Warren Alpert Medical School of Brown University, 55 Claverick St, Providence, RI, 02903, USA.
Perelman School of Medicine, University of Pennsylvania, Ground Silverstein, Rm 260, 3400 Spruce Street, Philadelphia, PA, 19104, USA.
Drug Alcohol Depend. 2021 Oct 1;227:108994. doi: 10.1016/j.drugalcdep.2021.108994. Epub 2021 Aug 28.
Understanding sex differences in toxicological etiologies of opioid-related drug overdose death could inform future sex- and gender-specific approaches to prevention and treatment.
A retrospective review of accidental or undetermined opioid-involved overdose deaths in Rhode Island 2016-2019 was performed using the Rhode Island Department of Health State Unintentional Drug Overdose Reporting System (SUDORS) database. Decedent toxicology data was linked with state Prescription Drug Monitoring Program (PDMP) records.
Of 766 cases in the analytical sample, 568 cases were in men (74.2%) and 198 cases were in women (25.6%). Median age was 40.0 years for males and 42.0 years for females. Statistically significant sex-differences in drug exposures were found. Compared to men, women were more likely have exposure to benzodiazepine, antipsychotic, and antidepressant drug classes and less likely to have fentanyl and alcohol co-exposure. No sex differences were found in cocaine and amphetamine exposure. Female decedents were more likely than male decedents to have a prescription for benzodiazepines or opioids in the 30 days before death (40% vs 21%). The proportion of decedents with a benzodiazepine on post-mortem toxicology testing in combination with a benzodiazepine prescription (p < 0.001) or an opioid prescription (p = 0.005) was over two times higher in women than men.
Higher rates of controlled substance prescription prior to death and prescription drug co-exposures suggest that female opioid-involved drug overdose decedents are often in contact with the health care system immediately preceding their death, presenting the opportunity to create patient-centric approaches for prevention, harm reduction, and substance use treatment.
了解阿片类药物相关药物过量死亡中毒病因学中的性别差异,可以为未来预防和治疗的性别和性别特定方法提供信息。
使用罗德岛健康部州意外药物过量报告系统 (SUDORS) 数据库,对 2016 年至 2019 年罗德岛的意外或未确定与阿片类药物相关的过量死亡进行回顾性审查。死者毒理学数据与州处方药物监测计划 (PDMP) 记录相关联。
在分析样本中的 766 例病例中,568 例为男性 (74.2%),198 例为女性 (25.6%)。男性的中位年龄为 40.0 岁,女性为 42.0 岁。在药物暴露方面发现了具有统计学意义的性别差异。与男性相比,女性更有可能接触到苯二氮卓类、抗精神病药和抗抑郁药类药物,而不太可能同时接触芬太尼和酒精。在可卡因和安非他命暴露方面未发现性别差异。女性死者在死亡前 30 天内开有苯二氮卓类或阿片类药物处方的可能性高于男性死者 (40%比 21%)。在死后毒理学检测中同时开有苯二氮卓类药物和苯二氮卓类药物处方 (p < 0.001) 或阿片类药物处方 (p = 0.005) 的死者比例,女性是男性的两倍多。
死亡前更高的受控物质处方率和处方药物共暴露率表明,女性阿片类药物相关药物过量死亡者在死亡前经常与医疗保健系统接触,为预防、减少伤害和药物使用治疗创造以患者为中心的方法提供了机会。