Postoperative Hemodynamics Comparison After High Spinal Block With or Without Intrathecal Morphine.
Vasoplegia
About this trial
This is an interventional diagnostic trial for Vasoplegia
Eligibility Criteria
Inclusion Criteria: - Adult patients with valvular heart disease and coronary artery disease of New York Heart Association class II-III aged 18 to 60 years undergoing elective cardiac surgery (Valve replacement/CABG).
Exclusion Criteria:
• All the standard contraindications for spinal anaesthesia which includes local site infection, spinal deformity, coagulopathy (platelet count<80,000, INR>1.5) patients on anticoagulant medication continued upto the day of the surgery as per the third edition of the American Society of Regional Anesthesia and Pain Medicine Evidence-Based Guidelines (Regional Anesthesia in the Patient Receiving Antithrombotic or Thrombolytic Therapy)
- Redo surgery/emergency surgeries.
- Patients having co-morbidities such as obesity (BMI more than 30), COPD, asthma, that are likely to require prolonged post operative mechanical ventilation.
- Total surgery time > 6 hours.
- History of opioid drug abuse or patients on opioids for treatment of chronic pain.
- Known or anticipated difficult airway
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Bupivacaine
Bupivacaine + Morphine
Intrathecal 8 ml single dose of 0.5% heavy Bupivacaine (Anawin heavy 0.5%).
Intrathecal 8 ml single dose of 0.5% heavy Bupivacaine (Anawin heavy 0.5%) and 250 microgram of preservative free Morphine (VERMOR).