Do interruptions to the continuity of methadone maintenance treatment in specialist addiction settings increase the risk of drug-related poisoning deaths? A retrospective cohort study
Autor: | Benedict K. Ryan, Gráinne Cousins, Kathleen Bennett, Denis O'Driscoll, Louise Durand, Tom Fahey, Eamon Keenan, Fiona Boland, Joseph Barry |
---|---|
Rok vydání: | 2019 |
Předmět: |
Adult
Male Narcotics Patient Transfer Research Report medicine.medical_specialty Methadone maintenance Population 030508 substance abuse Medicine (miscellaneous) opioid substitution treatment Cohort Studies 03 medical and health sciences 0302 clinical medicine Risk Factors drug‐related poisoning mortality Internal medicine Cause of Death medicine Risk of mortality Opiate Substitution Treatment Humans 030212 general & internal medicine education Retrospective Studies education.field_of_study business.industry All‐cause mortality Mortality rate Retrospective cohort study Opioid use disorder Research Reports Middle Aged medicine.disease Opioid-Related Disorders Psychiatry and Mental health methadone maintenance treatment Relative risk Female opioid‐use disorder Drug Overdose 0305 other medical science business heroin Ireland transfer Methadone medicine.drug |
Zdroj: | Addiction (Abingdon, England) |
ISSN: | 1360-0443 |
Popis: | Aims To examine the risk of mortality associated with interruptions to the continuity of methadone maintenance treatment (MMT), including transfers between services, in opioid‐dependent individuals attending specialist addiction services. Design Retrospective cohort study using addiction services and primary care dispensing records, the National Methadone Register and National Drug‐Related Death Index (NDRDI). Setting Geographically defined population in Dublin, Ireland. Participants A total of 2899 people prescribed and dispensed methadone in specialist addiction services between January 2010 and December 2015. There were five exposure groups: weeks 1–4 following transfer between treatment providers; weeks 1–4 out of treatment; weeks 5–52 out of treatment; weeks 1–4 of treatment initiation; and weeks 5+ of continuous treatment (reference category). Measurements Primary outcome: drug‐related poisoning (DRP) deaths. Secondary outcome: all‐cause mortality (ACM). Mortality rates calculated by dividing number of deaths (DRP; ACM) in exposure groups by person‐years exposure. Unadjusted and adjusted Poisson regression (covariates age, sex, incarceration, methadone dose and comorbidities) estimated differences in mortality rates. Findings There were 154 ACM deaths, 55 (35.7%) identified as DRP deaths. No deaths were observed in the first month following transfer between treatment providers. The risk of DRP mortality was highest in weeks 1–4 out of treatment [adjusted relative risk (aRR = 4.04, 95% confidence interval (CI) = 1.43–11.43, P = 0.009] and weeks 1–4 of treatment initiation (ARR = 3.4, 95% CI = 1.2–9.64, P = 0.02). Similarly, risk of ACM was highest in weeks 1–4 out of treatment (ARR = 11.78, 95% CI = 7.73–17.94, P |
Databáze: | OpenAIRE |
Externí odkaz: |