Does Pre-operative Carbohydrate Loading Reduce Insulin Resistance and Improve Outcomes in Elective Surgical Patients? (Preop)

This study has been completed.
Sponsor:
Information provided by:
St. Michael's Hospital, Toronto
ClinicalTrials.gov Identifier:
NCT00618592
First received: February 8, 2008
Last updated: July 21, 2010
Last verified: February 2009
  Purpose

The recent development of an oral carbohydrate drink for consumption prior to elective surgical procedures has been shown to improve insulin sensitivity. However, these studies have not investigated the use of this carbohydrate supplement in patients undergoing cardiac and spinal surgery.

Hypothesis: The administration of 100g of carbohydrates the evening before and 50g of carbohydrates two hours before elective coronary artery bypass graft (CABG) or spinal surgery will reduce postoperative insulin resistance by 40% compared to those undergoing the standard of care of fasting the evening before and the day of surgery.


Condition Intervention
Coronary Artery Bypass Graft Surgery
Spine Surgery
Dietary Supplement: PreOp carbohydrate drink

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Does Pre-operative Carbohydrate Loading Reduce Insulin Resistance and Improve Outcomes in Elective Surgical Patients?

Resource links provided by NLM:


Further study details as provided by St. Michael's Hospital, Toronto:

Primary Outcome Measures:
  • Insulin sensitivity [ Time Frame: baseline and postoperatively ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Markers of inflammation e.g., CRP, IL-6, free fatty acids [ Time Frame: baseline, in ICU, and 24, 48 and 72 hours postoperatively ] [ Designated as safety issue: No ]
  • Glucose metabolism e.g., insulin-mediated glucose uptake and GLUT 4 translocation [ Time Frame: onset of surgery ] [ Designated as safety issue: No ]
  • Clinical outcomes e.g., length of stay in ICU and hospital, blood transfusions [ Time Frame: during surgery and postoperatively ] [ Designated as safety issue: No ]
  • Preoperative patient discomfort [ Time Frame: baseline and preoperatively ] [ Designated as safety issue: No ]
  • IGF-1 [ Time Frame: baseline, in ICU and 24, 48 and 72 hours postoperatively ] [ Designated as safety issue: No ]

Estimated Enrollment: 60
Study Start Date: February 2008
Study Completion Date: August 2009
Primary Completion Date: August 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: CHO Dietary Supplement: PreOp carbohydrate drink
800 mL of PreOp evening before surgery, 400 mL at least two hours before surgery
Other Name: PreOp, Nutricia
No Intervention: FAST

Detailed Description:

In many Western hospitals, including St. Michael's Hospital, fasting for 12-14 hours is the standard protocol for patients entering elective surgery. Fasting results in a depletion of energy stores and consequently, a patient enters surgery in a catabolic state. Furthermore, the human body reacts to surgery by producing a variety of stress hormones and other hormone-like proteins that enable the body to react to stress or injury appropriately. One of the changes that occurs with surgery is related to how the body stores and metabolizes glucose. During and after surgery, muscle and adipose tissue become less sensitive to the action of insulin (insulin resistant). Insulin resistance results in a reduced uptake of glucose by these tissues and subsequently to a rise in circulating blood glucose levels. Sustained high levels of blood glucose have been associated with post-surgical complications and less favourable outcomes. Previous studies have found that fasting before surgery exacerbates insulin resistance during and after surgery. The recent development of a carbohydrate drink for consumption prior to elective surgical procedures has been shown to be well tolerated and pose no additional risk of pulmonary aspiration when ingested two hours prior to surgery. Furthermore, there appears to be metabolic, psychological and possibly clinical benefits in pre-operative carbohydrate loading compared to fasting, including improvements in insulin resistance. However, the studies done to date have been limited by their small sample size, their lack of clinical outcome data and their reliance upon predominantly surgeries of shorter duration and reduced metabolic stress where insulin resistance is lower. Therefore, there is a need to investigate the effect of carbohydrate loading on insulin resistance and clinical outcomes in patients undergoing surgery of extended duration and complexity.

Patients undergoing major cardiac and spinal surgery are ideal for studying the effects of pre-operative carbohydrate loading since this type of operation is of long duration and relatively high surgical stress resulting in the development of significant insulin resistance, and thus potentially benefit from pre-operative carbohydrate loading. Therefore, we will be conducting a larger randomized trial investigating the effects of pre-operative carbohydrate loading in comparison with fasting on insulin resistance and clinical outcomes in patients undergoing invasive cardiac and spinal surgery at St. Michael's Hospital.

We hypothesize that consumption of a pre-operative carbohydrate load will reduce postoperative insulin resistance by 40% (measured by the standardized short insulin tolerance test). As secondary outcomes, we hypothesize that pre-operative carbohydrate loading will reduce circulating markers of inflammation and stress as well as improve clinical outcomes such as blood product utilization, incidence of hyperglycemia, rates of adverse events and length of stay in comparison with standard pre-operative fasting. This study will provide important information regarding the clinical benefits associated with the consumption of a pre-operative carbohydrate load. Many European centres have already liberalized their pre-operative treatments; this study will help to optimize the perioperative management and outcomes of surgical patients at our institution.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adult patients undergoing elective coronary artery bypass graft or spinal (decompression and fusion) surgery
  • Ability to provide informed consent

Exclusion Criteria:

  • Patients undergoing associated cardiac procedures such as valve replacement or valve repair
  • Patients undergoing spinal surgery without fusion
  • Conditions likely to impair gastrointestinal motility or enhance gastrointestinal reflux
  • On medications likely to delay gastric emptying
  • BMI > 40
  • Existing Type I or Type II diabetes
  • Participated in another study in the past 30 days
  • Entering surgery greater than five hours after ingestion of morning drink
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00618592

Locations
Canada, Ontario
St. Michael's Hospital
Toronto, Ontario, Canada, M5B 1W8
Sponsors and Collaborators
St. Michael's Hospital, Toronto
Investigators
Principal Investigator: C. David Mazer, MD St. Michael's Hospital, Toronto
  More Information

No publications provided by St. Michael's Hospital, Toronto

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: C. David Mazer, St. Michael's Hospital
ClinicalTrials.gov Identifier: NCT00618592     History of Changes
Other Study ID Numbers: REB 02-117
Study First Received: February 8, 2008
Last Updated: July 21, 2010
Health Authority: Canada: Ethics Review Committee

Keywords provided by St. Michael's Hospital, Toronto:
carbohydrate supplementation
cardiac surgery
spine surgery
insulin resistance
insulin sensitivity
short insulin tolerance test
HOMA
outcomes

Additional relevant MeSH terms:
Insulin Resistance
Hyperinsulinism
Glucose Metabolism Disorders
Metabolic Diseases
Insulin
Hypoglycemic Agents
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on August 19, 2014