Congenital Heart Disease, Disorder of Fetus or Newborn
Conditions
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
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.
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
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With a Clinically Derived Composite Morbidity-mortality Outcome | Participants will be followed for the duration of hospital stay, an expected average of 5 weeks | 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
| Measure | Time frame | Description |
|---|---|---|
| Duration of Mechanical Ventilation Post Cardiac Surgery. | Participants will be followed for the duration of hospital stay, an expected average of 5 weeks | Amount of time on mechanical ventilation following cardiac surgery |
| Intensive Care Unit Stay | Participants will be followed for the duration of hospital stay, an expected average of 5 weeks | Amount of time in the intensive care unit following cardiac surgery |
| Hospital Stay | Participants will be followed for the duration of hospital stay, an expected average of 5 weeks | Total duration of hospital stay following cardiac surgery |
| Neurodevelopmental Outcome | 1 year | 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. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| 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 |
| Total | 176 |
Baseline characteristics
| Characteristic | Intraoperative Methylprednisone | Total | Placebo |
|---|---|---|---|
| Age, Continuous | 9.1 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 Participants | 12 Participants | 8 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 77 Participants | 164 Participants | 87 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 1 Participants | 1 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 2 Participants | 2 Participants |
| Race (NIH/OMB) Black or African American | 22 Participants | 49 Participants | 27 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 4 Participants | 9 Participants | 5 Participants |
| Race (NIH/OMB) White | 55 Participants | 115 Participants | 60 Participants |
| Region of Enrollment United States | 81 participants | 176 participants | 95 participants |
| Sex: Female, Male Female | 35 Participants | 70 Participants | 35 Participants |
| Sex: Female, Male Male | 46 Participants | 106 Participants | 60 Participants |
| Weight at surgery | 3.2 Kg STANDARD_DEVIATION 0.5 | 3.3 Kg STANDARD_DEVIATION 0.5 | 3.4 Kg STANDARD_DEVIATION 0.5 |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 5 / 81 | 6 / 95 |
| other Total, other adverse events | 2 / 81 | 2 / 95 |
| serious Total, serious adverse events | 4 / 81 | 11 / 95 |
Outcome results
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Intraoperative Methylprednisone | Number of Participants With a Clinically Derived Composite Morbidity-mortality Outcome | 27 Participants |
| Placebo | Number of Participants With a Clinically Derived Composite Morbidity-mortality Outcome | 40 Participants |
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
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Intraoperative Methylprednisone | Duration of Mechanical Ventilation Post Cardiac Surgery. | 4 Days |
| Placebo | Duration of Mechanical Ventilation Post Cardiac Surgery. | 5 Days |
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
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Intraoperative Methylprednisone | Hospital Stay | 20 Days |
| Placebo | Hospital Stay | 22 Days |
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
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Intraoperative Methylprednisone | Intensive Care Unit Stay | 11 Days |
| Placebo | Intensive Care Unit Stay | 11 Days |
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
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Intraoperative Methylprednisone | Neurodevelopmental Outcome | Cognitive Domain | 105 score on a scale | Standard Deviation 15 |
| Intraoperative Methylprednisone | Neurodevelopmental Outcome | Language Domain | 101 score on a scale | Standard Deviation 15 |
| Intraoperative Methylprednisone | Neurodevelopmental Outcome | Motor Domain | 90 score on a scale | Standard Deviation 16 |
| Placebo | Neurodevelopmental Outcome | Cognitive Domain | 104 score on a scale | Standard Deviation 14 |
| Placebo | Neurodevelopmental Outcome | Language Domain | 100 score on a scale | Standard Deviation 13 |
| Placebo | Neurodevelopmental Outcome | Motor Domain | 91 score on a scale | Standard Deviation 19 |