OPUM: Quantity of Opioids for Acute Pain and Limit Unused Medication
Study Details
Study Description
Brief Summary
Opioids (morphine and morphine-like substances) are often prescribed to patients to manage pain after an emergency department visit. In the past 20 years, opioid prescriptions have risen sharply, accompanied by a significant rise in opioid misuse (e.g., recreational or non-medical use, potentially leading to addiction or overdose). One explanation for this crisis is the availability and easy access of leftover opioid pills in Canadian homes, allowing family members (including children) and friends to take them for reasons other than pain relief.
Canada has no recommendations for the dosage, duration, or quantity of opioids that physicians should prescribe to manage acute pain at home. Physicians are therefore left guessing as to how much to prescribe when a patient with a condition like a fracture or renal colic is discharged from the emergency department. Our preliminary study showed that two-thirds of the pills from the initial opioid prescription to treat acute pain actually remained unused and were therefore available for potential misuse.
The investigators propose to determine how many opioid pills are consumed by patients who suffer from acute pain as they recover at home. The investigators will ask 2,580 patients (from 6 Canadian hospitals) to record their pain medication consumption in a 14-day diary. The investigators will also determine, their pain intensity level, whether or not they had new opioid prescriptions, and health services revisits. In case of missing information, patients will be contacted by phone at 2 weeks. The overall aim is to help emergency department physicians prescribe the right number of pills in order to manage patients' pain and at the same time reduce substantially leftovers available for potential misuse.
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Detailed Description
Introduction
Prescription opioid overdoses have quadrupled in the last 15 years, and are now the leading cause of accidental death, surpassing motor vehicle accidents. The drastic rise in opioid prescription rates in Canada and the US could be the driving force behind this higher mortality. It was shown that 71% of opioid misusers (i.e., intentional users for nonmedical purposes) received their drugs through the diversion of unused prescribed opioids (transfer of opioids to someone other than the holder of the initial prescription). Emergency department (ED) physicians are among the top opioid prescribers for patients under 40, and there are currently no prospective studies on how many opioid pills should be prescribed to patients discharged from the ED with common pain conditions in order to limit unused pills. Preliminary results from our group revealed that two-thirds of the total prescribed opioids were not consumed and remained available for misuse.
Objectives
The ultimate goal of this research program is to decrease opioid misuse by lowering the quantity of unused medications. The primary objective of this project is to determine the quantity of opioids consumed during the acute pain phase (2 weeks) by ED-discharged patients treated for an acute pain condition. The secondary objectives are to inventory the quantity of opioids prescribed and unused after ED visits, use of co-analgesics, pain intensity, health services revisits during the 2-week follow-up, and chronic pain prevalence at 3 months.
Methods
The investigators propose a multicentre prospective observational cohort study in 2,580 consecutive ED patients recruited from 6 Canadian hospitals. The study will include patients aged ≥18 years, treated for an acute pain condition present for less than 2 weeks (usual acute pain definition), and discharged from the ED with an opioid prescription. Pain at triage and at ED discharged, diagnosis, and complete pain medication prescription will be initially listed. Patients will complete a 14-day electronic diary using the REDCap web-based system to document their daily pain medication consumption, pain intensity, new opioid prescriptions, and health services revisits. Patients will also answer questionnaires at 2 weeks and 3 months for our various secondary objectives. To validate the patient self-report opioid consumption, a randomized subset of patients will come back to the emergency for a follow-up visit and a manual count of the remaining opioids. As mitigation strategies (validated in our pilot study), non-responders to the diary will be contacted by phone at 2 weeks to answered questions summing diary information, and paper versions will be available for patients without Internet access.
Feasibility
The investigators demonstrated the study feasibility in a successful pilot study with 627 patients at our academic ED. Additionally, our project brings together a committed, multidisciplinary research team, and all proposed study sites have collaborated previously on large multicentre studies. Finally, all instruments have been successfully tested, allowing rapid study implementation.
Impact
Our results will determine the quantity of opioids consumed during the acute pain phase (2 weeks) to ED-discharged patients treated for acute pain conditions. Our team members from relevant provincial and national stakeholders and patient associations, our strong evidence, and our extensive knowledge transfer strategy have the potential to impact physicians' opioid prescription practices. Consequently, fewer unused prescription opioids should lead to a substantial decrease in the currently high rate of opioid misuse.
