Repositori URV

Autor segons l'article: Grillo, Sara; Cuervo, Guillermo; Carratala, Jordi; San-Juan, Rafael; Aguado, Jose M.; Morata, Laura; Gomez-Zorrilla, Silvia; Lopez-Contreras, Joaquin; Gasch, Oriol; Gomila-Grange, Aina; Iftimie, Simona; Garcia-Pardo, Graciano; Calbo, Esther; Boix-Palop, Lucia; Orio, Isabel; Jover-Saenz, Alfredo; Eduardo Lopez-Cortes, Luis; Euba, Gorane; Aguirregabiria, Malen; Jose Garcia-pais, Maria; Gioia, Francesca; Ramon Pano, Jose; Luisa Pedro-Botet, Maria; Maria Benitez, Rosa; Teresa Perez-Rodriguez, Maria; Meije, Yolanda; Belen Loeches-Yague, Maria; Horna, Gertrudis; Berbel, Damaris; Angeles Dominguez, Maria; Padulles, Ariadna; Cobo, Sara; Hereu, Pilar; Videla, Sebastian; Tebe, Cristian; Pallares, Natalia; Miro, Josep M.; Pujol, Miquel;Safo Study Grp; Spanish Network Res Infect Dis

Departament: Medicina i Cirurgia

Autor/s de la URV: Garcia Pardo, Graciano / Iftimie Iftimie, Simona Mihaela / TEBÉ CORDOMÍ, CRISTIAN

Paraules clau: Mortality Microbiology Infectious diseases Endocarditis Clinical trials

Resum: Introduction Methicillin-susceptible Staphylococcus aureus (MSSA) bacteraemia is a frequent condition, with high mortality rates. There is a growing interest in identifying new therapeutic regimens able to reduce therapeutic failure and mortality observed with the standard of care of beta-lactam monotherapy. In vitro and small-scale studies have found synergy between cloxacillin and fosfomycin against S. aureus. Our aim is to test the hypothesis that cloxacillin plus fosfomycin achieves higher treatment success than cloxacillin alone in patients with MSSA bacteraemia.Methods We will perform a superiority, randomised, open-label, phase IV-III, two-armed parallel group (1:1) clinical trial at 20 Spanish tertiary hospitals. Adults (>= 18 years) with isolation of MSSA from at least one blood culture <= 72 hours before inclusion with evidence of infection, will be randomly allocated to receive either cloxacillin 2 g/4-hour intravenous plus fosfomycin 3 g/6-hour intravenous or cloxacillin 2 g/4-hour intravenous alone for 7 days. After the first week, sequential treatment and total duration of antibiotic therapy will be determined according to clinical criteria by the attending physician. Primary endpoints: (1) Treatment success at day 7, a composite endpoint comprising all the following criteria: patient alive, stable or with improved quick-Sequential Organ Failure Assessment score, afebrile and with negative blood cultures for MSSA at day 7. (2) Treatment success at test of cure (TOC) visit: patient alive and no isolation of MSSA in blood culture or at another sterile site from day 8 until TOC (12 weeks after randomisation). We assume a rate of treatment success of 74% in the cloxacillin group. Accepting alpha risk of 0.05 and beta risk of 0.2 in a two-sided test, 183 subjects will be required in each of the control and experimental groups to obtain statistically significant difference of 12% (considered clinically significant).Ethics and dissemination Ethical approval has been obtained from the Ethics Committee of Bellvitge University Hospital (AC069/18) and from the Spanish Medicines and Healthcare Product Regulatory Agency (AEMPS, AC069/18), and is valid for all participating centres under existing Spanish legislation. The results will be presented at international meetings and will be made available to patients and funders.

Àrees temàtiques: Saúde coletiva Psicología Odontología Nutrição Medicine, general & internal Medicine (miscellaneous) Medicine (all) Medicina veterinaria Medicina iii Medicina ii Medicina i Interdisciplinar General medicine Farmacia Ensino Enfermagem Educação física Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Ciências ambientais Ciência da computação Biotecnología

Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/

Adreça de correu electrònic de l'autor: graciano.garcia@urv.cat simonamihaela.iftime@urv.cat

Identificador de l'autor: 0000-0003-0714-8414

Data d'alta del registre: 2024-07-27

Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion

Enllaç font original: https://bmjopen.bmj.com/content/11/8/e051208.long

URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/

Referència a l'article segons font original: Bmj Open. 11 (8): e051208-

Referència de l'ítem segons les normes APA: Grillo, Sara; Cuervo, Guillermo; Carratala, Jordi; San-Juan, Rafael; Aguado, Jose M.; Morata, Laura; Gomez-Zorrilla, Silvia; Lopez-Contreras, Joaquin; (2021). Multicentre, randomised, open-label, phase IV-III study to evaluate the efficacy of cloxacillin plus fosfomycin versus cloxacillin alone in adult patients with methicillin-susceptible Staphylococcus aureus bacteraemia: study protocol for the SAFO trial. Bmj Open, 11(8), e051208-. DOI: 10.1136/bmjopen-2021-051208

DOI de l'article: 10.1136/bmjopen-2021-051208

Entitat: Universitat Rovira i Virgili

Any de publicació de la revista: 2021

Tipus de publicació: Journal Publications