Design and rationale of safe pediatric euglycemia After cardiac surgery: A randomized controlled trial of tight glycemic control After pediatric cardiac surgery

Michael G. Gaies, Monica Langer, Jamin Alexander, Garry M. Steil, Janice Ware, David Wypij, Peter C. Laussen, Jane W. Newburger, Caren S. Goldberg, Frank A. Pigula, Avinash C. Shukla, Christopher P. Duggan, Michael S.D. Agus, John M. Costello, Martha A. Curley, Pedro J. Del Nido, Tom Jaksic, Anjali Sadhwani

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Objectives: To describe the design of a clinical trial testing the hypothesis that children randomized to tight glycemic control with intensive insulin therapy after cardiac surgery will have improved clinical outcomes compared to children randomized to conventional blood glucose management. Design: Two-center, randomized controlled trial. Setting: Cardiac ICUs at two large academic pediatric centers. Patients: Children from birth to those aged 36 months recovering in the cardiac ICU after surgery with cardiopulmonary bypass. Interventions: Subjects in the tight glycemic control (intervention) group receive an intravenous insulin infusion titrated to achieve normoglycemia (target blood glucose range of 80-110 mg/dL; 4.4-6.1 mmol/L). The intervention begins at admission to the cardiac ICU from the operating room and terminates when the patient is ready for discharge from the ICU. Continuous glucose monitoring is performed during insulin infusion to minimize the risks of hypoglycemia. The standard care group has no target blood glucose range. Measurements and Main Results: The primary outcome is the development of any nosocomial infection (bloodstream, urinary tract, and surgical site infection or nosocomial pneumonia). Secondary outcomes include mortality, measures of cardiorespiratory function and recovery, laboratory indices of nutritional balance, immunologic, endocrinologic, and neurologic function, cardiac ICU and hospital length of stay, and neurodevelopmental outcome at 1 and 3 yrs of age. A total of 980 subjects will be enrolled (490 in each treatment arm) for sufficient power to show a 50% reduction in the prevalence of the primary outcome.

Original languageEnglish (US)
Pages (from-to)148-156
Number of pages9
JournalPediatric Critical Care Medicine
Volume14
Issue number2
DOIs
StatePublished - Feb 1 2013

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Critical Care and Intensive Care Medicine

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