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SPECS: Safe Pediatric Euglycemia in Cardiac Surgery (SPECS)

Primary Purpose

Heart Defects, Congenital, Hyperglycemia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Insulin
Usual Care
Sponsored by
Boston Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Defects, Congenital focused on measuring Congenital Heart Defects, Insulin, Euglycemia, Normoglycemia

Eligibility Criteria

undefined - 36 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Undergoing heart surgery with cardiopulmonary bypass
  • Recovering in the Cardiac ICU

Exclusion Criteria:

  • Enrolled in another interventional clinical trial with related study outcomes

Sites / Locations

  • Children's Hospital Boston
  • C.S. Mott Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Insulin

Usual Care

Arm Description

Insulin was infused to target a blood glucose concentration of 80-110 mg/dL

Insulin was infused according to the discretion of the treating clinical team.

Outcomes

Primary Outcome Measures

Incidence of Nosocomial Infections in the Cardiac ICU
Nosocomial infections that are attributable to the subject's stay in the Cardiac ICU, according to Center for Disease Control-defined criteria. These definitions are extensive and cannot be accurately condensed to fit within this space. Current CDC/NHSN criteria may be accessed through this URL: https://www.cdc.gov/nhsn/pdfs/pscmanual/17pscnosinfdef_current.pdf.

Secondary Outcome Measures

Cardiac Index (CI)
Cardiac index is a measure of cardiac function, relating the cardiac output from the left ventricle in one minute to body surface area. It is calculated using the Fick principle, using oxygen consumption measured with a metabolic cart, hemoglobin levels, and the difference between arterial and superior vena cava oxygen saturation measured by co-oximetry.
Duration of ICU Stay
Duration of ICU stay spans from post-operative cardiac ICU admission to cardiac ICU discharge.
Duration of Hospital Stay
Duration of hospital stay spans from post-operative cardiac ICU admission to hospital discharge.
Duration of Endotracheal Intubation
Duration of endotracheal intubation spans from endotracheal tube intubation/initiation of mechanical ventilation to endotracheal tube extubation.
Mortality at Hospital Discharge.
Mortality is assessed at hospital discharge and at 30 days.
Mortality at 30 Days.
Mortality is assessed at hospital discharge and at 30 days. If the participant is discharged from the hospital prior to 30 days, status is determined by a follow-up phone call to the family.
Cardiac Function
Cardiac function is assessed by duration of vasoactive support.
Immune Function
Immune function is assessed by C-reactive protein (CRP) on post-operative day 7.
Endocrine Function
Endocrine function is assessed by total triiodothyronine (T3) on post-operative day 7.
Nutritional Status
Nutritional status assessed by percentage of total caloric intake as enteral nutrition during critical illness period.
Neurodevelopmental Evaluation, Cognitive
Neurodevelopmental follow-up includes in-person testing using the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III), measured at one year of age. Bayley-III cognitive composite score ranges from 55-145, Bayley-III language composite score ranges from 47-153, and Bayley-III motor composite score ranges from 46-154. Higher values indicate better neurodevelopmental outcomes. These three composite scores cannot be combined and are presented as separate scores in the literature.
Neurodevelopmental Evaluation, Language
Neurodevelopmental follow-up includes in-person testing using the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III), measured at one year of age. Bayley-III cognitive composite score ranges from 55-145, Bayley-III language composite score ranges from 47-153, and Bayley-III motor composite score ranges from 46-154. Higher values indicate better neurodevelopmental outcomes. These three composite scores cannot be combined and are presented as separate scores in the literature.
Neurodevelopmental Evaluation, Motor
Neurodevelopmental follow-up includes in-person testing using the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III), measured at one year of age. Bayley-III cognitive composite score ranges from 55-145, Bayley-III language composite score ranges from 47-153, and Bayley-III motor composite score ranges from 46-154. Higher values indicate better neurodevelopmental outcomes. These three composite scores cannot be combined and are presented as separate scores in the literature.

