Clearance of penicillin allergies via direct oral provocation testing (DOPT): a systematic review.

Michael Dore, Ashley Otto, Annie Wang, Carly Heintz, Sarah Cantrell, Daniel Shields, Allyson Burkhart
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Abstract

Objective: Penicillin allergies are reported in 10-15% of the US population, but the actual rate is less than 1%. Inappropriate penicillin allergies are associated with adverse patient outcomes, poor antimicrobial stewardship, and increased healthcare costs. Direct oral provocation testing (DOPT) is a safe and cost-effective way to remove false penicillin allergy labels (PAL). However, widespread implementation is currently limited due to inadequate safety data and protocol variations. This systematic review evaluates the safety of single-dose, nongraded DOPT by the nonallergist.

Design: Systematic review. MEDLINE, Embase, Web of Science, and the Cochrane Central Register of Controlled Trials were searched from inception to May 2025.

Setting: Inpatient (Intensive care unit (ICU) and general medical ward) and outpatient.

Participants: Adults with self-reported penicillin allergies deemed low risk by a validated scoring system.

Interventions: DOPT by nonallergists with single-dose oral amoxicillin 250 mg with a 60-minute observation period.

Results: 3 352 studies were identified, 15 were included in the analysis. Of the 1786 patients who completed DOPT, 66 (3.7%) experienced any reaction: 27 (1.5%) immediate rashes, 24 (1.3%) delayed rashes, and 15 (.8%) other reactions. No cases of anaphylaxis, angioedema, or epinephrine use were reported.

Conclusion: The use of single-dose DOPT in patients deemed low risk, using a validated risk scoring tool, is safe, with low rates of mild reactions and no serious adverse events. A nonallergist can significantly improve penicillin delabeling rates and patient outcomes using this approach.

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通过直接口服激发试验(DOPT)清除青霉素过敏:一项系统综述。
目的:美国10-15%的人口报告青霉素过敏,但实际发生率不到1%。不适当的青霉素过敏与不良的患者结果、不良的抗菌药物管理和增加的医疗费用有关。直接口服激发试验(DOPT)是一种安全且经济有效的去除假青霉素过敏标签(PAL)的方法。然而,由于安全数据不足和协议变化,目前广泛实施受到限制。本系统综述评估了非过敏专科医师单剂量、非分级DOPT的安全性。设计:系统回顾。检索了MEDLINE、Embase、Web of Science和Cochrane Central Register of Controlled Trials从成立到2025年5月。环境:住院(重症监护病房(ICU)和普通病房)和门诊。参与者:经验证的评分系统认为自我报告青霉素过敏的成年人风险较低。干预措施:由非过敏专科医生采用单剂量口服阿莫西林250 mg,观察时间为60分钟。结果:共纳入3 352项研究,其中15项纳入分析。在完成DOPT的1786例患者中,66例(3.7%)出现了任何反应:27例(1.5%)立即皮疹,24例(1.3%)延迟皮疹,15例(0.8%)其他反应。没有过敏反应、血管性水肿或肾上腺素使用的病例报告。结论:使用经过验证的风险评分工具,在低风险患者中使用单剂量DOPT是安全的,轻度反应发生率低,无严重不良事件。使用这种方法,非过敏专科医师可以显著提高青霉素去标签率和患者预后。
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