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Continuous vs Intermittent ß-Lactam Antibiotic Infusions in Critically Ill Patients With Sepsis: The BLING III Randomized Clinical Trial.
Dulhunty, Joel M; Brett, Stephen J; De Waele, Jan J; Rajbhandari, Dorrilyn; Billot, Laurent; Cotta, Menino O; Davis, Joshua S; Finfer, Simon; Hammond, Naomi E; Knowles, Serena; Liu, Xiaoqiu; McGuinness, Shay; Mysore, Jayanthi; Paterson, David L; Peake, Sandra; Rhodes, Andrew; Roberts, Jason A; Roger, Claire; Shirwadkar, Charudatt; Starr, Therese; Taylor, Colman; Myburgh, John A; Lipman, Jeffrey.
Afiliação
  • Dulhunty JM; Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
  • Brett SJ; Redcliffe Hospital, Brisbane, Queensland, Australia.
  • De Waele JJ; The University of Queensland, Brisbane, Queensland, Australia.
  • Rajbhandari D; Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Billot L; Department of Surgery and Cancer, Imperial College London, London, United Kingdom.
  • Cotta MO; Department of Critical Care Medicine, Ghent University Hospital, Ghent, Belgium.
  • Davis JS; The George Institute for Global Health, The University of New South Wales, Sydney, New South Wales, Australia.
  • Finfer S; The George Institute for Global Health, The University of New South Wales, Sydney, New South Wales, Australia.
  • Hammond NE; Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
  • Knowles S; The University of Queensland, Brisbane, Queensland, Australia.
  • Liu X; Infection Research Program, Hunter Medical Research Institute, University of Newcastle, Newcastle, New South Wales, Australia.
  • McGuinness S; Department of Infectious Diseases, John Hunter Hospital, Newcastle, New South Wales, Australia.
  • Mysore J; The George Institute for Global Health, The University of New South Wales, Sydney, New South Wales, Australia.
  • Paterson DL; School of Public Health, Imperial College London, United Kingdom.
  • Peake S; The George Institute for Global Health, The University of New South Wales, Sydney, New South Wales, Australia.
  • Rhodes A; Malcolm Fisher Department of Intensive Care, Royal North Shore Hospital, Sydney, New South Wales, Australia.
  • Roberts JA; The George Institute for Global Health, The University of New South Wales, Sydney, New South Wales, Australia.
  • Roger C; The George Institute for Global Health, The University of New South Wales, Sydney, New South Wales, Australia.
  • Shirwadkar C; Auckland City Hospital, Auckland, New Zealand.
  • Starr T; Medical Research Institute of New Zealand, Wellington, New Zealand.
  • Taylor C; The George Institute for Global Health, The University of New South Wales, Sydney, New South Wales, Australia.
  • Myburgh JA; Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
  • Lipman J; The University of Queensland, Brisbane, Queensland, Australia.
JAMA ; 332(8): 629-637, 2024 08 27.
Article em En | MEDLINE | ID: mdl-38864155
ABSTRACT
Importance Whether ß-lactam antibiotics administered by continuous compared with intermittent infusion reduces the risk of death in patients with sepsis is uncertain.

Objective:

To evaluate whether continuous vs intermittent infusion of a ß-lactam antibiotic (piperacillin-tazobactam or meropenem) results in decreased all-cause mortality at 90 days in critically ill patients with sepsis. Design, Setting, and

Participants:

An international, open-label, randomized clinical trial conducted in 104 intensive care units (ICUs) in Australia, Belgium, France, Malaysia, New Zealand, Sweden, and the United Kingdom. Recruitment occurred from March 26, 2018, to January 11, 2023, with follow-up completed on April 12, 2023. Participants were critically ill adults (≥18 years) treated with piperacillin-tazobactam or meropenem for sepsis. Intervention Eligible patients were randomized to receive an equivalent 24-hour dose of a ß-lactam antibiotic by either continuous (n = 3498) or intermittent (n = 3533) infusion for a clinician-determined duration of treatment or until ICU discharge, whichever occurred first. Main Outcomes and

Measures:

The primary outcome was all-cause mortality within 90 days after randomization. Secondary outcomes were clinical cure up to 14 days after randomization; new acquisition, colonization, or infection with a multiresistant organism or Clostridioides difficile infection up to 14 days after randomization; ICU mortality; and in-hospital mortality.

Results:

Among 7202 randomized participants, 7031 (mean [SD] age, 59 [16] years; 2423 women [35%]) met consent requirements for inclusion in the primary analysis (97.6%). Within 90 days, 864 of 3474 patients (24.9%) assigned to receive continuous infusion had died compared with 939 of 3507 (26.8%) assigned intermittent infusion (absolute difference, -1.9% [95% CI, -4.9% to 1.1%]; odds ratio, 0.91 [95% CI, 0.81 to 1.01]; P = .08). Clinical cure was higher in the continuous vs intermittent infusion group (1930/3467 [55.7%] and 1744/3491 [50.0%], respectively; absolute difference, 5.7% [95% CI, 2.4% to 9.1%]). Other secondary outcomes were not statistically different. Conclusions and Relevance The observed difference in 90-day mortality between continuous vs intermittent infusions of ß-lactam antibiotics did not meet statistical significance in the primary analysis. However, the confidence interval around the effect estimate includes the possibility of both no important effect and a clinically important benefit in the use of continuous infusions in this group of patients. Trial Registration ClinicalTrials.gov Identifier NCT03213990.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sepse / Combinação Piperacilina e Tazobactam / Meropeném / Antibióticos beta Lactam / Unidades de Terapia Intensiva Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sepse / Combinação Piperacilina e Tazobactam / Meropeném / Antibióticos beta Lactam / Unidades de Terapia Intensiva Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Ano de publicação: 2024 Tipo de documento: Article