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Corticosteroid Therapy in Neonates Undergoing Cardiopulmonary Bypass

Corticosteroid Therapy in Neonates Undergoing Cardiopulmonary Bypass

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01579513
Enrollment
190
Registered
2012-04-18
Start date
2012-06-30
Completion date
2018-12-19
Last updated
2019-12-09

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

Conditions

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

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

Interventions

DRUGMethylprednisolone

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.

DRUGPlacebo

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.

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
National Institutes of Health (NIH)
CollaboratorNIH
Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
No minimum to 30 Days
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants With a Clinically Derived Composite Morbidity-mortality OutcomeParticipants will be followed for the duration of hospital stay, an expected average of 5 weeksThe 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

MeasureTime frameDescription
Duration of Mechanical Ventilation Post Cardiac Surgery.Participants will be followed for the duration of hospital stay, an expected average of 5 weeksAmount of time on mechanical ventilation following cardiac surgery
Intensive Care Unit StayParticipants will be followed for the duration of hospital stay, an expected average of 5 weeksAmount of time in the intensive care unit following cardiac surgery
Hospital StayParticipants will be followed for the duration of hospital stay, an expected average of 5 weeksTotal duration of hospital stay following cardiac surgery
Neurodevelopmental Outcome1 yearBayley 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.

Countries

United States

Participant flow

Participants by arm

ArmCount
Intraoperative Methylprednisone
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. Methylprednisolone: 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.
81
Placebo
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. Placebo: 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.
95
Total176

Baseline characteristics

CharacteristicIntraoperative MethylprednisoneTotalPlacebo
Age, Continuous9.1 days
STANDARD_DEVIATION 5.4
8.6 days
STANDARD_DEVIATION 5.5
8.2 days
STANDARD_DEVIATION 5.6
Ethnicity (NIH/OMB)
Hispanic or Latino
4 Participants12 Participants8 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
77 Participants164 Participants87 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants1 Participants1 Participants
Race (NIH/OMB)
Asian
0 Participants2 Participants2 Participants
Race (NIH/OMB)
Black or African American
22 Participants49 Participants27 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
4 Participants9 Participants5 Participants
Race (NIH/OMB)
White
55 Participants115 Participants60 Participants
Region of Enrollment
United States
81 participants176 participants95 participants
Sex: Female, Male
Female
35 Participants70 Participants35 Participants
Sex: Female, Male
Male
46 Participants106 Participants60 Participants
Weight at surgery3.2 Kg
STANDARD_DEVIATION 0.5
3.3 Kg
STANDARD_DEVIATION 0.5
3.4 Kg
STANDARD_DEVIATION 0.5

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
5 / 816 / 95
other
Total, other adverse events
2 / 812 / 95
serious
Total, serious adverse events
4 / 8111 / 95

Outcome results

Primary

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.

Time frame: Participants will be followed for the duration of hospital stay, an expected average of 5 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intraoperative MethylprednisoneNumber of Participants With a Clinically Derived Composite Morbidity-mortality Outcome27 Participants
PlaceboNumber of Participants With a Clinically Derived Composite Morbidity-mortality Outcome40 Participants
Secondary

Duration of Mechanical Ventilation Post Cardiac Surgery.

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

ArmMeasureValue (MEDIAN)
Intraoperative MethylprednisoneDuration of Mechanical Ventilation Post Cardiac Surgery.4 Days
PlaceboDuration of Mechanical Ventilation Post Cardiac Surgery.5 Days
Secondary

Hospital Stay

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

ArmMeasureValue (MEAN)
Intraoperative MethylprednisoneHospital Stay20 Days
PlaceboHospital Stay22 Days
Secondary

Intensive Care Unit Stay

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

ArmMeasureValue (MEAN)
Intraoperative MethylprednisoneIntensive Care Unit Stay11 Days
PlaceboIntensive Care Unit Stay11 Days
Secondary

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.

Time frame: 1 year

ArmMeasureGroupValue (MEAN)Dispersion
Intraoperative MethylprednisoneNeurodevelopmental OutcomeCognitive Domain105 score on a scaleStandard Deviation 15
Intraoperative MethylprednisoneNeurodevelopmental OutcomeLanguage Domain101 score on a scaleStandard Deviation 15
Intraoperative MethylprednisoneNeurodevelopmental OutcomeMotor Domain90 score on a scaleStandard Deviation 16
PlaceboNeurodevelopmental OutcomeCognitive Domain104 score on a scaleStandard Deviation 14
PlaceboNeurodevelopmental OutcomeLanguage Domain100 score on a scaleStandard Deviation 13
PlaceboNeurodevelopmental OutcomeMotor Domain91 score on a scaleStandard Deviation 19

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026