Kim Min-Hye, Kang Dong Yoon, Nam Young-Hee, Sim Da Woon, Kim Sujeong, Lee Jun Kyu, Park Jung-Won, Park Hye-Kyung, Jung Jae-Woo, Kim Cheol-Woo, Yang Min-Suk, Kim Joo-Hee, Ye Young-Min, Koh Young-Il, Kang Hye-Ryun, Park Seoung Ju, Kim Sae-Hoon
Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.
Department of Preventive Medicine, Ulsan University Hospital, Ulsan, Korea.
World Allergy Organ J. 2023 Jan 12;16(1):100738. doi: 10.1016/j.waojou.2022.100738. eCollection 2023 Jan.
Although beta-lactams are 1 of the major causative agents of severe cutaneous adverse reactions (SCAR), their epidemiology and clinical aspects have been poorly studied. This study aimed to investigate the characteristics of SCAR caused by beta-lactams in the Korean SCAR registry.
We retrospectively analyzed beta-lactam-induced SCAR cases collected from 28 tertiary university hospitals in Korea between 2010 and 2015. The SCAR phenotypes included Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), SJS-TEN overlap, and drug reaction with eosinophilia and systemic symptoms (DRESS). Beta-lactams were classified according to their chemical structures: penicillins, cephalosporins, and carbapenems. The causative beta-lactams, clinical and laboratory features, treatments, and outcomes were evaluated.
Among the 275 antibiotic-induced SCAR cases, 170 patients developed SCAR induced by beta-lactams. Beta-lactam antibiotic-induced SCAR showed more frequent SJS/TEN compared to SCAR induced by non-beta-lactam antibiotics (SJS/TEN/SJS-TEN overlap/DRESS: 36.5/11.2/5.9/46.5% vs. 23.8/10.5/2.9/62.9%, = 0.049). Cephalosporin was the most common culprit drug. Particularly, 91 and 79 patients presented with SJS/TEN and DRESS, respectively. The odds ratio (OR) for poor prognosis, such as sequelae and death, was significantly increased in subjects with SJS-TEN overlap and TEN and carbapenem as culprit drug in the multivariate analysis (OR, 35.61; = 0.016, OR, 28.07; = 0.006, OR 30.46; = 0.027).
Among antibiotic-induced SCAR, clinical features were different depending on whether the culprit drug was a beta-lactam antibiotic or SCAR type. The poor prognosis was related to SJS-TEN overlap, TEN type, and carbapenem as the culprit drug.
尽管β-内酰胺类药物是严重皮肤不良反应(SCAR)的主要致病因素之一,但其流行病学和临床特征尚未得到充分研究。本研究旨在调查韩国SCAR登记处中由β-内酰胺类药物引起的SCAR的特征。
我们回顾性分析了2010年至2015年间从韩国28家三级大学医院收集的β-内酰胺类药物引起的SCAR病例。SCAR的表型包括史蒂文斯-约翰逊综合征(SJS)、中毒性表皮坏死松解症(TEN)、SJS-TEN重叠型以及伴有嗜酸性粒细胞增多和全身症状的药物反应(DRESS)。β-内酰胺类药物根据其化学结构分类:青霉素类、头孢菌素类和碳青霉烯类。对致病的β-内酰胺类药物、临床和实验室特征、治疗方法及结果进行了评估。
在275例抗生素引起的SCAR病例中,有170例患者是由β-内酰胺类药物引起的SCAR。与非β-内酰胺类抗生素引起的SCAR相比,β-内酰胺类抗生素引起的SCAR中SJS/TEN更为常见(SJS/TEN/SJS-TEN重叠型/DRESS:36.5/11.2/5.9/46.5% 对 23.8/10.5/2.9/62.9%,P = 0.049)。头孢菌素是最常见的致病药物。特别是,分别有91例和79例患者出现SJS/TEN和DRESS。在多变量分析中,SJS-TEN重叠型、TEN型以及以碳青霉烯类药物作为致病药物的患者出现后遗症和死亡等不良预后的比值比(OR)显著升高(OR,35.61;P = 0.016,OR,28.07;P = 0.006,OR 30.46;P = 0.027)。
在抗生素引起的SCAR中,临床特征因致病药物是β-内酰胺类抗生素还是SCAR类型而异。不良预后与SJS-TEN重叠型、TEN型以及以碳青霉烯类药物作为致病药物有关。