Trial Outcomes & Findings for Opioid Use After Thyroid and Parathyroid Surgeries (NCT NCT04955444)

NCT ID: NCT04955444

Last Updated: 2023-09-05

Results Overview

Proportion of patients who receive new opioid discharge prescriptions at discharge following a thyroidectomy or parathyroidectomy procedure. This outcome excludes continuation of previous, chronic opioid therapy.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

240 participants

Primary outcome timeframe

Up to 2 days

Results posted on

2023-09-05

Participant Flow

Participant milestones

Participant milestones
Measure
Historical Control Group
The historical control group underwent a thyroidectomy or parathyroidectomy procedure prior to implementation of the quality improvement bundle.
Post-implementation Group
The post-implementation group underwent a thyroidectomy or parathyroidectomy procedure after bundle implementation and received care that is enhanced by the quality improvement bundle. Quality improvement bundle: The quality improvement bundle consists of (1) patient education, (2) provider education, and (3) EHR enhancements including order sets and best practice alerts.
Overall Study
STARTED
160
80
Overall Study
COMPLETED
160
80
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Opioid Use After Thyroid and Parathyroid Surgeries

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Historical Control Group
n=160 Participants
The historical control group underwent a thyroidectomy or parathyroidectomy procedure prior to implementation of the quality improvement bundle.
Post-implementation Group
n=80 Participants
The post-implementation group underwent a thyroidectomy or parathyroidectomy procedure after bundle implementation and received care that is enhanced by the quality improvement bundle. Quality improvement bundle: The quality improvement bundle consists of (1) patient education, (2) provider education, and (3) EHR enhancements including order sets and best practice alerts.
Total
n=240 Participants
Total of all reporting groups
Age, Continuous
56 years
STANDARD_DEVIATION 14 • n=99 Participants
57 years
STANDARD_DEVIATION 14 • n=107 Participants
57 years
STANDARD_DEVIATION 14 • n=206 Participants
Sex: Female, Male
Female
132 Participants
n=99 Participants
65 Participants
n=107 Participants
197 Participants
n=206 Participants
Sex: Female, Male
Male
28 Participants
n=99 Participants
15 Participants
n=107 Participants
43 Participants
n=206 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
21 Participants
n=99 Participants
14 Participants
n=107 Participants
35 Participants
n=206 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
139 Participants
n=99 Participants
66 Participants
n=107 Participants
205 Participants
n=206 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race/Ethnicity, Customized
Race · White
109 Participants
n=99 Participants
49 Participants
n=107 Participants
158 Participants
n=206 Participants
Race/Ethnicity, Customized
Race · Black or African American
33 Participants
n=99 Participants
23 Participants
n=107 Participants
56 Participants
n=206 Participants
Race/Ethnicity, Customized
Race · Asian
10 Participants
n=99 Participants
6 Participants
n=107 Participants
16 Participants
n=206 Participants
Race/Ethnicity, Customized
Race · Other
8 Participants
n=99 Participants
2 Participants
n=107 Participants
10 Participants
n=206 Participants
Opioid use within 1 week prior to surgery
8 Participants
n=99 Participants
2 Participants
n=107 Participants
10 Participants
n=206 Participants
Surgery performed
Parathyroidectomy
82 Participants
n=99 Participants
39 Participants
n=107 Participants
121 Participants
n=206 Participants
Surgery performed
Thyroidectomy
90 Participants
n=99 Participants
46 Participants
n=107 Participants
136 Participants
n=206 Participants

PRIMARY outcome

Timeframe: Up to 2 days

Proportion of patients who receive new opioid discharge prescriptions at discharge following a thyroidectomy or parathyroidectomy procedure. This outcome excludes continuation of previous, chronic opioid therapy.

