- Design
- Scoping review (executive summary) with a pharmacokinetic-factors checklist
- Population
- 96 studies of antimicrobial pharmacokinetics in critically ill patients on CRRT
- Primary outcome
- Factors influencing antimicrobial pharmacokinetics during CRRT
- Effect
- Clearance altered by CRRT, patient and drug factors; evidence-based dosing guidance still lacking
A scoping review mapped 96 studies of antimicrobial pharmacokinetics in critically ill patients on continuous renal replacement therapy (CRRT), summarising why reliable dosing guidance is still missing and producing a checklist of the factors that matter.
CRRT substantially alters drug clearance, and on top of that the ICU population is highly variable; many pharmacokinetic studies exclude CRRT patients or are small and methodologically limited, leaving a genuine evidence gap. The review groups the determinants into CRRT-related (modality, flow rates, filter), patient-related and drug-related factors.
The usable message for prescribers is caution: do not assume a standard antibiotic, antifungal or antiviral dose is right for a patient on CRRT. Account for the CRRT prescription and the drug's properties, and use therapeutic drug monitoring where it is available, especially for agents with a narrow margin. This is a methods and gap-mapping review, not a new dosing guideline.
- CRRT markedly changes antimicrobial clearance, and dosing evidence remains thin.
- Many pharmacokinetic studies exclude CRRT patients or are small and limited.
- Dosing depends on CRRT settings, patient factors and the drug itself.
- Do not assume standard doses on CRRT; individualise and use monitoring.
- Prioritise therapeutic drug monitoring for narrow-margin agents.
Why it matters
Under- or over-dosing antimicrobials in CRRT risks treatment failure, resistance or toxicity, and standard doses are often wrong.
Don't overread it
This is a scoping and methods review that maps the gap; it does not itself provide validated dose recommendations.
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