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.

Recruitment status

COMPLETED

Target enrollment

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)

Results posted on

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Tofacitinib IR

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Adalimumab

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Certolizumab Pegol

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Etanercept

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Infliximab

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Golimumab

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Rituximab

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Tocilizumab

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Abatacept

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Pfizer ClinicalTrials.gov Call Center

Pfizer Inc.

Phone: 1-800-718-1021

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