Skip to main content
Clinical Trials/NCT00394303
NCT00394303
Terminated
Phase 4

Tight Intra-Operative Glucose Control Using Continuous Insulin Infusion During Coronary Artery Bypass Surgery: Randomized Controlled Trial

Rabin Medical Center1 site in 1 country1,400 target enrollmentFebruary 2007

Overview

Phase
Phase 4
Intervention
Intraoperative continuous insulin infusion
Conditions
Coronary Artery Bypass
Sponsor
Rabin Medical Center
Enrollment
1400
Locations
1
Primary Endpoint
30-day all-cause mortality.
Status
Terminated
Last Updated
17 years ago

Overview

Brief Summary

Blood glucose levels increase in response to stress, infection or other conditions faced by patients in the hospital. This occurs commonly among patients with known diabetes, but also among non-diabetic hospitalized patients. Tight glucose control, the maintenance of blood glucose levels within normal limits (80-120 mg/dl), has been shown to improve patient outcomes in the hospital in several settings, mainly among critically ill patients hospitalized in intensive care units.

We plan to assess the importance of tight glucose control during open-heart surgery. The prevalence of hyperglycemia (elevated blood glucose) during this operation is high. Hyperglycemia may be associated with increased vulnerability to surgical site infections, neurological damage, cardiac and renal injury. Conversely, tight glucose control may be associated with hypoglycemia (pathologically low glucose levels) that may results in neurological injury. We hypothesize that tight glucose control will improve patient outcomes following surgery.

Detailed Description

Current evidence supports intensive glucose control for patients in the intensive care unit post-cardiac surgery. The risk-benefit ratio of tight glucose control using continuous insulin infusion during surgery has not been established. Pros for tight control include the association of hyperglycemia with neurological injury, cardiac ischemia, white blood cell dysfunction and renal failure. The cons include adverse effects, mainly hypoglycemia and hypokalemia. As with any intervention in medicine, tight intra-operative glucose control should be assessed in a randomized controlled trial. Objectives:to assess whether tight intra-operative tight glucose control using continuous insulin infusion reduces morbidity and mortality following cardiac surgery, defined as the incidence rate of surgical site infections, adverse neurological events, renal failure and 30-day mortality following CABG. Additional outcomes will include the effect of continuous insulin infusion on longer-term mortality; other infectious complications and antibiotic use during hospitalization; cardiovascular outcomes; the need for re-operations; length of hospital stay; readmission; hypoglycemia and other adverse events. Design: randomized controlled trial, with blinding of outcome assessors. Participants: all consecutive patients \>18 years undergoing CABG, without or without additional valve or other surgery at Rabin Medical Center; Beilinson campus, providing informed consent. Exclusion criteria: patients with diabetic ketoacidosis, or hyperosmolar coma. Intervention: Continuous insulin infusion throughout the operation aimed to maintain normoglycemia using a nomogram Control: Glucose management according to the discretion of the anesthesiologist (continuous or bolus infusion) During the early post-operative period (ICU-stay following surgery), all patients will be treated with intensive glucose control targeting glucose levels between 80-110.

Registry
clinicaltrials.gov
Start Date
February 2007
End Date
August 2009
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All consecutive patients \>18 years undergoing CABG, without or without additional valve or other surgery at Rabin Medical Center; Beilinson campus, providing informed consent.

Exclusion Criteria

  • Patients with diabetic ketoacidosis, or hyperosmolar coma

Arms & Interventions

1

Intervention

Intervention: Intraoperative continuous insulin infusion

2

Control

Intervention: Control

Outcomes

Primary Outcomes

30-day all-cause mortality.

Time Frame: 30-day

Deep or organ/ space (mediastinitis) surgical site infections.

Time Frame: 90 days

Acute renal failure during post-operative ICU stay, defined as: doubling of serum creatinine from baseline; or >50% reduction from baseline glomerular filtration rate; or need for renal replacement therapy.

Time Frame: 30 days

Perioperative cerebrovascular event defined as any new, temporary or permanent, focal or global neurological deficit.

Time Frame: 30 days

Secondary Outcomes

  • Individual components of the composite primary outcome(30 days)
  • Other infectious complications during ICU stay including pneumonia and bloodstream infections according to CDC criteria(ICU stay)
  • Other post-operative complications occurring during ICU stay, including re-intubation, re-operation(ICU stay)
  • Occurrence of hypoglycemia, defined as blood glucose level of 50mg/ dl or less, during surgery and up to the first glucose measurement in ICU.(during surgery)
  • Occurrence of severe hypokalemia, defined as K<2.5 mEq/l, during surgery(during surgery)
  • 6-months and long-term survival.(6 ans 12 months)
  • Durations of intubation, ICU and hospital stay(hospital stay)
  • Antibiotic use(30 days)
  • Glucose control in ICU, during the first 2 post-operative days(2 post-operative days)
  • Neurological status before surgery, at discharge and 3 months following surgery:(3 months)
  • Adverse cardiac events occurring during ICU stay(ICU stay)
  • Re-hospitalizations(30 days)

Study Sites (1)

Loading locations...

Similar Trials