BLING III
Beta-lactam antibiotics infusion group study
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Beta-lactam antibiotics infusion group study
Last updated
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Population: ICU patients receiving Tazocin or meropenem for sepsis
Interventions: Continuous infusions of beta-lactam antibiotics
Comparison: Usual care
Outcomes: 90-day mortality, unit-acquired infections
Inclusion criteria
Exclusion criteria
Documented/strong suspicion of infection
Expected to be in ICU >24h
Started Tazocin or meropenem
≥1 organ dysfunction in previous 24h
Aged < 18 years
Recieved Tazocin or meropenem for >24h during current infection
Pregnant
Tazocin/meropenem allergy
Need for RRT
Planned withdrawal within 48h
Previously enrolled in this trial.
Principle investigator: Dan Harvey
Trainee-lead:
DREEAM: Martin Dent
Website: