Study the postoperative pain reducing anesthetic technique known as ultrasound guided erector spinae block in cardiac surgery in children.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Pediatric patients between age 6 months to 12 years, ASA Grade I or II with congenital heart diseases i.e. ASD, VSD, TOF, TAPVC, requiring elective sternotomy for surgical correction or repair.Health Condition 2: Q213- Tetralogy of Fallot
- Registration Number
- CTRI/2018/02/011763
- Lead Sponsor
- Department of Cardiac Anesthesia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
patients of either sex in the age group of 06 months -12 years, patients with congenital heart disease with normal LV function for elective surgery.
Exclusion Criteria
emergency surgery, redo surgery, moderate to severe LV dysfunction, bleeding disorder or abnormal coagulation profile, patients planned for thoracotomy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the assessment of postoperative analgesia by the Modified Objective Pain Score (MOPS) and duration of postoperative analgesia of bilateral erector spinae plane block as compared to standard institutional practices.Timepoint: Modified Objective pain score assessed after extubation and the 2,4,6,8,10,12 hours after extubation
- Secondary Outcome Measures
Name Time Method To compare duration of mechanical ventilation, rescue analgesia (fentanyl) consumption / total opioid consumption and duration of ICU stay.Timepoint: Extubation time, monitoring of pulse rate, blood pressure SpO2, ECG, Respiratory rate, total fentanyl consumption, duration of mechanical ventilation and duration of ICU stay will be recorded every 2,4,6,8,10 and 12 hours.