Department of Pharmacology, Wayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA.
Department of Pharmacology, Wayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA.
Drug Alcohol Depend. 2021 Aug 1;225:108854. doi: 10.1016/j.drugalcdep.2021.108854. Epub 2021 Jun 24.
A high proportion of opioid drug deaths involve concurrent benzodiazepine use. To reduce the risk of drug overdose, various prescription drug monitoring programs have been implemented. This study examined the impact of concurrent benzodiazepine use on opioid-related deaths, and the utility of the Michigan Automated Prescription System (MAPS) in predicting risk of opioid death.
Wayne County Medical Examiner's Office cases from 2018 were examined in terms of MAPS data and MAPS-derived drug risk scores, as well as postmortem toxicology. Opioid death cases with concurrent benzodiazepine use were compared to non-drug deaths.
For cases with a MAPS history for 6 months preceding death, the incidence of opioid prescriptions filled did not differ between groups. In contrast, significantly more opioid death cases had filled a benzodiazepine prescription; alprazolam prescription was the single best predictor of opioid drug death. Groups differed in MAPS-calculated drug risk scores, though these were less predictive of opioid death than some individual measures of prescription drug use. In terms of postmortem toxicology, fentanyl was the best discriminator between cohorts, with significant associations seen for morphine, benzodiazepine, or cocaine use. Similar results were obtained in the subset of subjects filling a prescription within a month of death, except that MAPS risk scores no longer predicted drug deaths.
MAPS scores did not adequately predict risk of opioid-related death. Contrary to expectations, prescription opioid use was not correlated with opioid-related death, whereas concurrent use of opioids and benzodiazepines represented a highly significant risk factor.
阿片类药物死亡中,相当大的比例涉及同时使用苯二氮䓬类药物。为降低药物过量风险,实施了各种处方药物监测计划。本研究调查了同时使用苯二氮䓬类药物对阿片类相关死亡的影响,以及密歇根州自动处方系统(MAPS)在预测阿片类药物死亡风险中的效用。
检查 2018 年韦恩县法医办公室病例的 MAPS 数据和 MAPS 衍生的药物风险评分,以及死后毒理学。将同时使用苯二氮䓬类药物的阿片类药物死亡病例与非药物死亡病例进行比较。
对于在死亡前 6 个月有 MAPS 病史的病例,两组之间开具阿片类药物处方的发生率没有差异。相比之下,阿片类药物死亡病例开具苯二氮䓬类药物处方的情况明显更多;阿普唑仑处方是阿片类药物死亡的最佳预测指标。两组的 MAPS 计算药物风险评分存在差异,但与某些处方药使用的个别指标相比,这些评分对阿片类药物死亡的预测性较差。就死后毒理学而言,芬太尼是区分队列的最佳指标,吗啡、苯二氮䓬类或可卡因的使用均存在显著关联。在死亡前一个月内开具处方的受试者亚组中也得到了类似的结果,只是 MAPS 风险评分不再预测药物死亡。
MAPS 评分不能充分预测与阿片类药物相关的死亡风险。与预期相反,处方类阿片类药物的使用与阿片类药物相关的死亡无关,而同时使用阿片类药物和苯二氮䓬类药物则是一个非常显著的风险因素。