Feeding Study - Effects Post-cardiac Surgery
Primary Purpose
Heart Disease, Dietary Modification, Insulin Resistance
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Rapid advancement of feeds
Standard advancement of feeds
Sponsored by
About this trial
This is an interventional treatment trial for Heart Disease focused on measuring systemic inflammation, glucose metabolism, glucose-insulin ratio
Eligibility Criteria
Inclusion Criteria:
- less than 6 months of age
- weight > 2.5kg
- surgery using cardiopulmonary bypass
- expected duration of ventilation > 6 hours
Exclusion Criteria:
- cardiac transplantation
- prematurity (<37 weeks gestation AND under 28 days of life)
- intrauterine growth restriction
- NEC
- structural gastrointestinal anomalies
- known preoperative feeding intolerance
- diabetes or known metabolic disorder
- preoperative liver or renal dysfunction
- postoperative contraindication to enteral feeding as determined by clinical team
- previous enrollment at an earlier operation
- in the opinion of the clinical or research team the patient is too well to participate, such that slow escalation to feeds would lead to hunger and therefore be considered inappropriate.
Sites / Locations
- The Hospital for Sick Children
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
No Intervention
Arm Label
Rapid Advancement of Feeds
Average feeding protocol
Feeds not affected
Arm Description
Postoperative feeds are initiated on first postoperative day and rapidly advanced over 27 hours.
Postoperative feeds are initiated on first postoperative day and advanced in using a standardized protocol that best-reflects current feeding practice. Maximum feeding volume is reached at 60 hours.
Postoperative feeds for patients not eligible for randomization are initiated by the treating clinical team and increased as per clinical team's preference.
Outcomes
Primary Outcome Measures
Insulin resistance
Plasma insulin concentrations and glucose-insulin ratio (GIR) - GIR will be calculated at each time point and used to reflect insulin resistance, with lower values representing increased resistance
Secondary Outcome Measures
Postoperative systemic inflammation
Serial measurements of postoperative cytokine (IL-1beta, IL-6, IL-8, IL-10 and TNFalpha) concentrations
Cardiac output
Postoperative cardiac output measured by respiratory mass spectrometry and Fick equation
Morbidity score
Postoperative morbidity assessed by a composite morbidity score that includes death, cardiac arrest, use of extracorporeal membrane oxygenation, cardiogenic shock, acute kidney injury, hepatic injury, or hospital-acquired infection.
Number of subjects achieving goal feeds
Number of subjects with NEC/feeding intolerance/protocol violations
Full Information
NCT ID
NCT02274220
First Posted
October 20, 2014
Last Updated
May 23, 2018
Sponsor
The Hospital for Sick Children
1. Study Identification
Unique Protocol Identification Number
NCT02274220
Brief Title
Feeding Study - Effects Post-cardiac Surgery
Official Title
Randomized Study of Early Nutritional Delivery on Glucose Control, Insulin Resistance and Systemic Inflammation Following Pediatric Cardiac Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
October 2014 (Actual)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
April 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hospital for Sick Children
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this randomized trial is to clarify the role of enteral nutrition (EN) on the relationship between cardiopulmonary bypass-induced inflammation and insulin resistance by investigating the effects of two different feeding strategies in infants following cardiac surgery. The study's primary objective is to determine if early and higher volume feeding modifies the relationship between the severity of postoperative systemic inflammation and insulin resistance.
Detailed Description
Good nutrition is important for patients after surgery. Patients who are given food tend to have fewer infections, better wound healing, and are possibly discharged more quickly from the intensive care unit and hospital. However, the best time to start feeds and the speed at which they can be increased is unclear. This may be particularly true for young children who have undergone heart surgery using a heart-lung bypass machine (bypass surgery). Bypass surgery can cause inflammation that can change the way the body uses energy and nutrients. Specifically, after bypass the body can become insensitive to insulin (insulin resistant), which means that the cells in the body don't take up sugar from the blood like they are supposed to, and this may lead to complications from the surgery. In a recent study we found that inflammation and insulin resistance was not associated with as many complications in children who were being fed. We are not sure if feeding changed the way in which the body responded after surgery or if doctors chose to feed only patients who were already recovering well. In general, doctors often hesitate to feed patients immediately after surgery because they worry that the body may not be ready for food although there is not much information to prove that this worry is correct. Starting feeds early using a structured feeding plan may be good during the recovery from heart surgery, even in our most vulnerable patients. We therefore designed this study to see if starting feeds early after bypass surgery and increasing them more quickly than our usual routine would decrease inflammation and insulin resistance. We will only study children younger than 6 months of age because they are at higher risk of complications from bypass surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Disease, Dietary Modification, Insulin Resistance
Keywords
systemic inflammation, glucose metabolism, glucose-insulin ratio
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
86 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Rapid Advancement of Feeds
Arm Type
Experimental
Arm Description
Postoperative feeds are initiated on first postoperative day and rapidly advanced over 27 hours.
