Case-control Investigation of Previously Undiagnosed Diabetes in the Critically Ill

Author:

Krinsley James S1ORCID,Roberts Gregory2,Brownlee Michael3,Schwartz Michael4,Preiser Jean-Charles5,Rule Peter6,Wang Yu1,Bahgat Joseph1,Umpierrez Guillermo E7,Hirsch Irl B4

Affiliation:

1. Department of Medicine, Stamford Hospital and Columbia Vagelos Columbia College of Physicians and Surgeons , Stamford, CT 06902 , USA

2. Department of Pharmacology, Flinders Medical Centre , Bedford Park, SA 5042 , Australia

3. Department of Medicine, Albert Einstein College of Medicine , Bronx, NY 10461 , USA

4. Department of Medicine, University of Washington School of Medicine , Seattle, WA 98195 , USA

5. Department of Intensive Care, Erasme University Hospital , Brussels 1070 , Belgium

6. PRI Consultants , Los Altos Hills, CA 94024 , USA

7. Department of Medicine, Emory University School of Medicine , Atlanta, GA 30307 , USA

Abstract

Abstract Context The outcome of patients requiring intensive care can be influenced by the presence of previously undiagnosed diabetes (undiagDM). Objective This work aimed to define the clinical characteristics, glucose control metrics, and outcomes of patients admitted to the intensive care unit (ICU) with undiagDM, and compare these to patients with known DM (DM). Methods This case-control investigation compared undiagDM (glycated hemoglobin A1c [HbA1c] ≥ 6.5%, no history of diabetes) to patients with DM. Glycemic ratio (GR) was calculated as the quotient of mean ICU blood glucose (BG) and estimated preadmission glycemia, based on HbA1c ([28.7 × HbA1c] – 46.7 mg/dL). GR was analyzed by bands: less than 0.7, 0.7 to less than or equal to 0.9, 0.9 to less than 1.1, and greater than or equal to 1.1. Risk-adjusted mortality was represented by the Observed:Expected mortality ratio (OEMR), calculated as the quotient of observed mortality and mortality predicted by the severity of illness (APACHE IV prediction of mortality). Results Of 5567 patients 294 (5.3%) were undiagDM. UndiagDM had lower ICU mean BG (P < .0001) and coefficient of variation (P < .0001) but similar rates of hypoglycemia (P = .08). Mortality and risk-adjusted mortality were similar in patients with GR less than 1.1 comparing undiagDM and DM. However, for patients with GR greater than or equal to 1.1, mortality (38.5% vs 10.3% [P = .0072]) and risk-adjusted mortality (OEMR 1.18 vs 0.52 [P < .0001]) were higher in undiagDM than in DM. Conclusion These data suggest that DM patients may develop tolerance to hyperglycemia that occurs during critical illness, a protective mechanism not observed in undiagDM, for whom hyperglycemia remains strongly associated with higher risk of mortality. These results may shed light on the natural history of diabetes.

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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