Outcome measures

Outcome measures
Measure
Historical Control Group
n=160 Participants
The historical control group underwent a thyroidectomy or parathyroidectomy procedure prior to implementation of the quality improvement bundle.
Post-implementation Group
n=80 Participants
The post-implementation group underwent a thyroidectomy or parathyroidectomy procedure after bundle implementation and received care that is enhanced by the quality improvement bundle. Quality improvement bundle: The quality improvement bundle consists of (1) patient education, (2) provider education, and (3) EHR enhancements including order sets and best practice alerts.
New Opioid Discharge Prescriptions
128 Participants
28 Participants

SECONDARY outcome

Timeframe: Up to 2 days

Proportion of thyroidectomy and parathyroidectomy postoperative patients with opioid discharge prescriptions exceeding the recommended dose of 112.5 oral MMEs

Outcome measures

Outcome measures
Measure
Historical Control Group
n=160 Participants
The historical control group underwent a thyroidectomy or parathyroidectomy procedure prior to implementation of the quality improvement bundle.
Post-implementation Group
n=80 Participants
The post-implementation group underwent a thyroidectomy or parathyroidectomy procedure after bundle implementation and received care that is enhanced by the quality improvement bundle. Quality improvement bundle: The quality improvement bundle consists of (1) patient education, (2) provider education, and (3) EHR enhancements including order sets and best practice alerts.
Opioid Discharge Prescriptions Exceeding 112.5 Oral Morphine Milligram Equivalents (MMEs)
52 Participants
8 Participants

SECONDARY outcome

Timeframe: Up to 2 days

Proportion of thyroidectomy and parathyroidectomy postoperative patients with opioid discharge prescriptions exceeding 5 days of therapy

Outcome measures

Outcome measures
Measure
Historical Control Group
n=160 Participants
The historical control group underwent a thyroidectomy or parathyroidectomy procedure prior to implementation of the quality improvement bundle.
Post-implementation Group
n=80 Participants
The post-implementation group underwent a thyroidectomy or parathyroidectomy procedure after bundle implementation and received care that is enhanced by the quality improvement bundle. Quality improvement bundle: The quality improvement bundle consists of (1) patient education, (2) provider education, and (3) EHR enhancements including order sets and best practice alerts.
Opioid Discharge Prescriptions Exceeding 5 Days
27 Participants
5 Participants

SECONDARY outcome

Timeframe: Up to 7 days

Proportion of thyroidectomy and parathyroidectomy postoperative patients who receive new opioid prescriptions from the surgeon's office within 7 days of surgery including discharge prescriptions. This outcome excludes continuation of previous, chronic opioid therapy.

Outcome measures

Outcome measures
Measure
Historical Control Group
n=160 Participants
The historical control group underwent a thyroidectomy or parathyroidectomy procedure prior to implementation of the quality improvement bundle.
Post-implementation Group
n=80 Participants
The post-implementation group underwent a thyroidectomy or parathyroidectomy procedure after bundle implementation and received care that is enhanced by the quality improvement bundle. Quality improvement bundle: The quality improvement bundle consists of (1) patient education, (2) provider education, and (3) EHR enhancements including order sets and best practice alerts.
New Opioid Prescriptions From the Surgeon's Office Within 7 Days of Surgery
0 Participants
0 Participants

SECONDARY outcome

Timeframe: Up to 2 days

Proportion of thyroidectomy and parathyroidectomy postoperative patients with opioid prescriptions exceeding 50 oral MMEs/day when new, postoperative discharge prescriptions are added to existing opioid therapy

Outcome measures

Outcome measures
Measure
Historical Control Group
n=160 Participants
The historical control group underwent a thyroidectomy or parathyroidectomy procedure prior to implementation of the quality improvement bundle.
Post-implementation Group
n=80 Participants
The post-implementation group underwent a thyroidectomy or parathyroidectomy procedure after bundle implementation and received care that is enhanced by the quality improvement bundle. Quality improvement bundle: The quality improvement bundle consists of (1) patient education, (2) provider education, and (3) EHR enhancements including order sets and best practice alerts.
Opioid Prescriptions Exceeding 50 Oral MMEs/Day When New Discharge Prescriptions Are Added to Existing Opioid Therapy
9 Participants
0 Participants

Adverse Events

Historical Control Group

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

Post-implementation Group

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

Elsie Rizk

The Methodist Hospital Research Institute

Phone: 7134412557

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place