Acute respiratory distress syndrome.

Sat Sharma
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Abstract

INTRODUCTION Acute respiratory distress syndrome (ARDS) is characterised by lung inflammation with severe hypoxia, which usually develops over 4-48 hours and persists for days or weeks. The main causes of ARDS are infections, aspiration of gastric contents, and trauma. Between a third and a half of people with ARDS die from the disease, but mortality depends on the underlying cause. Some survivors have long-term respiratory or cognitive problems. METHODS AND OUTCOMES We conducted a systematic review and aimed to answer the following clinical question: What are the effects of interventions in adults with acute respiratory distress syndrome? We searched: Medline, Embase, The Cochrane Library and other important databases up to August 2006 (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 21 systematic reviews, RCTs, or observational studies that met our inclusion criteria. CONCLUSIONS In this systematic review we present information relating to the effectiveness and safety of the following interventions: corticosteroids, low tidal volume mechanical ventilation, nitric oxide, prone position, and protective ventilation.
急性呼吸窘迫综合征。
急性呼吸窘迫综合征(ARDS)以肺部炎症伴严重缺氧为特征,通常发展超过4-48小时,持续数天或数周。急性呼吸窘迫综合征的主要原因是感染、胃内容物误吸和创伤。三分之一到一半的ARDS患者死于该疾病,但死亡率取决于潜在的原因。一些幸存者有长期的呼吸或认知问题。方法和结果我们进行了一项系统回顾,旨在回答以下临床问题:干预措施对成人急性呼吸窘迫综合征的影响是什么?我们检索了Medline、Embase、The Cochrane Library等重要数据库,检索时间截止到2006年8月(临床证据综述定期更新,请查看我们的网站获取最新版本的综述)。我们纳入了来自相关组织的危害警报,如美国食品和药物管理局(FDA)和英国药品和保健产品监管局(MHRA)。结果我们发现21项系统综述、随机对照试验或观察性研究符合我们的纳入标准。结论:在这篇系统综述中,我们介绍了以下干预措施的有效性和安全性:皮质激素、低潮气量机械通气、一氧化氮、俯卧位和保护性通气。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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