Diabetes complications

Mean amplitude of glycemic excursion and mortality in critically ill patients: A retrospective analysis using the MIMIC ‐ IV database

Diabetes Obes MetabPublished Retrospective cohort study

Authors' conclusion

MAGE exhibits effective predictive value for mortality in ICU patients, with distinct thresholds for diabetic and non-diabetic populations. These findings underscore the importance of tailored GV management strategies in critical care settings and support the adoption of MAGE as a standardised metric for GV assessment in ICU settings.

Study context

Population
Critically ill adults with intensive care unit (ICU) stays exceeding 24 h, MIMIC-IV database
Participants
13,852 adults
Exposure
Mean Amplitude of Glycemic Excursion (MAGE) quartiles
Outcome
Mortality (ICU, in-hospital and 28-day)
Methodological detailsMIMIC-IV database, multivariable-adjusted
  • MIMIC-IV database
  • Multivariable-adjusted

Main finding

As reported in the abstract

Mortality, highest MAGE quartile

ICU mortality, highest MAGE quartile: HR

3.59

95% CI 2.99–4.31

In-hospital mortality, highest MAGE quartile: HR

3.43

95% CI 2.92–4.02

28-day mortality, highest MAGE quartile: HR

2.04

95% CI 1.47–2.82

Observational data: associations, not effects.

Further findings

MAGE and mortality by diabetes status

Non-diabetic patients: HR
3.36 (95% CI 2.90-3.89)
Diabetic patients: HR
1.59 (95% CI 1.33-1.91)

Optimal MAGE thresholds (restricted cubic spline)

Overall population
44.28 mg/dL
Diabetic patients
58.97 mg/dL
Non-diabetic patients
17.11 and 37.72 mg/dL

Predictive performance of MAGE for all-cause mortality

AUC
0.6286 (95% CI 0.6171-0.6400)
Adding MAGE to SAPS II and SOFA: Net reclassification improvement (NRI)
0.238
Adding MAGE to SAPS II and SOFA: Integrated discrimination improvement (IDI)
0.008

Original publication

Mean amplitude of glycemic excursion and mortality in critically ill patients: A retrospective analysis using the MIMIC ‐ IV database. Diabetes Obes Metab. Published 21 April 2025. doi:10.1111/dom.16410

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