Efficacy of extended infusion of β-lactam antibiotics for the treatment of febrile neutropenia in haematologic patients (BEATLE): a randomised, multicentre, open-label, superiority clinical trial.

Cefepime Extended infusion Febrile neutropenia Meropenem Piperacillin-tazobactam Randomised controlled trial β-lactam antibiotics

Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
19 Oct 2024
Historique:
received: 25 07 2024
revised: 02 10 2024
accepted: 05 10 2024
medline: 22 10 2024
pubmed: 22 10 2024
entrez: 21 10 2024
Statut: aheadofprint

Résumé

The efficacy of extended infusions (EI) of β-lactam antibiotics for optimising outcomes in febrile neutropenia is unclear. We assessed whether the administration of β-lactams was more effective in EI than in intermittent infusion (II) for the treatment of febrile neutropenia. We performed a randomised, open-label, superiority clinical trial of patients with febrile neutropenia at four Spanish university hospitals. Patients undergoing haematopoietic stem cell transplantation or with acute leukaemia receiving chemotherapy who required empirical antibiotic treatment for febrile neutropenia were randomly assigned (1:1) to receive EI of β-lactam or II after a first dose in bolus. The choice of antipseudomonal β-lactam was left to the discretion of the attending physician. The primary endpoint was treatment success at day 5, defined as defervescence without modifying the antibiotic treatment. Secondary endpoints included adverse events, attainment of the pharmacokinetic/pharmacodynamic target of 50, 75 and 100%ƒ Between November 19, 2019 and June 22, 2022, 295 patients we screened for eligibility, of whom 150 were randomly assigned to receive EI (n=77) or II (n=73) of the antipseudomonal β-lactam of choice. In the intention-to-treat analysis, treatment success at day 5 was achieved in 39/77 patients (50.6%) receiving EI versus 46/73 patients (63.0%) receiving II (risk difference -12.4%; 95% confidence interval, -29.4 to 4.7, p=0.17). The pharmacokinetic/pharmacodynamic targets of 75 and 100% ƒ Our findings do not support the routine use of empirical EI of β-lactams in febrile neutropenia. Further studies should consider the clinical heterogeneity of febrile neutropenia and focus on patients with sepsis/septic shock and microbiologically documented infections, particularly those with infections caused by microorganisms less susceptible to β-lactams.

Identifiants

pubmed: 39433124
pii: S1198-743X(24)00488-9
doi: 10.1016/j.cmi.2024.10.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests We declare no competing interests regarding the BEATLE trial and its publication.

Auteurs

Julia Laporte-Amargos (J)

Department of Infectious Diseases, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain. Electronic address: j.laporte@bellvitgehospital.cat.

Francisco Carmona-Torre (F)

Department of Infectious Diseases, Clínica Universidad de Navarra, Navarra Institute for Health Research (IdiSNA), Pamplona, Spain.

Maria Huguet (M)

Department of Clinical Haematology, Institut Català d'Oncologia-Badalona, Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Badalona, Spain.

Pedro Puerta-Alcalde (P)

Infectious Diseases Department, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clínic de Barcelona, Barcelona, Spain.

Raul Rigo-Bonnin (R)

Department of Clinical Laboratory, Bellvitge University Hospital, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.

Marta Ulldemolins (M)

Department of Infectious Diseases, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain.

Montserrat Arnan (M)

Department of Clinical Haematology, Institut Català d'Oncologia-Hospitalet, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain; University of Barcelona, Barcelona, Spain.

Jose Luis Del Pozo (JL)

Department of Infectious Diseases, Clínica Universidad de Navarra, Navarra Institute for Health Research (IdiSNA), Pamplona, Spain; Department of Clinical Microbiology, Clínica Universidad de Navarra, Pamplona, Spain.

Anna Torrent (A)

Department of Clinical Haematology, Institut Català d'Oncologia-Badalona, Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Badalona, Spain.

Carolina Garcia-Vidal (C)

Infectious Diseases Department, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clínic de Barcelona, Barcelona, Spain.

Natàlia Pallarès (N)

University of Barcelona, Barcelona, Spain; Biostatistics Unit, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.

Cristian Tebé (C)

Biostatistics Unit, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.

Carme Muñoz (C)

Department of Pharmacy, Institut Català d'Oncologia-Hospitalet, IDIBELL, Barcelona, Spain.

Fe Tubau (F)

Department of Microbiology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.

Ariadna Padullés (A)

Department of Pharmacy, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain; Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.

Ana-Maria Sureda (AM)

Department of Clinical Haematology, Institut Català d'Oncologia-Hospitalet, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.

Jordi Carratalà (J)

Department of Infectious Diseases, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain; University of Barcelona, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain; Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.

Carlota Gudiol (C)

Department of Infectious Diseases, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain; University of Barcelona, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain; Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain; Institut Català d'Oncologia, Barcelona, Spain.

Classifications MeSH