Department of Allergy, Hospital Universitario Virgen del Rocío, Sevilla, Spain.
Department of Allergy, Hospital Universitario Virgen del Rocío, Sevilla, Spain.
Aten Primaria. 2024 Nov;56(11):102925. doi: 10.1016/j.aprim.2024.102925. Epub 2024 May 24.
To determine whether the β-lactam allergy delabeling was safe and cost-saving in Primary Care (PC) patients.
We have conducted a retrospective chart review of PC patients with β-lactam allergy label evaluated in our Allergy Unit between 2017 and 2022. SITE: Allergy Department. Hospital Virgen del Rocio (Sevilla).
A total of 391 patients labeled for β-lactam allergy in PC were studied.
(a) Outcome evaluation of a β-lactam allergy delabeling procedure. (b) A ratio between the total e-prescribed antibiotic cost and the number of treatment days (the experimental daily antibiotic cost or EDAC) before and after delabeling was analyzed in delabeled and truly allergic patients.
The results of skin testing were positive in 9.2% of the reported cases (36 of 391 patients). The reactions to oral provocation challenge (OPC) occurred in 2.14% of the patients who underwent negative skin testing to offending β-lactam (in 15 of 699 OPC). A total of 307 patients (78.5%) were delabeled; 70 (17.9%) had a β-lactam selective response and 14 (3.59%) reacted to both penicillin and cephalosporin. The EDAC before and after the procedure in delabeled patients was significantly lower (0.88 € vs 0.62 €, p<10), than that observed in truly allergic group (0.87 € vs. 0.76 €, p=not significant).
To delabel β-lactam allergy in Primary Care patients is safe in most patients, cost-saving in antibioticotherapy, and allows identify the main clinical β-lactam allergy phenotypes that benefit from this procedure.
确定在初级保健(PC)患者中进行β-内酰胺类药物过敏去标签化是否安全和节省成本。
我们对 2017 年至 2022 年期间在我们过敏科评估的 PC 中具有β-内酰胺类药物过敏标签的患者进行了回顾性图表审查。
过敏科。Virgen del Rocio 医院(塞维利亚)。
共研究了 391 名在 PC 中被标记为β-内酰胺类药物过敏的患者。
(a)β-内酰胺类药物过敏去标签程序的结果评估。(b)在去标签化前后,分析去标签化和真正过敏患者的总电子处方抗生素费用与治疗天数(实验性每日抗生素费用或 EDAC)之间的比值。
报告病例中有 9.2%(36/391 例)的皮肤试验结果阳性。对β-内酰胺类药物进行阴性皮肤试验的患者中,有 2.14%(15/699 例)发生口服激发挑战(OPC)反应。共有 307 名患者(78.5%)被去标签化;70 名(17.9%)对β-内酰胺类药物有选择性反应,14 名(3.59%)对青霉素和头孢菌素均有反应。去标签化患者的 EDAC 在程序前后显著降低(0.88 欧元与 0.62 欧元,p<10),明显低于真正过敏组(0.87 欧元与 0.76 欧元,p=无统计学意义)。
在大多数患者中,在 PC 患者中去标签β-内酰胺类药物过敏是安全的,可以节省抗生素治疗费用,并可以确定从该程序中受益的主要临床β-内酰胺类药物过敏表型。