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To evaluate the accuracy of functioning of heart using two different methods namely Electrical Cardiometry and Arterial pressure used during the operation under general anaesthesia

Not Applicable
Conditions
Health Condition 1: C00-D49- Neoplasms
Registration Number
CTRI/2019/08/020543
Lead Sponsor
A
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Adult patients who give written informed consent to allow data collection.(70 yrs 18 yrs )

2.Elective major surgeries under general anaesthesia

3.Patients in whom CO is being monitored with Arterial Pressure Based Cardiac Output Device (Flotrac•) or EV1000• monitor

Exclusion Criteria

1.Patients who refuse consent

2.Age under 18 years

3.Presence of arrhythmias

4.Burns over areas of impedance electrodes

5.Pt having pacemakers

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the precision and limits of agreement in the cardiac output measurement using Electric Cardiometry with Arterial Pressure based cardiac output method in patients undergoing major surgeries undergoing General anaesthesiaTimepoint: 1.Baseline (immediately after connecting the devices for CO monitoring) <br/ ><br>2.Intraoperative period <br/ ><br>3.Before and <br/ ><br>4.After completion of a fluid bolus (5mL/kg which is the standard fluid bolus in our institute), administered in case of hemodynamic instability as decided by the treating anaesthesiologist. <br/ ><br>5.Immediately after extubation
Secondary Outcome Measures
NameTimeMethod
Assessment of Variation of Index of Contractility ( VIC), Thoracic Fluid Content (TFC), Systolic Time Ratio (STR)-Pre ejection period(PEP)/ LV Ejection time(LVET), Index of Contractility( ICON )Timepoint: 1.Baseline (immediately after connecting the devices for CO monitoring) <br/ ><br>2.Intraoperative period <br/ ><br>3.Before and <br/ ><br>4.After completion of a fluid bolus (5mL/kg which is the standard fluid bolus in our institute), administered in case of hemodynamic instability as decided by the treating anaesthesiologist. <br/ ><br>5.Immediately after extubation
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