Postmortem toxicological analyses of blood samples from 107 patients receiving opioid agonist treatment: substances detected and pooled opioid and benzodiazepine concentrations

被引:16
|
作者
Bech, Anne Berit [1 ,2 ]
Clausen, Thomas [2 ]
Waal, Helge [2 ,3 ]
Vindenes, Vigdis [4 ,5 ]
Edvardsen, Hilde Eroy [4 ]
Frost, Joachim [6 ]
Skeie, Ivar [1 ,2 ]
机构
[1] Innlandet Hosp Trust, Dept Mental Hlth, Natl Advisory Unit Concurrent Subst Abuse & Menta, POB 104, N-2381 Brumunddal, Norway
[2] Univ Oslo, Inst Clin Med, Norwegian Ctr Addict Res SERAF, Oslo, Norway
[3] Oslo Univ Hosp, Natl Advisory Unit Subst Use Disorder Treatment, Oslo, Norway
[4] Oslo Univ Hosp, Dept Forens Sci, Oslo, Norway
[5] Univ Oslo, Inst Clin Med, Oslo, Norway
[6] Trondheim Reg & Univ Hosp, St Olavs Hosp, Dept Clin Pharmacol, Trondheim, Norway
关键词
Autopsy; benzodiazepine; buprenorphine; drug-induced; forensic; methadone; opioid agonist treatment; overdose; polydrug; toxicology; METHADONE-RELATED FATALITIES; BUPRENORPHINE-NALOXONE; MAINTENANCE TREATMENT; MORTALITY; ABUSE; DIVERSION; PATTERNS; MORPHINE; DEATHS; HEROIN;
D O I
10.1111/add.15211
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Aims To present the substances and their concentrations detected postmortem in patients receiving opioid agonist treatment (OAT) stratified by cause of death, estimate the pooled opioid and benzodiazepine concentrations using established conversion factors for blood concentrations from the Norwegian Road Traffic Act and explore the association between drug-induced cause of death and the pooled opioid and benzodiazepine concentrations. Design Cross-sectional nation-wide study. Setting Norway. Participants One hundred and seven patients who died during OAT (i.e. within 5 days after the last intake of OAT medication) between 1 January 2014 and 31 December 2015, with postmortem femoral blood available for toxicology. Data were collected from hospital records, the Norwegian Cause of Death Registry and autopsy reports. Measurements Presence of alcohol and non-alcohol substances in the bloodstream postmortem, determined through records of toxicology of postmortem femoral blood. Findings A median of four substances was detected across the causes of death. At least one benzodiazepine was detected in 81 (76%) patients. The median pooled opioid concentration was significantly higher in drug-induced deaths compared with other causes of death (362 versus 182 ng/ml,P < 0.001), in contrast to the pooled benzodiazepine concentration (5466 versus 5701 ng/ml,P = 0.353). The multivariate regression analysis showed that only increasing pooled opioid concentration (ng/ml) was associated with increased odds of a drug-induced cause of death (odds ratio = 1.003; 95% confidence interval = 1.001-1.006). Conclusions In Norway, overall opioid concentration seems to play an important role in drug-induced deaths during opioid agonist treatment in patients prescribed methadone or buprenorphine. Patients prescribed buprenorphine tend to replace their agonist with full agonists, while patients prescribed methadone tend to have high opioid concentrations from methadone as the only opioid.
引用
收藏
页码:845 / 855
页数:11
相关论文
共 3 条
  • [1] Concentrations of psychoactive substances in blood samples from non-fatal and fatal opioid overdoses
    Edvardsen, Hilde Marie Eroy
    Aamodt, Carl
    Bogstrand, Stig Tore
    Krajci, Peter
    Vindenes, Vigdis
    Rognli, Eline Borger
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2022, 88 (10) : 4494 - 4504
  • [2] Organ pathologies detected post-mortem in patients receiving opioid agonist treatment for opioid use disorder: a nation-wide 2-year cross-sectional study
    Bech, Anne Berit
    Clausen, Thomas
    Waal, Helge
    Delaveris, Gerd Jorunn Moller
    Skeie, Ivar
    ADDICTION, 2022, 117 (04) : 977 - 985
  • [3] DRUG USE AND REINFECTION DURING AND FOLLOWING HCV TREATMENT WITH ELBASVIR/GRAZOPREVIR AMONG PATIENTS RECEIVING OPIOID AGONIST THERAPY: FINAL RESULTS FROM THE CO-STAR STUDY
    Grebely, Jason
    Conway, Brian
    Litwin, Alain H.
    Dalgard, Olav
    Shibolet, Oren
    Nahass, Ronald G.
    Altice, Frederick
    Gane, Edward J.
    Luetkemeyer, Annie
    Peng, Cheng-Yuan
    Iser, David
    Gendrano, Isaias Noel, III
    Kelly, Michelle
    Hwang, Peggy
    Asante-Appiah, Ernest
    Barr, Eliav
    Robertson, Michael Newton
    Platt, Heather
    Dore, Gregory
    HEPATOLOGY, 2019, 70 : 955A - 956A