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

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 d...

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Veröffentlicht in:Clinical microbiology and infection 2022-04, Vol.28 (4), p.550-557
Hauptverfasser: Molina, José, Montero-Mateos, Enrique, Praena-Segovia, Julia, León-Jiménez, Eva, Natera, Clara, López-Cortés, Luis E., Valiente, Lucía, Rosso-Fernández, Clara M., Herrero, Marta, Aller-García, Ana I., Cano, Ángela, Gutiérrez-Gutiérrez, Belén, Márquez-Gómez, Ignacio, Álvarez-Marín, Rocío, Infante, Carmen, Roca, Cristina, Valiente-Méndez, Adoración, Pachón, Jerónimo, Reguera, José María, Corzo-Delgado, Juan Enrique, Torre-Cisneros, Julián, Rodríguez-Baño, Jesús, Cisneros, José Miguel, Solano, Blanca, González-Galán, Verónica, Hinojosa, Esteban, López-Bernal, Francisco, Suñer, Marta, Noval, José Ángel, Giráldez, Álvaro, Navarro, Antonio, Rodríguez-Hernández, María Jesús, Borrego, Yolanda, Gil, Paloma, Lepe, José Antonio, Morales, Isabel, Retamar, Pilar, de Cueto, Marina, Castón, Juan José, Vidal, Elisa
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Sprache:eng
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Zusammenfassung: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.
ISSN:1198-743X
1469-0691
DOI:10.1016/j.cmi.2021.09.001