Research Design: Pilot-study for a large prospective, randomized, single-blinded, clinical trial.
This study is a parallel-arm, randomized, single-blinded clinical trial based on a hemodynamic outcome that will inform a subsequent larger randomized trial based on clinical outcomes.
Main research question: Does continuous BiVp for up to 48 hours in infants with EMD after CHD surgery increase CI as measured every 1-3 hours by the Fick method using an AMIS2000 mass spectrometer for VO2 measurement? Primary Hypothesis: Continuous BiVp increases the mean change in CI from baseline to 48 hours in infants with EMD following CHD surgery compared to standard care alone.
Primary objective: The primary objective of this pilot study is to provide physiologic proof of principle data by testing the hypothesis that continuous BiVp increases the mean change in CI from baseline to 48 hours in infants with EMD following CHD surgery. Although this is suggested by our preliminary data, the number of infants with wide QRS was small and statistically underpowered. The current study will expand the target population and provide preliminary data for sample size calculation and outcome measures for a subsequent, larger, clinical trial based on clinical outcomes such as duration of mechanical ventilation, length of ICU stay and vasoactive-inotropic score.
Secondary Hypotheses:
1. BiVp reduces the maximum vasoactive-inotropic score over the 1st 48 hours after CHD surgery in infants with EMD compared to standard therapy.
2. BiVp improves end-organ perfusion: cerebral NIRS, serum lactate, kidney (time to negative fluid balance, creatinine clearance and neutrophil gelatinase-associated lipocalin (NGAL)), liver function (AST, ALT) and brain natiuretic peptide (BNP) in the 1st 48 hours in infants with EMD after CHD surgery compared to standard therapy.
3. BiVp reduces duration of mechanical ventilation in infants with EMD after CHD surgery.
Study population Screening: Potentially eligible patients will be screened by the study coordinator, Ms Rita Nobile, using the cardiovascular surgical schedule at SickKids. Consecutive patients will be enrolled to maximize representation of the target population. All screened patients will be registered in a screening log according to the CONSORT statement.60 Inclusion criteria-infants must meet all inclusion criteria to be enrolled: 1. Post-operative QRS duration ≥ 98th centile for age based on Davignon.61 2. 0-1 year of age undergoing biventricular repair of CHD under CPB. Based on a recent population undergoing CHD surgery over a 1-year period at SickKids, wthe investigators expect the following types of CHD to be included (Table 2, p.23): tetralogy of Fallot (40%), transposition of the great arteries (30%), complete atrioventricular septal defect (15%), interrupted aortic arch (4%), other (10%).
Exclusion criteria- Exclusion criteria will be assessed before and after surgery by the study coordinator and investigators. The presence of any criterion will exclude an infant from the study:
1\. Extubation in operating room or expected extubation \<12 hours after surgery. 2. Functionally univentricular heart disease (lack of septation into 2 ventricles each supporting pulmonary or systemic circulations). 3. Major extra-cardiac anomalies (expected to affect mechanical ventilation, ICU stay, 30-day mortality, expected to require intervention within 30-days, lethal genetic abn.(e.g. trisomy 13/18)). 4. Surgery without CPB or palliative surgery (e.g systemic-pulmonary shunt). 5. Weight \<2.5 kg at time of surgery. 6. ECMO (at time of the ICU admission), infants expected to die or require ECMO within 12 hours after operation (judged by surgeon or ICU responsible physician); brain death within 12 hours after surgery (declared by ICU responsible physician). 7. Previous cardiac operation on CPB. 8. Junctional, atrial ectopic or ventricular tachycardia.
If BiVp (time zero in controls) has started and an arrhythmia precluding BiVp (listed above) or ECMO occurs ≤ 8 hrs after surgery, the patient will be excluded; if \>8 hrs -analysis will be 'intention-to-treat'.
Study Groups: Following these inclusion/ exclusion criteria there will be 3 study groups:
1. Intervention group: Consented infants with wide QRS randomized to BiVp.
2. Control group 1: Consented infants with wide QRS randomized to the control group.
3. Control group 2 (observation group): Consented infants with narrow QRS will enter control group 2 without randomization. All study outcome measurements will be performed on this group. Enrolment, informed consent, randomization and definition of time zero: Informed signed consent will be obtained by the PIs and research coordinator from the infant's legal guardians prior to surgery. At surgery all consented patients will receive 3 temporary epicardial pacing leads: standard right atrial and RV leads, LV apical lead. On return to the intensive care unit, QRS width will be manually evaluated from an unpaced 12-lead ECG by Dr Stephenson, Friedberg or Schwartz. Children with prolonged QRS (≥98 centile61 by the longest QRS duration from any lead) (expected in \~48% of infants (Fig. 2, p.18) will be randomized in a 1:1 pacing: control ratio by computer-generated allocation (www.random.org) to receive either standard of care plus BiVp or to standard of care alone. Consented patients with QRS duration \<98 centile will be allocated to the narrow QRS control group (control group 2). For the BiVp group time zero is defined by the start of pacing. For controls, time zero is 1 hour after arrival in the ICU (expected time BiVp will start in the intervention group).
