Department of Infectious Diseases and Clinical Microbiology, University of Health Sciences, Bakirkoy Dr. Sadi Konuk Education and Research Hospital, Istanbul, Turkey.
Curr HIV Res. 2020;18(6):415-425. doi: 10.2174/1574885515666200812215140.
Long life expectancy in people living with human immunodeficiency virus (PLWH) caused an increase in comorbidities and co-medications. We aimed to analyse comedications and drug-drug interactions (DDIs) in antiretroviral therapy (ART)-naive PLWH in the era of integrase inhibitors.
A retrospective observational study was conducted between January 2016-August 2019. Patients' characteristics and chronic co-medications were recorded. The University of Liverpool HIV drug interaction database was used for DDIs.
Among 745 patients, the chronic co-medication rate was 30.9%. Older age (p<0.001, OR:6.66, 95% CI: 3.86-11.49) and female gender (p=002, OR:2.25, 95%:1.14-4.44) were independently associated with co-medication. Cardiovascular system (CVS) and central nervous system (CNS) drugs were the most common co-medications. Older age patients (p<0.001, OR:12.04, 95% CI:4.63-36.71), having heterosexual (HS) contact (p=0.003, OR:3.8, 95% CI:1.57-9.22) were independently associated with CVS drugs use, while being men who have sex with men (MSM) (p=0.03, OR:2.59, 95% CI:1.11-6.03) were associated with CNS drugs use. DDIs were seen in 37.4% of patients with co-medications. Antidiabetics (23.3%), CNS (22.1%) and CVS drugs (19.8%) most commonly had DDIs. Contraindication was most commonly seen between inhaled corticosteroids and elvitegravir/cobicistat. A number of non-ART drugs, elvitegravir/cobicistat, antidiabetics, vitamins were independently associated with the presence of DDIs.
Results suggested the need for attention about co-medication in PLWH regardless of whether they are young or older. CNS drugs should be questioned more detailed in MSM, as well as CVS drugs in older HS patients. Elvitegravir/cobicistat is significantly associated with DDIs and switching to an unboosted INSTI should be considered in patients with multiple comorbidities.
人类免疫缺陷病毒(HIV)感染者的预期寿命延长导致合并症和合并用药增加。我们旨在分析整合酶抑制剂时代初治 HIV 感染者的合并用药和药物相互作用(DDI)。
这是一项回顾性观察性研究,于 2016 年 1 月至 2019 年 8 月进行。记录患者的特征和慢性合并用药情况。使用利物浦大学 HIV 药物相互作用数据库来检测 DDI。
在 745 名患者中,慢性合并用药率为 30.9%。年龄较大(p<0.001,OR:6.66,95%CI:3.86-11.49)和女性(p=0.02,OR:2.25,95%:1.14-4.44)与合并用药独立相关。心血管系统(CVS)和中枢神经系统(CNS)药物是最常见的合并用药。年龄较大的患者(p<0.001,OR:12.04,95%CI:4.63-36.71)、异性性接触(p=0.003,OR:3.8,95%CI:1.57-9.22)与 CVS 药物使用独立相关,而男男性接触(p=0.03,OR:2.59,95%CI:1.11-6.03)与 CNS 药物使用相关。合并用药的患者中,有 37.4%出现药物相互作用。抗糖尿病药(23.3%)、CNS 药物(22.1%)和 CVS 药物(19.8%)最常见的药物相互作用。最常见的药物相互作用是吸入性皮质类固醇和艾维雷格/考比司他之间的相互作用。许多非抗逆转录病毒药物、艾维雷格/考比司他、抗糖尿病药和维生素与药物相互作用的发生独立相关。
结果表明,无论 HIV 感染者年龄大小,都需要关注合并用药的问题。应更详细地询问男男性接触者中的 CNS 药物,以及老年异性性接触者中的 CVS 药物。艾维雷格/考比司他与药物相互作用显著相关,应考虑在合并多种合并症的患者中换用无增效剂的整合酶抑制剂。