349 Participants
|
89 Participants
n=304 Participants
|
768 Participants
n=2728 Participants
|
60 Participants
n=192 Participants
|
518 Participants
n=1948 Participants
|
122 Participants
n=349 Participants
|
114 Participants
n=376 Participants
|
107 Participants
n=325 Participants
|
75 Participants
n=204 Participants
|
157 Participants
n=533 Participants
|
2092 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Methylprednisolone
|
79 Participants
n=349 Participants
|
61 Participants
n=304 Participants
|
684 Participants
n=2728 Participants
|
38 Participants
n=192 Participants
|
503 Participants
n=1948 Participants
|
81 Participants
n=349 Participants
|
89 Participants
n=376 Participants
|
52 Participants
n=325 Participants
|
39 Participants
n=204 Participants
|
112 Participants
n=533 Participants
|
1738 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Tramadol Hydrochloride
|
58 Participants
n=349 Participants
|
64 Participants
n=304 Participants
|
604 Participants
n=2728 Participants
|
37 Participants
n=192 Participants
|
462 Participants
n=1948 Participants
|
79 Participants
n=349 Participants
|
89 Participants
n=376 Participants
|
84 Participants
n=325 Participants
|
44 Participants
n=204 Participants
|
124 Participants
n=533 Participants
|
1645 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Azithromycin
|
89 Participants
n=349 Participants
|
64 Participants
n=304 Participants
|
592 Participants
n=2728 Participants
|
50 Participants
n=192 Participants
|
430 Participants
n=1948 Participants
|
74 Participants
n=349 Participants
|
94 Participants
n=376 Participants
|
67 Participants
n=325 Participants
|
38 Participants
n=204 Participants
|
126 Participants
n=533 Participants
|
1624 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Meloxicam
|
59 Participants
n=349 Participants
|
47 Participants
n=304 Participants
|
647 Participants
n=2728 Participants
|
29 Participants
n=192 Participants
|
448 Participants
n=1948 Participants
|
73 Participants
n=349 Participants
|
81 Participants
n=376 Participants
|
41 Participants
n=325 Participants
|
36 Participants
n=204 Participants
|
89 Participants
n=533 Participants
|
1550 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Levothyroxine Sodium
|
67 Participants
n=349 Participants
|
55 Participants
n=304 Participants
|
498 Participants
n=2728 Participants
|
35 Participants
n=192 Participants
|
363 Participants
n=1948 Participants
|
65 Participants
n=349 Participants
|
73 Participants
n=376 Participants
|
62 Participants
n=325 Participants
|
43 Participants
n=204 Participants
|
119 Participants
n=533 Participants
|
1380 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Gabapentin
|
52 Participants
n=349 Participants
|
34 Participants
n=304 Participants
|
373 Participants
n=2728 Participants
|
31 Participants
n=192 Participants
|
315 Participants
n=1948 Participants
|
64 Participants
n=349 Participants
|
64 Participants
n=376 Participants
|
53 Participants
n=325 Participants
|
37 Participants
n=204 Participants
|
114 Participants
n=533 Participants
|
1137 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Omeprazole
|
42 Participants
n=349 Participants
|
50 Participants
n=304 Participants
|
367 Participants
n=2728 Participants
|
22 Participants
n=192 Participants
|
320 Participants
n=1948 Participants
|
62 Participants
n=349 Participants
|
62 Participants
n=376 Participants
|
67 Participants
n=325 Participants
|
40 Participants
n=204 Participants
|
92 Participants
n=533 Participants
|
1124 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Albuterol Sulfate
|
52 Participants
n=349 Participants
|
48 Participants
n=304 Participants
|
411 Participants
n=2728 Participants
|
25 Participants
n=192 Participants
|
282 Participants
n=1948 Participants
|
54 Participants
n=349 Participants
|
42 Participants
n=376 Participants
|
47 Participants
n=325 Participants
|
36 Participants
n=204 Participants
|
92 Participants
n=533 Participants
|
1089 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Diclofenac Sodium
|
47 Participants
n=349 Participants
|
42 Participants
n=304 Participants
|
410 Participants
n=2728 Participants
|
27 Participants
n=192 Participants
|
294 Participants
n=1948 Participants
|
62 Participants
n=349 Participants
|
64 Participants
n=376 Participants
|
34 Participants
n=325 Participants
|
28 Participants
n=204 Participants
|
77 Participants
n=533 Participants
|
1085 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Leflunomide
|
56 Participants
n=349 Participants
|
50 Participants
n=304 Participants
|
356 Participants
n=2728 Participants
|
27 Participants
n=192 Participants
|
283 Participants
n=1948 Participants
|
60 Participants
n=349 Participants
|
62 Participants
n=376 Participants
|
44 Participants
n=325 Participants
|
27 Participants
n=204 Participants
|
94 Participants
n=533 Participants
|
1059 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Amoxicillin
|
52 Participants
n=349 Participants
|
41 Participants
n=304 Participants
|
365 Participants
n=2728 Participants
|
25 Participants
n=192 Participants
|
286 Participants
n=1948 Participants
|
47 Participants
n=349 Participants
|
62 Participants
n=376 Participants
|
47 Participants
n=325 Participants
|
29 Participants
n=204 Participants
|
94 Participants
n=533 Participants
|
1048 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Cyclobenzaprine Hydrochloride
|
46 Participants
n=349 Participants
|
43 Participants
n=304 Participants
|
367 Participants
n=2728 Participants
|
25 Participants
n=192 Participants
|
286 Participants
n=1948 Participants
|
45 Participants
n=349 Participants
|
55 Participants
n=376 Participants
|
40 Participants
n=325 Participants
|
35 Participants
n=204 Participants
|
73 Participants
n=533 Participants
|
1015 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Fluticasone Propionate
|
55 Participants
n=349 Participants
|
51 Participants
n=304 Participants
|
329 Participants
n=2728 Participants
|
29 Participants
n=192 Participants
|
259 Participants
n=1948 Participants
|
51 Participants
n=349 Participants
|
46 Participants
n=376 Participants
|
47 Participants
n=325 Participants
|
25 Participants
n=204 Participants
|
70 Participants
n=533 Participants
|
962 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Amoxicillin/Clavulanate Potassium
|
60 Participants
n=349 Participants
|
34 Participants
n=304 Participants
|
380 Participants
n=2728 Participants
|
19 Participants
n=192 Participants
|
228 Participants
n=1948 Participants
|
52 Participants
n=349 Participants
|
36 Participants
n=376 Participants
|
40 Participants
n=325 Participants
|
28 Participants
n=204 Participants
|
80 Participants
n=533 Participants
|
957 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Acetaminophen/Oxycodone Hydrochloride
|
40 Participants
n=349 Participants
|
39 Participants
n=304 Participants
|
294 Participants
n=2728 Participants
|
23 Participants
n=192 Participants
|
229 Participants
n=1948 Participants
|
56 Participants
n=349 Participants
|
41 Participants
n=376 Participants
|
49 Participants
n=325 Participants
|
32 Participants
n=204 Participants
|
82 Participants
n=533 Participants
|
885 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Ibuprofen
|
36 Participants
n=349 Participants
|
40 Participants
n=304 Participants
|
318 Participants
n=2728 Participants
|
20 Participants
n=192 Participants
|
233 Participants
n=1948 Participants
|
59 Participants
n=349 Participants
|
50 Participants
n=376 Participants
|
29 Participants
n=325 Participants
|
27 Participants
n=204 Participants
|
62 Participants
n=533 Participants
|
874 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Ergocalciferol
|
48 Participants
n=349 Participants
|
32 Participants
n=304 Participants
|
322 Participants
n=2728 Participants
|
25 Participants
n=192 Participants
|
206 Participants
n=1948 Participants
|
40 Participants
n=349 Participants
|
56 Participants
n=376 Participants
|
36 Participants
n=325 Participants
|
28 Participants
n=204 Participants
|
60 Participants
n=533 Participants
|
853 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Duloxetine Hydrochloride
|
36 Participants
n=349 Participants
|
34 Participants
n=304 Participants
|
289 Participants
n=2728 Participants
|
22 Participants
n=192 Participants
|
222 Participants
n=1948 Participants
|
47 Participants
n=349 Participants
|
51 Participants
n=376 Participants
|
30 Participants
n=325 Participants
|
28 Participants
n=204 Participants
|
75 Participants
n=533 Participants
|
834 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Ciprofloxacin Hydrochloride
|
40 Participants
n=349 Participants
|
38 Participants
n=304 Participants
|
249 Participants
n=2728 Participants
|
16 Participants
n=192 Participants
|
219 Participants
n=1948 Participants
|
41 Participants
n=349 Participants
|
42 Participants
n=376 Participants
|
52 Participants
n=325 Participants
|
23 Participants
n=204 Participants
|
80 Participants
n=533 Participants
|
800 Participants
n=7308 Participants
|
|
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Atorvastatin Calcium
|
54 Participants
n=349 Participants
|
26 Participants
n=304 Participants
|
285 Participants
n=2728 Participants
|
20 Participants
n=192 Participants
|
190 Participants
n=1948 Participants
|
51 Participants
n=349 Participants
|
41 Participants
n=376 Participants
|
33 Participants
n=325 Participants
|
29 Participants
n=204 Participants
|
64 Participants
n=533 Participants
|
793 Participants
n=7308 Participants
|
|
Number of Participants Who Used Opioids or NSAIDs During 12 Months Pre-Index Baseline Period
|
214 Participants
n=349 Participants
|
236 Participants
n=304 Participants
|
1,867 Participants
n=2728 Participants
|
134 Participants
n=192 Participants
|
1,360 Participants
n=1948 Participants
|
265 Participants
n=349 Participants
|
277 Participants
n=376 Participants
|
229 Participants
n=325 Participants
|
157 Participants
n=204 Participants
|
380 Participants
n=533 Participants
|
5119 Participants
n=7308 Participants
|
|
Mean Number of Pharmacy Claims for Opioids and NSAIDS During 12 Months Pre-Index Baseline Period
|
4.04 pharmacy claims
STANDARD_DEVIATION 6.39 • n=214 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
5.31 pharmacy claims
STANDARD_DEVIATION 6.85 • n=236 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
4.08 pharmacy claims
STANDARD_DEVIATION 5.84 • n=1867 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
4.15 pharmacy claims
STANDARD_DEVIATION 6.09 • n=134 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
4.45 pharmacy claims
STANDARD_DEVIATION 5.80 • n=1360 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
4.84 pharmacy claims
STANDARD_DEVIATION 5.92 • n=265 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
4.46 pharmacy claims
STANDARD_DEVIATION 5.38 • n=277 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
4.14 pharmacy claims
STANDARD_DEVIATION 5.23 • n=229 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
5.05 pharmacy claims
STANDARD_DEVIATION 6.21 • n=157 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
4.58 pharmacy claims
STANDARD_DEVIATION 5.94 • n=380 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
4.35 pharmacy claims
STANDARD_DEVIATION 5.89 • n=5119 Participants • Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
|
|
Number of Participants Who Used Oral Corticosteroids During 12 Months Pre-Index Baseline Period
|
254 Participants
n=349 Participants
|
222 Participants
n=304 Participants
|
2,138 Participants
n=2728 Participants
|
134 Participants
n=192 Participants
|
1,515 Participants
