Université Paris Descartes, Hôpital Necker Enfants Malades, Service de Maladies Infectieuses et Tropicales, Paris, France; Groupe Hospitalier Paris Saint-Joseph, Equipe Mobile de Microbiologie Clinique, Paris, France.
Université Paris XII, Hôpital Henri Mondor, Unité de Contrôle Épidémiologique et Prévention de l'Infection, Créteil, France.
Int J Infect Dis. 2015 Oct;39:62-7. doi: 10.1016/j.ijid.2015.08.011. Epub 2015 Sep 12.
To avoid the use of carbapenems, alternatives such as cephamycin, piperacillin-tazobactam, and others are suggested for the treatment of extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-PE) infections. The aim of this study was to evaluate the frequency and the feasibility of antimicrobial de-escalation for ESBL-PE-related infections.
A prospective observational, bi centric cohort study was conducted. All patients with ESBL-PE infections were included. De-escalation was systematically suggested if patients were clinically stable and the isolate was susceptible to possible alternatives.
Seventy-nine patients were included: 36 (45.6%) were children, 27 (34.1%) were hospitalized in intensive care units, and 37 (47%) were immunocompromised. Urinary tract infections, pneumonia, and catheter-related bloodstream infections accounted for 45.6%, 19%, and 10%, respectively, of the cohort. Escherichia coli, Klebsiella pneumoniae, and Enterobacter cloacae were the three most frequent causative organisms isolated. On day 5, 47 (59.2%) of the patients were still receiving carbapenems. Antimicrobial resistance (44.7%), infection relapse (26.9%), and clinical instability (19.2%) were the most important reasons for not prescribing alternatives. E. coli-related infections appeared to be a protective factor against maintaining the carbapenem prescription (odds ratio 0.11, 95% confidence interval 0.041-0.324; p=0.0013).
In clinical practice, less than 50% of patients with ESBL-PE-related infections were de-escalated after empirical treatment with carbapenems.
为避免使用碳青霉烯类药物,建议使用头孢菌素、哌拉西林他唑巴坦等替代药物治疗产超广谱β-内酰胺酶(ESBL)肠杆菌科(ESBL-PE)感染。本研究旨在评估 ESBL-PE 相关感染中抗菌药物降级治疗的频率和可行性。
前瞻性观察性、双中心队列研究。纳入所有 ESBL-PE 感染患者。如果患者临床稳定且分离株对可能的替代药物敏感,则系统建议降级治疗。
共纳入 79 例患者:36 例(45.6%)为儿童,27 例(34.1%)住院于重症监护病房,37 例(47%)免疫功能低下。尿路感染、肺炎和导管相关血流感染分别占队列的 45.6%、19%和 10%。最常见的病原体依次为大肠埃希菌、肺炎克雷伯菌和阴沟肠杆菌。第 5 天,仍有 47 例(59.2%)患者接受碳青霉烯类药物治疗。抗菌药物耐药(44.7%)、感染复发(26.9%)和临床不稳定(19.2%)是未开替代药物的最重要原因。与大肠埃希菌相关的感染似乎是维持碳青霉烯类药物处方的保护因素(比值比 0.11,95%置信区间 0.041-0.324;p=0.0013)。
在临床实践中,接受经验性碳青霉烯类药物治疗后,不到 50%的 ESBL-PE 相关感染患者进行了降级治疗。