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Multicenter Study
. 2024 Jul 14;196(25):E866-E874.
doi: 10.1503/cmaj.231640.

Opioid prescribing requirements to minimize unused medications after an emergency department visit for acute pain: a prospective cohort study

Affiliations
Multicenter Study

Opioid prescribing requirements to minimize unused medications after an emergency department visit for acute pain: a prospective cohort study

Raoul Daoust et al. CMAJ. .

Abstract

Background: Unused opioid prescriptions can be a driver of opioid misuse. Our objective was to determine the optimal quantity of opioids to prescribe to patients with acute pain at emergency department discharge, in order to meet their analgesic needs while limiting the amount of unused opioids.

Methods: In a prospective, multicentre cohort study, we included consecutive patients aged 18 years and older with an acute pain condition present for less than 2 weeks who were discharged from emergency department with an opioid prescription. Participants completed a pain medication diary for real-time recording of quantity, doses, and names of all analgesics consumed during a 14-day follow-up period.

Results: We included 2240 participants, who had a mean age of 51 years; 48% were female. Over 14 days, participants consumed a median of 5 (quartiles, 1-14) morphine 5 mg tablet equivalents, with significant variation across pain conditions (p < 0.001). Most opioid tablets prescribed (63%) were unused. To meet the opioid need of 80% of patients for 2 weeks, we found that those experiencing renal colic or abdominal pain required fewer opioid tablets (8 morphine 5 mg tablet equivalents) than patients who had fractures (24 tablets), back pain (21 tablets), neck pain (17 tablets), or other musculoskeletal pain (16 tablets).

Interpretation: Two-thirds of opioid tablets prescribed at emergency department discharge for acute pain were unused, whereas opioid requirements varied significantly based on the cause of acute pain. Smaller, cause-specific opioid prescriptions could provide adequate pain management while reducing the risk of opioid misuse.

Trial registration: ClinicalTrials.gov, no. NCT03953534.

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Conflict of interest statement

Competing interests:: Justin Yan reports receiving funding from the Spring 2021 Innovation Fund from the Academic Medical Organization of Southwestern Ontario, and the 2021 Internal Research Fund for Pilot Studies from the Lawson Health Research Institute. Dr. Yan has also served as the chair of the data safety monitoring boards of the RAFF4 Study and the REMOSYNCED Study, and vice-chair of the Canadian Association of the Emergency Physicians Research Committee. Jeffrey Perry reports receiving a peer review salary support grant from the Heart and Stroke Foundation of Ontario. Gilles Lavigne reports receiving consulting fees from Straumann Suisse related to a sleep bruxism device, and an oral appliance for sleep apnea from Panthera Dental. Dr. Lavigne is also a board member of the Canadian Academy of Health Sciences. No other competing interests were declared.

Figures

Figure 1:
Figure 1:
Flow chart of patient enrolment in the study. Note: ED = emergency department.
Figure 2:
Figure 2:
Number of morphine 5 mg tablet equivalents to prescribe to meet the needs of 80% of patients for 14 days and for 7 days for each pain condition category.
Figure 3:
Figure 3:
Cumulative distribution of quantity of 5 mg morphine tablet equivalents to prescribe to meet the need of patients with (A) renal colic, abdominal pain, and other pain conditions, and (B) fracture, back pain, neck pain, and other musculoskeletal pain.
Figure 4:
Figure 4:
Percentage of morphine 5 mg tablet equivalents that remained unused after the 2-week follow-up for each pain condition category. Note: Mean ± standard error of the mean is reported.
Figure 5:
Figure 5:
Percentage of patients consuming opioids, nonsteroidal anti-inflammatory drugs (NSAIDs), and acetaminophen for each day of the 14-day follow-up after emergency department (ED) discharge. Data extracted from diary only (1798 patients).

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