n=1948 Participants
|
276 Participants
n=349 Participants
|
280 Participants
n=376 Participants
|
249 Participants
n=325 Participants
|
167 Participants
n=204 Participants
|
400 Participants
n=533 Participants
|
5635 Participants
n=7308 Participants
|
|
Mean Number of Visits to Rheumatologist During 12 Months Pre-Index Baseline Period
|
4.53 visits
STANDARD_DEVIATION 2.38 • n=349 Participants
|
4.92 visits
STANDARD_DEVIATION 2.90 • n=304 Participants
|
4.65 visits
STANDARD_DEVIATION 2.47 • n=2728 Participants
|
5.26 visits
STANDARD_DEVIATION 2.88 • n=192 Participants
|
4.76 visits
STANDARD_DEVIATION 2.62 • n=1948 Participants
|
5.60 visits
STANDARD_DEVIATION 2.88 • n=349 Participants
|
5.89 visits
STANDARD_DEVIATION 3.59 • n=376 Participants
|
5.41 visits
STANDARD_DEVIATION 3.06 • n=325 Participants
|
5.79 visits
STANDARD_DEVIATION 3.94 • n=204 Participants
|
5.92 visits
STANDARD_DEVIATION 4.19 • n=533 Participants
|
4.97 visits
STANDARD_DEVIATION 2.89 • n=7308 Participants
|
|
Mean Number of Visits to Rheumatologist During Variable-Length Pre-Index Baseline Period
|
11.28 visits
STANDARD_DEVIATION 8.45 • n=349 Participants
|
12.12 visits
STANDARD_DEVIATION 8.56 • n=304 Participants
|
8.21 visits
STANDARD_DEVIATION 5.98 • n=2728 Participants
|
11.43 visits
STANDARD_DEVIATION 9.51 • n=192 Participants
|
8.39 visits
STANDARD_DEVIATION 6.03 • n=1948 Participants
|
10.79 visits
STANDARD_DEVIATION 7.79 • n=349 Participants
|
11.25 visits
STANDARD_DEVIATION 8.36 • n=376 Participants
|
13.01 visits
STANDARD_DEVIATION 9.69 • n=325 Participants
|
13.75 visits
STANDARD_DEVIATION 11.80 • n=204 Participants
|
12.43 visits
STANDARD_DEVIATION 8.90 • n=533 Participants
|
9.61 visits
STANDARD_DEVIATION 7.45 • n=7308 Participants
|
|
Disease Duration During Variable-Length Pre-Index Baseline Period
|
882.61 days
STANDARD_DEVIATION 558.81 • n=349 Participants
|
919.71 days
STANDARD_DEVIATION 437.63 • n=304 Participants
|
570.38 days
STANDARD_DEVIATION 481.35 • n=2728 Participants
|
730.28 days
STANDARD_DEVIATION 536.06 • n=192 Participants
|
568.98 days
STANDARD_DEVIATION 474.54 • n=1948 Participants
|
661.66 days
STANDARD_DEVIATION 513.64 • n=349 Participants
|
651.11 days
STANDARD_DEVIATION 482.93 • n=376 Participants
|
888.34 days
STANDARD_DEVIATION 541.51 • n=325 Participants
|
806.50 days
STANDARD_DEVIATION 527.20 • n=204 Participants
|
789.95 days
STANDARD_DEVIATION 498.75 • n=533 Participants
|
648.91 days
STANDARD_DEVIATION 504.69 • n=7308 Participants
|
|
Out of Pocket Health Care Costs for Healthcare Services During 12 Months Pre-Index Baseline Period
|
1803.44 dollars
STANDARD_DEVIATION 1789.99 • n=349 Participants
|
2154.86 dollars
STANDARD_DEVIATION 1828.01 • n=304 Participants
|
2152.95 dollars
STANDARD_DEVIATION 1741.99 • n=2728 Participants
|
2013.10 dollars
STANDARD_DEVIATION 1714.01 • n=192 Participants
|
2251.93 dollars
STANDARD_DEVIATION 1800.59 • n=1948 Participants
|
2287.63 dollars
STANDARD_DEVIATION 2494.77 • n=349 Participants
|
2174.31 dollars
STANDARD_DEVIATION 1782.74 • n=376 Participants
|
2797.43 dollars
STANDARD_DEVIATION 2975.36 • n=325 Participants
|
2174.18 dollars
STANDARD_DEVIATION 1553.37 • n=204 Participants
|
2453.28 dollars
STANDARD_DEVIATION 2389.53 • n=533 Participants
|
2217.74 dollars
STANDARD_DEVIATION 1931.29 • n=7308 Participants
|
|
Out of Pocket Health Care Costs for Healthcare Services During Variable Length Pre-Index Period
|
6626.03 dollars
STANDARD_DEVIATION 5819.96 • n=349 Participants
|
6549.23 dollars
STANDARD_DEVIATION 4717.18 • n=304 Participants
|
6270.02 dollars
STANDARD_DEVIATION 5087.71 • n=2728 Participants
|
6453.01 dollars
STANDARD_DEVIATION 5204.02 • n=192 Participants
|
6510.77 dollars
STANDARD_DEVIATION 5550.34 • n=1948 Participants
|
6856.14 dollars
STANDARD_DEVIATION 6946.33 • n=349 Participants
|
6841.01 dollars
STANDARD_DEVIATION 6423.20 • n=376 Participants
|
8934.99 dollars
STANDARD_DEVIATION 12740.35 • n=325 Participants
|
7331.39 dollars
STANDARD_DEVIATION 5037.30 • n=204 Participants
|
7636.47 dollars
STANDARD_DEVIATION 6096.75 • n=533 Participants
|
6672.79 dollars
STANDARD_DEVIATION 6042.90 • n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Cardiovascular disease
|
198 Participants
n=349 Participants
|
189 Participants
n=304 Participants
|
1315 Participants
n=2728 Participants
|
110 Participants
n=192 Participants
|
992 Participants
n=1948 Participants
|
205 Participants
n=349 Participants
|
208 Participants
n=376 Participants
|
210 Participants
n=325 Participants
|
133 Participants
n=204 Participants
|
328 Participants
n=533 Participants
|
3888 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
COPD
|
33 Participants
n=349 Participants
|
33 Participants
n=304 Participants
|
248 Participants
n=2728 Participants
|
23 Participants
n=192 Participants
|
188 Participants
n=1948 Participants
|
46 Participants
n=349 Participants
|
38 Participants
n=376 Participants
|
47 Participants
n=325 Participants
|
34 Participants
n=204 Participants
|
74 Participants
n=533 Participants
|
764 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Asthma
|
35 Participants
n=349 Participants
|
38 Participants
n=304 Participants
|
272 Participants
n=2728 Participants
|
16 Participants
n=192 Participants
|
210 Participants
n=1948 Participants
|
45 Participants
n=349 Participants
|
30 Participants
n=376 Participants
|
35 Participants
n=325 Participants
|
26 Participants
n=204 Participants
|
71 Participants
n=533 Participants
|
778 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Kidney disease
|
37 Participants
n=349 Participants
|
30 Participants
n=304 Participants
|
257 Participants
n=2728 Participants
|
27 Participants
n=192 Participants
|
192 Participants
n=1948 Participants
|
38 Participants
n=349 Participants
|
43 Participants
n=376 Participants
|
55 Participants
n=325 Participants
|
30 Participants
n=204 Participants
|
81 Participants
n=533 Participants
|
790 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Diabetes
|
54 Participants
n=349 Participants
|
54 Participants
n=304 Participants
|
424 Participants
n=2728 Participants
|
33 Participants
n=192 Participants
|
283 Participants
n=1948 Participants
|
65 Participants
n=349 Participants
|
56 Participants
n=376 Participants
|
62 Participants
n=325 Participants
|
33 Participants
n=204 Participants
|
114 Participants
n=533 Participants
|
1178 Participants
n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 12
|
866.68 dollars
STANDARD_DEVIATION 6,397.79 • n=349 Participants
|
1,513.38 dollars
STANDARD_DEVIATION 4,866.04 • n=304 Participants
|
245.94 dollars
STANDARD_DEVIATION 1,376.47 • n=2728 Participants
|
1,154.62 dollars
STANDARD_DEVIATION 5,835.03 • n=192 Participants
|
428.33 dollars
STANDARD_DEVIATION 3,467.75 • n=1948 Participants
|
636.49 dollars
STANDARD_DEVIATION 1,859.90 • n=349 Participants
|
523.41 dollars
STANDARD_DEVIATION 2,603.76 • n=376 Participants
|
1,481.59 dollars
STANDARD_DEVIATION 4,925.66 • n=325 Participants
|
1,404.77 dollars
STANDARD_DEVIATION 5,959.49 • n=204 Participants
|
946.24 dollars
STANDARD_DEVIATION 3,371.70 • n=533 Participants
|
572.10 dollars
STANDARD_DEVIATION 3,361.14 • n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Depression
|
54 Participants
n=349 Participants
|
58 Participants
n=304 Participants
|
450 Participants
n=2728 Participants
|
30 Participants
n=192 Participants
|
376 Participants
n=1948 Participants
|
60 Participants
n=349 Participants
|
67 Participants
n=376 Participants
|
58 Participants
n=325 Participants
|
35 Participants
n=204 Participants
|
117 Participants
n=533 Participants
|
1305 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Anxiety
|
59 Participants
n=349 Participants
|
57 Participants
n=304 Participants
|
412 Participants
n=2728 Participants
|
32 Participants
n=192 Participants
|
343 Participants
n=1948 Participants
|
60 Participants
n=349 Participants
|
58 Participants
n=376 Participants
|
50 Participants
n=325 Participants
|
18 Participants
n=204 Participants
|
98 Participants
n=533 Participants
|
1187 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Liver disease
|
18 Participants
n=349 Participants
|
17 Participants
n=304 Participants
|
143 Participants
n=2728 Participants
|
17 Participants
n=192 Participants
|
111 Participants
n=1948 Participants
|
24 Participants
n=349 Participants
|
19 Participants
n=376 Participants
|
31 Participants
n=325 Participants
|
19 Participants
n=204 Participants
|
41 Participants
n=533 Participants
|
440 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Sleep disorders
|
44 Participants
n=349 Participants
|
31 Participants
n=304 Participants
|
307 Participants
n=2728 Participants
|
18 Participants
n=192 Participants
|
209 Participants
n=1948 Participants
|
45 Participants
n=349 Participants
|
49 Participants
n=376 Participants
|
34 Participants
n=325 Participants
|
26 Participants
n=204 Participants
|
79 Participants
n=533 Participants
|
842 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Hypertension
|
157 Participants
n=349 Participants
|
153 Participants
n=304 Participants
|
1053 Participants
n=2728 Participants
|
96 Participants
n=192 Participants
|
790 Participants
n=1948 Participants
|
169 Participants
n=349 Participants
|
172 Participants
n=376 Participants
|
158 Participants
n=325 Participants
|
104 Participants
n=204 Participants
|
268 Participants
n=533 Participants
|
3120 Participants
n=7308 Participants
|
|
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
Hyperlipidemia
|
150 Participants
n=349 Participants
|
120 Participants
n=304 Participants
|
931 Participants
n=2728 Participants
|
73 Participants
n=192 Participants
|
682 Participants
n=1948 Participants
|
155 Participants
n=349 Participants
|
147 Participants
n=376 Participants
|
115 Participants
n=325 Participants
|
88 Participants
n=204 Participants
|
223 Participants
n=533 Participants
|
2684 Participants
n=7308 Participants
|
|
All cause Inpatient, Outpatient and Emergency Room Visits Costs During 12 Months Pre-Index Period
Inpatient visits costs
|
6,439.48 dollars
STANDARD_DEVIATION 24,897.59 • n=349 Participants
|
5,918.18 dollars
STANDARD_DEVIATION 31,820.77 • n=304 Participants
|
2796.16 dollars
STANDARD_DEVIATION 13970.41 • n=2728 Participants
|
5745.63 dollars
STANDARD_DEVIATION 21990.52 • n=192 Participants
|
2908.83 dollars
STANDARD_DEVIATION 13624.11 • n=1948 Participants
|
2802.86 dollars
STANDARD_DEVIATION 9813.21 • n=349 Participants
|
5593.85 dollars
STANDARD_DEVIATION 28885.69 • n=376 Participants
|
10287.84 dollars
STANDARD_DEVIATION 32246.91 • n=325 Participants
|
9475.99 dollars
STANDARD_DEVIATION 32796.53 • n=204 Participants
|
4661.57 dollars
STANDARD_DEVIATION 16089.35 • n=533 Participants
|
4007.49 dollars
STANDARD_DEVIATION 18785.55 • n=7308 Participants
|
|
All cause Inpatient, Outpatient and Emergency Room Visits Costs During 12 Months Pre-Index Period
Outpatient visits costs
|
11,764.03 dollars
STANDARD_DEVIATION 27,775.60 • n=349 Participants
|
12,056.68 dollars
STANDARD_DEVIATION 19,456.56 • n=304 Participants
|
8235.49 dollars
STANDARD_DEVIATION 14916.40 • n=2728 Participants
|
10585.64 dollars
STANDARD_DEVIATION 13522.28 • n=192 Participants
|
8989.76 dollars
STANDARD_DEVIATION 18037.61 • n=1948 Participants
|
13625.70 dollars
STANDARD_DEVIATION 23,398.43 • n=349 Participants
|
11200.01 dollars
STANDARD_DEVIATION 20002.68 • n=376 Participants
|
25746.57 dollars
STANDARD_DEVIATION 46437.00 • n=325 Participants
|
15879.61 dollars
STANDARD_DEVIATION 26952.93 • n=204 Participants
|
14260.86 dollars
STANDARD_DEVIATION 19512.63 • n=533 Participants
