Grant: CIHR Fellowship
University of British Columbia
$140,000.00
Does initiation of outpatient opioid agonist therapy after hospital departure reduce overdose risk? A target trial emulation study
EF 2024-25
Résumé
The opioid epidemic is a critical public health issue in Canada, particularly in British Columbia (BC), where overdose events have surged, exceeding 16,000 in 2023 alone. Individuals with opioid use disorder (OUD) face heightened risks of overdose in the vulnerable period following hospital discharge. Our research indicates that patients who depart the hospital "before medically advised" (BMA) are about ten times more likely to experience an overdose in the first 30 days post-discharge compared to physician-advised discharges. Alarmingly, BMA discharges are three times more frequent among OUD patients and have risen in recent years, yet effective support for these individuals remains scarce. This proposal aims to determine whether initiating opioid agonist therapy (OAT) within seven days after hospital discharge can reduce the risk of overdose among patients with opioid use disorder. We will examine both physician-advised discharges and BMA discharges. OAT, which includes medications like methadone and Suboxone, has been shown to significantly lower drug-related mortality rates. Our study will analyze approximately 180,000 physician-advised and 6,000 BMA discharges using a comprehensive dataset from BC's Provincial Overdose Cohort. We will use a new technique called target trial emulation, which involves applying the principles of a randomized clinical trial to real-world data. By addressing biases through advanced statistical methods, we aim to provide robust evidence on the effectiveness of OAT for improving patient outcomes. Ultimately, this research seeks to inform healthcare practices and policies, potentially leading to better support for individuals at high risk of overdose during the critical post-discharge period.
Programme
CIHR Fellowship
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
513426
Name
Naik Hiten
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Population and Public Health
Theme2
Social / Cultural / Environmental / Population Health
Prcname2
Health Research Training B - HP
Projecttitle
Does initiation of outpatient opioid agonist therapy after hospital departure reduce overdose risk? A target trial emulation study
Programtype2
Fellowship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$140,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Addiction; Before Medically Advised Discharge; Drug Overdose; Transitions In Care
Abstract
The opioid epidemic is a critical public health issue in Canada, particularly in British Columbia (BC), where overdose events have surged, exceeding 16,000 in 2023 alone. Individuals with opioid use disorder (OUD) face heightened risks of overdose in the vulnerable period following hospital discharge. Our research indicates that patients who depart the hospital "before medically advised" (BMA) are about ten times more likely to experience an overdose in the first 30 days post-discharge compared to physician-advised discharges. Alarmingly, BMA discharges are three times more frequent among OUD patients and have risen in recent years, yet effective support for these individuals remains scarce. This proposal aims to determine whether initiating opioid agonist therapy (OAT) within seven days after hospital discharge can reduce the risk of overdose among patients with opioid use disorder. We will examine both physician-advised discharges and BMA discharges. OAT, which includes medications like methadone and Suboxone, has been shown to significantly lower drug-related mortality rates. Our study will analyze approximately 180,000 physician-advised and 6,000 BMA discharges using a comprehensive dataset from BC's Provincial Overdose Cohort. We will use a new technique called target trial emulation, which involves applying the principles of a randomized clinical trial to real-world data. By addressing biases through advanced statistical methods, we aim to provide robust evidence on the effectiveness of OAT for improving patient outcomes. Ultimately, this research seeks to inform healthcare practices and policies, potentially leading to better support for individuals at high risk of overdose during the critical post-discharge period.
Competitiondate
202410
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Naik, Hiten
Approvedterm
2 ans 0 mois
Cihrcontribution2
~ $140,000~ $0~