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万古霉素治疗复发性感染的临床疗效、安全性及耐受性——一项系统评价

The Clinical Efficacy, Safety, and Tolerability of Vancomycin for the Treatment of Recurrent Infection - A Systematic Review.

作者信息

Knudsen Maja Johanne Søndergaard, Rubin Ingrid Maria Cecilia, Petersen Andreas Munk

机构信息

Department of Clinical Microbiology, Copenhagen University Hospital - Amager and Hvidovre, Hvidovre, Denmark.

Department of Gastroenterology, Copenhagen University Hospital - Amager and Hvidovre, Hvidovre, Denmark.

出版信息

Drug Healthc Patient Saf. 2023 Mar 21;15:63-71. doi: 10.2147/DHPS.S348501. eCollection 2023.

Abstract

INTRODUCTION

The aim of this systematic review of randomized clinical trials (RCTs) was to examine the efficacy, safety, and tolerability of vancomycin for treatment of recurrent infection (rCDI).

METHODS

The PubMed database was searched from inception to August 23, 2022. An initial screening was performed followed by a full-text evaluation of the papers. Inclusion criteria were RCTs investigating vancomycin for treatment of rCDI.

RESULTS

A total of six studies and 269 patients were included in the review. Three studies used a fixed dose regimen of vancomycin, one study used pulse regimen, one study used a taper-and-pulse regimen, and one study used a taper-and-pulse regimen for the participants with two or more recurrences. The resolution of infection varied from 19% to 58.3% in five of six studies reporting this as an outcome. Four out of six studies reported new episodes of rCDI as an intervention outcome, in those studies 50-63% of participants experienced rCDI. Regarding the safety and tolerability of vancomycin treatment for rCDI, one study described several adverse events regarding gastrointestinal discomfort along with fatigue and skin rash. There were no records of serious adverse events in the included studies.

CONCLUSION

While oral vancomycin is mostly safe and well tolerated in the RCTs reviewed here, the efficacy for treating rCDI varies greatly from 19-58.3%, and 50-63% of participants experienced new episodes of rCDI.

摘要

引言

本随机临床试验(RCT)系统评价的目的是研究万古霉素治疗复发性艰难梭菌感染(rCDI)的疗效、安全性和耐受性。

方法

检索PubMed数据库自建库至2022年8月23日的文献。首先进行初步筛选,然后对文献进行全文评估。纳入标准为研究万古霉素治疗rCDI的随机对照试验。

结果

本评价共纳入6项研究和269例患者。3项研究使用了固定剂量的万古霉素方案,1项研究使用脉冲方案,1项研究使用递减和脉冲方案,1项研究对复发两次或更多次的参与者使用递减和脉冲方案。在将感染缓解作为结局指标报告的6项研究中的5项中,感染缓解率从19%到58.3%不等。6项研究中有4项将新的rCDI发作作为干预结局指标报告,在这些研究中,50%-63%的参与者出现了rCDI。关于万古霉素治疗rCDI的安全性和耐受性,1项研究描述了与胃肠道不适、疲劳和皮疹相关的几种不良事件。纳入研究中无严重不良事件记录。

结论

虽然在此回顾的随机对照试验中口服万古霉素大多安全且耐受性良好,但治疗rCDI的疗效差异很大,为19%-58.3%,且50%-63%的参与者出现了新的rCDI发作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e2/10039659/8e05790bdad8/DHPS-15-63-g0001.jpg

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