|
10667.28 dollars
STANDARD_DEVIATION 20794.73 • n=7308 Participants
|
|
All cause Inpatient, Outpatient and Emergency Room Visits Costs During 12 Months Pre-Index Period
Emergency Room visits costs
|
1,308.81 dollars
STANDARD_DEVIATION 3,867.67 • n=349 Participants
|
1,404.59 dollars
STANDARD_DEVIATION 5,254.09 • n=304 Participants
|
968.34 dollars
STANDARD_DEVIATION 3245.47 • n=2728 Participants
|
1035.11 dollars
STANDARD_DEVIATION 3080.83 • n=192 Participants
|
1094.48 dollars
STANDARD_DEVIATION 3219.72 • n=1948 Participants
|
1528.22 dollars
STANDARD_DEVIATION 3716.98 • n=349 Participants
|
1014.59 dollars
STANDARD_DEVIATION 2993.84 • n=376 Participants
|
1,519.68 dollars
STANDARD_DEVIATION 3770.18 • n=325 Participants
|
1721.96 dollars
STANDARD_DEVIATION 5667.52 • n=204 Participants
|
1413.05 dollars
STANDARD_DEVIATION 4290.22 • n=533 Participants
|
1145.23 dollars
STANDARD_DEVIATION 3581.14 • n=7308 Participants
|
|
RA Related Inpatient, Outpatient and ER Visits Costs During 12 Months Pre-Index Baseline Period
Inpatient visits cost
|
3,089.94 dollars
STANDARD_DEVIATION 14,786.15 • n=349 Participants
|
2,831.70 dollars
STANDARD_DEVIATION 14,317.53 • n=304 Participants
|
1151.57 dollars
STANDARD_DEVIATION 7901.71 • n=2728 Participants
|
1789.30 dollars
STANDARD_DEVIATION 8142.05 • n=192 Participants
|
1587.91 dollars
STANDARD_DEVIATION 9792.03 • n=1948 Participants
|
1309.07 dollars
STANDARD_DEVIATION 6851.41 • n=349 Participants
|
1838.26 dollars
STANDARD_DEVIATION 12154.86 • n=376 Participants
|
4505.60 dollars
STANDARD_DEVIATION 20528.63 • n=325 Participants
|
3468.19 dollars
STANDARD_DEVIATION 15523.54 • n=204 Participants
|
2353.90 dollars
STANDARD_DEVIATION 12328.42 • n=533 Participants
|
1791.46 dollars
STANDARD_DEVIATION 10793.10 • n=7308 Participants
|
|
RA Related Inpatient, Outpatient and ER Visits Costs During 12 Months Pre-Index Baseline Period
Outpatient visits costs
|
4,006.13 dollars
STANDARD_DEVIATION 19,532.04 • n=349 Participants
|
3,062.35 dollars
STANDARD_DEVIATION 11,564.95 • n=304 Participants
|
1727.93 dollars
STANDARD_DEVIATION 3936.67 • n=2728 Participants
|
2263.77 dollars
STANDARD_DEVIATION 6164.69 • n=192 Participants
|
1665.28 dollars
STANDARD_DEVIATION 2716.01 • n=1948 Participants
|
5686.02 dollars
STANDARD_DEVIATION 19928.57 • n=349 Participants
|
2601.07 dollars
STANDARD_DEVIATION 11012.98 • n=376 Participants
|
5363.37 dollars
STANDARD_DEVIATION 11254.35 • n=325 Participants
|
4237.16 dollars
STANDARD_DEVIATION 13758.63 • n=204 Participants
|
3272.09 dollars
STANDARD_DEVIATION 8075.92 • n=533 Participants
|
2467.90 dollars
STANDARD_DEVIATION 8644.57 • n=7308 Participants
|
|
RA Related Inpatient, Outpatient and ER Visits Costs During 12 Months Pre-Index Baseline Period
ER visits costs
|
349.64 dollars
STANDARD_DEVIATION 1,585.83 • n=349 Participants
|
328.19 dollars
STANDARD_DEVIATION 1,576.11 • n=304 Participants
|
219.03 dollars
STANDARD_DEVIATION 1206.08 • n=2728 Participants
|
277.53 dollars
STANDARD_DEVIATION 2140.86 • n=192 Participants
|
259.28 dollars
STANDARD_DEVIATION 1316.71 • n=1948 Participants
|
407.85 dollars
STANDARD_DEVIATION 1947.66 • n=349 Participants
|
212.55 dollars
STANDARD_DEVIATION 1251.78 • n=376 Participants
|
399.12 dollars
STANDARD_DEVIATION 1739.26 • n=325 Participants
|
363.43 dollars
STANDARD_DEVIATION 1481.07 • n=204 Participants
|
365.98 dollars
STANDARD_DEVIATION 1593.09 • n=533 Participants
|
273.51 dollars
STANDARD_DEVIATION 1411.57 • n=7308 Participants
|
|
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Pre-Index Period
Health care costs
|
24,420.92 dollars
STANDARD_DEVIATION 47,406.99 • n=349 Participants
|
30,416.53 dollars
STANDARD_DEVIATION 43,264.63 • n=304 Participants
|
16168.53 dollars
STANDARD_DEVIATION 25602.71 • n=2728 Participants
|
26501.73 dollars
STANDARD_DEVIATION 34187.93 • n=192 Participants
|
17580.75 dollars
STANDARD_DEVIATION 30240.41 • n=1948 Participants
|
23845.95 dollars
STANDARD_DEVIATION 30481.00 • n=349 Participants
|
24,401.11 dollars
STANDARD_DEVIATION 42,380.03 • n=376 Participants
|
48981.85 dollars
STANDARD_DEVIATION 75040.93 • n=325 Participants
|
40490.72 dollars
STANDARD_DEVIATION 57253.38 • n=204 Participants
|
30609.54 dollars
STANDARD_DEVIATION 35308.08 • n=533 Participants
|
21784.90 dollars
STANDARD_DEVIATION 36617.83 • n=7308 Participants
|
|
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Pre-Index Period
Medical costs
|
19,512.32 dollars
STANDARD_DEVIATION 44,212.78 • n=349 Participants
|
19,379.45 dollars
STANDARD_DEVIATION 40,053.13 • n=304 Participants
|
11999.99 dollars
STANDARD_DEVIATION 22939.57 • n=2728 Participants
|
17366.38 dollars
STANDARD_DEVIATION 29180.07 • n=192 Participants
|
12993.07 dollars
STANDARD_DEVIATION 26,623.07 • n=1948 Participants
|
17956.78 dollars
STANDARD_DEVIATION 26,894.74 • n=349 Participants
|
17808.46 dollars
STANDARD_DEVIATION 38710.40 • n=376 Participants
|
37554.08 dollars
STANDARD_DEVIATION 65360.94 • n=325 Participants
|
27077.56 dollars
STANDARD_DEVIATION 48487.39 • n=204 Participants
|
20335.48 dollars
STANDARD_DEVIATION 28896.19 • n=533 Participants
|
15820.00 dollars
STANDARD_DEVIATION 32082.59 • n=7308 Participants
|
|
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Pre-Index Period
Pharmacy costs
|
4,908.60 dollars
STANDARD_DEVIATION 9,860.95 • n=349 Participants
|
11,037.07 dollars
STANDARD_DEVIATION 15,244.06 • n=304 Participants
|
4168.54 dollars
STANDARD_DEVIATION 7951.66 • n=2728 Participants
|
9135.35 dollars
STANDARD_DEVIATION 13525.45 • n=192 Participants
|
4587.69 dollars
STANDARD_DEVIATION 11199.66 • n=1948 Participants
|
5889.17 dollars
STANDARD_DEVIATION 14361.93 • n=349 Participants
|
6592.65 dollars
STANDARD_DEVIATION 11444.46 • n=376 Participants
|
11427.76 dollars
STANDARD_DEVIATION 33915.60 • n=325 Participants
|
13413.16 dollars
STANDARD_DEVIATION 29104.61 • n=204 Participants
|
10274.06 dollars
STANDARD_DEVIATION 19612.35 • n=533 Participants
|
5964.90 dollars
STANDARD_DEVIATION 14230.43 • n=7308 Participants
|
|
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Pre-Index Period
Health care costs
|
8,833.52 dollars
STANDARD_DEVIATION 25,667.44 • n=349 Participants
|
14,943.61 dollars
STANDARD_DEVIATION 24,196.06 • n=304 Participants
|
4546.86 dollars
STANDARD_DEVIATION 10379.97 • n=2728 Participants
|
9807.20 dollars
STANDARD_DEVIATION 15314.26 • n=192 Participants
|
4935.77 dollars
STANDARD_DEVIATION 11793.45 • n=1948 Participants
|
10462.36 dollars
STANDARD_DEVIATION 22548.83 • n=349 Participants
|
8151.85 dollars
STANDARD_DEVIATION 18490.62 • n=376 Participants
|
15878.07 dollars
STANDARD_DEVIATION 31575.28 • n=325 Participants
|
15136.67 dollars
STANDARD_DEVIATION 23086.46 • n=204 Participants
|
11914.79 dollars
STANDARD_DEVIATION 20,244.11 • n=533 Participants
|
7230.81 dollars
STANDARD_DEVIATION 16,844.84 • n=7308 Participants
|
|
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Pre-Index Period
Medical costs
|
7,445.71 dollars
STANDARD_DEVIATION 25,437.86 • n=349 Participants
|
6,222.23 dollars
STANDARD_DEVIATION 18,623.00 • n=304 Participants
|
3098.53 dollars
STANDARD_DEVIATION 9170.64 • n=2728 Participants
|
4330.60 dollars
STANDARD_DEVIATION 10538.65 • n=192 Participants
|
3512.47 dollars
STANDARD_DEVIATION 10696.10 • n=1948 Participants
|
7402.94 dollars
STANDARD_DEVIATION 21149.65 • n=349 Participants
|
4651.88 dollars
STANDARD_DEVIATION 16484.62 • n=376 Participants
|
10268.09 dollars
STANDARD_DEVIATION 24816.89 • n=325 Participants
|
8068.79 dollars
STANDARD_DEVIATION 20919.77 • n=204 Participants
|
5,991.97 dollars
STANDARD_DEVIATION 15,427.73 • n=533 Participants
|
4,532.88 dollars
STANDARD_DEVIATION 14,350.99 • n=7308 Participants
|
|
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Pre-Index Period
Pharmacy costs
|
1,215.71 dollars
STANDARD_DEVIATION 2,974.03 • n=349 Participants
|
7,230.13 dollars
STANDARD_DEVIATION 13,414.82 • n=304 Participants
|
1361.31 dollars
STANDARD_DEVIATION 4448.33 • n=2728 Participants
|
4712.28 dollars
STANDARD_DEVIATION 11103.97 • n=192 Participants
|
1347.30 dollars
STANDARD_DEVIATION 4566.96 • n=1948 Participants
|
2272.80 dollars
STANDARD_DEVIATION 6908.41 • n=349 Participants
|
2399.30 dollars
STANDARD_DEVIATION 6306.26 • n=376 Participants
|
3413.49 dollars
STANDARD_DEVIATION 9249.18 • n=325 Participants
|
5537.26 dollars
STANDARD_DEVIATION 11303.84 • n=204 Participants
|
4,434.95 dollars
STANDARD_DEVIATION 10,153.34 • n=533 Participants
|
2,211.73 dollars
STANDARD_DEVIATION 6,758.38 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 1
|
1,472.00 dollars
STANDARD_DEVIATION 3,964.00 • n=349 Participants
|
1,585.23 dollars
STANDARD_DEVIATION 4,511.40 • n=304 Participants
|
1,195.47 dollars
STANDARD_DEVIATION 2,995.66 • n=2728 Participants
|
1,268.10 dollars
STANDARD_DEVIATION 2,070.32 • n=192 Participants
|
1,309.62 dollars
STANDARD_DEVIATION 3,241.11 • n=1948 Participants
|
1,223.86 dollars
STANDARD_DEVIATION 1,782.55 • n=349 Participants
|
1,654.98 dollars
STANDARD_DEVIATION 4,444.79 • n=376 Participants
|
5,422.21 dollars
STANDARD_DEVIATION 18,311.75 • n=325 Participants
|
2,578.36 dollars
STANDARD_DEVIATION 9,044.31 • n=204 Participants
|
1,697.90 dollars
STANDARD_DEVIATION 3,722.09 • n=533 Participants
|
1,545.44 dollars
STANDARD_DEVIATION 5,285.44 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 2
|
1,841.98 dollars
STANDARD_DEVIATION 5,672.40 • n=349 Participants
|
1,893.55 dollars
STANDARD_DEVIATION 5,349.66 • n=304 Participants
|
1,221.22 dollars
STANDARD_DEVIATION 3,437.40 • n=2728 Participants
|
1,302.98 dollars
STANDARD_DEVIATION 3,060.04 • n=192 Participants
|
1,358.67 dollars
STANDARD_DEVIATION 4,471.99 • n=1948 Participants
|
1,800.75 dollars
STANDARD_DEVIATION 3,735.34 • n=349 Participants
|
1,582.17 dollars
STANDARD_DEVIATION 5,171.59 • n=376 Participants
|
4,457.43 dollars
STANDARD_DEVIATION 17,260.29 • n=325 Participants
|
2,988.66 dollars
STANDARD_DEVIATION 8,177.26 • n=204 Participants
|
1,967.35 dollars
STANDARD_DEVIATION 3,994.51 • n=533 Participants
|
1,611.54 dollars
STANDARD_DEVIATION 5,610.29 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 3
|
1,950.72 dollars
STANDARD_DEVIATION 6,054.56 • n=349 Participants
|
1,967.88 dollars
STANDARD_DEVIATION 4,629.86 • n=304 Participants
|
1,413.62 dollars
STANDARD_DEVIATION 4,763.79 • n=2728 Participants
|
1,991.21 dollars
STANDARD_DEVIATION 3,653.14 • n=192 Participants
|
1,344.95 dollars
STANDARD_DEVIATION 4,357.56 • n=1948 Participants
|
1,945.43 dollars
STANDARD_DEVIATION 4,917.73 • n=349 Participants
|
1,456.25 dollars
STANDARD_DEVIATION 2,597.73 • n=376 Participants
|
4,999.71 dollars
STANDARD_DEVIATION 16,893.14 • n=325 Participants
|
3,142.42 dollars
STANDARD_DEVIATION 6,375.80 • n=204 Participants
|
2,568.07 dollars
STANDARD_DEVIATION 5,760.73 • n=533 Participants
|
1,778.72 dollars
STANDARD_DEVIATION 5,905.89 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 4
|
1,831.75 dollars
STANDARD_DEVIATION 6,783.17 • n=349 Participants
|
2,345.62 dollars
STANDARD_DEVIATION 5,547.80 • n=304 Participants
|
1,408.75 dollars
STANDARD_DEVIATION 4,353.81 • n=2728 Participants
|
2,483.09 dollars
STANDARD_DEVIATION 9,380.52 • n=192 Participants
|
1,505.32 dollars
STANDARD_DEVIATION 6,551.42 • n=1948 Participants
|
2,147.16 dollars
STANDARD_DEVIATION 4,807.09 • n=349 Participants
|
2,512.04 dollars
STANDARD_DEVIATION 10,555.29 • n=376 Participants
|
3,173.71 dollars
STANDARD_DEVIATION 6,536.49 • n=325 Participants
|
3,468.91 dollars
STANDARD_DEVIATION 9,562.43 • n=204 Participants
|
2,548.52 dollars
STANDARD_DEVIATION 6,278.21 • n=533 Participants
