Sepsis & infection

High-dose versus standard-dose intermittent meropenem in critically ill patients: An observational cohort study

Ann Intensive CarePublished Observational cohort study

Authors' conclusion

High-dose intermittent meropenem was independently associated with lower 90-day all-cause mortality compared with standard-dose therapy in critically ill patients.

Study context

Population
Critically ill patients with intensive care unit (ICU) stay ≥3 days treated with meropenem, Vienna, Austria, March 2014 to March 2024received meropenem
Participants
4,210 patients
Exposure
High-dose vs standard-dose intermittent meropenem
  • High-dosen = 1,144
  • Standard-dosen = 572reference
Outcome
All-cause mortality
Follow-up
90 days
Methodological details2:1 propensity score matching with covariate adjustment
  • 2:1 propensity score matching with covariate adjustment

Main finding

90-day all-cause mortality

Adjusted risk difference

9.4%

95% CI 4.8–14.1

P < 0.001

By group

High-dose vs Standard-dose
adjusted risk difference 9.4% (95% CI 4.8–14.1); P < 0.001

As reported in the abstract

Observational data: associations, not effects.

Secondary outcomes

ICU LOS

Hospital LOS

Adjusted risk

OutcomeHigh-doseStandard-dose
30-day mortality20.0%22.2%
Resistance emergence5.0%6.2%
ECMO initiation6.1%7.3%
New-onset ARDS20.8%24.9%

30-day mortality

No significant difference

Resistance emergence

No significant difference

Extracorporeal membrane oxygenation (ECMO) initiation

No significant difference

New-onset acute respiratory distress syndrome (ARDS)

No significant difference

ICU LOS

Comparable

Hospital LOS

Comparable

Safety

Adjusted risk

OutcomeHigh-doseStandard-dose
AKI60.6%68.2%

Acute kidney injury (AKI)

High-dose associated with lower adjusted risk of AKI

Original publication

High-dose versus standard-dose intermittent meropenem in critically ill patients: An observational cohort study. Ann Intensive Care. Published 16 January 2026. doi:10.1016/j.aicoj.2025.100022

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