Swiss Tropical and Public Health Institute, Basel, Switzerland.
University of Basel, Basel, Switzerland.
J Antimicrob Chemother. 2021 Sep 15;76(10):2681-2689. doi: 10.1093/jac/dkab254.
The extent to which drug-drug interactions (DDIs) between antiretrovirals (ARVs) and co-medications are recognized and managed has not been thoroughly evaluated in limited-resource settings.
This prospective questionnaire-based study aimed to determine the prevalence and risk factors for unrecognized/incorrectly managed DDIs in people living with HIV followed-up at the Chronic Diseases Clinic of Ifakara (CDCI) and enrolled in the Kilombero and Ulanga Antiretroviral Cohort (KIULARCO).
We prospectively included ARV-treated adults receiving ≥1 co-medication coming for a follow-up visit at the CDCI between March and July 2017. Using a structured questionnaire, physicians were requested to identify potentially clinically significant DDIs in the prescribed treatment, to provide recommendations for their management and to indicate any hurdles to implement the recommendations. Prescriptions were subsequently screened for DDIs using the Liverpool DDIs database. Identified clinically significant DDIs and their recommended management according to the DDIs database were compared with the information provided in the questionnaires.
Among 334 participants, the median age was 47 years (IQR = 40-56 years), 69% were female and 82% had ≥1 non-communicable disease (NCD). Overall, 129 participants had ≥1 clinically relevant DDI, which was not recognized and/or incorrectly managed in 56 participants (43%). Of those, 6 (11%) were due to limited monitoring options or medication affordability issues. In the multivariable logistic regression, the presence of ≥1 NCD was associated with an increased risk for unrecognized/incorrect DDI management (OR = 15.8; 95% CI = 1.8-139.6).
Recognition/appropriate management of DDIs is suboptimal, highlighting the need for educational programmes, pharmacovigilance activities and increased access to medications and monitoring options. This should become a focus of HIV programmes given the increasing burden of NCDs in sub-Saharan Africa.
在资源有限的环境中,尚未对抗逆转录病毒药物(ARV)与合并药物之间药物-药物相互作用(DDI)的识别和管理程度进行彻底评估。
本前瞻性基于问卷的研究旨在确定在伊法卡拉慢性疾病诊所(CDCI)接受随访并参与基洛姆贝罗和乌兰加抗逆转录病毒队列(KIULARCO)的艾滋病毒感染者中,未识别/不正确管理的 DDIs 的发生率和危险因素。
我们前瞻性地纳入了 2017 年 3 月至 7 月期间在 CDCI 接受至少一种合并药物治疗的接受 ARV 治疗的成年患者。使用结构化问卷,医生被要求识别处方治疗中可能具有临床意义的 DDIs,提供管理建议,并指出实施建议的任何障碍。随后使用利物浦 DDIs 数据库筛选处方以识别 DDIs。根据 DDIs 数据库识别出的具有临床意义的 DDIs 及其推荐的管理方法与问卷中提供的信息进行比较。
在 334 名参与者中,中位年龄为 47 岁(IQR=40-56 岁),69%为女性,82%患有≥1 种非传染性疾病(NCD)。总体而言,129 名参与者有≥1 种具有临床相关性的 DDI,其中 56 名(43%)未被识别和/或处理不当。其中,有 6 名(11%)是由于监测选择有限或药物可负担性问题所致。在多变量逻辑回归中,存在≥1 种 NCD 与未识别/处理不当的 DDI 管理风险增加相关(OR=15.8;95%CI=1.8-139.6)。
DDI 的识别/适当管理并不理想,这突出表明需要开展教育计划、药物警戒活动,并增加药物和监测选择的可及性。鉴于撒哈拉以南非洲地区非传染性疾病负担不断增加,这应成为艾滋病毒规划的重点。