Full Information

First Posted
March 5, 2007
Last Updated
July 21, 2022
Sponsor
Boston Children's Hospital
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT00443599
Brief Title
SPECS: Safe Pediatric Euglycemia in Cardiac Surgery
Acronym
SPECS
Official Title
Maintaining Normal Blood Sugar Levels in Children Undergoing Heart Surgery to Reduce the Risk of Infections and Improve Recovery (The SPECS Study)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston Children's Hospital
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Critically ill children, including children undergoing heart surgery, commonly develop elevated blood glucose (also known as "blood sugar") levels during their illness, which can lead to poor health outcomes and an increased risk of death. This study will examine the effectiveness of maintaining normal blood glucose levels at decreasing infections and improving recovery in young children undergoing heart surgery.
Detailed Description
Children undergoing heart surgery are under significant bodily stress, which can lead to higher than normal or lower than normal blood glucose levels. A synthetic form of insulin, a naturally occurring hormone in the body, can be injected into people to normalize blood glucose levels. Insulin is most commonly used to treat people with diabetes, but it is also used in hospitals to control blood glucose levels in patients. Previous studies of adult intensive care unit (ICU) patients have shown that patients whose blood sugar levels are maintained at normal levels with the use of insulin contract fewer infections and are released more quickly from the ICU than patients who do not maintain normal blood glucose levels. This study will use a continuous blood glucose monitoring system to detect changes in blood glucose levels. Intravenous insulin infusions will be used to then safely maintain normal blood glucose levels. The purpose of this study is to determine if maintaining normal blood glucose levels during an ICU stay will help decrease the incidence of infections and improve surgical recovery in young children following heart surgery. This study will enroll children who are undergoing heart surgery that requires a cardiopulmonary bypass procedure. Participants will be randomly assigned to either a control group or the treatment group. All participants will receive usual care while in the ICU and will undergo continuous glucose monitoring. Participants in the treatment group will receive intravenous insulin infusions to keep their blood glucose within the normal range. While in the ICU, blood will be collected from all participants once a day for the first 3 days and then once a week to monitor glucose levels, hormone levels, and measurements of nutrition and immune function. On days 1 and 5 following surgery, participants who are on a ventilator will have their breath measured to monitor heart function and energy use. Thirty days and 1 year following surgery, study researchers will contact the participant's parent or doctor to collect information on health status and any new infections at the surgical site. Children who enroll in the study will be asked to participate in follow-up neurodevelopmental evaluations at 1 and 3 years of age to assess longer term cognitive effects of tight glycemic control in the ICU.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Defects, Congenital, Hyperglycemia
Keywords
Congenital Heart Defects, Insulin, Euglycemia, Normoglycemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
989 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Insulin
Arm Type
Experimental
Arm Description
Insulin was infused to target a blood glucose concentration of 80-110 mg/dL
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Insulin was infused according to the discretion of the treating clinical team.
Intervention Type
Drug
Intervention Name(s)
Insulin
Other Intervention Name(s)
Human regular insulin, Humulin R, Novolin R
Intervention Description
Study drug is continuously infused intravenous insulin. Suggested dose is calculated by a computerized infusion algorithm using the participant's blood sugar concentration. The insulin infusion rate is titrated to maintain normal blood sugar. Participants are eligible to receive insulin while they have an in-dwelling arterial catheter.
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Participants receive standard Cardiac ICU care without tight blood glucose control.
Primary Outcome Measure Information:
Title
Incidence of Nosocomial Infections in the Cardiac ICU
Description
Nosocomial infections that are attributable to the subject's stay in the Cardiac ICU, according to Center for Disease Control-defined criteria. These definitions are extensive and cannot be accurately condensed to fit within this space. Current CDC/NHSN criteria may be accessed through this URL: https://www.cdc.gov/nhsn/pdfs/pscmanual/17pscnosinfdef_current.pdf.
Time Frame
Measured during participant's ICU stay, a median duration of 3 days.
