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淋病

Gonorrhoea.

作者信息

Creighton Sarah

机构信息

Department of Sexual Health, Homerton University Hospital, London, UK.

出版信息

BMJ Clin Evid. 2011 Mar 14;2011:1604.

Abstract

INTRODUCTION

In the UK, diagnosis rates for gonorrhoea in 2008 were 152/100,000 for men aged 20 to 24 years and 135/100,000 for women aged 16 to 19 years. Resistance to one or more antimicrobial agent is reported in more than one quarter of isolates. Co-infection with Chlamydia trachomatis is reported in 10% to 40% of people with gonorrhoea in the US and UK.

METHODS AND OUTCOMES

We conducted a systematic review and aimed to answer the following clinical questions: What are the effects of treatments for uncomplicated infections in men and non-pregnant women; and in pregnant women? What are the effects of treatments for disseminated gonococcal infection? What are the effects of dual treatment for gonorrhoea and chlamydia infection? We searched: Medline, Embase, The Cochrane Library, and other important databases up to March 2010 (Clinical Evidence reviews are updated periodically, please check our website for the most up-to-date version of this review). We included harms alerts from relevant organisations such as the US Food and Drug Administration (FDA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).

RESULTS

We found 24 systematic reviews, RCTs, or observational studies that met our inclusion criteria. We performed a GRADE evaluation of the quality of evidence for interventions.

CONCLUSIONS

In this systematic review we present information relating to the effectiveness and safety of the following interventions: antibiotic regimens (dual treatment, multiple dose, single dose).

摘要

引言

在英国,2008年20至24岁男性的淋病诊断率为每10万人中有152例,16至19岁女性的淋病诊断率为每10万人中有135例。超过四分之一的分离株报告对一种或多种抗菌药物耐药。在美国和英国,10%至40%的淋病患者报告同时感染沙眼衣原体。

方法和结果

我们进行了一项系统评价,旨在回答以下临床问题:针对男性和非孕妇以及孕妇的单纯性感染的治疗效果如何?播散性淋球菌感染的治疗效果如何?淋病和衣原体感染的联合治疗效果如何?我们检索了:截至2010年3月的Medline、Embase、Cochrane图书馆及其他重要数据库(Clinical Evidence综述会定期更新,请查看我们的网站获取本综述的最新版本)。我们纳入了来自美国食品药品监督管理局(FDA)和英国药品及保健品监管局(MHRA)等相关组织的危害警示。

结果

我们发现24项系统评价、随机对照试验或观察性研究符合我们的纳入标准。我们对干预措施的证据质量进行了GRADE评估。

结论

在本系统评价中,我们提供了以下干预措施的有效性和安全性相关信息:抗生素治疗方案(联合治疗、多剂量、单剂量)。

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