|
1,833.05 dollars
STANDARD_DEVIATION 6,224.14 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 5
|
1,675.13 dollars
STANDARD_DEVIATION 6,088.40 • n=349 Participants
|
3,392.53 dollars
STANDARD_DEVIATION 15,825.28 • n=304 Participants
|
1,527.09 dollars
STANDARD_DEVIATION 5,071.51 • n=2728 Participants
|
1,758.14 dollars
STANDARD_DEVIATION 3,461.89 • n=192 Participants
|
1,591.72 dollars
STANDARD_DEVIATION 5,506.24 • n=1948 Participants
|
2,114.46 dollars
STANDARD_DEVIATION 5,180.05 • n=349 Participants
|
2,218.34 dollars
STANDARD_DEVIATION 5,995.86 • n=376 Participants
|
4,185.96 dollars
STANDARD_DEVIATION 11,773.79 • n=325 Participants
|
2,948.97 dollars
STANDARD_DEVIATION 6,648.21 • n=204 Participants
|
2,808.88 dollars
STANDARD_DEVIATION 6,605.37 • n=533 Participants
|
1,950.09 dollars
STANDARD_DEVIATION 6,657.06 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 6
|
1,795.34 dollars
STANDARD_DEVIATION 5,425.88 • n=349 Participants
|
2,872.44 dollars
STANDARD_DEVIATION 8,354.65 • n=304 Participants
|
1,395.97 dollars
STANDARD_DEVIATION 4,745.83 • n=2728 Participants
|
2,739.15 dollars
STANDARD_DEVIATION 8,184.36 • n=192 Participants
|
1,494.42 dollars
STANDARD_DEVIATION 3,935.51 • n=1948 Participants
|
2,072.51 dollars
STANDARD_DEVIATION 4,611.54 • n=349 Participants
|
1,917.33 dollars
STANDARD_DEVIATION 4,986.30 • n=376 Participants
|
4,055.38 dollars
STANDARD_DEVIATION 11,882.81 • n=325 Participants
|
3,514.88 dollars
STANDARD_DEVIATION 8,666.83 • n=204 Participants
|
2,314.86 dollars
STANDARD_DEVIATION 4,419.75 • n=533 Participants
|
1,841.56 dollars
STANDARD_DEVIATION 5,579.06 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 7
|
2,065.20 dollars
STANDARD_DEVIATION 5,994.05 • n=349 Participants
|
2,748.68 dollars
STANDARD_DEVIATION 5,793.90 • n=304 Participants
|
1,338.57 dollars
STANDARD_DEVIATION 4,608.86 • n=2728 Participants
|
3,155.53 dollars
STANDARD_DEVIATION 8,765.16 • n=192 Participants
|
1,613.11 dollars
STANDARD_DEVIATION 4,861.36 • n=1948 Participants
|
2,300.37 dollars
STANDARD_DEVIATION 5,609.29 • n=349 Participants
|
1,853.74 dollars
STANDARD_DEVIATION 8,578.01 • n=376 Participants
|
3,973.03 dollars
STANDARD_DEVIATION 11,780.35 • n=325 Participants
|
2,888.53 dollars
STANDARD_DEVIATION 7,052.99 • n=204 Participants
|
3,161.07 dollars
STANDARD_DEVIATION 10,088.12 • n=533 Participants
|
1,918.63 dollars
STANDARD_DEVIATION 6,333.24 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 8
|
1,821.27 dollars
STANDARD_DEVIATION 5,436.36 • n=349 Participants
|
2,573.90 dollars
STANDARD_DEVIATION 5,934.45 • n=304 Participants
|
1,426.81 dollars
STANDARD_DEVIATION 5,137.29 • n=2728 Participants
|
2,851.54 dollars
STANDARD_DEVIATION 6,973.89 • n=192 Participants
|
1,494.05 dollars
STANDARD_DEVIATION 6,412.22 • n=1948 Participants
|
1,979.07 dollars
STANDARD_DEVIATION 4,586.50 • n=349 Participants
|
2,276.07 dollars
STANDARD_DEVIATION 6,439.26 • n=376 Participants
|
3,345.52 dollars
STANDARD_DEVIATION 9,676.74 • n=325 Participants
|
4,544.99 dollars
STANDARD_DEVIATION 15,057.51 • n=204 Participants
|
2,907.13 dollars
STANDARD_DEVIATION 5,677.67 • n=533 Participants
|
1,899.12 dollars
STANDARD_DEVIATION 6,435.26 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 9
|
2,811.19 dollars
STANDARD_DEVIATION 11,684.53 • n=349 Participants
|
2,647.26 dollars
STANDARD_DEVIATION 5,787.01 • n=304 Participants
|
1,300.85 dollars
STANDARD_DEVIATION 4,397.94 • n=2728 Participants
|
1,799.68 dollars
STANDARD_DEVIATION 4,360.96 • n=192 Participants
|
1,469.14 dollars
STANDARD_DEVIATION 5,540.05 • n=1948 Participants
|
2,225.15 dollars
STANDARD_DEVIATION 6,382.76 • n=349 Participants
|
2,220.71 dollars
STANDARD_DEVIATION 12,367.62 • n=376 Participants
|
4,008.30 dollars
STANDARD_DEVIATION 9,388.11 • n=325 Participants
|
3,462.03 dollars
STANDARD_DEVIATION 9,018.17 • n=204 Participants
|
2,355.49 dollars
STANDARD_DEVIATION 5,254.45 • n=533 Participants
|
1,836.07 dollars
STANDARD_DEVIATION 6,502.79 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 10
|
2,255.16 dollars
STANDARD_DEVIATION 10,002.22 • n=349 Participants
|
2,471.86 dollars
STANDARD_DEVIATION 7,969.85 • n=304 Participants
|
1,460.94 dollars
STANDARD_DEVIATION 7,614.63 • n=2728 Participants
|
2,441.32 dollars
STANDARD_DEVIATION 6,726.25 • n=192 Participants
|
1,504.17 dollars
STANDARD_DEVIATION 6,658.33 • n=1948 Participants
|
2,320.68 dollars
STANDARD_DEVIATION 4,945.91 • n=349 Participants
|
2,275.94 dollars
STANDARD_DEVIATION 10,695.17 • n=376 Participants
|
3,353.37 dollars
STANDARD_DEVIATION 7,098.15 • n=325 Participants
|
4,993.31 dollars
STANDARD_DEVIATION 21,871.26 • n=204 Participants
|
2,729.46 dollars
STANDARD_DEVIATION 7,803.62 • n=533 Participants
|
1,936.48 dollars
STANDARD_DEVIATION 8,342.23 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 11
|
2,531.08 dollars
STANDARD_DEVIATION 10,352.92 • n=349 Participants
|
2,789.28 dollars
STANDARD_DEVIATION 10,384.81 • n=304 Participants
|
1,308.22 dollars
STANDARD_DEVIATION 5,002.82 • n=2728 Participants
|
1,584.63 dollars
STANDARD_DEVIATION 2,672.79 • n=192 Participants
|
1,503.62 dollars
STANDARD_DEVIATION 4,509.59 • n=1948 Participants
|
1,886.96 dollars
STANDARD_DEVIATION 4,857.36 • n=349 Participants
|
2,574.77 dollars
STANDARD_DEVIATION 11,572.01 • n=376 Participants
|
3,795.88 dollars
STANDARD_DEVIATION 10,458.45 • n=325 Participants
|
2,986.24 dollars
STANDARD_DEVIATION 7,461.79 • n=204 Participants
|
2,705.38 dollars
STANDARD_DEVIATION 5,841.53 • n=533 Participants
|
1,839.75 dollars
STANDARD_DEVIATION 6,472.03 • n=7308 Participants
|
|
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 12
|
2,370.10 dollars
STANDARD_DEVIATION 10,163.97 • n=349 Participants
|
3,128.29 dollars
STANDARD_DEVIATION 6,951.00 • n=304 Participants
|
1,171.01 dollars
STANDARD_DEVIATION 3,347.20 • n=2728 Participants
|
3,126.35 dollars
STANDARD_DEVIATION 8,734.75 • n=192 Participants
|
1,391.97 dollars
STANDARD_DEVIATION 4,685.03 • n=1948 Participants
|
1,829.55 dollars
STANDARD_DEVIATION 4,212.90 • n=349 Participants
|
1,858.76 dollars
STANDARD_DEVIATION 5,981.09 • n=376 Participants
|
4,211.34 dollars
STANDARD_DEVIATION 8,924.43 • n=325 Participants
|
2,973.41 dollars
STANDARD_DEVIATION 7,460.54 • n=204 Participants
|
2,845.43 dollars
STANDARD_DEVIATION 6,831.07 • n=533 Participants
|
1,794.44 dollars
STANDARD_DEVIATION 5,550.54 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 1
|
406.83 dollars
STANDARD_DEVIATION 1,619.24 • n=349 Participants
|
703.28 dollars
STANDARD_DEVIATION 3,907.43 • n=304 Participants
|
439.11 dollars
STANDARD_DEVIATION 1,589.58 • n=2728 Participants
|
322.11 dollars
STANDARD_DEVIATION 844.32 • n=192 Participants
|
469.85 dollars
STANDARD_DEVIATION 2,199.09 • n=1948 Participants
|
441.39 dollars
STANDARD_DEVIATION 1,290.59 • n=349 Participants
|
539.47 dollars
STANDARD_DEVIATION 2,768.24 • n=376 Participants
|
1,962.14 dollars
STANDARD_DEVIATION 13,284.62 • n=325 Participants
|
430.25 dollars
STANDARD_DEVIATION 1,111.69 • n=204 Participants
|
473.64 dollars
STANDARD_DEVIATION 1,356.24 • n=533 Participants
|
528.95 dollars
STANDARD_DEVIATION 3,402.02 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 2
|
566.83 dollars
STANDARD_DEVIATION 3,826.74 • n=349 Participants
|
882.34 dollars
STANDARD_DEVIATION 4,120.86 • n=304 Participants
|
469.92 dollars
STANDARD_DEVIATION 2,658.20 • n=2728 Participants
|
531.40 dollars
STANDARD_DEVIATION 2,601.98 • n=192 Participants
|
431.85 dollars
STANDARD_DEVIATION 2,771.90 • n=1948 Participants
|
928.87 dollars
STANDARD_DEVIATION 3,291.21 • n=349 Participants
|
549.71 dollars
STANDARD_DEVIATION 2,069.01 • n=376 Participants
|
1,192.36 dollars
STANDARD_DEVIATION 7,180.33 • n=325 Participants
|
1,325.06 dollars
STANDARD_DEVIATION 6,068.59 • n=204 Participants
|
654.37 dollars
STANDARD_DEVIATION 1,876.46 • n=533 Participants
|
578.64 dollars
STANDARD_DEVIATION 3,258.34 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 3
|
655.66 dollars
STANDARD_DEVIATION 4,004.11 • n=349 Participants
|
1,056.77 dollars
STANDARD_DEVIATION 3,824.32 • n=304 Participants
|
454.12 dollars
STANDARD_DEVIATION 2,803.31 • n=2728 Participants
|
1,142.03 dollars
STANDARD_DEVIATION 3,334.59 • n=192 Participants
|
456.38 dollars
STANDARD_DEVIATION 3,023.11 • n=1948 Participants
|
756.09 dollars
STANDARD_DEVIATION 2,747.09 • n=349 Participants
|
560.10 dollars
STANDARD_DEVIATION 1,714.80 • n=376 Participants
|
1,649.74 dollars
STANDARD_DEVIATION 10,509.93 • n=325 Participants
|
1,020.45 dollars
STANDARD_DEVIATION 2,905.01 • n=204 Participants
|
921.59 dollars
STANDARD_DEVIATION 3,769.16 • n=533 Participants
|
630.44 dollars
STANDARD_DEVIATION 3,714.50 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 4
|
730.91 dollars
STANDARD_DEVIATION 5,246.45 • n=349 Participants
|
1,303.00 dollars
STANDARD_DEVIATION 4,313.06 • n=304 Participants
|
442.85 dollars
STANDARD_DEVIATION 2,018.74 • n=2728 Participants
|
798.63 dollars
STANDARD_DEVIATION 2,432.86 • n=192 Participants
|
482.37 dollars
STANDARD_DEVIATION 4,554.79 • n=1948 Participants
|
958.05 dollars
STANDARD_DEVIATION 3,302.16 • n=349 Participants
|
1,202.34 dollars
STANDARD_DEVIATION 9,855.61 • n=376 Participants
|
757.71 dollars
STANDARD_DEVIATION 2,576.49 • n=325 Participants
|
1,277.46 dollars
STANDARD_DEVIATION 3,232.57 • n=204 Participants
|
1,119.77 dollars
STANDARD_DEVIATION 4,721.57 • n=533 Participants
|
662.62 dollars
STANDARD_DEVIATION 4,133.73 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 5
|
685.73 dollars
STANDARD_DEVIATION 5,135.95 • n=349 Participants
|
1,062.30 dollars
STANDARD_DEVIATION 2,928.13 • n=304 Participants
|
486.22 dollars
STANDARD_DEVIATION 3,038.35 • n=2728 Participants
|
765.62 dollars
STANDARD_DEVIATION 2,130.63 • n=192 Participants
|
521.77 dollars
STANDARD_DEVIATION 3,323.80 • n=1948 Participants
|
954.68 dollars
STANDARD_DEVIATION 3,610.34 • n=349 Participants
|
1,048.93 dollars
STANDARD_DEVIATION 4,863.81 • n=376 Participants
|
1,273.15 dollars
STANDARD_DEVIATION 5,820.90 • n=325 Participants
|
1,164.43 dollars
STANDARD_DEVIATION 3,669.03 • n=204 Participants
|
825.12 dollars
STANDARD_DEVIATION 2,359.95 • n=533 Participants
|
666.50 dollars
STANDARD_DEVIATION 3,506.75 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 6
|
660.86 dollars
STANDARD_DEVIATION 3,687.69 • n=349 Participants
|
1,153.03 dollars
STANDARD_DEVIATION 3,383.39 • n=304 Participants
|
380.78 dollars
STANDARD_DEVIATION 2,221.36 • n=2728 Participants
|
1,149.35 dollars
STANDARD_DEVIATION 3,733.45 • n=192 Participants
|
420.73 dollars
STANDARD_DEVIATION 2,016.61 • n=1948 Participants
|
1,179.18 dollars
STANDARD_DEVIATION 4,190.03 • n=349 Participants
|
683.35 dollars
STANDARD_DEVIATION 2,716.99 • n=376 Participants
|
1,336.14 dollars
STANDARD_DEVIATION 4,584.60 • n=325 Participants
|
1,512.57 dollars
STANDARD_DEVIATION 4,394.90 • n=204 Participants
|
886.98 dollars
STANDARD_DEVIATION 2,654.20 • n=533 Participants
|
621.82 dollars
STANDARD_DEVIATION 2,779.38 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 7
|
795.24 dollars
STANDARD_DEVIATION 3,635.05 • n=349 Participants
|
1,595.90 dollars
STANDARD_DEVIATION 5,028.76 • n=304 Participants
|
300.98 dollars
STANDARD_DEVIATION 1,305.66 • n=2728 Participants
|
1,084.32 dollars
STANDARD_DEVIATION 4,484.62 • n=192 Participants
|
371.06 dollars
STANDARD_DEVIATION 1,888.55 • n=1948 Participants
|
1,043.14 dollars
STANDARD_DEVIATION 4,077.61 • n=349 Participants
|
528.57 dollars
STANDARD_DEVIATION 1,611.21 • n=376 Participants
|
1,535.64 dollars
STANDARD_DEVIATION 4,984.93 • n=325 Participants
|
