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过敏反应的药物治疗:能否加强证据基础?

Pharmacologic treatment of anaphylaxis: can the evidence base be strengthened?

机构信息

Department of Pediatrics & Child Health, Department of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

出版信息

Curr Opin Allergy Clin Immunol. 2010 Aug;10(4):384-93. doi: 10.1097/ACI.0b013e32833c2038.

Abstract

PURPOSE OF REVIEW

To evaluate the evidence base for the pharmacologic treatment of anaphylaxis.

RECENT FINDINGS

In this review, we focus on four classes of medications (the alpha/beta-agonist epinephrine (adrenaline), H1-antihistamines, H2-antihistamines, and glucocorticoids) that are used in healthcare settings for the initial treatment of anaphylaxis. Epinephrine and many H1-antihistamines and glucocorticoids were introduced before the era of randomized controlled trials and before the era of evidence-based medicine. In anaphylaxis, no randomized controlled trials that are free from methodological problems and meet current standards have been performed with these medications, or with H2-antihistamines. The evidence base for epinephrine injection is stronger than the evidence base for use of other medications in anaphylaxis. Guidelines unanimously recommend prompt injection of epinephrine as the life-saving first-line medication in anaphylaxis; however, they differ in their recommendations for H1-antihistamines, H2-antihistamines, and glucocorticoids. Epinephrine is the only medication that is universally available for anaphylaxis treatment in healthcare settings worldwide. Paradoxically, it is underused in anaphylaxis treatment.

SUMMARY

For ethical reasons, there should never be a placebo-controlled trial of epinephrine in anaphylaxis. We discuss why the possibility of conducting randomized placebo-controlled trials with H1-antihistamines, H2-antihistamines, and particularly with glucocorticoids in anaphylaxis should be considered in order to improve the evidence base for treatment and guide clinical decision-making. We also describe the precautions that will be needed if randomized controlled trials are conducted in anaphylaxis.

摘要

目的综述

评估过敏反应治疗的药理学基础。

最近的发现

在这篇综述中,我们重点关注了四类药物(α/β-激动剂肾上腺素(epinephrine)、H1 抗组胺药、H2 抗组胺药和糖皮质激素),这些药物在医疗环境中用于过敏反应的初始治疗。肾上腺素和许多 H1 抗组胺药和糖皮质激素是在随机对照试验时代和循证医学时代之前引入的。在过敏反应中,没有针对这些药物或 H2 抗组胺药进行的、无方法学问题且符合当前标准的随机对照试验。肾上腺素注射的证据基础强于过敏反应中其他药物的证据基础。指南一致推荐迅速注射肾上腺素作为过敏反应的救命一线药物;然而,它们在 H1 抗组胺药、H2 抗组胺药和糖皮质激素的推荐上存在差异。肾上腺素是全球医疗环境中治疗过敏反应的唯一普遍可用的药物。具有讽刺意味的是,它在过敏反应治疗中的使用不足。

总结

出于伦理原因,在过敏反应中永远不应该进行肾上腺素的安慰剂对照试验。我们讨论了为什么应该考虑在过敏反应中进行 H1 抗组胺药、H2 抗组胺药,特别是糖皮质激素的随机安慰剂对照试验的可能性,以改善治疗的证据基础并指导临床决策。我们还描述了如果在过敏反应中进行随机对照试验需要注意的事项。

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