Key result
Elevated glycemic variability (highest vs lowest quartile) was independently associated with a significantly increased risk of 28-day all-cause mortality (HR 2.00) in critically ill patients with mitral valve disease.
Why the study?
Glycemic variability indicates outcomes in critically ill patients, but its effect on ICU patients with mitral valve disease was unclear.
Does high glycemic variability increase all-cause mortality in critically ill patients with mitral valve disease?
Cohort (n=3,378)
No
Does high glycemic variability increase all-cause mortality in critically ill patients with mitral valve disease?
Elevated glycemic variability is an independent predictor of short-term mortality in critically ill patients with mitral valve disease, highlighting its potential utility in risk stratification.
Answers are grounded in this paper and cite their sources.
Supports glycemic variability for risk stratification in critically ill mitral valve patients; leaves open causal effects and intervention benefits.
Background: Mitral valve disease is associated with higher cardiovascular morbidity and mortality. Glycemic variability (GV), reflecting blood glucose fluctuations, acts as an independent indicator for results in critically ill patients. However, it's effect on patients in the ICU with mitral valve disease is unclear. Methods: All blood glucose measurements of patients with mitral valve disease were extracted from MIMIC-IV database. GV was assessed using the coefficient of variation of glucose levels. Cox hazard regression models and restrictive cubic spline (RCS) were applied to examine the link between GV and outcomes. A threshold effect analysis was also conducted to explore potential inflection points. Subgroup analyses were performed to assess consistency across demographics and clinical subgroups. Results: The study of 3,378 adults with mitral valve disease found that higher GV was significantly associated with increased 28-day and 90-day mortality, as shown by Cox regression analysis. Subgroup analyses confirmed these findings. Conclusions: For ICU patients with mitral valve disease, elevated GV was an independent predictor of short-term mortality. GV was recommended for consideration in risk stratification and glucose management strategies, particularly in non-diabetic critically ill populations. Monitoring and targeting GV were proposed to new avenues for improving clinical outcomes in this high-risk group.
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Peng et al. (2025) conducted a cohort in Mitral valve disease (n=3,378). Glycemic variability vs. Lowest quartile of glycemic variability was evaluated on 28-day all-cause mortality (HR 2.00, 95% CI 1.53-2.61, p=<0.001). Elevated glycemic variability (highest vs lowest quartile) was independently associated with a significantly increased risk of 28-day all-cause mortality (HR 2.00) in critically ill patients with mitral valve disease.
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