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Corticosteroid Therapy in Neonates Undergoing Cardiopulmonary Bypass

Primary Purpose

Congenital Heart Disease, Disorder of Fetus or Newborn

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Methylprednisolone
Placebo
Sponsored by
Medical University of South Carolina
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Congenital Heart Disease focused on measuring Cardiopulmonary Bypass (CPB), System Inflammatory Response, inflammation, Methylprednisolone, Neonates, Steroid, Cardiac Surgical Procedures, Children, Infants, Pediatrics, Glucocorticoid, Heart Disease, Heart Defects, Congenital, Cardiovascular Diseases, Cardiovascular Abnormalities, Corticosteroid, methylprednisolone Hemisuccinate, Hormones, Physiological Effects of Drugs, Randomized Clinical Trial

Eligibility Criteria

undefined - 30 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age < 1 month
  • Male and female patients who are scheduled to undergo cardiac surgery involving CPB

Exclusion Criteria:

  • Prematurity: < 37 weeks post gestational age at time of surgery
  • Treatment with intravenous steroids within the two days prior to scheduled surgery.
  • Participation in research studies involving the evaluation of investigational drugs within 30 days of randomization.
  • Suspected infection that would contraindicate steroid use (eg - Herpes)
  • Known hypersensitivity to IVMP or one of its components or other contraindication to steroid therapy (eg - gastrointestinal bleeding).
  • Preoperative use of mechanical circulatory support or active resuscitation at the time of proposed randomization.

Sites / Locations

  • Children's Healthcare of Atlanta/Emory University
  • Medical University of South Carolina, Pediatric Cardiology

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Intraoperative Methylprednisone

Placebo

Arm Description

Neonates with congenital heart disease requiring surgery utilizing cardiopulmonary bypass(CPB) in the first month of life that receive one dose of intravenous methylprednisolone (30 mg/kg) during anesthetic induction.

Neonates with congenital heart disease requiring surgery utilizing cardiopulmonary bypass (CPB) in the first month of life that receive one dose of placebo (normal saline) during anesthetic induction.

Outcomes

Primary Outcome Measures

Number of Participants With a Clinically Derived Composite Morbidity-mortality Outcome
The composite morbidity-mortality outcome will be met if any of the following occur after surgery but before hospital discharge: death, cardiac arrest, extracorporeal membrane oxygenation, renal insufficiency (creatinine more than two times normal), hepatic insufficiency (aspartate aminotransferase or alanine aminotransferase more than two times normal), or rising lactic acidosis (>5mmol/L). This outcome was choosen because death rarely occurs in this population. We have found this endpoint to be highly associated with other important clinical outcomes in this population.

Secondary Outcome Measures

Duration of Mechanical Ventilation Post Cardiac Surgery.
Amount of time on mechanical ventilation following cardiac surgery
Intensive Care Unit Stay
Amount of time in the intensive care unit following cardiac surgery
Hospital Stay
Total duration of hospital stay following cardiac surgery
Neurodevelopmental Outcome
Bayley Scales of Infant and Toddler Development version 3 at 1 year. Cognitive, language, and motor composite scores will be used. The general population has a mean of 100 with a standard deviation of 15 for each composite score. Higher scores are better. The minimum composite score is 46 and maximum 154.

