Maisat Wiriya, Bermudez Marie, Yuki Koichi
Cardiac Anesthesia Division, Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Boston, United States of America.
Department of Anaesthesia, Harvard Medical School, Boston, United States of America.
Perioper Care Oper Room Manag. 2022 Sep;28. doi: 10.1016/j.pcorm.2022.100278. Epub 2022 Jul 13.
Clindamycin serves as an alternative surgical prophylactic antibiotic in patients with penicillin (PCN) or cephalosporin allergy labels. In the previous reports, the use of clindamycin was associated with higher incidences of surgical site infections (SSIs). We aimed to determine the characteristics of PCN or cephalosporin allergic reactions to stratify patient's risk and indicate subsequent management; leading to de-labeling of PCN or cephalosporin allergy.
We conducted a prospective cohort study of patients receiving clindamycin as surgical antibiotic prophylaxis from September 2021 to March 2022. Data were collected from electronic medical records; included demographic data, antibiotic allergy labels, allergic reaction, and allergy testing.
Clindamycin was administered in 445 patients who underwent 451 operations. Among these patients, 53.0% ( = 236) were female with a median age of 15 years (range; 0.5-57.0 years). PCN and cephalosporin allergies were labelled in 83.8% ( = 373) and 25.6% ( = 114) patients, respectively; 11.4% ( = 51) of patients were allergic to both classes of the antibiotics. There were 191 (51.2%) and 73 (64.0%) possible hypersensitivity reactions (HSRs) in PCN and cephalosporin groups, respectively. The most common reactions were rash (PCN: = 99, 26.5%; cephalosporin: = 35, 30.7%), and hives (PCN: = 71, 19.0%; cephalosporin: = 24, 21.1%). Severe reactions included angioedema (PCN: = 7, 1.9%; cephalosporin: = 5, 4.4%), anaphylaxis (PCN: = 8, 2.1%; cephalosporin: = 7, 6.1%), bronchospasm (cephalosporin: = 1, 0.9%), airway involvement (PCN: = 1, 0.3%; cephalosporin: = 1, 0.9%), serum sickness (PCN: = 1, 0.3%), blisters (PCN: = 1, 0.3%), and drug reaction with eosinophilia and systemic symptoms (DRESS) (PCN: = 1, 0.3%). Low-risk history of allergy included gastrointestinal side effects (PCN: = 9, 2.4%; cephalosporin: = 3, 2.7%), positive family history (PCN: = 7, 1.9%; cephalosporin: = 1, 0.9%), and remote history of allergy (PCN: = 2, 0.5%). There were 201 (53.9%) and 53 (46.5%) unknown reactions in PCN and cephalosporin groups, respectively. In the overall cohort, 3 patients (0.7%) were skin tested for drug allergy (PCN: = 2, 0.5%; cephalosporin: = 2, 1.8%).
Clindamycin was largely administered in patients with non-severe HSRs, low-risk history or unknown reactions to PCN or cephalosporin, whom cefazolin could have been administered safely. Obtaining a detailed history of antibiotic allergy, allergy testing and/or direct oral challenge can de-label unsubstantiated PCN or cephalosporin allergy and ultimately reduce the incidence of SSIs by optimizing the rate of more effective antibiotic administration.
对于有青霉素(PCN)或头孢菌素过敏标识的患者,克林霉素可作为外科预防性抗生素的替代药物。在既往报告中,使用克林霉素与手术部位感染(SSI)的较高发生率相关。我们旨在确定PCN或头孢菌素过敏反应的特征,以对患者风险进行分层并指导后续管理,从而去除PCN或头孢菌素过敏标识。
我们对2021年9月至2022年3月期间接受克林霉素作为外科抗生素预防用药的患者进行了一项前瞻性队列研究。数据从电子病历中收集,包括人口统计学数据、抗生素过敏标识、过敏反应和过敏试验。
445例患者接受了451次手术并使用了克林霉素。在这些患者中,53.0%(n = 236)为女性,中位年龄为15岁(范围:0.5 - 57.0岁)。分别有83.8%(n = 373)和25.6%(n = 114)的患者有PCN和头孢菌素过敏标识;11.4%(n = 51)的患者对这两类抗生素均过敏。PCN组和头孢菌素组分别有191例(51.2%)和73例(64.0%)可能的超敏反应(HSR)。最常见的反应是皮疹(PCN组:n = 99,26.5%;头孢菌素组:n = 35,30.7%)和荨麻疹(PCN组:n = 71,19.0%;头孢菌素组:n = 24,21.1%)。严重反应包括血管性水肿(PCN组:n = 7,1.9%;头孢菌素组:n = 5,4.4%)、过敏反应(PCN组:n = 8,2.1%;头孢菌素组:n = 7,6.1%)、支气管痉挛(头孢菌素组:n = 1,0.9%)、气道受累(PCN组:n = 1,0.3%;头孢菌素组:n = 1,0.9%)、血清病(PCN组:n = 1,0.3%)、水疱(PCN组:n = 1,0.3%)以及伴有嗜酸性粒细胞增多和全身症状的药物反应(DRESS)(PCN组:n = !,0.3%)。低风险过敏史包括胃肠道副作用(PCN组:n = 9,2.4%;头孢菌素组:n = 3,2.7%)、阳性家族史(PCN组:n = 7,1.9%;头孢菌素组:n = 1,0.9%)和既往过敏史(PCN组:n = 2,0.5%)。PCN组和头孢菌素组分别有201例(53.9%)和53例(46.5%)反应不明。在整个队列中,3例患者(0.7%)进行了药物过敏皮肤试验(PCN组:n = 2,0.5%;头孢菌素组:n = 2,1.8%)。
克林霉素主要用于对PCN或头孢菌素发生非严重HSR、低风险过敏史或反应不明的患者,而这些患者原本可以安全地使用头孢唑林。获取详细的抗生素过敏史、进行过敏试验和/或直接口服激发试验可以去除未经证实的PCN或头孢菌素过敏标识,并最终通过优化更有效抗生素的给药率来降低SSI的发生率。