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Grant: Project Grant

University of British Columbia

$1,184,681.00

Evaluating Microdosing in Emergency Departments: A Randomized Controlled Trial Comparing the Effectiveness of Buprenorphine/Naloxone Microdosing vs. Standard Dosing (EMED Study)

EF 2021-22

Résumé
Buprenorphine/naloxone (commonly known as Suboxone) is a life-saving medication for people with opioid addiction. Studies show that Suboxone works when started from emergency departments (EDs), which is important because many people make ED visits before they overdose. However, Suboxone is hard to start, because it can cause people to experience bad withdrawal symptoms (vomiting, sweating, pain) if it is started too soon after a person has used other opioids like heroin or morphine. This is called precipitated withdrawal and makes many people afraid of starting Suboxone at all. To prevent this complication, doctors tell patients to wait for 12-24 hours since they last used other opioids and to already be in withdrawal before starting, which is very uncomfortable for patients. A new method, called microdosing, tries to improve patient comfort by avoiding precipitated withdrawal and withdrawal altogether. This method starts people on very small Suboxone doses that gradually increase while they continue to use other opioids. Microdosing has never been evaluated in a formal study. This study will identify adult patients with opioid addiction in EDs in BC and Alberta. We will provide them with either take-home Suboxone microdosing or standard dosing packages to start after they are discharged. We will look at whether patients who receive microdosing are more likely to stay on Suboxone than those who receive a standard dosing package. We will also look at whether people who receive microdosing are more likely to take any opioid agonist therapy in the future, and we will compare deaths, overdoses, and healthcare use between the groups. We are working with health regions, provincial policy makers, public health, and people with lived experience with opioid use to make sure that we share our findings with EDs and patients across Canada. We hope that EDs will use our study results to develop Suboxone programs that are most likely to help patients at risk for overdose.
Programme
Project Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
443382
Name
Moe Jessica
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Clinical
Prcname2
Randomized Controlled Trials 2
Projecttitle
Evaluating Microdosing in Emergency Departments: A Randomized Controlled Trial Comparing the Effectiveness of Buprenorphine/Naloxone Microdosing vs. Standard Dosing (EMED Study)
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$1,184,681
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Buprenorphine/Naloxone; Emergency Departments; Opioid-Related Disorders; Randomized Controlled Trial
Abstract
Buprenorphine/naloxone (commonly known as Suboxone) is a life-saving medication for people with opioid addiction. Studies show that Suboxone works when started from emergency departments (EDs), which is important because many people make ED visits before they overdose. However, Suboxone is hard to start, because it can cause people to experience bad withdrawal symptoms (vomiting, sweating, pain) if it is started too soon after a person has used other opioids like heroin or morphine. This is called precipitated withdrawal and makes many people afraid of starting Suboxone at all. To prevent this complication, doctors tell patients to wait for 12-24 hours since they last used other opioids and to already be in withdrawal before starting, which is very uncomfortable for patients. A new method, called microdosing, tries to improve patient comfort by avoiding precipitated withdrawal and withdrawal altogether. This method starts people on very small Suboxone doses that gradually increase while they continue to use other opioids. Microdosing has never been evaluated in a formal study. This study will identify adult patients with opioid addiction in EDs in BC and Alberta. We will provide them with either take-home Suboxone microdosing or standard dosing packages to start after they are discharged. We will look at whether patients who receive microdosing are more likely to stay on Suboxone than those who receive a standard dosing package. We will also look at whether people who receive microdosing are more likely to take any opioid agonist therapy in the future, and we will compare deaths, overdoses, and healthcare use between the groups. We are working with health regions, provincial policy makers, public health, and people with lived experience with opioid use to make sure that we share our findings with EDs and patients across Canada. We hope that EDs will use our study results to develop Suboxone programs that are most likely to help patients at risk for overdose.
Competitiondate
202104
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Moe, Jessica; Carter, Connie I; Davison, Carolyn; Hohl, Corinne M; Holroyd, Brian R; Lock, Kurt; Nosyk, Bohdan P; Slaunwhite, Amanda K; Wong, Hubert H
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $1,184,681~ $0~