About this trial
Group (A): This group will receive fentanyl infusion at a dose of (0.5μg/kg/h) all through the whole operation plus ultrasound guided bilateral superficial parasternal intercostal Plane block which will be done by injecting 0.4ml/kg (1:1 solution of bupivacaine 0.25% and lidocaine 1%) at each side3.
Group (B): This group will receive fentanyl infusion at a dose of (0.5μg/kg/h) all through the whole operation plus Ultrasound guided bilateral ESPB which will be done by injecting 0.4ml/kg (1:1 solution of bupivacaine 0.25% and lidocaine 1%) at each side .
Eligibility criteria
Qualifiers
RACHS-1: Categories 1, 2 and 3
Patients undergoing corrective cardiac surgeries with midline sternotomy incision.
Redo surgeries.
Disqualifiers
Patients whose parents or legal guardians refuse to participate.
Preoperative mechanical ventilation.
Preoperative inotropic drug infusion.
Coagulopathy.
Trial design
Treatments tested in this trial
- superficial parasternal intercostal Plane block
- Erecto spinea plane block