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Early oral antibiotic switch in Staphylococcus aureus bacteraemia: The Staphylococcus aureus Network Adaptive Platform (SNAP) Trial Early Oral Switch Protocol.
de Kretser, Dana; Mora, Jocelyn; Bloomfield, Max; Campbell, Anita; Cheng, Matthew P; Guy, Stephen; Hensgens, Marjolein; Kalimuddin, Shirin; Lee, Todd C; Legg, Amy; Mahar, Robert K; Marks, Michael; Marsh, Julie; McGlothlin, Anna; Morpeth, Susan C; Sud, Archana; Ten Oever, Jaap; Yahav, Dafna; Tong, Steven Yc; Davis, Joshua S; Walls, Genevieve; Goodman, Anna L; Bonten, Marc.
Afiliación
  • de Kretser D; Medical Research Council Clinical Trials Unit, University College London, London, United Kingdom.
  • Mora J; Department of Infectious Diseases University of Melbourne, Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
  • Bloomfield M; Department of Infection Services, Wellington Regional Hospital, New Zealand.
  • Campbell A; Telethon Kids Institute, Wesfarmers Centre of Infectious Diseases and Vaccines, The University of Western Australia, Perth, Australia.
  • Cheng MP; Divisions of Infectious Diseases and Medical Microbiology, McGill University Health Centre, Montreal, Canada.
  • Guy S; Department of Infectious Diseases, Eastern Health, Box Hill, 3128, Australia.
  • Hensgens M; Monash University (including Australian and New Zealand Intensive Care Research Centre), Clayton, 3800, Australia, Australia.
  • Kalimuddin S; UMC Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Lee TC; Julius Center for Health Sciences and Primary Care, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Legg A; Department of Infectious Diseases, Singapore General Hospital, 169608, Singapore, Singapore.
  • Mahar RK; Program in Emerging Infectious Diseases, Duke-NUS Medical School, 169857, Singapore, Singapore.
  • Marks M; Clinical Practice Assessment Unit and Division of Infectious Diseases, McGill University, Montreal, Canada.
  • Marsh J; Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
  • McGlothlin A; Herston Infectious Diseases Institute, Herston, Brisbane, Australia.
  • Morpeth SC; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, Australia.
  • Sud A; Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Parkville, Australia.
  • Ten Oever J; Department of Clinical Research, London School of Hygiene & Tropical Medicine, London, United Kingdom.
  • Yahav D; Hospital for Tropical Diseases, University College London Hospital, London.
  • Tong SY; Division of Infection and Immunity, University College London, London.
  • Davis JS; Telethon Kids Institute &/Department of Infectious Diseases &/Wesfarmers Centre for Vaccines and Infectious Diseases, Perth Children's Hospital, Perth, Australia.
  • Walls G; Berry Consultants, LLC, Austin, Texas, USA.
  • Goodman AL; Middlemore Hospital, Auckland, New Zealand.
  • Bonten M; Department of Infectious Diseases, University of Sydney, Nepean Hospital, Kingswood, New South Wales, Australia.
Clin Infect Dis ; 2023 Oct 31.
Article en En | MEDLINE | ID: mdl-37921609
ABSTRACT

BACKGROUND:

Staphylococcus aureus bloodstream infection (bacteraemia) is traditionally treated with at least two weeks of IV antibiotics in adults, 3-7 days in children, and often longer for those with complicated disease. The current practice of treating S. aureus bacteraemia (SAB) with prolonged IV antibiotics (rather than oral antibiotics) is based on historical observational research and expert opinion. Prolonged IV antibiotic therapy has significant disadvantages for patients and healthcare systems, and there is growing interest in whether a switch to oral antibiotics following an initial period of IV therapy is a safe alternative for clinically stable patients. PROTOCOL The early oral switch (EOS) domain of the S. aureus Network Adaptive Platform (SNAP) trial will assess early switch to oral antibiotics compared with continued IV treatment in clinically stable patients with SAB. The primary endpoint is 90-day all-cause mortality. Hospitalised SAB patients are assessed at platform day 7 +/- 2 (uncomplicated SAB) and day 14 +/-2 (complicated SAB) to determine their eligibility for randomisation to EOS (intervention) or continued IV treatment (current standard of care).

DISCUSSION:

Recruitment is occurring to the EOS domain of the SNAP trial. As of August 2023, 21% of all SNAP participants had been randomised to the EOS domain, a total of 264 participants across 77 centres, with an aim to recruit at least 1000 participants. We describe challenges and facilitators to enrolment in this domain to aid those planning similar trials.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido