Masaki Tetsuhiro, Ishikawa Kazuhiro, Fujino Takahisa, Koyamada Ryosuke, Kawai Fujimi, Ota Erika, Mori Shinichiro
Department of Haematology, St Luke's International Hospital, Chuo-ku, Tokyo, Japan.
Department of Infectious Diseases, St Luke's International Hospital, Chuo-ku, Tokyo, Japan.
Open Forum Infect Dis. 2024 Sep 2;11(9):ofae499. doi: 10.1093/ofid/ofae499. eCollection 2024 Sep.
In immunocompromised individuals, trimethoprim/sulfamethoxazole (TMP/SMX) for pneumonia (PCP) prophylaxis has adverse events, and the optimal dosage is unclear. The objective of this study was to assess efficacy and safety of intermittent versus daily TMP/SMX for PCP prophylaxis.
This systematic review included randomized controlled trials (RCTs) indexed in the Cochrane Central Register of Controlled Trials, PubMed, Ichushi, or Embase databases, published from database inception to September 2023. The inclusion criteria were adults taking intermittent or daily TMP/SMX for PCP prophylaxis. Risk of bias was assessed using the Cochrane risk-of-bias tool. The primary outcomes were PCP incidence, PCP-related mortality, and adverse events requiring temporary or permanent TMP/SMX discontinuation.
Four RCTs (N = 2808 patients) were included. PCP incidence did not differ significantly between the intermittent and daily regimen groups (risk ratio [RR], 1.17 [95% confidence interval {CI}, .89-1.53]; certainty: very low). There was no PCP-related mortality in the 3 RCTs reporting its outcome. Compared with the daily regimen group, the intermittent regimen group experienced significantly fewer adverse events requiring temporary or permanent TMP/SMX discontinuation (RR, 0.51 [95% CI, .42-.61]; certainty: low).
This systematic review and meta-analysis suggests that intermittent TMP/SMX regimens for PCP prophylaxis may be more tolerable than daily regimens and may have similar efficacy. Further RCTs are needed to apply this to current practice. PROSPERO (CRD42022359102).
在免疫功能低下的个体中,用于预防肺炎(肺孢子菌肺炎,PCP)的甲氧苄啶/磺胺甲恶唑(TMP/SMX)存在不良事件,且最佳剂量尚不清楚。本研究的目的是评估间歇性与每日服用TMP/SMX预防PCP的疗效和安全性。
本系统评价纳入了Cochrane对照试验中心注册库、PubMed、Ichushi或Embase数据库中索引的随机对照试验(RCT),这些试验发表时间从数据库建立至2023年9月。纳入标准为成年患者采用间歇性或每日服用TMP/SMX预防PCP。使用Cochrane偏倚风险工具评估偏倚风险。主要结局为PCP发病率、PCP相关死亡率以及需要暂时或永久停用TMP/SMX的不良事件。
纳入了4项RCT(共2808例患者)。间歇性给药方案组和每日给药方案组的PCP发病率无显著差异(风险比[RR]为1.17[95%置信区间{CI}为0.89 - 1.53];确定性:非常低)。在报告该结局的3项RCT中,无PCP相关死亡病例。与每日给药方案组相比,间歇性给药方案组需要暂时或永久停用TMP/SMX的不良事件显著更少(RR为0.51[95%CI为0.42 - 0.61];确定性:低)。
本系统评价和荟萃分析表明,间歇性TMP/SMX方案预防PCP可能比每日给药方案更具耐受性,且疗效可能相似。需要进一步的RCT将此应用于当前实践。国际前瞻性系统评价注册库(PROSPERO)登记号(CRD42022359102)。