Secondary Outcome Measure Information:
Title
Cardiac Index (CI)
Description
Cardiac index is a measure of cardiac function, relating the cardiac output from the left ventricle in one minute to body surface area. It is calculated using the Fick principle, using oxygen consumption measured with a metabolic cart, hemoglobin levels, and the difference between arterial and superior vena cava oxygen saturation measured by co-oximetry.
Time Frame
Day 2 (day after cardiopulmonary bypass surgery).
Title
Duration of ICU Stay
Description
Duration of ICU stay spans from post-operative cardiac ICU admission to cardiac ICU discharge.
Time Frame
The duration of cardiac ICU stay was evaluated from the date of postoperative cardiac ICU admission until the date of cardiac ICU discharge or date of death from any cause, whichever came first, assessed up to 30 days.
Title
Duration of Hospital Stay
Description
Duration of hospital stay spans from post-operative cardiac ICU admission to hospital discharge.
Time Frame
The duration of hospital stay was evaluated from the day of postoperative cardiac ICU admission until the day of hospital discharge or day of death from any cause, whichever came first, assessed up to 30 days.
Title
Duration of Endotracheal Intubation
Description
Duration of endotracheal intubation spans from endotracheal tube intubation/initiation of mechanical ventilation to endotracheal tube extubation.
Time Frame
The duration of endotracheal intubation (mechanical ventilation) was evaluated from the day of postoperative cardiac ICU admission until the day of extubation or day of death from any cause, whichever came first, assessed up to 30 days.
Title
Mortality at Hospital Discharge.
Description
Mortality is assessed at hospital discharge and at 30 days.
Time Frame
Mortality at hospital discharge (In-hospital mortality) was evaluated on the day of hospital discharge or day of death from any cause, whichever came first (no upper limit).
Title
Mortality at 30 Days.
Description
Mortality is assessed at hospital discharge and at 30 days. If the participant is discharged from the hospital prior to 30 days, status is determined by a follow-up phone call to the family.
Time Frame
Measured at 30 days.
Title
Cardiac Function
Description
Cardiac function is assessed by duration of vasoactive support.
Time Frame
The duration of vasoactive support was evaluated from the day of postoperative cardiac ICU admission until the last day of vasoactive support or day of death from any cause, whichever came first, assessed up to 30 days.
Title
Immune Function
Description
Immune function is assessed by C-reactive protein (CRP) on post-operative day 7.
Time Frame
Post-operative day 7.
Title
Endocrine Function
Description
Endocrine function is assessed by total triiodothyronine (T3) on post-operative day 7.
Time Frame
Measured during participant's ICU stay on Day 7.
Title
Nutritional Status
Description
Nutritional status assessed by percentage of total caloric intake as enteral nutrition during critical illness period.
Time Frame
The percentage of total caloric intake was evaluated from the day of postoperative cardiac ICU admission until the last day of the critical illness period, as defined by the presence of the arterial catheter, assessed up to 30 days.
Title
Neurodevelopmental Evaluation, Cognitive
Description
Neurodevelopmental follow-up includes in-person testing using the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III), measured at one year of age. Bayley-III cognitive composite score ranges from 55-145, Bayley-III language composite score ranges from 47-153, and Bayley-III motor composite score ranges from 46-154. Higher values indicate better neurodevelopmental outcomes. These three composite scores cannot be combined and are presented as separate scores in the literature.
Time Frame
Measured at one year of age.
Title
Neurodevelopmental Evaluation, Language
Description
Neurodevelopmental follow-up includes in-person testing using the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III), measured at one year of age. Bayley-III cognitive composite score ranges from 55-145, Bayley-III language composite score ranges from 47-153, and Bayley-III motor composite score ranges from 46-154. Higher values indicate better neurodevelopmental outcomes. These three composite scores cannot be combined and are presented as separate scores in the literature.
Time Frame
Measured at one year of age.
Title
Neurodevelopmental Evaluation, Motor
Description
Neurodevelopmental follow-up includes in-person testing using the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III), measured at one year of age. Bayley-III cognitive composite score ranges from 55-145, Bayley-III language composite score ranges from 47-153, and Bayley-III motor composite score ranges from 46-154. Higher values indicate better neurodevelopmental outcomes. These three composite scores cannot be combined and are presented as separate scores in the literature.
Time Frame
Measured at one year of age.

