Beta-lactam antibiotics administration among adult inpatients with a beta-lactam allergy label: incidence, predictors, and outcomes

• Published in: Antimicrobial stewardship & healthcare epidemiology : ASHE 2024, Vol.4 (1), p.e68-e68, Article e68
• Main Authors: Epstein-Rigbi, Naama, Ziv, Sharon, Bulanenkova, Marina, Bouganim, Ruth, Tal-Jasper, Ruthy, Marchaim, Dror
• Format: Article
• Language: English
• Subjects: Allergies; Anaphylaxis; Antibiotics; Antimicrobial agents; Asthma; Clinical outcomes; Dermatitis; Food allergies; Hay fever; Hospitalization; Hypersensitivity; Labeling; Medical records; Original; Patients; Penicillin; Rhinitis
• ISSN: 2732-494X; 2732-494X
• DOI: 10.1017/ash.2024.68

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.