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ARTICLE

Intensive Intraoperative Insulin Therapy versus Conventional Glucose Management during Cardiac Surgery

A Randomized Trial

right arrow Gunjan Y. Gandhi, MD, MSc; Gregory A. Nuttall, MD; Martin D. Abel, MD; Charles J. Mullany, MD; Hartzell V. Schaff, MD; Peter C. O'Brien, PhD; Matthew G. Johnson, MPH; Arthur R. Williams, PhD; Susanne M. Cutshall, RN; Lisa M. Mundy, RN; Robert A. Rizza, MD; and M. Molly McMahon, MD

20 February 2007 | Volume 146 Issue 4 | Pages 233-243

Background: It is not known whether rigorous intraoperative glycemic control reduces death and morbidity in cardiac surgery patients.

Objective: To compare outcomes of intensive insulin therapy during cardiac surgery with those of conventional intraoperative glucose management.

Design: A randomized, open-label, controlled trial with blinded end point assessment.

Setting: Tertiary care center.

Patients: Adults with and without diabetes who were undergoing on-pump cardiac surgery.

Measurements: The primary outcome was a composite of death, sternal infections, prolonged ventilation, cardiac arrhythmias, stroke, and renal failure within 30 days after surgery. Secondary outcome measures were length of stay in the intensive care unit and hospital.

Intervention: Patients were randomly assigned to receive continuous insulin infusion to maintain intraoperative glucose levels between 4.4 (80 mg/dL) and 5.6 mmol/L (100 mg/dL) (n = 199) or conventional treatment (n = 201). Patients in the conventional treatment group were not given insulin during surgery unless glucose levels were greater than 11.1 mmol/L (>200 mg/dL). Both groups were treated with insulin infusion to maintain normoglycemia after surgery.

Results: Mean glucose concentrations were statistically significantly lower in the intensive treatment group at the end of surgery (6.3 mmol/L [SD, 1.6] [114 mg/dL {SD, 29}] in the intensive treatment group vs. 8.7 mmol/L [SD, 2.3] [157 mg/dL {SD, 42}] in the conventional treatment group; difference, –2.4 mmol/L [95% CI, –2.8 to –1.9 mmol/L] [–43 mg/dL {CI, –50 to –35 mg/dL}]). Eighty two of 185 patients (44%) in the intensive treatment group and 86 of 186 patients (46%) in the conventional treatment group had an event (risk ratio, 1.0 [CI, 0.8 to 1.2]). More deaths (4 deaths vs. 0 deaths; P = 0.061) and strokes (8 strokes vs. 1 strokes; P = 0.020) occurred in the intensive treatment group. Length of stay in the intensive care unit (mean, 2 days [SD, 2] vs. 2 days [SD, 3]; difference, 0 days [CI, –1 to 1 days]) and in the hospital (mean, 8 days [SD, 4] vs. 8 days [SD, 5]; difference, 0 days [CI, –1 to 0 days]) was similar for both groups.

Limitations: This single-center study used a composite end point and could not examine whether outcomes differed by diabetes status.

Conclusions: Intensive insulin therapy during cardiac surgery does not reduce perioperative death or morbidity. The increased incidence of death and stroke in the intensive treatment group raises concern about routine implementation of this intervention.


Editors' Notes
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Context

  • Intensive insulin therapy used to maintain normoglycemia during intensive care after cardiac surgery improves perioperative outcomes. Its effect during cardiac surgery is unknown.

Contributions

  • The authors randomly assigned 400 cardiac surgical patients to tight glycemic control (blood glucose level, 4.4 to 5.6 mmol/L [80 to 100 mg/dL]) during surgery or usual intraoperative care. All patients received tight glycemic control in the cardiac intensive care unit. The groups had the same risk for perioperative adverse events (risk ratio, 1.0 [95% CI, 0.8 to 1.2]). The intensive treatment group had more strokes (8 vs. 1) and more deaths (4 vs. 0) than the conventional treatment group.

Caution

  • The authors performed the study at a single center.

Implications

  • Maintaining normoglycemia during cardiac surgery does not improve outcomes and might worsen them.

—The Editors

 

Author and Article Information
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From the Mayo Clinic College of Medicine, Rochester, Minnesota.

ClinicalTrials.gov registration number: NCT00282698.

Acknowledgments: The authors thank Nicole Henderson, Laurie Olsen, and Lisa Schrader for recruitment of study participants, data collection and entry, and project management; Victor Montori, MD, MSc, for providing methodological expertise; and Darrell Schroeder, MS, for statistical support.

Potential Financial Conflicts of Interest: Consultancies: R.A. Rizza (Abbott, Takeda, Symphony Capital, Eli Lilly Inc.), M.M. McMahon (Baxter Healthcare); Honoraria: R.A. Rizza (Merck & Co. Inc., Novo Nordisk, Takeda, Mankind, Eli Lilly Inc.); Stock ownership or options (other than mutual funds): R.A. Rizza (Diobex); Grants received: H.V. Schaff (AstraZeneca, Atricure Inc., Avant Immunotherapeutics Inc., Baxter, Boston Scientific, Cryolife Inc., Edwards Lifesciences, Jarvik Heart Inc., Medtronic Inc., Sorin Group/Carbomedics, St. Jude Medical, Thoratec Corporation, TransTech Pharma Inc., W.L. Gore and Associates Inc.).

Requests for Single Reprints: Gunjan Y. Gandhi, MD, MSc, Mayo Clinic College of Medicine, 200 First Street Southwest, Rochester, MN 55905; e-mail, gandhi.gunjan{at}mayo.edu.

Current Author Addresses: Drs. Gandhi, Nuttall, Abel, Mullany, Schaff, O'Brien, Williams, Rizza, and McMahon; Mr. Johnson, Ms. Cutshall, and Ms. Mundy: Mayo Clinic College of Medicine, 200 First Street Southwest, Rochester, MN 55905.

Author Contributions: Conception and design: G.Y. Gandhi, G.A. Nuttall, M.D. Abel, P.C. O'Brien, A.R. Williams, S.M. Cutshall, L.M. Mundy, R.A. Rizza, M.M. McMahon.

Analysis and interpretation of the data: G.Y. Gandhi, G.A. Nuttall, P.C. O'Brien, R.A. Rizza, M.M. McMahon.

Drafting of the article: G.Y. Gandhi, R.A. Rizza, M.M. McMahon.

Critical revision of the article for important intellectual content: G.Y. Gandhi, G.A. Nuttall, M.D. Abel, C.J. Mullany, P.C. O'Brien, A.R. Williams, R.A. Rizza, M.M. McMahon.

Final approval of the article: G.Y. Gandhi, R.A. Rizza, M.M. McMahon.

Provision of study materials or patients: C.J. Mullany, H.V. Schaff.

Statistical expertise: P.C. O'Brien, M.G. Johnson.

Obtaining of funding: A.R. Williams, R.A. Rizza, M.M. McMahon.

Administrative, technical, or logistic support: G.A. Nuttall, M.D. Abel, C.J. Mullany, H.V. Schaff, S.M. Cutshall, L.M. Mundy.

Collection and assembly of data: G.Y. Gandhi.

 

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Rapid Responses:

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Intensive Insulin Therapy Isn't For Everyone
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