Cooper Lesley, Harbour Jenny, Sneddon Jacqueline, Seaton R Andrew
Scottish Antimicrobial Prescribing Group, Healthcare Improvement Scotland, Delta House, 50 West Nile Street, Glasgow G1 2NP, UK.
Healthcare Improvement Scotland, Delta House, 50 West Nile Street, Glasgow G1 2NP, UK.
JAC Antimicrob Resist. 2021 Jan 27;3(1):dlaa123. doi: 10.1093/jacamr/dlaa123. eCollection 2021 Mar.
Approximately 10% of people have an unverified penicillin allergy, with multiple personal and public health consequences.
To assess the efficacy and safety of direct oral challenge, without prior skin testing, in this population.
MEDLINE, EMBASE, CINAHL, the Cochrane Library and Google Scholar were searched from inception to 28 June 2020 (updated November 2020) to find published and unpublished studies that reported direct oral challenge for the purpose of removal of penicillin allergy labels. Population weighted mean was used to calculate the proportion of patients who developed an immediate or delayed reaction to direct oral challenge across the studies.
Thirteen studies were included in the review, with a sample size of 1202 (range 7-328). Studies included inpatient and outpatient cohorts assessed as low risk for true allergy. In pooled analysis of all 13 studies there were 41/1202 (3.41%) mild immediate or delayed reactions to direct oral challenge. The population-weighted mean incidence of immediate or delayed reaction to an oral challenge across studies was also 3.41% (95% CI: 2.38%-4.43%). There were no reports of serious adverse reactions, 96.5% of patients could be de-labelled and many were subsequently successfully treated with penicillin.
Direct oral challenge is safe and effective for de-labelling patients assessed as low risk for true allergy. Non-specialist clinicians competent in using an assessment algorithm can offer evaluation of penicillin allergy labels using direct oral challenge in appropriate patients. These measures will facilitate optimal infection treatment for patients, support antimicrobial stewardship, and minimize antimicrobial resistance.
约10%的人存在未经证实的青霉素过敏,这会对个人和公共健康产生多种后果。
评估在该人群中不进行预先皮肤试验而直接口服激发试验的有效性和安全性。
检索MEDLINE、EMBASE、CINAHL、Cochrane图书馆和谷歌学术,检索时间从建库至2020年6月28日(2020年11月更新),以查找报告直接口服激发试验以去除青霉素过敏标签的已发表和未发表研究。采用总体加权均值计算各项研究中对直接口服激发试验出现即刻或延迟反应的患者比例。
该综述纳入了13项研究,样本量为1202例(范围7 - 328例)。研究纳入了被评估为真正过敏低风险的住院和门诊队列。在对所有13项研究的汇总分析中,有41/1202例(3.41%)对直接口服激发试验出现轻度即刻或延迟反应。各项研究中口服激发试验即刻或延迟反应的总体加权平均发生率也为3.41%(95%CI:2.38% - 4.43%)。未报告严重不良反应,96.5%的患者可去除过敏标签,许多患者随后成功接受了青霉素治疗。
对于被评估为真正过敏低风险的患者,直接口服激发试验用于去除过敏标签是安全有效的。具备使用评估算法能力的非专科临床医生可在合适患者中采用直接口服激发试验对青霉素过敏标签进行评估。这些措施将有助于为患者实现最佳感染治疗,支持抗菌药物管理,并最大限度减少抗菌药物耐药性。