Temocillin versus meropenem for the targeted treatment of bacteraemia due to third-generation cephalosporin-resistant Enterobacterales (ASTARTÉ): protocol for a randomised, pragmatic trial.

dc.contributor.authorMarín-Candón, Alicia
dc.contributor.authorRosso-Fernández, Clara M
dc.contributor.authorBustos de Godoy, Natalia
dc.contributor.authorLópez-Cerero, Lorena
dc.contributor.authorGutiérrez-Gutiérrez, Belén
dc.contributor.authorLópez-Cortés, Luis Eduardo
dc.contributor.authorBarrera Pulido, Lydia
dc.contributor.authorBorreguero Borreguero, Irene
dc.contributor.authorLeón, María José
dc.contributor.authorMerino, Vicente
dc.contributor.authorCamean-Fernández, Manuel
dc.contributor.authorRetamar, Pilar
dc.contributor.authorSalamanca, Elena
dc.contributor.authorPascual, Alvaro
dc.contributor.authorRodriguez-Baño, Jesús
dc.contributor.authorASTARTÉ Study Group
dc.date.accessioned2025-01-07T16:05:31Z
dc.date.available2025-01-07T16:05:31Z
dc.date.issued2021-09-27
dc.description.abstractAlternatives to carbapenems are needed in the treatment of third-generation cephalosporin-resistant Enterobacterales (3GCR-E). Temocillin is a suitable candidate, but comparative randomised studies are lacking. The objective is to investigate if temocillin is non-inferior to carbapenems in the targeted treatment of bacteraemia due to 3GCR-E. Multicentre, open-label, randomised, controlled, pragmatic phase 3 trial. Patients with bacteraemia due to 3GCR-E will be randomised to receive intravenously temocillin (2 g three times a day) or carbapenem (meropenem 1 g three times a day or ertapenem 1 g once daily). The primary endpoint will be clinical success 7-10 days after end of treatment with no recurrence or death at day 28. Adverse events will be collected; serum levels of temocillin will be investigated in a subset of patients. For a 10% non-inferiority margin, 334 patients will be included (167 in each study arm). For the primary analysis, the absolute difference with one-sided 95% CI in the proportion of patients reaching the primary endpoint will be compared in the modified intention-to-treat population. The study started after approval of the Spanish Regulatory Agency and the reference institutional review board. Data will be published in peer-reviewed journals. NCT04478721.
dc.identifier.doi10.1136/bmjopen-2021-049481
dc.identifier.essn2044-6055
dc.identifier.pmcPMC8477313
dc.identifier.pmid34580096
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC8477313/pdf
dc.identifier.unpaywallURLhttps://bmjopen.bmj.com/content/bmjopen/11/9/e049481.full.pdf
dc.identifier.urihttps://hdl.handle.net/10668/27611
dc.issue.number9
dc.journal.titleBMJ open
dc.journal.titleabbreviationBMJ Open
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen del Rocío
dc.organizationSAS - Hospital Universitario Virgen Macarena
dc.organizationSAS - Hospital Universitario Virgen Macarena
dc.page.numbere049481
dc.pubmedtypeClinical Trial Protocol
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectbacteriology
dc.subjectclinical pharmacology
dc.subjectinfection control
dc.subjectinfectious diseases
dc.subjectmicrobiology
dc.subject.meshBacteremia
dc.subject.meshCephalosporins
dc.subject.meshClinical Trials, Phase III as Topic
dc.subject.meshEnterobacteriaceae
dc.subject.meshHumans
dc.subject.meshMeropenem
dc.subject.meshMulticenter Studies as Topic
dc.subject.meshPenicillins
dc.subject.meshPragmatic Clinical Trials as Topic
dc.subject.meshRandomized Controlled Trials as Topic
dc.titleTemocillin versus meropenem for the targeted treatment of bacteraemia due to third-generation cephalosporin-resistant Enterobacterales (ASTARTÉ): protocol for a randomised, pragmatic trial.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number11

Files

Original bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
PMC8477313.pdf
Size:
288.26 KB
Format:
Adobe Portable Document Format