Impact of dexmedetomidine on mortality in critically ill patients with acute kidney injury: a retrospective propensity score matching analysis.
retrospective_cohort · Level III
Where this comes from
- Record sourced from PubMed, PMID 37968013.
- Also identified by DOI 10.1136/bmjopen-2023-073675 and PMC identifier 10660201.
- Licence recorded as CC BY-NC.
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Abstract
This study sought to estimate the effect of dexmedetomidine (DEX) administration on mortality in critically ill patients with acute kidney injury (AKI). A retrospective cohort study. The study sourced its data from the Multiparameter Intelligent Monitoring in Intensive Care Database IV (MIMIC-IV), a comprehensive database of intensive care unit patients. A total of 15 754 critically ill patients with AKI were enrolled from the MIMIC-IV database. Primary outcome was in-hospital mortality and secondary outcome was 180-day mortality. 15 754 critically ill AKI patients were included in our analysis. We found that DEX use decreased in-hospital mortality risk by 38% (HR 0.62, 95% CI 0.55 to 0.70) and 180-day mortality risk by 23% (HR 0.77, 95% CI 0.69 to 0.85). After adjusting for confounding factors, DEX can reduce all three stages of AKI in in-hospital mortality. Our retrospective cohort study suggests that DEX significantly correlates with decreased risk-adjusted in-hospital and 180-day mortality in critically ill AKI patients. Nonetheless, future randomised controlled trials are warranted to validate our findings.
Medical subject headings
- Dexmedetomidine
- Acute Kidney Injury