Epstein-Rigbi Naama, Ziv Sharon, Bulanenkova Marina, Bouganim Ruth, Tal-Jasper Ruthy, Marchaim Dror
The Institute of Allergy, Immunology and Pediatric Pulmonology, Shamir (Assaf Harofeh) Medical Center, Beer Yaacov, Israel.
Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Antimicrob Steward Healthc Epidemiol. 2024 Apr 30;4(1):e68. doi: 10.1017/ash.2024.68. eCollection 2024.
A beta-lactam antibiotics (BLA) allergy label is common, resulting in disadvantageous outcomes due to the usage of second-line antimicrobial agents. Noncontrolled case-series analyses report low rates of hypersensitivity reactions, following intentional/non-intentional BLA challenges among labeled inpatients. The study aims were to explore predictors and outcomes associated with hypersensitivity reactions following BLA challenge among BLA-allergic labeled inpatients.
Retrospective cohort study (2019-2020) of adult (≥18 years) inpatients (Shamir Medical Center, Israel), labeled as allergic to ≥1 BLA, who received ≥1 dose/s of BLA during their stay. Independent predictors to develop allergic reactions and the independent associations of allergic reactions with clinical outcomes were queried by logistic and Cox regressions.
Of 9,670 inpatients (14,088 hospitalizations), 3,570 (37%) were labeled as allergic to ≥1 BLA. Of those, 1,171 (33%) patients received ≥1 BLA. The majority were women (67%), and the mean age was 69.3 ± 19.4 years. Only 30 patients (2.6%) developed a reaction, all mild. Independent predictors to develop an allergic reaction were documented reactions in the past, atopic background, antihistamines administration prior to the BLA challenge, and high risk for cross-reactivity, based on the BLA side chains, between the labeled and the challenged agents. Reaction upon the BLA challenge was not independently associated with any worse outcome.
Despite the commonality of allergy labeling, and the commonality of BLA administration to labeled inpatients, hypersensitivity reactions were mild and rare. Interventional stewardship strategies for active BLA de-labeling among low-risk patients should be promoted, to improve patients' and institutional health and fiscal outcomes.
β-内酰胺类抗生素(BLA)过敏标签很常见,由于使用二线抗菌药物会导致不利后果。非对照病例系列分析报告称,在有标签的住院患者中,有意/无意进行BLA激发试验后,过敏反应发生率较低。本研究的目的是探讨BLA过敏标签的住院患者在进行BLA激发试验后与过敏反应相关的预测因素和结果。
对以色列沙米尔医疗中心2019 - 2020年成年(≥18岁)住院患者进行回顾性队列研究,这些患者被标记为对≥1种BLA过敏,且在住院期间接受了≥1剂BLA。通过逻辑回归和Cox回归分析发生过敏反应的独立预测因素以及过敏反应与临床结果的独立关联。
在9670名住院患者(14088次住院)中,3570名(37%)被标记为对≥1种BLA过敏。其中,1171名(33%)患者接受了≥1剂BLA。大多数为女性(67%),平均年龄为69.3±19.4岁。只有30名患者(2.6%)出现反应,均为轻度。发生过敏反应的独立预测因素包括既往有记录的反应、特应性背景、在BLA激发试验前使用抗组胺药,以及根据BLA侧链判断,标记的药物和激发试验使用的药物之间存在高交叉反应风险。BLA激发试验后的反应与任何更差的结果均无独立关联。
尽管过敏标签很常见,且对有标签住院患者使用BLA也很常见,但过敏反应轻微且罕见。应推广针对低风险患者积极去除BLA过敏标签的干预管理策略,以改善患者和机构的健康及财务状况。