Suppr超能文献

口服疫苗(OM-89)用于预防复发性尿路感染:一项包含荟萃分析的实用系统评价

Oral vaccine (OM-89) in the recurrent urinary tract infection prophylaxis: a realistic systematic review with meta-analysis.

作者信息

Taha Neto K A, Nogueira Castilho L, Reis L O

机构信息

Faculty of Medicine, Center of Life Sciences, Pontifical Catholic University of Campinas, PUC-Campinas, Campinas, São Paulo, Brasil.

Radium Institute, Campinas, São Paulo, Brasil.

出版信息

Actas Urol Esp. 2016 May;40(4):203-8. doi: 10.1016/j.acuro.2015.04.008. Epub 2015 Oct 24.

Abstract

OBJECTIVE

To evaluate the efficacy of Escherichia Coli extract (OM-89) in the prophylaxis of recurrent uncomplicated urinary tract infection (UTI) through a contemporary systematic review and meta-analysis.

METHODS

Inclusion criteria were double-blind randomized trials using orally administrated OM-89, 6mg daily, during three months with a minimum of three months of monitoring. Outcomes were the frequency of bacteriuria in 3 and 6 months, dysuria in 6 months and UTI in 6 months.

DATABASES

PubMed, MEDLINE, Cochrane Collaboration and their key references. After analysis by three independent reviewers, 15 double-blind randomized trials were identified, 10 papers excluded due to methods flaws and 5 used for data analysis due to double blinding and reporting drop-outs.

RESULTS

Among 5 selected studies the date of publication ranged from 1985 to 2005, totalizing 396 patients in the OM-89 group and 392 in the control group. Overall, there were 61 dropouts in the control group and 76 in the OM-89 group. As a major limitation there was no appropriate description of their methodologies and none of the studies described conflict of interest or commitment to the pharmaceutical industry. All studies were multi-centric, except for two, which showed no clarity on allocation concealment. All studies show benefit in favor of vaccine.

CONCLUSIONS

Current literature on prospective randomized controlled trials evaluating the use of oral OM-89 vaccine in the recurrent UTI prophylaxis is of low quality, limited to the first six months only and with variable definition of bacteriuria and UTI. Although all studies show benefit in favor of vaccine, no robust trial was identified, resulting in a high heterogeneity in the data analyzed. Also, publication bias could not be excluded and future higher quality studies are warranted adding intermediate (>12 months) and long-term follow-up.

摘要

目的

通过当代系统评价和荟萃分析评估大肠杆菌提取物(OM-89)预防复发性单纯性尿路感染(UTI)的疗效。

方法

纳入标准为双盲随机试验,每日口服6mg OM-89,为期三个月,并至少监测三个月。观察指标为3个月和6个月时的菌尿频率、6个月时的排尿困难以及6个月时的UTI。

数据库

PubMed、MEDLINE、Cochrane协作网及其关键参考文献。经三位独立评审员分析后确定了15项双盲随机试验,其中10篇因方法缺陷被排除,5篇因双盲和报告失访情况而用于数据分析。

结果

在5项入选研究中,发表日期从1985年至2005年不等,OM-89组共有396例患者,对照组有392例。总体而言,对照组有6项失访,OM-89组有76项失访。作为一个主要局限性,其方法学没有得到恰当描述,且没有一项研究描述利益冲突或与制药行业的关系。除两项研究外,所有研究均为多中心研究,这两项研究在分配隐藏方面不明确。所有研究均显示疫苗有益。

结论

目前关于评估口服OM-89疫苗预防复发性UTI的前瞻性随机对照试验的文献质量较低,仅局限于前六个月,且菌尿和UTI的定义各不相同。尽管所有研究均显示疫苗有益,但未发现有力的试验,导致所分析的数据存在高度异质性。此外,不能排除发表偏倚,因此有必要开展未来更高质量的研究,并增加中期(>12个月)和长期随访。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验