Seven-versus 14-day course of antibiotics for the treatment of bloodstream infections by Enterobacterales: a randomized, controlled trial

医学 临床终点 随机对照试验 抗生素 临床试验 内科学 意向治疗分析 外科 儿科 生物 微生物学
作者
José Antonio Molina,Enrique Montero-Mateos,Julia Praena-Segovia,E. León-Jiménez,Clara Nátera,Luis Eduardo López-Cortés,Lucía Dolores Mesa Valiente,Clara Rosso-Fernández,Marta Herrero,Ana Isabel Aller-García,Ángela Cano,Belén Gutiérrez‐Gutiérrez,Ignacio Márquez-Gómez,Rocío Álvarez‐Marín,Carmen Infante,Cristina Roca,Adoración Valiente-Méndez,Jerónimo Pachón,J.M. Reguera,Juan E. Corzo-Delgado,Julián Torre‐Cisneros,Jesús Rodríguez-Baño,José Miguel Cisneros,B. Solano,Verónica González-Galán,Esteban Fernández Hinojosa,Francisco López-Bernal,Marta Suñer,José Ángel Noval,Álvaro Giráldez,Antonio José Navarro,María Jesús Rodríguez-Hernández,Yolanda Borrego,Paloma Gil,José Antonio Suárez Lepe,Isabel Morales,Pilar Retamar,Marina de Cueto,Juan José Castón,Elisa Vidal
出处
期刊:Clinical Microbiology and Infection [Elsevier BV]
卷期号:28 (4): 550-557 被引量:60
标识
DOI:10.1016/j.cmi.2021.09.001
摘要

To prove that 7-day courses of antibiotics for bloodstream infections caused by members of the Enterobacterales (eBSIs) allow a reduction in patients' exposure to antibiotics while achieving clinical outcomes similar to those of 14-day schemes.A randomized trial was performed. Adult patients developing eBSI with appropriate source control were assigned to 7 or 14 days of treatment, and followed 28 days after treatment cessation; treatments could be resumed whenever necessary. The primary endpoint was days of treatment at the end of follow-up. Clinical outcomes included clinical cure, relapse of eBSI and relapse of fever. A superiority margin of 3 days was set for the primary endpoint, and a non-inferiority margin of 10% was set for clinical outcomes. Efficacy and safety were assessed together with a DOOR/RADAR (desirability of outcome ranking and response adjusted for duration of antibiotic risk) analysis.248 patients were assigned to 7 (n = 119) or 14 (n = 129) days of treatment. In the intention-to-treat analysis, median days of treatment at the end of follow-up were 7 and 14 days (difference 7, 95%CI 7-7). The non-inferiority margin was also met for clinical outcomes, except for relapse of fever (-0.2%, 95%CI -10.4 to 10.1). The DOOR/RADAR showed that 7-day schemes had a 77.7% probability of achieving better results than 14-day treatments.7-day schemes allowed a reduction in antibiotic exposure of patients with eBSI while achieving outcomes similar to those of 14-day schemes. The possibility of relapsing fever in a limited number of patients, without relevance to final outcomes, may not be excluded, but was overcome by the benefits of shortening treatments.
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