医学
不利影响
内科学
随机对照试验
相对风险
巨细胞病毒
荟萃分析
无症状的
中性粒细胞减少症
置信区间
免疫学
人类免疫缺陷病毒(HIV)
病毒性疾病
疱疹病毒科
化疗
作者
Prenali Dwisthi Sattwika,Yanri Wijayanti Subronto,Heni Retnowulan,Karina Ambar Sattwika,Detty Siti Nurdiati
标识
DOI:10.1080/23744235.2023.2165708
摘要
Background HIV patients are at higher risk of contracting and developing into an asymptomatic form of CMV infection. This review aimed to evaluate the efficacy and safety of preemptive therapy for preventing CMV disease in HIV patients.Methods The electronic search was conducted in MEDLINE/PubMed and CENTRAL from inception until 9 September 2022. Studies were included if they assessed the efficacy or safety of anti-CMV preemptive therapy compared to placebo or no therapy. Risk of bias were assessed using the Cochrane Risk of Bias tool for randomized trials version 2 or the Cochrane Collaboration Risk of Bias in Non-randomized Studies of Interventions. The random-effects model was used to calculate effect sizes.Results We identified six RCTs (2135 participants) and four observational studies (395 participants), with five RCTs were performed before highly active antiretroviral therapy (HAART) era. Preemptive therapy did not reduce the incidence of CMV disease (RR 0.84, 95% CI: 0.59–1.18), yet reduced the RR of all-cause mortality rate by 26% (RR 0.85, 95% CI: 0.74–0.97) with a low quality of evidence. The incidence of neutropenia as an adverse event increased significantly (RR 2.47, 95% CI: 1.12–5.45) with moderate quality of evidence.Conclusions With the advent of HAART, a limited number of studies have been performed to explore anti-CMV preemptive therapy due to the improved outcomes of HIV patients with CMV viremia. Therefore, optimal HAART should take precedence over anti-CMV preemptive therapy. The protocol for this review was registered in the Prospective Register of Systematic Reviews (CRD42020145765).
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