Utility of a prediction model for delirium in intensive care unit patients (PRE-DELIRIC) in mechanically ventilated patients with sepsis
- PMID: 33173589
- PMCID: PMC7640736
- DOI: 10.1002/ams2.589
Utility of a prediction model for delirium in intensive care unit patients (PRE-DELIRIC) in mechanically ventilated patients with sepsis
Abstract
Aim: Delirium frequently develops in patients with sepsis during their intensive care unit (ICU) stay, which is associated with increased morbidity and mortality. A prediction model for delirium in patients in ICU, PRE-DELIRIC, has been utilized in overall ICU patients, but its utility is uncertain among patients with sepsis. This study aims to examine the utility of PRE-DELIRIC to predict delirium in mechanically ventilated patients with sepsis.
Methods: This is a post hoc analysis of a randomized clinical trial in eight Japanese ICUs, which aimed to evaluate the sedative strategy with/without dexmedetomidine in adult mechanically ventilated patients with sepsis. The Confusion Assessment Method for the ICU was used every day to assess for delirium throughout their ICU stay. We excluded patients who were delirious on the first day of ICU, those who were under sustained coma throughout their ICU stay, and those who stayed in the ICU less than 24 h. The discriminative ability of PRE-DELIRIC was evaluated by measuring the area under the receiver operating characteristic curve (AUROC).
Results: Of the 201 patients enrolled in the trial, we analyzed 158 patients. The mean age was 69.4 ± 14.0 years, and 99 patients (63%) were men. Delirium occurred at least once during the ICU stay of 63 patients (40%). The AUROC of PRE-DELIRIC was 0.60 (95% confidence interval, 0.50-0.69). Subgroup analyses indicated that PRE-DELIRIC was useful in those with Sequential Organ Failure Assessment score >8 with AUROC of 0.65 (95% confidence interval, 0.51-0.77).
Conclusions: The PRE-DELIRIC model could not predict delirium in mechanically ventilated patients with sepsis.
Keywords: Clinical prediction rule; PRE‐DELIRIC; delirium; mechanical ventilation; sepsis.
© 2020 The Authors. Acute Medicine & Surgery published by John Wiley & Sons Australia, Ltd on behalf of Japanese Association for Acute Medicine.
Conflict of interest statement
Approval of the research protocol: This study was a post hoc analysis of the DESIRE trial, which was a randomized controlled trial undertaken among eight ICUs in Japan. The participating institutions were Osaka City University, Osaka City General Hospital, Hyogo College of Medicine, Saga University Hospital, National Hospital Organization Kyoto Medical Center, Sapporo Medical University, Yamaguchi Grand Medical Center, and Wakayama Medical University. The ethical review boards of all relevant institutions approved the study protocol. Informed consent: Written informed consent was obtained from all participants or legally authorized guardians before study enrollment. Registry and registration no. of the trial: This trial was registered on ClinicalTrials.gov (NCT01760967) on 1 January, 2013. Animal studies: N/A. Conflict of interests: None.
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