Full Information

First Posted
April 13, 2012
Last Updated
November 25, 2019
Sponsor
Medical University of South Carolina
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT01579513
Brief Title
Corticosteroid Therapy in Neonates Undergoing Cardiopulmonary Bypass
Official Title
Corticosteroid Therapy in Neonates Undergoing Cardiopulmonary Bypass
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
June 2012 (undefined)
Primary Completion Date
May 25, 2018 (Actual)
Study Completion Date
December 19, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of South Carolina
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Although cardiopulmonary bypass (heart-lung machine) is a necessary component of heart surgery, it is not without consequences. Cardiopulmonary bypass initiates a potent inflammatory response secondary to the body's recognition of the abnormal environment of the heart-lung machine. This inflammatory response may lead to poor heart, lung and kidney function after the heart surgery. This is turn can lead to longer times on the ventilator (breathing machine), the need for higher doses of heart medications, a longer stay in the intensive care unit and even death. This is particularly true in infants less than one month of age due to their size and the immaturity of their organs. The appreciation of the post-cardiopulmonary bypass inflammatory response has resulted in a number of interventions directed at its reduction. No therapy has been recognized as the standard of care; however steroid therapy has been applied most often despite unclear evidence of a benefit. This study aims to determine if steroids improve the outcomes of babies undergoing heart surgery.
Detailed Description
This study is a multi-institutional randomized double-blind placebo controlled trial of the use of glucocorticoids to improve the clinical course of neonates following cardiac surgery. Cardiopulmonary bypass (CPB) is critical to cardiac surgery, but the pathophysiologic processes engendered by CPB play an important role in post-operative recovery. The use, doses and schedule of glucocortiocoid administration to ameliorate these CPB induced processes is highly variable and without clear data to provide direction. The Primary Aim of this study is to compare the effects of intraoperative methylprednisolone to placebo on a composite morbidity-mortality outcome following neonatal CPB. Secondary Endpoints include: inotropic requirements, incidence of low cardiac output syndrome, fluid balance, ICU stay parameters, levels of inflammatory molecules, neuro-developmental outcomes, and safety parameters. The study will focus on neonates because their post-CPB clinical course is typically more severe, and that high level of severity itself provides a substrate for identifying the positive effects of a particular therapy. Finally, a therapy identified as beneficial has the greatest potential for benefit in this vulnerable population

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease, Disorder of Fetus or Newborn
Keywords
Cardiopulmonary Bypass (CPB), System Inflammatory Response, inflammation, Methylprednisolone, Neonates, Steroid, Cardiac Surgical Procedures, Children, Infants, Pediatrics, Glucocorticoid, Heart Disease, Heart Defects, Congenital, Cardiovascular Diseases, Cardiovascular Abnormalities, Corticosteroid, methylprednisolone Hemisuccinate, Hormones, Physiological Effects of Drugs, Randomized Clinical Trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
190 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intraoperative Methylprednisone
Arm Type
Active Comparator
Arm Description
Neonates with congenital heart disease requiring surgery utilizing cardiopulmonary bypass(CPB) in the first month of life that receive one dose of intravenous methylprednisolone (30 mg/kg) during anesthetic induction.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Neonates with congenital heart disease requiring surgery utilizing cardiopulmonary bypass (CPB) in the first month of life that receive one dose of placebo (normal saline) during anesthetic induction.
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone
Other Intervention Name(s)
Solulmedrol, Medrol, Corticosteroid, Steroid, Glucocorticoid
Intervention Description
Methylprednisolone at a dose of 30 mg/kg body weight and a concentration of 62.5 mg/cc. The study drug will be delivered in a blinded fashion to the anesthesiologist and will be administered intravenously with the induction of anesthesia.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Normal Saline
Intervention Description
Normal saline will be drawn up in an identical volume to that needed for active study drug. The study drug will be delivered in a blinded fashion to the anesthesiologist and will be administered intravenously with the induction of anesthesia.
Primary Outcome Measure Information:
Title
Number of Participants With a Clinically Derived Composite Morbidity-mortality Outcome
Description
The composite morbidity-mortality outcome will be met if any of the following occur after surgery but before hospital discharge: death, cardiac arrest, extracorporeal membrane oxygenation, renal insufficiency (creatinine more than two times normal), hepatic insufficiency (aspartate aminotransferase or alanine aminotransferase more than two times normal), or rising lactic acidosis (>5mmol/L). This outcome was choosen because death rarely occurs in this population. We have found this endpoint to be highly associated with other important clinical outcomes in this population.
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Secondary Outcome Measure Information:
Title
Duration of Mechanical Ventilation Post Cardiac Surgery.
Description
Amount of time on mechanical ventilation following cardiac surgery
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Intensive Care Unit Stay
Description
Amount of time in the intensive care unit following cardiac surgery
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Hospital Stay
Description
Total duration of hospital stay following cardiac surgery
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Neurodevelopmental Outcome
Description
Bayley Scales of Infant and Toddler Development version 3 at 1 year. Cognitive, language, and motor composite scores will be used. The general population has a mean of 100 with a standard deviation of 15 for each composite score. Higher scores are better. The minimum composite score is 46 and maximum 154.
Time Frame
1 year

