Antepartum vs postpartum amoxicillin oral challenge in pregnant patients with a reported penicillin allergy: A two-center prospective cohort study

IF 3.5 2区 医学 Q1 OBSTETRICS & GYNECOLOGY Acta Obstetricia et Gynecologica Scandinavica Pub Date : 2024-09-10 DOI:10.1111/aogs.14964
Jeffrey Man Hay Wong, Xiaoqing Liu, Raymond Mak, Stephanie C. Erdle, Colin Barber, Julianne van Schalkwyk, Melissa Watt, Sudharsana Rao Ande, Dozie Ochulor, Chelsea Elwood, Vanessa Poliquin
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Abstract

Introduction

While 10% of pregnant individuals report a penicillin allergy, there is no established best practice for penicillin allergy delabeling in pregnancy. To better understand options for penicillin delabeling, we aimed to evaluate two penicillin allergy delabeling protocols in pregnancy regarding efficacy, adverse events, and patient satisfaction.

Material and Methods

From July 2019 to December 2022, we completed a two-center prospective cohort study, where each site recruited pregnant patients over 24 weeks gestational age with a reported penicillin allergy. One center offered antepartum amoxicillin oral challenges, either directly or after negative skin testing (i.e., antepartum oral challenge site). Our other centers completed a two-step approach with antepartum penicillin skin testing only and deferred oral challenges to the postpartum period (i.e., postpartum oral challenge site). Our primary outcome was the rate of penicillin allergy delabeling, defined as tolerating an antibiotic challenge with penicillin or amoxicillin. Univariate analyses were completed using chi-squared, Fisher's exact, and Wilcoxon rank tests.

Results

During the study period, 276 pregnant patients were assessed, with 207 in the antepartum oral challenge site and 69 in the postpartum oral challenge site. Among the 204 patients who completed antepartum oral challenges, 201 (98%) passed without reactions. Deferring oral challenges to the postpartum period led to a loss of follow-up for 37/53 (70%) of eligible individuals. Overall, 97% (201/207) of patients at the antepartum oral challenge site were delabeled from their penicillin allergy—compared to 38% (26/69) of patients referred to the postpartum oral challenge site (p < 0.0001). Three antepartum oral challenge reactions were noted, including two mild cutaneous reactions and a case of transient abdominal discomfort.

Conclusions

Antepartum amoxicillin oral challenge is a more effective method to delabel pregnant patients from their penicillin allergy. Deferral of oral challenges to the postpartum period introduces a significant barrier for penicillin allergy delabeling.

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对已报告青霉素过敏的孕妇进行产前与产后阿莫西林口服试验:双中心前瞻性队列研究
导言虽然有 10% 的孕妇报告对青霉素过敏,但目前还没有确定妊娠期青霉素过敏脱敏的最佳实践。为了更好地了解青霉素脱敏的选择,我们旨在评估两种妊娠期青霉素过敏脱敏方案的疗效、不良事件和患者满意度。材料与方法从 2019 年 7 月到 2022 年 12 月,我们完成了一项双中心前瞻性队列研究,每个研究地点都招募了胎龄超过 24 周且报告青霉素过敏的孕妇患者。其中一个中心提供产前阿莫西林口服挑战,可直接进行或在皮试阴性后进行(即产前口服挑战点)。我们的其他中心采用了两步法,仅在产前进行青霉素皮试,并将口服试验推迟到产后进行(即产后口服试验点)。我们的主要结果是青霉素过敏脱敏率,即能耐受青霉素或阿莫西林的抗生素挑战。结果在研究期间,共有 276 名孕妇接受了评估,其中 207 人接受了产前口腔挑战,69 人接受了产后口腔挑战。在完成产前口服挑战的 204 名患者中,201 人(98%)无反应通过。将口服挑战推迟到产后进行会导致 37/53 人(70%)失去随访资格。总体而言,97%(201/207)的产前口服药物过敏患者与青霉素过敏脱敏,而 38%(26/69)的产后口服药物过敏患者与青霉素过敏脱敏(p <0.0001)。结论:产前阿莫西林口服试验是解除孕妇青霉素过敏的更有效方法。将口服试验推迟到产后进行会给青霉素过敏脱敏带来很大的障碍。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
180
审稿时长
3-6 weeks
期刊介绍: Published monthly, Acta Obstetricia et Gynecologica Scandinavica is an international journal dedicated to providing the very latest information on the results of both clinical, basic and translational research work related to all aspects of women’s health from around the globe. The journal regularly publishes commentaries, reviews, and original articles on a wide variety of topics including: gynecology, pregnancy, birth, female urology, gynecologic oncology, fertility and reproductive biology.
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