School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK; Public Health Scotland, Glasgow, UK.
School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK; Public Health Scotland, Glasgow, UK.
Psychiatry Res. 2024 Sep;339:116028. doi: 10.1016/j.psychres.2024.116028. Epub 2024 Jun 12.
Prescribing of gabapentinoids and Z-drug-hypnotics has increased in the population and among people receiving opioid-agonist treatment (OAT) for opioid dependence. Evidence is mixed on whether co-prescribing of sedatives such as gabapentinoids and Z-drugs during OAT increases risk of drug-related death (DRD).
We conducted a retrospective cohort study of individuals prescribed OAT between 2011 and 2020 in Scotland. Prescribing records were linked to mortality data and other healthcare datasets (sociodemographic, comorbidity). We identified episodes of treatment with gabapentinoids/Z-drugs and used multivariable quasi-Poisson regression to model associations between co-prescription and DRD risk.
Among 46,602 individuals with 304,783 person-years of follow-up, we found that co-prescription was common, with 25 % and 34 % ever being co-prescribed gabapentinoids and Z-drugs, respectively. Gabapentinoid exposure was strongly associated (adjusted hazard ratio (aHR)=2·18, 95 % CI=1·92, 2·46) and Z-drug exposure moderately associated (aHR=1·39, 95 % CI=1·15, 1·66) with elevated risk of DRD. Gabapentinoid exposure was associated with DRD risk on and off OAT; Z-drug exposure was less strongly associated with DRD risk when on OAT.
Co-prescription of gabapentinoids and Z-drugs is common among OAT patients. However, co-prescription is associated with increased risk of DRD. Alternatives to prescribing sedative medications to OAT patients and/or greater monitoring - if prescribed - are needed.
加巴喷丁类药物和 Z 类药物催眠剂在人群中以及接受阿片类激动剂治疗(OAT)的阿片类药物依赖患者中的使用有所增加。关于在 OAT 期间同时开具镇静剂(如加巴喷丁类药物和 Z 类药物)是否会增加与药物相关的死亡(DRD)风险,证据不一。
我们对 2011 年至 2020 年期间在苏格兰接受 OAT 治疗的个体进行了回顾性队列研究。将处方记录与死亡率数据和其他医疗保健数据集(社会人口统计学、合并症)相关联。我们确定了治疗加巴喷丁类药物/Z 类药物的治疗阶段,并使用多变量拟泊松回归模型来模拟共同处方与 DRD 风险之间的关联。
在 46602 名患者中,有 304783 人年的随访时间,我们发现共同处方很常见,分别有 25%和 34%的患者曾经同时开具加巴喷丁类药物和 Z 类药物。加巴喷丁类药物暴露与 DRD 风险显著相关(调整后的危险比[aHR]=2.18,95%CI=1.92,2.46),而 Z 类药物暴露与 DRD 风险中度相关(aHR=1.39,95%CI=1.15,1.66)。加巴喷丁类药物暴露与 OAT 期间和 OAT 之外的 DRD 风险相关;Z 类药物暴露与 OAT 期间的 DRD 风险相关性较弱。
OAT 患者中同时开具加巴喷丁类药物和 Z 类药物的情况很常见。然而,共同处方与 DRD 风险增加相关。需要为 OAT 患者提供替代镇静药物处方的方案,或者如果处方镇静药物,需要加强监测。