TY - JOUR
T1 - The impact of opioid agonist treatment on fatal and non-fatal drug overdose among people with a history of opioid dependence in NSW, Australia, 2001–2018
T2 - Findings from the OATS retrospective linkage study
AU - Jones, Nicola R.
AU - Hickman, Matthew
AU - Nielsen, Suzanne
AU - Larney, Sarah
AU - Dobbins, Timothy
AU - Ali, Robert
AU - Degenhardt, Louisa
N1 - Funding Information:
SL is supported by a Fonds de recherche du Qu?bec ? Sant??career award (#296569). MH acknowledges funding from NIHR Health Protection Research Unit (HPRU) in Behavioural Science and Evaluation, NIHR School of Public Health Research (SPHR), and NIHR Biomedical Research Centre (BRC) at Bristol. This paper presents independent research. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care. The OATS study is funded by the National Institutes of Health (R01 DA144740 PI: Degenhardt). SN and LD are supported by Australian National Health and Medical Research Council Research Fellowships [1135991,1163961]. NDARC is supported by funding from the Australian Government Department of Health under the Drug and Alcohol Program.
Funding Information:
SL is supported by a Fonds de recherche du Québec – Santé career award ( #296569 ). MH acknowledges funding from NIHR Health Protection Research Unit ( HPRU ) in Behavioural Science and Evaluation, NIHR School of Public Health Research (SPHR), and NIHR Biomedical Research Centre (BRC) at Bristol. This paper presents independent research. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care. The OATS study is funded by the National Institutes of Health ( R01 DA144740 PI: Degenhardt). SN and LD are supported by Australian National Health and Medical Research Council Research Fellowships [ 1135991 , 1163961 ]. NDARC is supported by funding from the Australian Government Department of Health under the Drug and Alcohol Program.
Funding Information:
This work was supported by the National Institutes of Health (R01 DA144740 PI: Degenhardt). SN and LD are supported by Australian National Health and Medical Research Council Research Fellowships (grant numbers 1163961, 1135991). The National Drug and Alcohol Research Centre is supported by funding from the Australian Government Department of Health under the Drug and Alcohol Program. SL is supported by a Fonds de recherche du Québec – Santé career award (#296569). MH acknowledges funding from NIHR Health Protection Research Unit (HPRU) in Behavioural Science and Evaluation, NIHR School of Public Health Research (SPHR), and NIHR Biomedical Research Centre (BRC) at Bristol. This paper presents independent research. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care.
Publisher Copyright:
© 2022
PY - 2022/7/1
Y1 - 2022/7/1
N2 - Background: There are critical periods of mortality risk at onset and cessation of opioid agonist treatment. We aim to determine whether non-fatal overdose followed the same pattern as fatal overdose, comparing the first 4 weeks of treatment and treatment cessation and the remainder time off treatment, with the remainder treatment time, to determine intervention markers. Methods: Retrospective cohort study of people with a history of opioid agonist treatment using linked New South Wales data. The incidence of non-fatal overdose hospitalization; emergency department presentation; and fatal overdose from national death records were compared. Rates were calculated using generalized estimating equations adjusting for demographics, year, and recent health and incarceration events. Results: The remainder time in OAT had the lowest incidence of overdose for all outcomes and is the reference level for the adjusted incident rate ratios (aIRR). Fatal overdose was lowest in treatment and highest in the first four weeks out of treatment, aIRR of 12.83 (95% CI 10.0–16.4). Whereas the highest overdose rate for non-fatal opioid overdose was in the first four weeks in treatment, aIRR of 3.11 (95% CI 2.19–4.42). Conclusions: Retention on opioid agonist treatment is protective against drug related overdose. There is elevated risk of non-fatal overdose at treatment initiation that is not evident for fatal overdose, but the first month of treatment cessation is a critical period for both non-fatal and fatal overdose. These findings emphasize the importance of treatment retention and interventions for polysubstance overdose at cessation.
AB - Background: There are critical periods of mortality risk at onset and cessation of opioid agonist treatment. We aim to determine whether non-fatal overdose followed the same pattern as fatal overdose, comparing the first 4 weeks of treatment and treatment cessation and the remainder time off treatment, with the remainder treatment time, to determine intervention markers. Methods: Retrospective cohort study of people with a history of opioid agonist treatment using linked New South Wales data. The incidence of non-fatal overdose hospitalization; emergency department presentation; and fatal overdose from national death records were compared. Rates were calculated using generalized estimating equations adjusting for demographics, year, and recent health and incarceration events. Results: The remainder time in OAT had the lowest incidence of overdose for all outcomes and is the reference level for the adjusted incident rate ratios (aIRR). Fatal overdose was lowest in treatment and highest in the first four weeks out of treatment, aIRR of 12.83 (95% CI 10.0–16.4). Whereas the highest overdose rate for non-fatal opioid overdose was in the first four weeks in treatment, aIRR of 3.11 (95% CI 2.19–4.42). Conclusions: Retention on opioid agonist treatment is protective against drug related overdose. There is elevated risk of non-fatal overdose at treatment initiation that is not evident for fatal overdose, but the first month of treatment cessation is a critical period for both non-fatal and fatal overdose. These findings emphasize the importance of treatment retention and interventions for polysubstance overdose at cessation.
KW - Data linkage
KW - Non-fatal and fatal drug overdose
KW - Opioid agonist
KW - Opioid agonist treatment
KW - Opioid dependence
UR - http://www.scopus.com/inward/record.url?scp=85129548457&partnerID=8YFLogxK
U2 - 10.1016/j.drugalcdep.2022.109464
DO - 10.1016/j.drugalcdep.2022.109464
M3 - Article
C2 - 35523111
AN - SCOPUS:85129548457
VL - 236
JO - Drug and Alcohol Dependence
JF - Drug and Alcohol Dependence
SN - 0376-8716
M1 - 109464
ER -