10. Eligibility

Sex
All
Maximum Age & Unit of Time
36 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Undergoing heart surgery with cardiopulmonary bypass Recovering in the Cardiac ICU Exclusion Criteria: Enrolled in another interventional clinical trial with related study outcomes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Agus, MD
Organizational Affiliation
Boston Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital Boston
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
C.S. Mott Children's Hospital
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Will share with investigators based upon specific requests
Citations:
PubMed Identifier
16998362
Citation
Agus MS, Javid PJ, Piper HG, Wypij D, Duggan CP, Ryan DP, Jaksic T. The effect of insulin infusion upon protein metabolism in neonates on extracorporeal life support. Ann Surg. 2006 Oct;244(4):536-44. doi: 10.1097/01.sla.0000237758.93186.c8.
Results Reference
background
PubMed Identifier
16951013
Citation
Piper HG, Alexander JL, Shukla A, Pigula F, Costello JM, Laussen PC, Jaksic T, Agus MS. Real-time continuous glucose monitoring in pediatric patients during and after cardiac surgery. Pediatrics. 2006 Sep;118(3):1176-84. doi: 10.1542/peds.2006-0347.
Results Reference
background
PubMed Identifier
15929674
Citation
Javid PJ, Halwick DR, Betit P, Thompson JE, Long K, Zhang Y, Jaksic T, Agus MS. The first use of live continuous glucose monitoring in patients on extracorporeal life support. Diabetes Technol Ther. 2005 Jun;7(3):431-9. doi: 10.1089/dia.2005.7.431.
Results Reference
background
PubMed Identifier
15185208
Citation
Agus MS, Javid PJ, Ryan DP, Jaksic T. Intravenous insulin decreases protein breakdown in infants on extracorporeal membrane oxygenation. J Pediatr Surg. 2004 Jun;39(6):839-44; discussion 839-44. doi: 10.1016/j.jpedsurg.2004.02.013.
Results Reference
background
PubMed Identifier
22805161
Citation
Gaies MG, Langer M, Alexander J, Steil GM, Ware J, Wypij D, Laussen PC, Newburger JW, Goldberg CS, Pigula FA, Shukla AC, Duggan CP, Agus MS; Safe Pediatric Euglycemia after Cardiac Surgery Study Group. Design and rationale of safe pediatric euglycemia after cardiac surgery: a randomized controlled trial of tight glycemic control after pediatric cardiac surgery. Pediatr Crit Care Med. 2013 Feb;14(2):148-56. doi: 10.1097/PCC.0b013e31825b549a.
Results Reference
background
PubMed Identifier
22957521
Citation
Agus MS, Steil GM, Wypij D, Costello JM, Laussen PC, Langer M, Alexander JL, Scoppettuolo LA, Pigula FA, Charpie JR, Ohye RG, Gaies MG; SPECS Study Investigators. Tight glycemic control versus standard care after pediatric cardiac surgery. N Engl J Med. 2012 Sep 27;367(13):1208-19. doi: 10.1056/NEJMoa1206044. Epub 2012 Sep 7.
Results Reference
result
PubMed Identifier
36071424
Citation
Sadhwani A, Asaro LA, Goldberg CS, Ware J, Butcher J, Gaies M, Smith C, Alexander JL, Wypij D, Agus MSD. Impact of tight glycemic control and hypoglycemia after pediatric cardiac surgery on neurodevelopmental outcomes at three years of age: Findings from a randomized clinical trial. BMC Pediatr. 2022 Sep 7;22(1):531. doi: 10.1186/s12887-022-03556-z.
Results Reference
derived
PubMed Identifier
27112038
Citation
Sadhwani A, Asaro LA, Goldberg C, Ware J, Butcher J, Gaies M, Smith C, Alexander JL, Wypij D, Agus MS. Impact of Tight Glycemic Control on Neurodevelopmental Outcomes at 1 Year of Age for Children with Congenital Heart Disease: A Randomized Controlled Trial. J Pediatr. 2016 Jul;174:193-198.e2. doi: 10.1016/j.jpeds.2016.03.048. Epub 2016 Apr 23.
Results Reference
derived
PubMed Identifier
25850865
Citation
Fisher JG, Sparks EA, Khan FA, Alexander JL, Asaro LA, Wypij D, Gaies M, Modi BP, Duggan C, Agus MS, Yu YM, Jaksic T. Tight Glycemic Control With Insulin Does Not Affect Skeletal Muscle Degradation During the Early Postoperative Period Following Pediatric Cardiac Surgery. Pediatr Crit Care Med. 2015 Jul;16(6):515-21. doi: 10.1097/PCC.0000000000000413.
Results Reference
derived
PubMed Identifier
24671945
Citation
Agus MS, Asaro LA, Steil GM, Alexander JL, Silverman M, Wypij D, Gaies MG; SPECS Investigators. Tight glycemic control after pediatric cardiac surgery in high-risk patient populations: a secondary analysis of the safe pediatric euglycemia after cardiac surgery trial. Circulation. 2014 Jun 3;129(22):2297-304. doi: 10.1161/CIRCULATIONAHA.113.008124. Epub 2014 Mar 26.
Results Reference
derived

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SPECS: Safe Pediatric Euglycemia in Cardiac Surgery

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