None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age group 18 years to 65 years. Patients undergoing neurosurgery using propofol for induction of anaesthesia. Patient willing to participate in the study
Exclusion criteria
Exclusion criteria: Patients with haemodynamic instability, patients on ionotropic support. Patients with cardiac failure, arrythmias, valvular heart disease. Patients with peripheral vascular disease. Patients with abdominal pathologies. Patients in sepsis. Patients on positive pressure ventilation. Patients with Glassgow Coma Scale (GCS) score Patients not giving consent to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) To calculate IVCCI and IVC:AO index in patients undergoing neurosurgery. 2) To correlate IVCCI for predicting post-propofol induction hypotension. 3) To correlate IVC:AO index for predicting post-propofol induction hypotension. Timepoint: 1) Measurement of preoperative IVCCI and IVC:AO indices. 2) Measurement of hemodynamic parameters to correlate with post-propofol induction hypotension. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To compare the predictive values of both IVCCI and IVC:AO index. 2)To find success rate for Ultrasound evaluation of IVC and aorta. Timepoint: 1) Measurement of preoperative IVCCI and IVC:AO indices. 2) Ultrasound duration for measuring IVC and Aorta diameters preoperatively. 3) Measurement of hemodynamic parameters to correlate with post-propofol induction hypotension. | — |
Countries
India
Contacts
LTMGH Sion Hospital