1,580.73 dollars
STANDARD_DEVIATION 6,155.27 • n=204 Participants
|
1,506.72 dollars
STANDARD_DEVIATION 8,975.05 • n=533 Participants
|
643.43 dollars
STANDARD_DEVIATION 3,600.63 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 8
|
684.64 dollars
STANDARD_DEVIATION 3,744.93 • n=349 Participants
|
1,562.50 dollars
STANDARD_DEVIATION 5,568.83 • n=304 Participants
|
354.75 dollars
STANDARD_DEVIATION 1,946.36 • n=2728 Participants
|
976.85 dollars
STANDARD_DEVIATION 3,453.52 • n=192 Participants
|
335.36 dollars
STANDARD_DEVIATION 1,750.03 • n=1948 Participants
|
954.47 dollars
STANDARD_DEVIATION 3,523.14 • n=349 Participants
|
860.95 dollars
STANDARD_DEVIATION 3,660.07 • n=376 Participants
|
1,164.74 dollars
STANDARD_DEVIATION 4,182.09 • n=325 Participants
|
1,179.40 dollars
STANDARD_DEVIATION 3,792.58 • n=204 Participants
|
1,276.16 dollars
STANDARD_DEVIATION 4,023.91 • n=533 Participants
|
612.85 dollars
STANDARD_DEVIATION 2,877.18 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 9
|
1,146.75 dollars
STANDARD_DEVIATION 8,152.88 • n=349 Participants
|
1,167.06 dollars
STANDARD_DEVIATION 2,588.52 • n=304 Participants
|
323.44 dollars
STANDARD_DEVIATION 2,680.72 • n=2728 Participants
|
628.15 dollars
STANDARD_DEVIATION 1,892.34 • n=192 Participants
|
448.58 dollars
STANDARD_DEVIATION 4,363.20 • n=1948 Participants
|
1,000.19 dollars
STANDARD_DEVIATION 4,066.02 • n=349 Participants
|
472.76 dollars
STANDARD_DEVIATION 1,867.06 • n=376 Participants
|
1,562.92 dollars
STANDARD_DEVIATION 6,092.02 • n=325 Participants
|
1,152.80 dollars
STANDARD_DEVIATION 2,780.05 • n=204 Participants
|
957.33 dollars
STANDARD_DEVIATION 3,882.14 • n=533 Participants
|
603.72 dollars
STANDARD_DEVIATION 3,917.33 • n=7308 Participants
|
|
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
Month 10
|
840.51 dollars
STANDARD_DEVIATION 5,804.19 • n=349 Participants
|
1,202.02 dollars
STANDARD_DEVIATION 2,951.84 • n=304 Participants
|
279.40 dollars
STANDARD_DEVIATION 2,115.08 • n=2728 Participants
|
618.40 dollars
STANDARD_DEVIATION 1,892.74 • n=192 Participants
|
248.11 dollars
STANDARD_DEVIATION 1,494.89 • n=1948 Participants
|
877.15 dollars
STANDARD_DEVIATION 3,123.73 • n=349 Participants
|
518.84 dollars
STANDARD_DEVIATION 2,090.45 • n=376 Participants
|
962.51 dollars
STANDARD_DEVIATION 3,276.90 • n=325 Participants
|
2,010.47 dollars
STANDARD_DEVIATION 10,949.32 • n=204 Participants
|
1,217.53 dollars
STANDARD_DEVIATION 6,154.58 • n=533 Participants
|
533.13 dollars
STANDARD_DEVIATION 3,428.70 • n=7308 Participants
|
PRIMARY outcome
Timeframe: Within 90 days after index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
In this outcome measure number of participants who were on combination therapy with index medication and who were on monotherapy during 12 months pre-index date were reported. Participants with a use of at least 1 of 4 specific csDMARDs (methotrexate, sulfasalazine, hydroxychloroquine, leflunomide) within 90 days on or after the index date were considered as being treated with combination therapy. Participants who did not take any csDMARDs along with index medication were considered being treated with monotherapy.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Were on Combination Therapy and Monotherapy During 90 Days After Index Date
Monotherapy
|
166 Participants
|
136 Participants
|
727 Participants
|
73 Participants
|
575 Participants
|
83 Participants
|
97 Participants
|
131 Participants
|
103 Participants
|
183 Participants
|
|
Number of Participants Who Were on Combination Therapy and Monotherapy During 90 Days After Index Date
Combination therapy
|
183 Participants
|
168 Participants
|
2001 Participants
|
119 Participants
|
1373 Participants
|
266 Participants
|
279 Participants
|
194 Participants
|
101 Participants
|
350 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Number of participants with most commonly used medications use during 12 months post index period are reported. The 25 most medications: 1) methotrexate sodium, 2) prednisone, 3) folic acid, 4) adalimumab, 5) etanercept, 6) acetaminophen/hydrocodone bitartrate, 7) hydroxychloroquine sulfate, 8) azithromycin, 9) levothyroxine sodium, 10) tramadol hydrochloride, 11) methylprednisolone, 12) gabapentin, 13) albuterol sulfate, 14) amoxicillin/clavulanate potassium, 15) omeprazole, 16) amoxicillin, 17) meloxicam, 18) tofacitinib citrate, 19) fluticasone propionate, 20) cyclobenzaprine hydrochloride, 21) diclofenac sodium, 22) duloxetine hydrochloride, 23) atorvastatin calcium, 24) leflunomide, 25) fluconazole. A participant could have received \>=1 most common medication.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Methotrexate Sodium
|
163 Participants
|
136 Participants
|
1,789 Participants
|
120 Participants
|
1,193 Participants
|
245 Participants
|
252 Participants
|
163 Participants
|
105 Participants
|
289 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Prednisone
|
161 Participants
|
185 Participants
|
1,473 Participants
|
106 Participants
|
1,053 Participants
|
221 Participants
|
214 Participants
|
191 Participants
|
129 Participants
|
306 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Acetaminophen/Hydrocodone Bitartrate
|
69 Participants
|
85 Participants
|
642 Participants
|
42 Participants
|
479 Participants
|
111 Participants
|
96 Participants
|
80 Participants
|
66 Participants
|
159 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Hydroxychloroquine Sulfate
|
74 Participants
|
75 Participants
|
665 Participants
|
36 Participants
|
501 Participants
|
72 Participants
|
92 Participants
|
82 Participants
|
39 Participants
|
163 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Azithromycin
|
75 Participants
|
87 Participants
|
621 Participants
|
33 Participants
|
447 Participants
|
76 Participants
|
89 Participants
|
78 Participants
|
44 Participants
|
151 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Levothyroxine Sodium
|
70 Participants
|
56 Participants
|
508 Participants
|
34 Participants
|
369 Participants
|
64 Participants
|
75 Participants
|
61 Participants
|
44 Participants
|
124 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Tramadol Hydrochloride
|
56 Participants
|
54 Participants
|
497 Participants
|
36 Participants
|
388 Participants
|
67 Participants
|
83 Participants
|
62 Participants
|
43 Participants
|
107 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Albuterol Sulfate
|
56 Participants
|
59 Participants
|
433 Participants
|
25 Participants
|
321 Participants
|
50 Participants
|
53 Participants
|
53 Participants
|
35 Participants
|
99 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Leflunomide
|
35 Participants
|
35 Participants
|
300 Participants
|
19 Participants
|
238 Participants
|
44 Participants
|
43 Participants
|
36 Participants
|
19 Participants
|
70 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Folic Acid
|
155 Participants
|
116 Participants
|
1,616 Participants
|
109 Participants
|
1,078 Participants
|
201 Participants
|
234 Participants
|
148 Participants
|
95 Participants
|
268 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Adalimumab
|
20 Participants
|
16 Participants
|
2,717 Participants
|
13 Participants
|
353 Participants
|
12 Participants
|
9 Participants
|
2 Participants
|
10 Participants
|
19 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Etanercept
|
12 Participants
|
11 Participants
|
327 Participants
|
7 Participants
|
1,943 Participants
|
6 Participants
|
11 Participants
|
1 Participants
|
8 Participants
|
25 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Methylprednisolone
|
66 Participants
|
64 Participants
|
503 Participants
|
49 Participants
|
357 Participants
|
61 Participants
|
67 Participants
|
50 Participants
|
30 Participants
|
104 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Gabapentin
|
58 Participants
|
48 Participants
|
397 Participants
|
38 Participants
|
341 Participants
|
66 Participants
|
64 Participants
|
58 Participants
|
40 Participants
|
113 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Amoxicillin/Clavulanate Potassium
|
49 Participants
|
51 Participants
|
427 Participants
|
33 Participants
|
289 Participants
|
41 Participants
|
61 Participants
|
55 Participants
|
32 Participants
|
90 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Omeprazole
|
47 Participants
|
50 Participants
|
387 Participants
|
20 Participants
|
314 Participants
|
68 Participants
|
58 Participants
|
56 Participants
|
38 Participants
|
89 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Amoxicillin
|
54 Participants
|
41 Participants
|
391 Participants
|
36 Participants
|
312 Participants
|
55 Participants
|
58 Participants
|
49 Participants
|
36 Participants
|
93 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Meloxicam
|
43 Participants
|
41 Participants
|
463 Participants
|
21 Participants
|
293 Participants
|
62 Participants
|
62 Participants
|
28 Participants
|
29 Participants
|
68 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Tofacitinib Citrate
|
349 Participants
|
304 Participants
|
180 Participants
|
11 Participants
|
123 Participants
|
3 Participants
|
12 Participants
|
7 Participants
|
9 Participants
|
33 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Fluticasone Propionate
|
47 Participants
|
49 Participants
|
322 Participants
|
25 Participants
|
269 Participants
|
62 Participants
|
56 Participants
|
45 Participants
|
26 Participants
|
83 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Cyclobenzaprine Hydrochloride
|
38 Participants
|
49 Participants
|
339 Participants
|
28 Participants
|
288 Participants
|
47 Participants
|
54 Participants
|
33 Participants
|
27 Participants
|
67 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Diclofenac Sodium
|
47 Participants
|
38 Participants
|
332 Participants
|
31 Participants
|
259 Participants
|
44 Participants
|
53 Participants
|
34 Participants
|
32 Participants
|
72 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Duloxetine Hydrochloride
|
30 Participants
|
41 Participants
|
318 Participants
|
23 Participants
|
253 Participants
|
45 Participants
|
55 Participants
|
37 Participants
|
31 Participants
|
75 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Atorvastatin Calcium
|
58 Participants
|
34 Participants
|
311 Participants
|
23 Participants
|
215 Participants
|
52 Participants
|
40 Participants
|
39 Participants
|
34 Participants
|
74 Participants
|
|
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Fluconazole
|
27 Participants
|
26 Participants
|
320 Participants
|
23 Participants
|
195 Participants
|
42 Participants
|
49 Participants
|
38 Participants
|
18 Participants
|
68 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Number of participants who used at least 1 opioid and NSAID during post-index period are reported.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Used Opioids and Non-steroidal Anti-inflammatory Drug (NSAIDs) During 12 Months Post Index Period
|
210 Participants
|
205 Participants
|
1,623 Participants
|
104 Participants
|
1,236 Participants
|
233 Participants
|
249 Participants
|
202 Participants
|
143 Participants
|
342 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study. Here, "overall number of participants analyzed" signifies participants evaluable for this outcome measure.
The mean number of pharmacy claims for opioids and NSAIDs during the post-index period are reported. A pharmacy claim was defined as a claim made by participants to their insurance provider in purchasing opioids and NSAIDs from the pharmacy.