10. Eligibility

Sex
All
Maximum Age & Unit of Time
30 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age < 1 month Male and female patients who are scheduled to undergo cardiac surgery involving CPB Exclusion Criteria: Prematurity: < 37 weeks post gestational age at time of surgery Treatment with intravenous steroids within the two days prior to scheduled surgery. Participation in research studies involving the evaluation of investigational drugs within 30 days of randomization. Suspected infection that would contraindicate steroid use (eg - Herpes) Known hypersensitivity to IVMP or one of its components or other contraindication to steroid therapy (eg - gastrointestinal bleeding). Preoperative use of mechanical circulatory support or active resuscitation at the time of proposed randomization.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eric M Graham, MD
Organizational Affiliation
Medical University of South Carolina
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Healthcare of Atlanta/Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30233
Country
United States
Facility Name
Medical University of South Carolina, Pediatric Cardiology
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21600592
Citation
Graham EM, Atz AM, Butts RJ, Baker NL, Zyblewski SC, Deardorff RL, DeSantis SM, Reeves ST, Bradley SM, Spinale FG. Standardized preoperative corticosteroid treatment in neonates undergoing cardiac surgery: results from a randomized trial. J Thorac Cardiovasc Surg. 2011 Dec;142(6):1523-9. doi: 10.1016/j.jtcvs.2011.04.019. Epub 2011 May 20.
Results Reference
background
PubMed Identifier
12903869
Citation
Seghaye MC. The clinical implications of the systemic inflammatory reaction related to cardiac operations in children. Cardiol Young. 2003 Jun;13(3):228-39. doi: 10.1017/s1047951103000465. No abstract available.
Results Reference
background
PubMed Identifier
9551188
Citation
Seghaye MC, Heyl W, Grabitz RG, Schumacher K, von Bernuth G, Rath W, Duchateau J. The production of pro- and anti-inflammatory cytokines in neonates assessed by stimulated whole cord blood culture and by plasma levels at birth. Biol Neonate. 1998;73(4):220-7. doi: 10.1159/000013980.
Results Reference
background
PubMed Identifier
15982431
Citation
Checchia PA, Bronicki RA, Costello JM, Nelson DP. Steroid use before pediatric cardiac operations using cardiopulmonary bypass: an international survey of 36 centers. Pediatr Crit Care Med. 2005 Jul;6(4):441-4. doi: 10.1097/01.PCC.0000163678.20704.C5.
Results Reference
background
PubMed Identifier
17943866
Citation
Robertson-Malt S, Afrane B, El Barbary M. Prophylactic steroids for pediatric open heart surgery. Cochrane Database Syst Rev. 2007 Oct 17;(4):CD005550. doi: 10.1002/14651858.CD005550.pub2.
Results Reference
background
PubMed Identifier
21060075
Citation
Pasquali SK, Hall M, Li JS, Peterson ED, Jaggers J, Lodge AJ, Marino BS, Goodman DM, Shah SS. Corticosteroids and outcome in children undergoing congenital heart surgery: analysis of the Pediatric Health Information Systems database. Circulation. 2010 Nov 23;122(21):2123-30. doi: 10.1161/CIRCULATIONAHA.110.948737. Epub 2010 Nov 8.
Results Reference
background
PubMed Identifier
22271697
Citation
Pasquali SK, Li JS, He X, Jacobs ML, O'Brien SM, Hall M, Jaquiss RD, Welke KF, Peterson ED, Shah SS, Gaynor JW, Jacobs JP. Perioperative methylprednisolone and outcome in neonates undergoing heart surgery. Pediatrics. 2012 Feb;129(2):e385-91. doi: 10.1542/peds.2011-2034. Epub 2012 Jan 23.
Results Reference
background
PubMed Identifier
21440149
Citation
Clarizia NA, Manlhiot C, Schwartz SM, Sivarajan VB, Maratta R, Holtby HM, Gruenwald CE, Caldarone CA, Van Arsdell GS, McCrindle BW. Improved outcomes associated with intraoperative steroid use in high-risk pediatric cardiac surgery. Ann Thorac Surg. 2011 Apr;91(4):1222-7. doi: 10.1016/j.athoracsur.2010.11.005.
Results Reference
background
PubMed Identifier
32374395
Citation
Everett AD, Buckley JP, Ellis G, Yang J, Graham D, Griffiths M, Bembea M, Graham EM. Association of Neurodevelopmental Outcomes With Environmental Exposure to Cyclohexanone During Neonatal Congenital Cardiac Operations: A Secondary Analysis of a Randomized Clinical Trial. JAMA Netw Open. 2020 May 1;3(5):e204070. doi: 10.1001/jamanetworkopen.2020.4070.
Results Reference
derived

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Corticosteroid Therapy in Neonates Undergoing Cardiopulmonary Bypass

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