用于预防致命性过敏性休克的肾上腺素自动注射器。

IF 6.3 2区 医学 Q1 ALLERGY Clinical and Experimental Allergy Pub Date : 2024-10-09 DOI:10.1111/cea.14565
Marcus Sim, Vibha Sharma, Karen Li, Mary H Gowland, Tomaz Garcez, Cassandra Shilladay, Richard Pumphrey, Nandinee Patel, Paul J Turner, Robert J Boyle
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引用次数: 0

摘要

在人的一生中,过敏性休克的发病率高达 5%。虽然过敏性休克通常不会对身体造成长期影响,但会导致焦虑和生活质量下降。罕见且不可预测的是,社区性过敏性休克可导致迅速的生理失调和死亡。肾上腺素(肾上腺素)是治疗过敏性休克的基石,提供肾上腺素自动注射器(AAI)已成为社区过敏性休克高危人群的标准护理方法。在本文中,我们利用从动物和人体体内研究以及流行病学中获得的信息,探讨了 AAI 在预防过敏性休克致命后果方面的有效性。我们发现,数据支持静脉注射肾上腺素可有效逆转过敏性休克的生理特征,通常剂量为 0.05 至 0.5 μg/kg/min,持续 1-2 小时,或总剂量约为 10 μg/kg。人体肌肉注射剂量接近 10 μg/kg,可产生与静脉注射相似的峰值血浆肾上腺素水平(100-500 pg/mL)。不过,肌肉注射肾上腺素后,这些水平通常持续时间较短,药代动力学和药效学结果可能无法预测。流行病学数据不支持增加 AAI 处方与减少致命性过敏性休克之间存在关联,尽管携带率和激活率仍然很低。总之,这些数据表明,目前的 AAI 对致命性过敏性休克的发生率影响不大,这可能是由于缺乏持续和足够的血浆肾上腺素浓度所致。AAI处方对生活质量的影响可能各不相同。有必要考虑可通过适当途径安全输注持续肾上腺素的替代品。
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Adrenaline Auto-Injectors for Preventing Fatal Anaphylaxis.

Anaphylaxis affects up to 5% of people during their lifetime. Although anaphylaxis usually resolves without long-term physical consequences, it can result in anxiety and quality of life impairment. Rarely and unpredictably, community anaphylaxis can cause rapid physiological decompensation and death. Adrenaline (epinephrine) is the cornerstone of anaphylaxis treatment, and provision of adrenaline autoinjectors (AAI) has become a standard of care for people at risk of anaphylaxis in the community. In this article, we explore the effectiveness of AAIs for preventing fatal outcomes in anaphylaxis, using information drawn from animal and human in vivo studies and epidemiology. We find that data support the effectiveness of intravenous adrenaline infusions for reversing physiological features of anaphylaxis, typically at doses from 0.05 to 0.5 μg/kg/min for 1-2 h, or ~ 10 μg/kg total dose. Intramuscular injection of doses approximating 10 μg/kg in humans can result in similar peak plasma adrenaline levels to intravenous infusions, at 100-500 pg/mL. However, these levels are typically short-lived following intramuscular adrenaline, and pharmacokinetic and pharmacodynamic outcomes can be unpredictable. Epidemiological data do not support an association between increasing AAI prescriptions and reduced fatal anaphylaxis, although carriage and activation rates remain low. Taken together, these data suggest that current AAIs have little impact on rates of fatal anaphylaxis, perhaps due to a lack of sustained and sufficient plasma adrenaline concentration. Effects of AAI prescription on quality of life may be variable. There is a need to consider alternatives, which can safely deliver a sustained adrenaline infusion via an appropriate route.

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来源期刊
CiteScore
10.40
自引率
9.80%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Clinical & Experimental Allergy strikes an excellent balance between clinical and scientific articles and carries regular reviews and editorials written by leading authorities in their field. In response to the increasing number of quality submissions, since 1996 the journals size has increased by over 30%. Clinical & Experimental Allergy is essential reading for allergy practitioners and research scientists with an interest in allergic diseases and mechanisms. Truly international in appeal, Clinical & Experimental Allergy publishes clinical and experimental observations in disease in all fields of medicine in which allergic hypersensitivity plays a part.
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