Adverse effects of daily oral pre-exposure prophylaxis in men who have sex with men and transgender women: a systematic review and meta-analysis

Marcos Pereira, C. Castro, Laio Magno, Tarcio de Almeida Oliveira, Fabiane Soares Gomes, Fabiane Maria Fernandes Neves, Pedro Rafael dos Santos do Nascimento, Inês Dourado
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Abstract

Abstract: The adverse effects of oral pre-exposure prophylaxis (PrEP) using tenofovir disoproxil fumarate are barriers to PrEP initiation and continuation. Although serious effects are rare and predictable, evidence for this assessment among men who have sex with men (MSM) and transgender women (TGW) is still limited. This study assesses the adverse effects of daily oral PrEP in MSM and TGW. This is a systematic review and meta-analysis of clinical trials and cohort studies on the use of daily oral PrEP selected from the PubMed/MEDLINE, Embase, LILACS, and Cochrane CENTRAL databases. Data extraction included adverse effects and changes in renal and hepatic markers. Random effects models were used to summarize the risk of adverse effects throughout the study. Heterogeneity was assessed using the Cochran’s Q test and the inconsistency test (I2). The risk of bias and the certainty of the evidence were assessed using the Cochrane Collaboration recommendations. The search identified 653 references. Of these, 10 were selected. All studies assessed the eligibility of renal and hepatic markers. The use of daily oral PrEP was not associated with grade 3 or 4 adverse events (RR = 0.99; 95%CI: 0.83-1.18; I2 = 26.1%), any serious adverse event (RR = 1.04; 95%CI: 0.58-1.87; I2 = 88.4%), grade 3+4 creatinine level (RR = 0.66; 95%CI: 0.24-1.84; I2 = 79.9%), and grade 3 or 4 hypophosphatemia (RR = 0.56; 95%CI: 0.15-2.10). The certainty of the evidence ranged from high to moderate for the outcomes analyzed. Daily oral PrEP is safe and well tolerated by MSM and TGW. Adverse effects were minimal and evenly distributed between intervention and control.
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男男性行为者和变性妇女每日口服暴露前预防药物的不良影响:系统回顾和荟萃分析
摘要:口服富马酸替诺福韦二氧吡酯暴露前预防(PrEP)的不良反应是PrEP开始和持续的障碍。尽管严重的影响是罕见和可预测的,但在男男性行为者(MSM)和变性女性(TGW)中进行这种评估的证据仍然有限。本研究评估每日口服PrEP对MSM和TGW的不良影响。这是从PubMed/MEDLINE、Embase、LILACS和Cochrane CENTRAL数据库中选择的关于每日口服PrEP使用的临床试验和队列研究的系统综述和荟萃分析。数据提取包括不良反应和肾脏和肝脏标志物的变化。随机效应模型用于总结整个研究过程中不良反应的风险。采用Cochran’s Q检验和不一致性检验(I2)评估异质性。使用Cochrane Collaboration推荐评估偏倚风险和证据的确定性。搜索确定了653个参考文献。其中10人入选。所有的研究都评估了肾脏和肝脏标志物的合格性。每日口服PrEP与3级或4级不良事件无关(RR = 0.99;95%置信区间:0.83—-1.18;I2 = 26.1%),严重不良事件(RR = 1.04;95%置信区间:0.58—-1.87;I2 = 88.4%), 3+4级肌酐水平(RR = 0.66;95%置信区间:0.24—-1.84;I2 = 79.9%), 3级或4级低磷血症(RR = 0.56;95%置信区间:0.15—-2.10)。对于分析的结果,证据的确定性从高到中等。每日口服PrEP对MSM和TGW是安全且耐受性良好的。干预组和对照组的不良反应最小且分布均匀。
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