医学
肾上腺素
哮喘
优势比
麻醉
恶化
急性重症哮喘
随机对照试验
过敏反应
兴奋剂
内科学
过敏
呼吸道疾病
受体
免疫学
肺
作者
Christina Baggott,Jo Hardy,Jenny Sparks,Doñah Sabbagh,Richard Beasley,Mark Weatherall,James Fingleton
出处
期刊:Thorax
[BMJ]
日期:2021-09-30
卷期号:77 (6): 563-572
被引量:24
标识
DOI:10.1136/thoraxjnl-2021-217124
摘要
Background International asthma guidelines recommend against epinephrine (adrenaline) administration in acute asthma unless associated with anaphylaxis or angio-oedema. However, administration of intramuscular epinephrine in addition to nebulised selective β 2 -agonist is recommended for acute severe or life-threatening asthma in many prehospital guidelines. We conducted a systematic review to determine the efficacy of epinephrine in comparison to selective β 2 -agonist in acute asthma. Methods We included peer-reviewed publications of randomised controlled trials (RCTs) that enrolled children or adults in any healthcare setting and compared epinephrine by any route to selective β 2 -agonist by any route for an acute asthma exacerbation. The primary outcome was treatment failure, including hospitalisation, need for intubation or death. Results Thirty-eight of 1140 studies were included. Overall quality of evidence was low. Seventeen studies contributed data on 1299 participants to the meta-analysis. There was significant statistical heterogeneity, I 2 =56%. The pooled Peto’s OR for treatment failure with epinephrine versus selective β 2 -agonist was 0.99 (0.75 to 1.32), p=0.95. There was strong evidence that recruitment age group was associated with different estimates of the odds of treatment failure; with studies recruiting adults-only having lower odds of treatment failure with epinephrine. It was not possible to determine whether epinephrine in addition to selective β 2 -agonist improved outcomes. Conclusion The low-quality evidence available suggests that epinephrine and selective β 2 -agonists have similar efficacy in acute asthma. There is a need for high-quality double-blind RCTs to determine whether addition of intramuscular epinephrine to inhaled or nebulised selective β 2 -agonist improves outcome. PROSPERO registration number CRD42017079472.
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