Outcome measures
| Measure |
Tofacitinib XR
n=210 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=205 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=1623 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=104 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1236 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=233 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=249 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=202 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=143 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=342 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Mean Number of Pharmacy Claims for Opioids and NSAIDS During 12 Months Post Index Period
|
3.68 pharmacy claims
Standard Deviation 6.04
|
4.99 pharmacy claims
Standard Deviation 6.87
|
3.78 pharmacy claims
Standard Deviation 5.98
|
3.80 pharmacy claims
Standard Deviation 6.00
|
4.13 pharmacy claims
Standard Deviation 6.00
|
4.30 pharmacy claims
Standard Deviation 6.04
|
4.08 pharmacy claims
Standard Deviation 5.37
|
3.83 pharmacy claims
Standard Deviation 5.63
|
5.19 pharmacy claims
Standard Deviation 6.52
|
4.50 pharmacy claims
Standard Deviation 6.23
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study. Here, "overall number of participants analyzed" signifies participants evaluable for this outcome measure.
Mean number of days from the index date to the first opioid and NSAIDs claim during post index period are reported.
Outcome measures
| Measure |
Tofacitinib XR
n=210 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=205 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=1623 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=104 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1236 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=233 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=249 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=202 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=143 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=342 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Mean Number of Days From The Index Date to the First Opioid and NSAIDs Claim During 12 Months Post Index Period
Days to First Opioid
|
85.35 days
Standard Deviation 94.49
|
83.31 days
Standard Deviation 95.78
|
95.67 days
Standard Deviation 98.71
|
99.05 days
Standard Deviation 105.20
|
94.05 days
Standard Deviation 99.55
|
101.04 days
Standard Deviation 102.35
|
88.81 days
Standard Deviation 89.79
|
98.71 days
Standard Deviation 101.38
|
81.58 days
Standard Deviation 92.36
|
93.31 days
Standard Deviation 96.62
|
|
Mean Number of Days From The Index Date to the First Opioid and NSAIDs Claim During 12 Months Post Index Period
Days to First NSAID
|
116.22 days
Standard Deviation 99.95
|
99.94 days
Standard Deviation 95.31
|
107.03 days
Standard Deviation 99.29
|
123.31 days
Standard Deviation 106.32
|
105.37 days
Standard Deviation 97.93
|
118.44 days
Standard Deviation 107.09
|
110.65 days
Standard Deviation 103.11
|
97.37 days
Standard Deviation 92.35
|
92.44 days
Standard Deviation 89.42
|
90.89 days
Standard Deviation 93.80
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Number of participants who used opioids and NSAIDs during tofacitinib persistency and post-persistency are reported. Persistence with the index medication was defined as not having a gap in therapy of at least 60 days between fills/infusions.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Used Opioids and NSAIDs While Persistent and After Persistent With Index Medication During 12 Months Post Index Period
Used NSAIDs While Persistent
|
94 Participants
|
85 Participants
|
769 Participants
|
43 Participants
|
535 Participants
|
100 Participants
|
122 Participants
|
39 Participants
|
60 Participants
|
146 Participants
|
|
Number of Participants Who Used Opioids and NSAIDs While Persistent and After Persistent With Index Medication During 12 Months Post Index Period
Used Opioids While Persistent
|
138 Participants
|
128 Participants
|
1,035 Participants
|
61 Participants
|
774 Participants
|
168 Participants
|
177 Participants
|
78 Participants
|
104 Participants
|
246 Participants
|
|
Number of Participants Who Used Opioids and NSAIDs While Persistent and After Persistent With Index Medication During 12 Months Post Index Period
Used Opioids After Persistent
|
22 Participants
|
31 Participants
|
182 Participants
|
20 Participants
|
167 Participants
|
23 Participants
|
18 Participants
|
85 Participants
|
17 Participants
|
41 Participants
|
|
Number of Participants Who Used Opioids and NSAIDs While Persistent and After Persistent With Index Medication During 12 Months Post Index Period
Used NSAIDs After Persistent
|
20 Participants
|
26 Participants
|
157 Participants
|
16 Participants
|
144 Participants
|
17 Participants
|
26 Participants
|
62 Participants
|
8 Participants
|
25 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
The number of participants who used at least 1 oral corticosteroid during the 12 months post-index period are reported.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Used Oral Corticosteroids During 12 Months Post-Index Period
|
198 Participants
|
216 Participants
|
1,713 Participants
|
126 Participants
|
1,225 Participants
|
241 Participants
|
241 Participants
|
217 Participants
|
138 Participants
|
356 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Non-persistence was defined as the gap of at least 60 days in treatment with the index medication or switching to other biologic.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Were Non-persistent to Index Medication
|
166 Participants
|
189 Participants
|
1381 Participants
|
117 Participants
|
1036 Participants
|
139 Participants
|
188 Participants
|
320 Participants
|
117 Participants
|
287 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Participants were classified as switched immediately if they initiated a non-index bDMARD before a 60-day gap in index medication treatment.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Switched Immediately From Index Medication
|
41 Participants
|
70 Participants
|
575 Participants
|
33 Participants
|
451 Participants
|
49 Participants
|
55 Participants
|
3 Participants
|
34 Participants
|
112 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Participants were classified as discontinued and then restarted index medication if there was a gap in the index therapy of at least 60 days and the first medication observed after the gap was the index medication.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Discontinued Then Restarted Index Medication
|
43 Participants
|
33 Participants
|
201 Participants
|
15 Participants
|
152 Participants
|
21 Participants
|
55 Participants
|
197 Participants
|
21 Participants
|
52 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Participants were classified as discontinued and then switched from index medication if there was a gap in the index therapy of at least 60 days and the first medication observed after the gap was a bDMARD (including tofacitinib) different from index medication.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Discontinued Then Switched From Index Medication
|
12 Participants
|
24 Participants
|
127 Participants
|
15 Participants
|
130 Participants
|
7 Participants
|
24 Participants
|
19 Participants
|
11 Participants
|
25 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Participants were classified as discontinued without switching or restarting index medication if they had a gap in therapy of at least 60 days and there were no claims for either the index medication or a different bDMARD for the remainder of the follow-up period.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Discontinued Without Switching or Restarting Index Medication
|
70 Participants
|
62 Participants
|
478 Participants
|
54 Participants
|
303 Participants
|
62 Participants
|
54 Participants
|
101 Participants
|
51 Participants
|
98 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Number of participants who switched from index medication to a biologic at any time during post-index period are reported.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Switched Any Time From Index Medication
|
55 Participants
|
96 Participants
|
727 Participants
|
48 Participants
|
599 Participants
|
56 Participants
|
84 Participants
|
26 Participants
|
45 Participants
|
140 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Participants who had a claim for the index medication any time after they were considered non-persistent with the index treatment (i.e, including after switching) during the 12-month follow-up are reported. Non-persistence was defined as the gap of at least 60 days in treatment with the index medication or switching to other biologic.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Re-started Index Medication at Any Time
|
25 Participants
|
25 Participants
|
132 Participants
|
6 Participants
|
78 Participants
|
13 Participants
|
25 Participants
|
188 Participants
|
9 Participants
|
31 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study. As per planned analysis MPR was not evaluated for Rituximab arm.
MPR was calculated as the total days supply of methotrexate between the first and including the last prescription/administration divided by the time between the first through and including last biologic prescription/administration days supply.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Mean Medication Possession Ratio (MPR) for Methotrexate
|
0.89 ratio
Standard Deviation 0.16
|
0.87 ratio
Standard Deviation 0.18
|
0.91 ratio
Standard Deviation 0.14
|
0.92 ratio
Standard Deviation 0.14
|
0.91 ratio
Standard Deviation 0.14
|
0.98 ratio
Standard Deviation 0.07
|
0.65 ratio
Standard Deviation 0.18
|
—
|
0.89 ratio
Standard Deviation 0.14
|
0.91 ratio
Standard Deviation 0.14
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
The PDC was calculated based on total days supply over the 12 months follow-up. The PDC was calculated by using the date of service and the day supply for each fill of the index medication.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Proportion of Days Covered (PDC)
|
0.65 proportion of days
Standard Deviation 0.32
|
0.55 proportion of days
Standard Deviation 0.32
|
0.66 proportion of days
Standard Deviation 0.31
|
0.56 proportion of days
Standard Deviation 0.32
|
0.63 proportion of days
Standard Deviation 0.32
|
0.77 proportion of days
Standard Deviation 0.28
|
0.46 proportion of days
Standard Deviation 0.20
|
0.63 proportion of days
Standard Deviation 0.48
|
0.60 proportion of days
Standard Deviation 0.31
|
0.63 proportion of days
Standard Deviation 0.31
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study. Here, "overall number of participants analyzed" signifies the participants who initiated treatment as monotherapy with index medication only.
Participants with monotherapy who used additional csDMARD during post index period are reported.
Outcome measures
| Measure |
Tofacitinib XR
n=166 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=136 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=727 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=73 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=575 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=83 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=97 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=131 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=103 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=183 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Addition of Conventional Synthetic Disease-modifying Antirheumatic Drug (Cs-DMARDs) in Participants With Monotherapy
|
48 Participants
|
37 Participants
|
247 Participants
|
29 Participants
|
193 Participants
|
28 Participants
|
31 Participants
|
39 Participants
|
36 Participants
|
70 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study. Here, "overall number of participants analyzed" signifies the participants who initiated treatment as combination therapy with index medication and cs-DMARDs.
Adherence was calculated as the total day supply for csDMARDs divided by the number of days from the first claim during the follow-up until the end of the follow-up.
Outcome measures
| Measure |
Tofacitinib XR
n=183 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=168 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2001 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=119 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1373 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=266 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=279 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=194 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=101 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=350 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Adherence to Cs-DMARDs in Participants With Combination Therapy
|
0.72 ratio
Standard Deviation 0.30
|
0.79 ratio
Standard Deviation 0.26
|
0.77 ratio
Standard Deviation 0.27
|
0.74 ratio
Standard Deviation 0.28
|
0.78 ratio
Standard Deviation 0.27
|
0.79 ratio
Standard Deviation 0.26
|
0.79 ratio
Standard Deviation 0.27
|
0.77 ratio
Standard Deviation 0.28
|
0.70 ratio
Standard Deviation 0.30
|
0.80 ratio
Standard Deviation 0.26
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
Adherence criteria: PDC \>=0.8, proportion of days of supply during post-index period of 12 months.Dose escalation criteria: no increase in dose for index drug compared to starting dose during post-index period. Switch criteria: no switching from index drug to (different) biologic agent during post-index period. DMARD criteria: no addition of new csDMARD to index drug during post-index period. Oral glucocorticoid criteria: Participants with no claims for oral glucocorticoids in 6 months pre-index cannot receive oral glucocorticoids for greater than (\>)30 days between (index date +91 days) to (index date + 365 days); or participants with claims for oral glucocorticoids in 6 months pre-index no increase in oral glucocorticoid dose during months 6-12 post-index.Injectable glucocorticoid criteria: at most 1 parenteral or intra-articular glucocorticoid joint injection on unique days after participant had been on bDMARD treatment for \>3 months between (index date + 91) to (index date + 365).