Arm Title
Average feeding protocol
Arm Type
Experimental
Arm Description
Postoperative feeds are initiated on first postoperative day and advanced in using a standardized protocol that best-reflects current feeding practice. Maximum feeding volume is reached at 60 hours.
Arm Title
Feeds not affected
Arm Type
No Intervention
Arm Description
Postoperative feeds for patients not eligible for randomization are initiated by the treating clinical team and increased as per clinical team's preference.
Intervention Type
Dietary Supplement
Intervention Name(s)
Rapid advancement of feeds
Intervention Description
Feeding is initiated on first postoperative day. Bolus feeds are started at 1 mL/kg every three hours and up-titrated by 1 mL/kg every feed (Q 3 hours) to a goal of 10 mL/kg/feed (equivalent to approximately 50 kcal/kg/day). Feeding volume will exceed 20 mL/kg/day by 6 hours following protocol initiation and reach target feeds by 27 hours of protocol initiation.
Intervention Type
Dietary Supplement
Intervention Name(s)
Standard advancement of feeds
Intervention Description
Feeding is initiated on first postoperative day. Bolus feeds are started at 3 mL every three hours for 24 hours. Bolus feeds then up-titrated by 1 mL/kg every-other feed (Q 6 hours) for 24 hours. Bolus feeds then up-titrated by 1mL/kg every feed for to a goal of 10 mL/kg/feed (equivalent to approximately 50 kcal/kg/day). Feeding volume will reach target feeds by 60-63 hours after protocol initiation.
Primary Outcome Measure Information:
Title
Insulin resistance
Description
Plasma insulin concentrations and glucose-insulin ratio (GIR) - GIR will be calculated at each time point and used to reflect insulin resistance, with lower values representing increased resistance
Time Frame
96 hours
Secondary Outcome Measure Information:
Title
Postoperative systemic inflammation
Description
Serial measurements of postoperative cytokine (IL-1beta, IL-6, IL-8, IL-10 and TNFalpha) concentrations
Time Frame
96 hours
Title
Cardiac output
Description
Postoperative cardiac output measured by respiratory mass spectrometry and Fick equation
Time Frame
96 hours
Title
Morbidity score
Description
Postoperative morbidity assessed by a composite morbidity score that includes death, cardiac arrest, use of extracorporeal membrane oxygenation, cardiogenic shock, acute kidney injury, hepatic injury, or hospital-acquired infection.
Time Frame
96 hours
Title
Number of subjects achieving goal feeds
Time Frame
96 hours
Title
Number of subjects with NEC/feeding intolerance/protocol violations
Time Frame
96 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Minute
Maximum Age & Unit of Time
6 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
less than 6 months of age
weight > 2.5kg
surgery using cardiopulmonary bypass
expected duration of ventilation > 6 hours
Exclusion Criteria:
cardiac transplantation
prematurity (<37 weeks gestation AND under 28 days of life)
intrauterine growth restriction
NEC
structural gastrointestinal anomalies
known preoperative feeding intolerance
diabetes or known metabolic disorder
preoperative liver or renal dysfunction
postoperative contraindication to enteral feeding as determined by clinical team
previous enrollment at an earlier operation
in the opinion of the clinical or research team the patient is too well to participate, such that slow escalation to feeds would lead to hunger and therefore be considered inappropriate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steve Schwartz, MD
Organizational Affiliation
The Hospital for Sick Children
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Hospital for Sick Children
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X8
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Feeding Study - Effects Post-cardiac Surgery
We'll reach out to this number within 24 hrs