Health Condition 1: C00-D49- Neoplasms
Conditions
Interventions
Intervention1: NA: NA
Control Intervention1: NA: NA
Sponsors
None listed
Eligibility
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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) 2. Intraoperative period 3. Before and 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. 5. Immediately after extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| 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) 2. Intraoperative period 3. Before and 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. 5. Immediately after extubation | — |
Countries
India
Contacts
Public ContactDr Resham Rathod
Tata Memorial Hospital
Outcome results
None listed