Dexmedetomidine and Magnesium Sulfate in Preventing Junctional Ectopic Tachycardia After Pediatric Cardiac Surgery
Post Operative Arrythmia
About this trial
This is an interventional prevention trial for Post Operative Arrythmia
Eligibility Criteria
Inclusion Criteria:
- Age: less than 5 yrs.
- Weight: more than 5 kg .
- Pathology :A-V canal ,VSD ,ASD undergoing corrective surgery with normal sinus rhythm, and stable hemodynamics.
Exclusion Criteria:
- a history of arrhythmias within the last 6 months, current use of antiarrhythmic medication such as amiodarone, digoxin.
- patients with pacemaker or atrioventricular (A-V) block.
- known allergy to dexmedetomidine or magnesium sulfate.
- patients with a history of re-do surgery.
Sites / Locations
- Kasralainy Faculty of MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
No Intervention
Active Comparator
Active Comparator
control group
dexmedetomidine group
Dexmedetomidine Mgso4 group
patients will receive normal saline instead of dexmedetomidine and MgSo4 .
patients will receive the same of dexmedetomidine as MD group in addition to normal saline instead of Magnesium Sulfate .
patients will receive dexmedetomidine 0.5 µg/kg diluted in 50 mL of normal saline intravenously over 20 minutes, After induction followed by 0.5 µg/kg per hour infusion for 72 hours postoperatively or ready for extubation prior to 72 hour time period (Precedex ; Hospira Worldwide ,Lake Forest, IL).(20) and receiving Magnesium Sulfate (50 mg/kg) bolus administered at the time of Aortic Cross Clamp Release. with continued administration for 72 hours postoperatively at a dose of 30 mg/kg/day