How low should you go? The limbo of glycemic control in intensive care units

Andrew C Faust1, Rebecca L Attridge, Laurajo Ryan

  • 1Methodist University Hospital, Dept of Pharmacy, Memphis, TN 38104, USA. rphfaust@gmail.com

Critical Care Nurse
|August 3, 2011
PubMed

Insights

Intensive insulin therapy for critically ill patients showed initial promise but later studies revealed increased mortality and hypoglycemia. Current guidelines suggest alternative blood glucose targets for better patient outcomes.

Area of Science:

  • Critical care medicine
  • Endocrinology
  • Clinical research

Background:

  • Hyperglycemia is common in critically ill patients and associated with adverse outcomes.
  • The initial Leuven I study (2001) suggested intensive insulin therapy reduced mortality in surgical ICUs.
  • Subsequent studies yielded mixed results, with some showing no significant mortality benefit.

Purpose of the Study:

  • To evaluate the efficacy and safety of intensive insulin therapy in critically ill patients.
  • To determine if the initial benefits observed in the Leuven I study are reproducible.
  • To assess the risk of hypoglycemia associated with intensive insulin therapy.

Main Methods:

  • Review of key clinical trials evaluating intensive insulin therapy in critically ill populations.
  • Comparison of mortality rates and hypoglycemia incidence between intensive insulin therapy and conventional glucose control.
  • Analysis of data from single-center, medical ICU, and multicenter studies.

Main Results:

  • The initial Leuven I study reported a 3.4% absolute mortality reduction.
  • Subsequent studies, including multicenter trials, showed no significant mortality benefit.
  • Some studies were halted early due to significantly higher rates of hypoglycemia with intensive insulin therapy, which was linked to increased mortality.
  • The largest prospective study found significantly higher mortality in the intensive therapy group (27.5%) versus control (24.9%).

Conclusions:

  • Intensive insulin therapy does not consistently benefit all critically ill patients.
  • The risk of hypoglycemia and associated increased mortality must be considered.
  • Alternative blood glucose targets (e.g., 140-180 mg/dL) are proposed to balance glycemic control and safety.

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