Clinical Infectious Diseases · 2023 · 22 citations · 28 references
PharmacyInfectious DiseasesPharmacotherapyAntimicrobial PharmacotherapyClinical PharmacologyMedical MicrobiologyDe-escalation Of Antimicrobial TherapyEmpiric Therapy SelectionIntravenous To Oral Switch PoliciesIntravenous-to-oral Switch TherapyPediatric Antibiotic TherapyPediatric Antimicrobial TherapyEarly Oral Switch TherapyEmpiric Antibiotic TherapyExpert Opinion EvidenceIntravenous-to-oral Antibiotic SwitchObservational MethodologyObservational Research DesignOral Antibiotic TherapyPediatric Bacteremia
BACKGROUND: Staphylococcus aureus bloodstream infection (bacteremia) is traditionally treated with at least 2 weeks of intravenous (IV) antibiotics in adults, 3-7 days in children, and often longer for those with complicated disease. The current practice of treating S. aureus bacteremia (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 randomization to EOS (intervention) or continued IV treatment (current standard of care). DISCUSSION: Recruitment is occurring in the EOS domain of the SNAP trial. As of August 2023, 21% of all SNAP participants had been randomized to the EOS domain, a total of 264 participants across 77 centers, 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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