Diarrhea associated with lopinavir/ritonavir-based therapy: results of a meta-analysis of 1469 HIV-1-infected participants.

Colleen M Wegzyn, Linda M Fredrick, Roxann O Stubbs, William C Woodward, Michael Norton
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引用次数: 11

Abstract

Background: Antiretroviral therapy is associated with adverse events (AEs). The most frequently reported AE associated with lopinavir/ritonavir (LPV/r) containing regimens is diarrhea. The objective of this meta-analysis is to describe the incidence, prevalence, and duration of diarrhea in individuals taking LPV/r.

Methods: This is a meta-analysis of Abbott-conducted clinical trials. Inclusion criteria included prospective randomized clinical trials with the LPV/r tablet formulation and had AE data (moderate/severe diarrhea) available through 48 weeks of treatment.

Results: Three trials (total 1469 participants) met the inclusion criteria. In all, 11.2% of participants reported moderate/severe diarrhea by week 8, with median time to resolution of 7.4 weeks. The overall 48-week incidence of moderate/severe diarrhea was 15.5%. The discontinuation rate due to moderate/severe diarrhea was 1.3%.

Conclusions: Moderate/severe diarrhea occurred in less than 1 in 6 participants taking LPV/r, typically started in the first 8 weeks of treatment and infrequently resulted in premature discontinuation.

基于洛匹那韦/利托那韦的治疗与腹泻相关:1469名hiv -1感染参与者的荟萃分析结果
背景:抗逆转录病毒治疗与不良事件(ae)相关。与含洛匹那韦/利托那韦(LPV/r)方案相关的最常报道的AE是腹泻。本荟萃分析的目的是描述服用LPV/r的个体腹泻的发生率、流行率和持续时间。方法:这是一项雅培进行的临床试验的荟萃分析。纳入标准包括LPV/r片剂配方的前瞻性随机临床试验,并在48周的治疗期间获得AE数据(中度/重度腹泻)。结果:3项试验(共1469名受试者)符合纳入标准。总的来说,11.2%的参与者在第8周报告了中度/重度腹泻,平均缓解时间为7.4周。48周中/重度腹泻的总发生率为15.5%。中度/重度腹泻导致的停药率为1.3%。结论:服用LPV/r的患者中,6人中不到1人出现中度/重度腹泻,通常在治疗的前8周开始,很少导致过早停药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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