Wednesday, January 30, 2013

Intensive Insulin Therapy for The Treatment of Hyperglycemia in Critically Ill Adults: A Qualitative Systematic Review and Critical Appraisal of the Evidence


ABSTRACT

Rattan Juneja MD; Michael E. Stuart, MD; Sheri A. Strite

Background: Hyperglycemia in intensive care patients is associated with high mortality, but optimal management of this population with insulin therapy is Methods: We utilized the extensive search from a recent published meta-analysis and conducted an updated search using MEDLINE (2008-2009), the Cochrane Central Register of Controlled Trials, and the Cochrane Database of Systematic Reviews. We assessed bias of trials using a detailed checklist to document the overall quality of the evidence for mortality and hypoglycemia in intensive care populations.
Findings: We included a total of 17 clinical trials totaling 12,345 patients. All included trials were rated as being at medium risk of bias. We identified eight groups of patients in which intensive insulin treatment has been compared to less intensive insulin therapy. Mortality rates varied by patient population with rates of < 16% in predominantly surgical patients with mixed conditions to nearly 75% in neurosurgical patients. Overall, mortality rates ranged from 4% to 74% but the overall level of evidence for mortality was inconclusive. Hypoglycemia rates ranged from 0% to 94% and the overall level of evidence for hypoglycemia was borderline.
Interpretation: The evidence is insufficient for determining the effect of intensive
insulin treatment compared to less intensive treatment in acutely ill hyperglycemic
patients. The evidence does not justify guideline recommendations for specific glycemic target ranges for adults being treated in intensive care units. Further research is needed, but should be carefully planned with attention to trial bias, populations, type of insulin protocols used, adherence, co-interventions, and frequency of blood glucose testing to avoid the heterogeneity and bias present in currently available research.

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