International recommendations on epinephrine auto-injector doses often differ from standard weight-based guidance: a review and clinical proposals.

Sten Dreborg, Graham Walter, Harold Kim
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引用次数: 0

Abstract

Background: In anaphylaxis, the dosing of injectable epinephrine in medical settings has been arbitrarily recommended to be 0.01 mg/kg of body weight. For ethical reasons, there have been no dose-response studies or double-blind studies performed on patients with active anaphylaxis. Intramuscular delivery of epinephrine has been the standard. Auto-injectors for use in the treatment of anaphylaxis are available in four strengths (0.1, 0.15, 0.3, and 0.5 mg). However, in many countries, only the 0.15 and 0.3 mg strengths are available. Consequently, many adult, heavy patients are prescribed the 0.3 mg dose, which may result in only one-fifth to one-third of the recommended weight-based dose being administered in heavy patients experiencing anaphylaxis. Underdosing may have therefore contributed to mortality in anaphylaxis.

Objective: To review the doses of epinephrine recommended for the treatment of anaphylaxis in the community, and assess whether recommendations should be made to increase dosing for heavy adult patients in hopes of avoiding future deaths from anaphylaxis.

Methods: We reviewed multiple national and international recommendations for the dosing of epinephrine. We also reviewed the literature on adverse drug reactions from epinephrine, lethal doses of epinephrine, and epinephrine dose-finding studies.

Results: The majority of national and regional professional societies and authorities recommend epinephrine delivered by auto-injectors at doses far lower than the generally accepted therapeutic dose of 0.01 mg/kg body weight. Furthermore, we found that the recommendations vary even within regions themselves.

Conclusions: We suggest prescribing more appropriate doses of epinephrine auto-injectors based on weight-based recommendations. There may be some exceptions, such as for patients with heart disease. We hypothesize that these recommendations will lead to improved outcomes of anaphylaxis.

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关于肾上腺素自动注射器剂量的国际建议往往不同于基于体重的标准指南:回顾与临床建议。
背景:在过敏性休克的医疗环境中,注射用肾上腺素的剂量被武断地推荐为 0.01 毫克/千克体重。出于伦理原因,目前尚未对活动性过敏性休克患者进行剂量反应研究或双盲研究。肌肉注射肾上腺素一直是标准用药。用于治疗过敏性休克的自动注射器有四种强度(0.1、0.15、0.3 和 0.5 毫克)。然而,在许多国家,只有 0.15 和 0.3 毫克两种强度的自动注射器。因此,许多体重较重的成年患者会被处方 0.3 毫克的剂量,这可能导致发生过敏性休克的体重较重患者的用药量仅为推荐剂量的五分之一到三分之一。因此,剂量不足可能会导致过敏性休克患者死亡:目的:回顾建议用于治疗社区过敏性休克的肾上腺素剂量,并评估是否应建议增加体重较重的成年患者的剂量,以避免今后因过敏性休克而死亡:我们回顾了多个国家和国际上关于肾上腺素剂量的建议。我们还查阅了有关肾上腺素药物不良反应、肾上腺素致死剂量和肾上腺素剂量测定研究的文献:结果:大多数国家和地区的专业协会和权威机构都建议使用自动注射器注射肾上腺素,其剂量远远低于公认的治疗剂量(0.01 毫克/千克体重)。此外,我们还发现,即使在同一地区,推荐的剂量也不尽相同:结论:我们建议根据基于体重的建议,处方更适当剂量的肾上腺素自动注射器。可能会有一些例外情况,如心脏病患者。我们假设这些建议将改善过敏性休克的治疗效果。
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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