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Early glucose variability in cardiogenic shock following acute myocardial infarction: a pilot study
Chiara Lazzeri1, Serafina Valente2, Marco Chiostri2
1Intensive Cardiac Care Unit, Heart and Vessel Department, Viale Morgagni 85, 50134 Florence, Italy lazzeric@libero.it.
Insights
Early high glucose variability in ST-elevation myocardial infarction patients with cardiogenic shock predicts mortality. Lower variability in survivors suggests a potential therapeutic target for improving outcomes.
Area of Science:
- Cardiology
- Endocrinology
- Intensive Care Medicine
Background:
- Limited data exists on the link between glucose variability and outcomes in ST-elevation myocardial infarction (STEMI) patients experiencing cardiogenic shock (CS).
- Understanding this association is crucial for identifying prognostic markers and potential interventions.
Purpose of the Study:
- To investigate the relationship between early glycaemic variability and mortality in patients with CS post-STEMI.
- To determine if glycaemic variability metrics are independent predictors of short-term and long-term mortality.
Main Methods:
- A cohort of 67 consecutive CS post-STEMI patients was studied.
- Glycaemic variability was assessed within the first 48 hours using standard deviation (SD) of glucose and mean absolute glucose change per hour (MAGC).
Main Results:
- Survivors exhibited significantly lower glycaemic variability (lower SD and MAGC) compared to non-survivors.
- Both MAGC and SD were identified as independent predictors of mortality (p=0.002 and p=0.003, respectively).
- Peak glycaemia also emerged as an independent predictor of death (adjusted HR: 1.95, p=0.007).
Conclusions:
- Early glycaemic variability serves as an independent predictor of mortality in CS patients following acute myocardial infarction.
- Further research in larger cohorts is warranted to validate these findings.
- Investigating strategies to reduce glucose variability may offer a novel therapeutic approach to improve patient outcomes.
Background:
No data are so far available on the association between glycaemic variability and outcomes in patients with cardiogenic shock (CS) following ST elevation myocardial infarction (STEMI).
Methods:
We assessed the relationship between glycaemic variability and mortality, both short term and long term, in 67 consecutive patients with cardiogenic shock following STEMI admitted to our Intensive Cardiac Care Unit. Glycaemic variability was measured in the first 48 h by means of standard deviation (SD) of glucose values and the mean absolute glucose change per hour (MAGC) defined as the sum of all absolute glucose change divided by the time in hours.
Results:
Lower glycaemic variability was observed in survivors when compared with nonsurvivors, as indicated by lower values of SD and MAGC, respectively. In Cox regression analysis, MAGC and SD were independent predictors of death (MAGC: adjusted hazard ratio [HR]: 8.60, 95% confidence interval [CI]: 2.21-33.41, p = 0.002; SD: adjusted HR: 6.64, 95% CI: 1.92-22.99, p = 0.003), as well as peak glycaemia (adjusted HR: 1.95, 95% CI: 1.20-3.15, p = 0.007).
Conclusions:
According to our results, in patients with CS following acute myocardial infarction, early glycaemic variability is an independent predictor of mortality. Further studies are needed to confirm our results in larger cohorts and eventually to assess the effect of strategies specifically targeting glucose variability reduction on mortality.
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