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Number of Participants Who Met Different Medication Effectiveness Criteria
Met DMARD criteria
|
316 Participants
|
270 Participants
|
2458 Participants
|
165 Participants
|
1727 Participants
|
314 Participants
|
339 Participants
|
298 Participants
|
185 Participants
|
462 Participants
|
|
Number of Participants Who Met Different Medication Effectiveness Criteria
Met adherence criteria
|
168 Participants
|
98 Participants
|
1249 Participants
|
64 Participants
|
843 Participants
|
222 Participants
|
30 Participants
|
206 Participants
|
72 Participants
|
223 Participants
|
|
Number of Participants Who Met Different Medication Effectiveness Criteria
Met dose escalation criteria
|
333 Participants
|
288 Participants
|
2362 Participants
|
190 Participants
|
1864 Participants
|
199 Participants
|
373 Participants
|
0 Participants
|
202 Participants
|
522 Participants
|
|
Number of Participants Who Met Different Medication Effectiveness Criteria
Met switch criteria
|
294 Participants
|
208 Participants
|
2001 Participants
|
144 Participants
|
1349 Participants
|
293 Participants
|
292 Participants
|
299 Participants
|
159 Participants
|
393 Participants
|
|
Number of Participants Who Met Different Medication Effectiveness Criteria
Met glucocorticoid oral criteria
|
285 Participants
|
240 Participants
|
2308 Participants
|
160 Participants
|
1652 Participants
|
288 Participants
|
316 Participants
|
269 Participants
|
167 Participants
|
429 Participants
|
|
Number of Participants Who Met Different Medication Effectiveness Criteria
Met glucocorticoid injection criteria
|
306 Participants
|
242 Participants
|
2263 Participants
|
149 Participants
|
1605 Participants
|
246 Participants
|
291 Participants
|
140 Participants
|
151 Participants
|
406 Participants
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause inpatient visits costs, outpatient visits costs and emergency room visits costs during 12 months post index period are reported. Inpatient visit costs consisted of expenses during hospital visit for formal admission. Outpatient visit costs consisted of expenses when participants visited hospital but not for formal admission. Emergency room visit costs consisted of expenses during visit to hospital emergency room.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
All Cause Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
Inpatient visits costs
|
5,301.85 dollars
Standard Deviation 20,548.39
|
4,326.53 dollars
Standard Deviation 18,879.99
|
3,863.95 dollars
Standard Deviation 20,664.73
|
4,691.74 dollars
Standard Deviation 18,400.58
|
3,856.57 dollars
Standard Deviation 17,506.77
|
5,260.88 dollars
Standard Deviation 18,311.36
|
3,482.13 dollars
Standard Deviation 15,539.56
|
11,204.53 dollars
Standard Deviation 46,080.79
|
5,929.53 dollars
Standard Deviation 21,129.94
|
5,995.50 dollars
Standard Deviation 25,570.37
|
|
All Cause Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
Outpatient visits costs
|
11,533.02 dollars
Standard Deviation 31,816.02
|
10,643.90 dollars
Standard Deviation 17,097.41
|
9,477.87 dollars
Standard Deviation 19,068.99
|
33,271.44 dollars
Standard Deviation 38,242.58
|
10,567.29 dollars
Standard Deviation 22,288.21
|
42,056.44 dollars
Standard Deviation 32,134.21
|
39,161.11 dollars
Standard Deviation 30,665.68
|
69,689.17 dollars
Standard Deviation 66,481.44
|
28,394.20 dollars
Standard Deviation 30,600.24
|
35,119.77 dollars
Standard Deviation 36,208.77
|
|
All Cause Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
ER visits costs
|
1,330.49 dollars
Standard Deviation 4,934.64
|
1,500.08 dollars
Standard Deviation 3,892.48
|
1,079.34 dollars
Standard Deviation 3,346.54
|
1,738.59 dollars
Standard Deviation 5,234.10
|
1,176.85 dollars
Standard Deviation 4,307.77
|
1,663.83 dollars
Standard Deviation 4,093.45
|
1,177.78 dollars
Standard Deviation 3,618.48
|
1,787.39 dollars
Standard Deviation 4,392.54
|
1,567.34 dollars
Standard Deviation 4,030.41
|
1,814.41 dollars
Standard Deviation 6,476.07
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related inpatient visit costs consisted of expenses during hospital visits for formal admission for RA. Outpatient visit costs consisted of expenses when participants visited hospital but not for formal admission for RA. ER visit costs consisted of expenses during visit to ER of hospital for RA.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Rheumatoid Arthritis (RA) Related Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
Inpatient visits costs
|
2,465.50 dollars
Standard Deviation 13,108.37
|
2,470.87 dollars
Standard Deviation 13,911.22
|
2,215.74 dollars
Standard Deviation 15,372.12
|
1,794.11 dollars
Standard Deviation 8,062.54
|
2,054.38 dollars
Standard Deviation 11,418.40
|
3,561.22 dollars
Standard Deviation 14,505.62
|
2,034.70 dollars
Standard Deviation 12,060.95
|
4,938.52 dollars
Standard Deviation 24,124.90
|
2,143.98 dollars
Standard Deviation 9,456.96
|
2,678.39 dollars
Standard Deviation 15,669.24
|
|
Rheumatoid Arthritis (RA) Related Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
Outpatient visits costs
|
2,257.47 dollars
Standard Deviation 8,687.34
|
1,773.11 dollars
Standard Deviation 2,446.67
|
2,060.29 dollars
Standard Deviation 5,605.48
|
3,540.19 dollars
Standard Deviation 5,886.92
|
2,122.31 dollars
Standard Deviation 6,842.63
|
5,412.86 dollars
Standard Deviation 7,401.70
|
3,348.09 dollars
Standard Deviation 6,632.70
|
9,991.58 dollars
Standard Deviation 18,160.69
|
4,176.44 dollars
Standard Deviation 7,257.25
|
4,166.63 dollars
Standard Deviation 8,262.58
|
|
Rheumatoid Arthritis (RA) Related Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
ER visits costs
|
335.97 dollars
Standard Deviation 1,902.64
|
359.62 dollars
Standard Deviation 1,397.80
|
374.24 dollars
Standard Deviation 1,940.56
|
351.14 dollars
Standard Deviation 1,187.24
|
356.14 dollars
Standard Deviation 1,979.50
|
569.19 dollars
Standard Deviation 2,702.12
|
416.68 dollars
Standard Deviation 1,933.80
|
403.89 dollars
Standard Deviation 1,807.54
|
345.85 dollars
Standard Deviation 1,771.27
|
485.19 dollars
Standard Deviation 2,931.20
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause total health care costs, medical costs, pharmacy costs during 12 months post-index period are reported. All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs).
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
Total health care costs
|
61,431.53 dollars
Standard Deviation 50,673.36
|
53,150.92 dollars
Standard Deviation 35,767.69
|
66,645.17 dollars
Standard Deviation 38,833.73
|
62,064.23 dollars
Standard Deviation 47,099.08
|
64,120.91 dollars
Standard Deviation 39,299.75
|
55,737.03 dollars
Standard Deviation 42,155.65
|
58,148.31 dollars
Standard Deviation 36,240.29
|
95,365.52 dollars
Standard Deviation 102,623.86
|
62,120.81 dollars
Standard Deviation 52,128.91
|
69,508.99 dollars
Standard Deviation 48,744.63
|
|
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
Medical costs
|
18,165.35 dollars
Standard Deviation 43,146.20
|
16,470.52 dollars
Standard Deviation 32,254.10
|
14,421.15 dollars
Standard Deviation 32,612.17
|
39,701.78 dollars
Standard Deviation 45,908.94
|
15,600.71 dollars
Standard Deviation 33,988.45
|
48,981.15 dollars
Standard Deviation 40,482.57
|
43,821.02 dollars
Standard Deviation 36,135.48
|
82,681.09 dollars
Standard Deviation 95,516.54
|
35,891.07 dollars
Standard Deviation 39,557.04
|
42,929.69 dollars
Standard Deviation 50,218.20
|
|
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
Pharmacy costs
|
43,266.17 dollars
Standard Deviation 25,298.33
|
36,680.40 dollars
Standard Deviation 19,244.84
|
52,224.02 dollars
Standard Deviation 23,822.84
|
22,362.45 dollars
Standard Deviation 22,762.52
|
48,520.21 dollars
Standard Deviation 21,330.02
|
6,755.88 dollars
Standard Deviation 12,128.67
|
14,327.29 dollars
Standard Deviation 21,609.36
|
12,684.43 dollars
Standard Deviation 35,574.58
|
26,229.74 dollars
Standard Deviation 39,070.32
|
26,579.30 dollars
Standard Deviation 27,293.48
|
PRIMARY outcome
Timeframe: During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care costs, medical costs, pharmacy costs during 12 months post-index period are reported. RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs).
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
Total health care costs
|
44,134.19 dollars
Standard Deviation 24,089.13
|
38,462.40 dollars
Standard Deviation 22,381.48
|
54,892.62 dollars
Standard Deviation 27,900.44
|
41,845.23 dollars
Standard Deviation 22,687.60
|
50,531.75 dollars
Standard Deviation 23,297.78
|
42,227.78 dollars
Standard Deviation 34,533.34
|
43,897.47 dollars
Standard Deviation 21,606.90
|
55,383.00 dollars
Standard Deviation 50,554.53
|
37,868.85 dollars
Standard Deviation 21,498.52
|
49,156.67 dollars
Standard Deviation 31,002.05
|
|
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
Medical costs
|
5,058.93 dollars
Standard Deviation 17,558.57
|
4,603.61 dollars
Standard Deviation 14,852.30
|
4,650.27 dollars
Standard Deviation 17,149.92
|
5,685.44 dollars
Standard Deviation 11,078.72
|
4,532.83 dollars
Standard Deviation 15,083.29
|
9,543.27 dollars
Standard Deviation 17,696.01
|
5,799.47 dollars
Standard Deviation 14,164.57
|
15,333.99 dollars
Standard Deviation 35,734.38
|
6,666.27 dollars
Standard Deviation 12,568.84
|
7,330.20 dollars
Standard Deviation 18,740.87
|
|
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
Pharmacy costs
|
38,526.59 dollars
Standard Deviation 18,005.41
|
32,697.22 dollars
Standard Deviation 17,139.97
|
48,872.33 dollars
Standard Deviation 22,384.60
|
17,384.65 dollars
Standard Deviation 21,700.87
|
45,093.62 dollars
Standard Deviation 19,352.72
|
3,679.43 dollars
Standard Deviation 10,548.26
|
9,565.34 dollars
Standard Deviation 17,476.03
|
3,667.78 dollars
Standard Deviation 10,132.59
|
18,471.52 dollars
Standard Deviation 20,373.61
|
20,603.02 dollars
Standard Deviation 22,860.86
|
PRIMARY outcome
Timeframe: Month 1 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 1 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 1 Post Index Date
|
7,985.18 dollars
Standard Deviation 5,870.38
|
6,989.92 dollars
Standard Deviation 3,627.60
|
9,290.98 dollars
Standard Deviation 4,894.97
|
10,394.75 dollars
Standard Deviation 5,480.85
|
8,777.27 dollars
Standard Deviation 5,155.60
|
8,794.60 dollars
Standard Deviation 6,778.97
|
11,036.55 dollars
Standard Deviation 6,382.95
|
27,231.41 dollars
Standard Deviation 20,230.94
|
7,265.53 dollars
Standard Deviation 7,175.27
|
10,278.66 dollars
Standard Deviation 7,509.70
|
PRIMARY outcome
Timeframe: Month 2 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 2 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 2 Post Index Date
|
4,805.26 dollars
Standard Deviation 8,465.89
|
3,207.83 dollars
Standard Deviation 2,974.52
|
4,661.95 dollars
Standard Deviation 5,512.59
|
4,734.42 dollars
Standard Deviation 6,655.08
|
4,735.15 dollars
Standard Deviation 7,341.43
|
4,915.29 dollars
Standard Deviation 4,993.19
|
3,205.10 dollars
Standard Deviation 6,755.35
|
5,169.15 dollars
Standard Deviation 12,056.54
|
4,244.12 dollars
Standard Deviation 6,081.42
|
4,716.32 dollars
Standard Deviation 7,099.03
|
PRIMARY outcome
Timeframe: Month 3 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 3 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 3 Post Index Date
|
5,093.95 dollars
Standard Deviation 7,838.08
|
4,551.06 dollars
Standard Deviation 5,175.57
|
5,975.14 dollars
Standard Deviation 6,404.19
|
6,950.34 dollars
Standard Deviation 20,526.66
|
5,674.03 dollars
Standard Deviation 7,388.21
|
3,047.15 dollars
Standard Deviation 7,044.98
|
5,139.77 dollars
Standard Deviation 6,311.03
|
5,857.31 dollars
Standard Deviation 14,795.16
|
5,861.37 dollars
Standard Deviation 11,900.93
|
6,395.67 dollars
Standard Deviation 14,460.70
|
PRIMARY outcome
Timeframe: Month 4 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 4 of post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 4 Post Index Date
|
5,079.28 dollars
Standard Deviation 10,071.92
|
3,969.48 dollars
Standard Deviation 5,061.60
|
5,301.22 dollars
Standard Deviation 6,550.05
|
5,014.75 dollars
Standard Deviation 6,964.19
|
5,120.19 dollars
Standard Deviation 7,544.90
|
5,346.93 dollars
Standard Deviation 11,012.15
|
4,221.26 dollars
Standard Deviation 10,606.65
|
5,344.44 dollars
Standard Deviation 13,741.05
|
5,977.41 dollars
Standard Deviation 12,963.41
|
5,412.70 dollars
Standard Deviation 5,751.93
|
PRIMARY outcome
Timeframe: Month 5 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 5 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 5 Post Index Date
|
4,122.15 dollars
Standard Deviation 6,848.85
|
4,874.41 dollars
Standard Deviation 9,227.40
|
4,828.27 dollars
Standard Deviation 5,749.33
|
4,102.21 dollars
Standard Deviation 6,198.56
|
4,915.71 dollars
Standard Deviation 7,978.40
|
3,363.56 dollars
Standard Deviation 5,474.43
|
5,709.69 dollars
Standard Deviation 9,306.48
|
4,837.39 dollars
Standard Deviation 7,827.14
|
4,489.84 dollars
Standard Deviation 5,244.84
|
4,951.42 dollars
Standard Deviation 6,353.78
|
PRIMARY outcome
Timeframe: Month 6 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 6 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 6 Post Index Date
|
4,867.20 dollars
Standard Deviation 11,052.21
|
3,826.79 dollars
Standard Deviation 6,801.85
|
5,997.83 dollars
Standard Deviation 13,221.77
|
4,830.11 dollars
Standard Deviation 7,660.60
|
4,982.15 dollars
