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N/A N=240 Health Services Research

Opioid Use After Thyroid and Parathyroid Surgeries

Thyroidectomy · Parathyroidectomy · Opioid Use · Pain, Postoperative

Enrolled (actual)
240
Serious AEs
Results posted
Sep 2023
Primary outcome: Primary: New Opioid Discharge Prescriptions — 128; 28 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Quality improvement bundle (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
The Methodist Hospital Research Institute
Primary completion
Dec 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
New Opioid Discharge Prescriptions
128; 28
SECONDARY
Opioid Discharge Prescriptions Exceeding 112.5 Oral Morphine Milligram Equivalents (MMEs)
52; 8
SECONDARY
Opioid Discharge Prescriptions Exceeding 5 Days
27; 5
SECONDARY
New Opioid Prescriptions From the Surgeon's Office Within 7 Days of Surgery
0; 0
SECONDARY
Opioid Prescriptions Exceeding 50 Oral MMEs/Day When New Discharge Prescriptions Are Added to Existing Opioid Therapy
9; 0

Summary

Unnecessary opioid prescriptions for postoperative pain can increase the risk for new, persistent opioid use and dependence. Published literature suggests that most patients undergoing thyroid or parathyroid surgery can have their pain effectively managed without opioids following hospital discharge. The purpose of this quasi-experimental, quality improvement study is to develop, implement, and measure the impact of a quality improvement bundle that consists of (1) patient education, (2) provider education, and (3) electronic health record (EHR) enhancements. The proportion of patients who receive new opioid discharge prescriptions for pain management following thyroid or parathyroid surgery at Houston Methodist Hospital for up to 6 months following bundle implementation will be compared to a historical control group.

Eligibility Criteria

Inclusion Criteria

  • Adult patients undergoing a primary thyroidectomy or parathyroidectomy procedure at Houston Methodist Hospital during the study period. Only index surgeries during the study time frame were included.

Exclusion Criteria

  • Patients with a hospital length of stay after surgery >2 days
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04955444). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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