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确定滴定疗法随机对照试验中的护理标准。

Defining the standard of care in randomized controlled trials of titrated therapies.

作者信息

Deans Katherine J, Minneci Peter C, Eichacker Peter Q, Natanson Charles

机构信息

Critical Care Medicine Department, Warren G. Magnuson Clinical Center, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Curr Opin Crit Care. 2004 Dec;10(6):579-82. doi: 10.1097/01.ccx.0000145097.36069.44.

Abstract

PURPOSE OF REVIEW

To discuss the appropriate standard of care in randomized controlled trials of titrated therapies in critically ill patients.

RECENT FINDINGS

The debate over the appropriate standard of care in randomized controlled trials was sparked by the Acute Respiratory Distress Syndrome Network trial of low tidal volume ventilation. In this trial, patients were randomized to either low or traditional tidal volume ventilation, and the investigators reported that low tidal volume ventilation significantly improved survival in patients with acute respiratory distress syndrome. However, it was argued that the control group used in this trial was not reflective of current practice patterns and that the improvement in survival may have been derived from patients in the control group being placed at increased risk. This debate forced intensivists to consider what defines an appropriate standard-of-care control group in randomized controlled trials of titrated therapies. If titrated therapies are to be studied safely, the mechanism behind the titration must be understood and incorporated into the control group. Failure to include a comparator group receiving current practice creates a study design that may jeopardize patient safety because there is no control group representing probable patient outcome outside of the trial. Additionally, randomizing patients to the extremes of a range of care without incorporation of a current practice control group prevents the investigators from making valid recommendations for changing current practice.

SUMMARY

The incorporation of current practice patterns into randomized controlled trials of titrated therapies is essential for producing generalizable results and safeguarding patients.

摘要

综述目的

探讨危重症患者滴定疗法随机对照试验中适当的护理标准。

最新研究结果

急性呼吸窘迫综合征网络低潮气量通气试验引发了关于随机对照试验中适当护理标准的争论。在该试验中,患者被随机分为低潮气量通气组或传统潮气量通气组,研究人员报告称低潮气量通气显著提高了急性呼吸窘迫综合征患者的生存率。然而,有人认为该试验中使用的对照组不能反映当前的实践模式,生存率的提高可能源于对照组患者面临的风险增加。这场争论促使重症监护医生思考在滴定疗法随机对照试验中,什么才是合适的护理标准对照组。如果要安全地研究滴定疗法,必须了解滴定背后的机制并将其纳入对照组。不纳入接受当前治疗方法的比较组会导致研究设计可能危及患者安全,因为没有代表试验外患者可能结局的对照组。此外,在不纳入当前治疗方法对照组的情况下,将患者随机分配到一系列治疗的极端情况,会使研究人员无法就改变当前治疗方法提出有效的建议。

总结

将当前实践模式纳入滴定疗法随机对照试验对于得出可推广的结果和保护患者至关重要。

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