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Outcomes of sevoflurane and propofol on left ventricular diastolic function in patients undergoing coronary artery bypass graft surgery.

Not Applicable
Conditions
Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery
Registration Number
CTRI/2024/04/065898
Lead Sponsor
ARMY HOSPITAL REASERCH AND REFERAL NEW DELHI India
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Adult patients undergoing elective coronary artery bypass graft surgery using cardiopulmonary bypass

Exclusion Criteria

LEFT VENTRICULAR EJECTION FRACTION LESS THAN 30%

CARDIOMYOPATHY

PRE EXISTING VALVULAR HEART DISEASE

GRADE 4 DIASTOLIC DYSFUNCTION

ATRIAL FIBRILLATION

SIGNIFICANT PULMONARY DISEASES (EG.ILD,PTE..)

EMERGENCY PROCEDURE

OESOPHAGEAL PATHOLOGY

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate left ventricular diastolic function by measuring Peak flow velocity of early diastolic filling E Early diastolic mitral annulus velocity e using Transesophageal echocardiography(TEE) under sevoflurane or propofol based anaesthesia in patients undergoing Coronary artery bypass graft on cardiopulmonary bypass <br/ ><br>Timepoint: 48hrs
Secondary Outcome Measures
NameTimeMethod
To compare other parameters of diastolic function between sevoflurane and propofol group ; <br/ ><br> Late diastolic filling(A), <br/ ><br> Deceleration time (DT) , <br/ ><br> Peak systolic flow velocity (S), <br/ ><br> Peak diastolic flow velocity (D), <br/ ><br> S/D ratio, <br/ ><br> Peak reversal atrial flow (Ar), <br/ ><br> Duration of reverse atrial flow (Ar dur), <br/ ><br> Late diastolic mitral annulus velocity(a’). <br/ ><br> <br/ ><br>To determine the Vasoactive inotropic Score (VIS ) between sevoflurane group and propofol group . <br/ ><br> <br/ ><br>To assess the duration of Mechanical ventilation & ICU stay between sevoflurane group and propofol group <br/ ><br>Timepoint: 7 days
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