Piloting a Novel Algorithm for Glucose Control in the Coronary Care Unit

Author:

Nerenberg Kara A.1,Goyal Abhinav2,Xavier Denis3,Sigamani Alben4,Ng Jennifer1,Mehta Shamir R.15,Díaz Rafael6,Kosiborod Mikhail7,Yusuf Salim1,Gerstein Hertzel C.158,

Affiliation:

1. Population Health Research Institute McMaster University, Hamilton, Ontario, Canada

2. Department of Medicine, Emory University, Atlanta, Georgia

3. Department of Pharmacology, St. John’s Medical School, Bangalore, India

4. Department of Pharmacology, St. John’s Research Institute, Bangalore, India

5. Department of Medicine, McMaster University, Hamilton, Ontario, Canada

6. Etudios Cardiologica Latin America, Rosario, Argentina

7. Mid-America Heart and Vascular Institute of Saint Luke’s Hospital and the Department of Medicine, University of Missouri, Kansas City, Missouri

8. Department of Clinical Epidemiology and Biostatistics, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada

Abstract

OBJECTIVE Elevated glucose levels are common after an acute myocardial infarction (AMI) and increase the risk of death. Prior trials of glucose control after AMI have been inconsistent in their ability to lower glucose levels and have reported mixed effects on mortality. We developed a paper-based glucose-lowering algorithm and assessed its feasibility and safety in the setting of AMI. RESEARCH DESIGN AND METHODS A total of 287 participants with an acute ST segment elevation myocardial infarction (STEMI) and a capillary glucose level ≥8.0 mmol/L were randomly allocated to glucose management with intravenous glulisine insulin using this algorithm in the coronary care unit (CCU), followed by once-daily subcutaneous insulin glargine for 30 days versus standard glycemic approaches. The primary outcome was a difference in mean glucose levels at 24 h. Participants were followed for clinical outcomes through 90 days. RESULTS At 24 h, the mean glucose level was 1.41 mmol/L (95% CI 0.69–2.13) lower in the insulin (6.53 vs. 7.94 mmol/L). Differences in glucose levels were maintained at 72 h and 30 days. A total of 22.7% of the insulin group versus 4.4% of the standard group had biochemical hypoglycemia (with neither signs nor symptoms) in the CCU because of lower glycemic goals. However, there were no differences in symptomatic hypoglycemia or clinical outcomes between the groups. CONCLUSIONS A paper-based insulin algorithm targeting glucose levels of 5.0–6.5 mmol/L (90–117 mg/dL) can be feasibly implemented in the CCU. A cardiovascular outcomes trial using this approach can determine whether targeted glucose lowering improves patient outcomes.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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