通过多学科团队确定的hiv感染患者队列中潜在药物相互作用的频率和严重程度。

Q2 Medicine
HIV Clinical Trials Pub Date : 2018-02-01 Epub Date: 2017-11-28 DOI:10.1080/15284336.2017.1404690
E Molas, S Luque, A Retamero, D Echeverría-Esnal, A Guelar, M Montero, R Guerri, L Sorli, E Lerma, J Villar, H Knobel
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引用次数: 22

摘要

目的:抗逆转录病毒治疗(ART)和药物之间的相互作用是艾滋病毒感染患者关注的问题。本研究旨在确定在我们的环境中与ART发生潜在药物-药物相互作用(pddi)的频率和严重程度。方法:多学科团队对1259例HIV患者(2015年3月- 2016年9月)进行观察性研究。收集了人口统计学、有毒习惯、合并症和当前抗逆转录病毒治疗的数据。一份结构化的问卷记录了伴随用药情况(包括偶尔用药和非处方药)。pddi分为四类:(1)无相互作用,(2)轻度(临床无显著性),(3)中度(需要密切监测或药物修改/剂量调整),(4)重度(禁忌)。统计分析:卡方检验、logistic回归分析。结果:881例(70%)患者服药,563例(44.7%)患者PDDI≥。41例(4.6%)患者有重度pddi, 522例(59.2%)有中度pddi。中度pddi主要涉及心血管(53.8%)和中枢神经系统(40.2%)药物。pddi的独立危险因素是ART含有增强的蛋白酶抑制剂(优势比[OR]=9.11, 95%可信区间[CI] 5.15-16.11;p = 0.0001)和/或非核苷逆转录酶(NNRTI) (or = 4.34, 95%CI 2.49-7.55;p = 0.0001),丙肝病毒合并感染(或= 3.26,95% ci 2.15 - -4.93;p = 0.0001),使用两种或两种以上药物(or = 3.36, 95%CI 2.27-4.97;p = 0.0001)。有和没有pddi的患者ART的依从性和有效性相似。该小组提出了133项与药物(药物改变或剂量调整)或ART(药物转换或改变给药计划)有关的建议。结论:系统评估发现,在接受抗逆转录病毒治疗的艾滋病毒患者中,有很大比例的pddi需要干预。对药物-药物相互作用的监测和建议应成为常规做法的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Frequency and severity of potential drug interactions in a cohort of HIV-infected patients Identified through a Multidisciplinary team.

Objectives: Interactions between antiretroviral treatment (ART) and comedications are a concern in HIV-infected patients. This study aimed to determine the frequency and severity of potential drug-drug interactions (PDDIs) with ART in our setting.

Methods: Observational study by a multidisciplinary team in 1259 consecutive HIV patients (March 2015-September 2016). Data on demographics, toxic habits, comorbidities, and current ART were collected. A structured questionnaire recorded concomitant medications (including occasional and over-the-counter drugs). PDDIs were classified into four categories: (1) no interactions, (2) mild (clinically non-significant), (3) moderate (requiring close monitoring or drug modification/dose adjustment), and (4) severe (contraindicated).

Statistical analysis: chi-square test, logistic regression analysis.

Results: In total, 881 (70%) patients took comedication, and 563 (44.7%) had ≥ PDDI. Forty-one comedicated patients (4.6%) had severe and 522 (59.2%) moderate PDDIs. Moderate PDDIs mainly involved cardiovascular (53.8%) and central nervous system (40.2%) drugs. Independent risk factors for PDDIs were ART containing a boosted protease inhibitor (odds ratio [OR]=9.11, 95% confidence interval [CI] 5.15-16.11; p = 0.0001) and/or non-nucleoside reverse transcriptase (NNRTI) (OR = 4.34, 95%CI 2.49-7.55; p = 0.0001), HCV co-infection (OR = 3.26, 95%CI 2.15-4.93; p = 0.0001), and use of two or more comedications (OR = 3.36, 95%CI 2.27-4.97; p = 0.0001). Adherence and effectiveness of ART were similar in patients with and without PDDIs. The team made 133 recommendations related to comedications (drug change or dose adjustment) or ART (drug switch or change in administration schedule).

Conclusions: Systematic evaluation detected a significant percentage of PDDIs requiring an intervention in HIV patients on ART. Monitoring and advice about drug-drug interactions should be part of routine practice.

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来源期刊
HIV Clinical Trials
HIV Clinical Trials 医学-传染病学
CiteScore
1.76
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: HIV Clinical Trials is devoted exclusively to presenting information on the latest developments in HIV/AIDS clinical research. This journal enables readers to obtain the most up-to-date, innovative research from around the world.
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