ICU sedation, delirium & recovery
Selected Serious Adverse Events in a Cohort of Adult Intensive Care Unit (ICU) Patients: Protocol for a Sub‐Study of the PATIENCE Cohort
Study context
- Population
- Acutely admitted adult ICU patients from 11 countries
- Participants
- 1,440 participants · 11 countries
- Planned comparison
- Patients with vs without prokinetic treatment
- Primary endpoint
- Proportion of patients experiencing selected SAEs, by exposure to prokinetic treatment
Methodological detailsdescriptive, Data presented descriptively, Secondary outcomes: proportion with each specific SAE, distribution by treatment duration, timing relative to ICU admission and prokinetic use; characteristics of patients with and without serious adverse events (SAEs)
- Descriptive
- Data presented descriptively
- Secondary outcomes: proportion with each specific SAE, distribution by treatment duration, timing relative to ICU admission and prokinetic use; characteristics of patients with and without SAEs
No results yet. This paper sets out the design of a trial; its results are to come.
Original publication
Selected Serious Adverse Events in a Cohort of Adult ICU Patients: Protocol for a Sub‐Study of the PATIENCE Cohort. Acta Anaesthesiol Scand. Published 18 September 2025. doi:10.
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