Study Design
Outcome Measures
Primary Outcome Measures
- Quantity of opioids consumed during the acute pain phase (2 weeks) following ED discharge for each pain condition [During 14 days]
This will allow us to define the quantity of opioids needed to manage acute pain while limiting the quantity of unused pills available for potential misuse.
Secondary Outcome Measures
- Quantity of opioids prescribed to ED-discharged patients treated for different acute pain conditions [Baseline]
From physicians' prescriptions
- Quantity of opioids to sufficiently supply a given percentage of patients for each pain condition [During 14 days]
Patient's questionnaire after 2 weeks and 14-diary on opioids consumption.
- Quantity of unused opioids [At day 14]
Patient's questionnaire after 2 weeks
- Quantity of patients that filled (initial or other) opioid prescriptions [At day 14]
Patient's questionnaire after 2 weeks
- Quantity of patients using of coanalgesics or other substances (alcohol, cannabis…) to manage pain [During 14 days]
Patient's questionnaire after 2 weeks
- Qualitative evaluation of the participants' reasons for stopping opioid consumption [During 14 days]
Patient's questionnaire after 2 weeks
- Incidence and type of medication side effects during the 2-week period [During 14 days]
Patient's questionnaire after 2 weeks
- Quantity of patients who revisit health services to obtain new prescription [During 14 days]
Patient's questionnaire after 2 weeks
- Quantitive validation of the patients' self-report opioid consumption [At day 14]
Comparison of self-report comsumption and in person pill count after 2 weeks
- Group-based trajectory modeling to determine pain intensity trajectory for each pain condition during the acute phase [During 14 days]
After 2 weeks. Average pain intensity for each patient will be measured using a 0-10 numerical rating scale for each of the 14-day diary. Group-based trajectory modeling will then be used to identify groups of patients with similar pattern of pain evolution over time without assuming the existence of a specific trend or number of groups.
- Evaluate the chronic pain prevalence at 3 months among study participants assessed if certain profiles of pain intensity evolution over the14-day after emergency department (ED) discharge are predictive of chronic pain 3 months later. [3 months]
After 90 days. Chronic pain will be defined as a pain intensity score at 3-month of >=4 and with moderate or severe functional disability using the pain disability index score (>40).
- Assessed if certain profiles of pain intensity evolution over the14-day after emergency department (ED) discharge are predictive of chronic pain 3 months later [3 months]
Pain intensity trajectories after 14 days and chronic pain at 3 months. Average pain intensity for each patient will be measured using a 0-10 numerical rating scale for each of the 14-day diary. Group-based trajectory modeling will then be used to identify groups of patients with similar pattern of pain evolution over time without assuming the existence of a specific trend or number of groups. Chronic pain will be defined as a pain intensity score at 3-month of >=4 and with moderate or severe functional disability using the pain disability index score (>40).
Other Outcome Measures
- Qualitative evaluation of participant's opioids storage and disposal [At day 14]
Patient's questionnaire after 2 weeks
- Evaluate the participants' perception of opioid analgesia (patient, physician, nurse, and pharmacist) with a likert scale type survey [Baseline]
Survey with Likert style questions administered before start of recruitment
Eligibility Criteria
Criteria
Inclusion Criteria:
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Opioid prescription at discharge
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Acute pain for less than 2 weeks
Exclusion Criteria:
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Language barrier
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Chronic pain under treatment
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Active Neoplasia
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Follow-up impossible / Unable to complete agenda
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Already on opioids
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Kingston General Hospital | Kingston | Ontario | Canada | K7L 2V7 |
| 2 | Sunnybrook Health Sciences Centre | Toronto | Ontario | Canada | M4N 3M5 |
| 3 | Hôpital Maisonneuve-Rosemont | Montréal | Quebec | Canada | H1T 2M4 |
| 4 | Hôpital du Sacré-Coeur de Montréal | Montréal | Quebec | Canada | H4J 1C4 |
| 5 | Hôpital régional de Saint-Jérôme | Saint-Jérôme | Quebec | Canada | J7Z 5T3 |
| 6 | Hôpital de l'Enfant-Jésus | Québec | Canada | G1J 1Z4 |
Sponsors and Collaborators
- Hopital du Sacre-Coeur de Montreal
- Kingston Health Sciences Centre
- Maisonneuve-Rosemont Hospital
- Sunnybrook Health Sciences Centre
- Hopital de l'Enfant-Jesus
Investigators
- Principal Investigator: Raoul Daoust, MD MSc, Université de Montréal
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2019-1684
- PJT-159808