British Columbia Centre for Excellence in HIV/AIDS.
Pharmacy Department, St Paul's Hospital.
AIDS. 2022 Jul 1;36(8):1105-1115. doi: 10.1097/QAD.0000000000003226. Epub 2022 Mar 11.
To characterize the annual prevalence of antiretroviral/nonantiretroviral drug interactions in relation to antiretroviral therapy (ART)-prescribing patterns, and to describe drug interaction-related ART changes.
DESIGN/METHODS: This cohort study included ART-treated adults in British Columbia, Canada between 01 January 2010 and 31 December 2016. Medication dispensing records were abstracted from a population-based, linked administrative-health dataset and used to identify antiretroviral-comedication drug interactions ('caution'/'avoid' drug interactions in HIV-focused drug interaction checkers). We identified temporal trends in annual drug interaction prevalence and quantified the association between taking higher drug interaction-risk ART and receiving nonrecommended antiretroviral-comedication combinations using Poisson regression models, modified for binary outcomes and correlated data. Clinician-reported, drug interaction-related ART changes and associated adverse events were abstracted from an HIV drug treatment registry and summarized descriptively.
Among 8571 ART-treated adults who received nonantiretroviral comedications, prevalence of having any drug interaction or receiving nonrecommended drug combination(s) significantly declined from 85 to 71% and 5.6 to 3.2%, respectively, between 2010 and 2016 ( P < 0.001). This paralleled a shift from higher drug interaction-risk ART (e.g. ritonavir/cobicistat-boosted protease inhibitors) to lower drug interaction-risk ART (e.g. unboosted integrase inhibitors). Risk of receiving a nonrecommended antiretroviral-comedication combination was greater for persons taking higher vs. lower drug interaction-risk ART [adjusted risk ratio (aRR) 3.12, 95% confidence interval (CI) 2.24-4.35]. Boosted antiretroviral-inhaled corticosteroid drug interactions accounted for the most commonly dispensed, nonrecommended drug combinations, and the most commonly reported drug interaction-related adverse events (adrenal insufficiency).
The prevalence of antiretroviral-comedication drug interactions is declining as ART shifts towards antiretrovirals with lower drug interaction potential but nonrecommended drug combinations remain a concern. Healthcare providers should screen for drug interactions whenever drugs are prescribed or dispensed.
描述与抗逆转录病毒治疗(ART)处方模式相关的抗逆转录病毒/非抗逆转录病毒药物相互作用的年度流行率,并描述药物相互作用相关的 ART 改变。
这项队列研究纳入了 2010 年 1 月 1 日至 2016 年 12 月 31 日期间在加拿大不列颠哥伦比亚省接受 ART 治疗的成年人。从一个基于人群的、关联的行政健康数据集提取药物配药记录,用于识别抗逆转录病毒联合用药的药物相互作用(在 HIV 药物相互作用检查器中为“注意”/“避免”药物相互作用)。我们使用泊松回归模型,根据二项结果和相关数据进行了修正,以确定年度药物相互作用流行率的时间趋势,并量化了服用高药物相互作用风险的 ART 与接受不推荐的抗逆转录病毒联合用药之间的关联。从 HIV 药物治疗登记处提取临床医生报告的、与药物相互作用相关的 ART 改变及其相关不良事件,并进行描述性总结。
在 8571 名接受非抗逆转录病毒合并用药的接受 ART 治疗的成年人中,有任何药物相互作用或接受不推荐的药物联合用药的比例从 2010 年的 85%显著下降至 2016 年的 71%和 5.6%降至 3.2%(P <0.001)。这与从高药物相互作用风险的 ART(如利托那韦/考比司他增强的蛋白酶抑制剂)向低药物相互作用风险的 ART(如未增强的整合酶抑制剂)的转变相一致。与服用低药物相互作用风险的 ART 相比,服用高药物相互作用风险的 ART 更有可能接受不推荐的抗逆转录病毒合并用药(调整后的风险比[aRR]3.12,95%置信区间[CI]2.24-4.35)。增强型抗逆转录病毒吸入皮质类固醇药物相互作用是最常开出的、不推荐的药物联合用药,也是最常报告的药物相互作用相关不良事件(肾上腺功能不全)。
随着 ART 向药物相互作用风险较低的抗逆转录病毒药物转变,抗逆转录病毒药物相互作用的流行率正在下降,但不推荐的药物联合用药仍然是一个问题。无论何时开出处方或配药,医护人员都应筛查药物相互作用。