Standard Deviation 5,627.02
|
4,626.76 dollars
Standard Deviation 8,140.63
|
3,115.80 dollars
Standard Deviation 4,317.17
|
5,442.79 dollars
Standard Deviation 13,221.86
|
4,359.39 dollars
Standard Deviation 4,986.93
|
5,059.37 dollars
Standard Deviation 5,983.06
|
PRIMARY outcome
Timeframe: Month 7 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 7 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 7 Post Index Date
|
4,950.36 dollars
Standard Deviation 8,724.15
|
4,939.24 dollars
Standard Deviation 11,793.47
|
5,004.78 dollars
Standard Deviation 6,780.50
|
4,392.10 dollars
Standard Deviation 5,205.06
|
4,817.34 dollars
Standard Deviation 5,794.22
|
3,067.81 dollars
Standard Deviation 4,192.17
|
4,677.76 dollars
Standard Deviation 4,306.25
|
8,433.49 dollars
Standard Deviation 13,389.18
|
4,465.05 dollars
Standard Deviation 7,021.43
|
5,874.66 dollars
Standard Deviation 10,684.51
|
PRIMARY outcome
Timeframe: Month 8 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 8 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 8 Post Index Date
|
3,815.56 dollars
Standard Deviation 5,915.52
|
4,139.87 dollars
Standard Deviation 6,027.39
|
5,021.37 dollars
Standard Deviation 6,364.92
|
5,095.74 dollars
Standard Deviation 8,352.05
|
5,068.81 dollars
Standard Deviation 9,110.42
|
4,943.14 dollars
Standard Deviation 7,251.38
|
3,709.37 dollars
Standard Deviation 5,334.43
|
8,202.13 dollars
Standard Deviation 13,851.24
|
4,886.07 dollars
Standard Deviation 6,342.07
|
5,745.10 dollars
Standard Deviation 8,591.42
|
PRIMARY outcome
Timeframe: Month 9 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 9 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 9 Post Index Date
|
4,300.84 dollars
Standard Deviation 5,689.33
|
4,399.74 dollars
Standard Deviation 7,749.58
|
5,335.04 dollars
Standard Deviation 7,227.68
|
3,921.54 dollars
Standard Deviation 4,739.81
|
5,210.21 dollars
Standard Deviation 9,459.88
|
5,064.33 dollars
Standard Deviation 9,371.11
|
5,292.97 dollars
Standard Deviation 8,820.67
|
5,049.22 dollars
Standard Deviation 9,633.49
|
5,716.07 dollars
Standard Deviation 12,032.48
|
5,249.20 dollars
Standard Deviation 8,523.88
|
PRIMARY outcome
Timeframe: Month 10 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 10 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 10 Post Index Date
|
5,670.69 dollars
Standard Deviation 21,678.99
|
3,939.86 dollars
Standard Deviation 4,973.50
|
5,186.08 dollars
Standard Deviation 11,341.01
|
3,998.95 dollars
Standard Deviation 5,348.32
|
4,698.56 dollars
Standard Deviation 5,971.85
|
4,147.01 dollars
Standard Deviation 5,145.78
|
3,975.54 dollars
Standard Deviation 9,056.34
|
6,545.01 dollars
Standard Deviation 14,883.32
|
3,938.69 dollars
Standard Deviation 4,406.49
|
5,073.34 dollars
Standard Deviation 7,324.79
|
PRIMARY outcome
Timeframe: Month 11 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 11 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 11 Post-index Date
|
4,244.03 dollars
Standard Deviation 6,261.71
|
4,083.34 dollars
Standard Deviation 7,378.37
|
5,032.88 dollars
Standard Deviation 6,919.38
|
4,500.99 dollars
Standard Deviation 5,936.52
|
5,202.71 dollars
Standard Deviation 9,216.69
|
4,334.84 dollars
Standard Deviation 6,332.45
|
4,861.39 dollars
Standard Deviation 6,362.99
|
6,109.10 dollars
Standard Deviation 17,250.46
|
5,248.98 dollars
Standard Deviation 13,994.80
|
5,180.75 dollars
Standard Deviation 6,145.81
|
PRIMARY outcome
Timeframe: Month 12 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 12 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total All Cause Monthly Health Care Cost at Month 12 Post Index Date
|
6,497.03 dollars
Standard Deviation 16,191.59
|
4,229.36 dollars
Standard Deviation 4,796.31
|
5,009.64 dollars
Standard Deviation 6,414.68
|
4,128.34 dollars
Standard Deviation 4,822.56
|
4,918.79 dollars
Standard Deviation 7,208.45
|
4,085.60 dollars
Standard Deviation 5,581.80
|
3,203.10 dollars
Standard Deviation 4,275.94
|
7,144.07 dollars
Standard Deviation 35,560.31
|
5,668.30 dollars
Standard Deviation 12,736.72
|
5,571.79 dollars
Standard Deviation 9,090.65
|
PRIMARY outcome
Timeframe: Month 1 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 1 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 1 Post Index Date
|
6,743.68 dollars
Standard Deviation 3,290.35
|
6,021.42 dollars
Standard Deviation 3,153.69
|
8,562.89 dollars
Standard Deviation 4,383.18
|
9,390.90 dollars
Standard Deviation 5,023.75
|
7,943.89 dollars
Standard Deviation 4,187.36
|
7,850.66 dollars
Standard Deviation 6,450.60
|
10,152.78 dollars
Standard Deviation 5,722.77
|
22,346.69 dollars
Standard Deviation 13,384.38
|
5,595.28 dollars
Standard Deviation 4,234.37
|
8,937.97 dollars
Standard Deviation 6,127.69
|
PRIMARY outcome
Timeframe: Month 2 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measurec RA related total all cause health care cost in dollars is reported for Month 2 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 2 Post Index Date
|
2,998.35 dollars
Standard Deviation 3,709.88
|
2,450.14 dollars
Standard Deviation 2,559.50
|
3,876.12 dollars
Standard Deviation 4,442.59
|
2,761.42 dollars
Standard Deviation 2,733.37
|
3,639.87 dollars
Standard Deviation 4,342.96
|
3,941.04 dollars
Standard Deviation 3,879.91
|
2,102.21 dollars
Standard Deviation 3,492.31
|
2,376.90 dollars
Standard Deviation 8,383.96
|
2,478.72 dollars
Standard Deviation 2,886.26
|
3,378.57 dollars
Standard Deviation 4,598.62
|
PRIMARY outcome
Timeframe: Month 3 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 3 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 3 Post Index Date
|
3,747.82 dollars
Standard Deviation 4,128.35
|
3,494.46 dollars
Standard Deviation 3,952.15
|
5,049.33 dollars
Standard Deviation 5,212.08
|
3,829.80 dollars
Standard Deviation 7,098.78
|
4,522.20 dollars
Standard Deviation 4,443.60
|
2,108.64 dollars
Standard Deviation 5,867.55
|
4,157.90 dollars
Standard Deviation 5,309.22
|
2,487.38 dollars
Standard Deviation 9,628.44
|
3,696.15 dollars
Standard Deviation 7,327.63
|
3,987.88 dollars
Standard Deviation 3,859.03
|
PRIMARY outcome
Timeframe: Month 4 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 4 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 4 Post Index Date
|
3,935.88 dollars
Standard Deviation 8,393.52
|
2,932.92 dollars
Standard Deviation 4,452.72
|
4,279.35 dollars
Standard Deviation 4,913.29
|
3,333.94 dollars
Standard Deviation 5,238.91
|
4,058.48 dollars
Standard Deviation 6,106.54
|
4,336.50 dollars
Standard Deviation 10,408.87
|
2,982.49 dollars
Standard Deviation 9,267.47
|
1,660.75 dollars
Standard Deviation 7,016.18
|
3,209.19 dollars
Standard Deviation 3,929.79
|
3,871.96 dollars
Standard Deviation 3,628.35
|
PRIMARY outcome
Timeframe: Month 5 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 5 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 5 Post Index Date
|
2,872.41 dollars
Standard Deviation 4,212.74
|
3,192.69 dollars
Standard Deviation 5,189.22
|
3,951.04 dollars
Standard Deviation 4,643.52
|
2,631.47 dollars
Standard Deviation 2,880.06
|
3,715.18 dollars
Standard Deviation 4,674.66
|
2,408.72 dollars
Standard Deviation 4,426.25
|
4,017.58 dollars
Standard Deviation 4,117.99
|
2,442.36 dollars
Standard Deviation 5,874.48
|
2,886.74 dollars
Standard Deviation 3,679.24
|
3,430.00 dollars
Standard Deviation 4,950.93
|
PRIMARY outcome
Timeframe: Month 6 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 6 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 6 Post Index Date
|
3,914.17 dollars
Standard Deviation 8,567.41
|
2,567.31 dollars
Standard Deviation 3,448.98
|
4,657.35 dollars
Standard Deviation 8,370.54
|
3,208.61 dollars
Standard Deviation 4,754.10
|
4,017.72 dollars
Standard Deviation 4,670.44
|
3,257.63 dollars
Standard Deviation 4,275.02
|
2,207.60 dollars
Standard Deviation 3,273.20
|
2,225.86 dollars
Standard Deviation 6,782.54
|
2,848.72 dollars
Standard Deviation 3,192.47
|
3,614.41 dollars
Standard Deviation 4,409.61
|
PRIMARY outcome
Timeframe: Month 7 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 7 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 7 Post Index Date
|
3,493.19 dollars
Standard Deviation 3,937.61
|
3,724.00 dollars
Standard Deviation 10,798.76
|
3,937.19 dollars
Standard Deviation 4,482.39
|
3,091.38 dollars
Standard Deviation 3,466.66
|
3,745.42 dollars
Standard Deviation 4,327.50
|
2,156.48 dollars
Standard Deviation 3,609.41
|
3,623.70 dollars
Standard Deviation 3,763.69
|
5,701.51 dollars
Standard Deviation 10,692.58
|
2,873.86 dollars
Standard Deviation 5,510.48
|
3,980.53 dollars
Standard Deviation 9,296.61
|
PRIMARY outcome
Timeframe: Month 8 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 8 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 8 Post Index Date
|
2,724.51 dollars
Standard Deviation 3,993.58
|
2,945.03 dollars
Standard Deviation 5,092.32
|
4,118.25 dollars
Standard Deviation 5,281.28
|
2,660.95 dollars
Standard Deviation 3,160.08
|
3,837.85 dollars
Standard Deviation 7,021.63
|
3,849.37 dollars
Standard Deviation 5,761.95
|
2,597.10 dollars
Standard Deviation 4,366.96
|
5,004.67 dollars
Standard Deviation 10,146.63
|
3,122.90 dollars
Standard Deviation 4,084.72
|
3,781.65 dollars
Standard Deviation 5,490.15
|
PRIMARY outcome
Timeframe: Month 9 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 9 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 9 Post Index Date
|
3,304.66 dollars
Standard Deviation 4,833.81
|
2,938.67 dollars
Standard Deviation 5,812.01
|
4,368.93 dollars
Standard Deviation 6,456.66
|
2,782.29 dollars
Standard Deviation 3,614.65
|
3,934.80 dollars
Standard Deviation 4,426.58
|
3,535.00 dollars
Standard Deviation 7,449.94
|
3,440.04 dollars
Standard Deviation 3,674.15
|
2,618.44 dollars
Standard Deviation 5,696.21
|
3,012.74 dollars
Standard Deviation 4,507.57
|
3,338.46 dollars
Standard Deviation 4,072.61
|
PRIMARY outcome
Timeframe: Month 10 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 10 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 10 Post Index Date
|
3,416.78 dollars
Standard Deviation 5,512.87
|
2,848.24 dollars
Standard Deviation 4,237.09
|
4,146.86 dollars
Standard Deviation 10,401.39
|
2,519.73 dollars
Standard Deviation 3,185.01
|
3,677.71 dollars
Standard Deviation 5,281.64
|
2,989.40 dollars
Standard Deviation 4,049.61
|
2,972.93 dollars
Standard Deviation 8,506.46
|
2,816.24 dollars
Standard Deviation 7,484.20
|
2,515.85 dollars
Standard Deviation 3,251.37
|
3,591.22 dollars
Standard Deviation 6,160.68
|
PRIMARY outcome
Timeframe: Month 11 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 11 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 11 Post-index Date
|
3,010.75 dollars
Standard Deviation 4,511.85
|
2,418.53 dollars
Standard Deviation 3,287.81
|
3,926.41 dollars
Standard Deviation 4,868.49
|
2,861.97 dollars
Standard Deviation 3,291.44
|
3,793.28 dollars
Standard Deviation 5,725.91
|
2,982.23 dollars
Standard Deviation 4,486.31
|
3,473.65 dollars
Standard Deviation 3,866.51
|
3,261.20 dollars
Standard Deviation 13,966.79
|
3,239.53 dollars
Standard Deviation 4,890.32
|
3,588.33 dollars
Standard Deviation 4,787.32
|
PRIMARY outcome
Timeframe: Month 12 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)Population: Analysis was performed on all participants included in the study.
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 12 post-index date.
Outcome measures
| Measure |
Tofacitinib XR
n=349 Participants
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
|
Tofacitinib IR
n=304 Participants
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
|
Adalimumab
n=2728 Participants
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor \[TNFI\]) during identification period were included in this arm.
|
Certolizumab Pegol
n=192 Participants
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
|
Etanercept
n=1948 Participants
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
|
Infliximab
n=349 Participants
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
|
Golimumab
n=376 Participants
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
|
Rituximab
n=325 Participants
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
|
Tocilizumab
n=204 Participants
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
|
Abatacept
n=533 Participants
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Total RA Related Monthly Health Care Cost at Month 12 Post Index Date
|
3,971.99 dollars
Standard Deviation 7,435.02
|
2,929.00 dollars
Standard Deviation 3,457.82
|
4,018.90 dollars
Standard Deviation 5,462.12
|
2,772.76 dollars
Standard Deviation 3,617.79
|
3,645.36 dollars
Standard Deviation 4,613.68
|
2,812.13 dollars
Standard Deviation 4,641.79
|
2,169.49 dollars
Standard Deviation 3,163.67
|
2,441.00 dollars
Standard Deviation 14,133.28
|
2,389.17 dollars
Standard Deviation 2,778.68
|
3,655.69 dollars
Standard Deviation 5,469.38
|
Adverse Events
Tofacitinib XR
Tofacitinib IR
Adalimumab
Certolizumab Pegol
Etanercept
Infliximab
Golimumab
Rituximab
Tocilizumab
Abatacept
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee Pfizer has the right to review disclosures, requesting a delay of less than 60 days. Investigator will postpone single center publications until after disclosure of pooled data (all sites), less than 12 months from study completion/termination at all participating sites. Investigator may not disclose previously undisclosed confidential information other than study results.
- Publication restrictions are in place
Restriction type: OTHER