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Tight Intra-Operative Glucose Control During Coronary Artery Bypass Surgery

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

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00394303
Enrollment
1400
Registered
2006-11-01
Start date
2007-02-28
Completion date
2009-08-31
Last updated
2009-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Bypass

Keywords

Open heart surgery, Diabetes mellitus, Hyperglycemia, Surgical site infection, Normoglycemia

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.

Interventions

DRUGIntraoperative continuous insulin infusion

Nomogram specified in appendix

OTHERControl

Glucose management according to the discretion of the anesthesiologist aimed to maintain glucose levels \<200 mg.dl, reflecting current practice.

Sponsors

Rabin Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
30-day all-cause mortality.30-day
Deep or organ/ space (mediastinitis) surgical site infections.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.30 days
Perioperative cerebrovascular event defined as any new, temporary or permanent, focal or global neurological deficit.30 days

Secondary

MeasureTime frame
Durations of intubation, ICU and hospital stayhospital stay
Other post-operative complications occurring during ICU stay, including re-intubation, re-operationICU 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 surgeryduring surgery
Individual components of the composite primary outcome30 days
Neurological status before surgery, at discharge and 3 months following surgery:3 months
Adverse cardiac events occurring during ICU stayICU stay
Re-hospitalizations30 days
Glucose control in ICU, during the first 2 post-operative days2 post-operative days
6-months and long-term survival.6 ans 12 months
Other infectious complications during ICU stay including pneumonia and bloodstream infections according to CDC criteriaICU stay
Antibiotic use30 days

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026