Health Condition 1: I428- Other cardiomyopathies
Conditions
Interventions
None listed
Sponsors
United CIIGMA Hopsital
Eligibility
Inclusion criteria
Inclusion criteria: 1)Adult patients referred from pre-anesthetic clinic or pre-anesthetic evaluation for 2D echocardiography as a part of preoperative workup before surgery. 2)Ability to complete a clinical echocardiogram on the same day before or after study procedures 3)Able and willing to provide informed consent · Outpatients and inpatients being evaluated before elective surgery
Exclusion criteria
Exclusion criteria: 1)Unwilling or unable to provide informed consent 2)Patients admitted in ICU on mechanical ventilator support and/or on vasoactive medications to maintain stable hemodynamics.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary end point of the study will be diagnostic accuracy of single-lead ECG based artificial intelligence algorithm to identify individuals with reduced EF (EF less than 40%) by comparing results from AI-based Eko Duo device with the actual measurements of LVEF by echocardiography.Timepoint: Before Elective Surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| The primary end point of the study will be diagnostic accuracy of single-lead ECG based artificial intelligence algorithm to identify individuals with reduced EF (EF less than 50%) by comparing results from AI-based Eko Duo device with the actual measurements of LVEF by echocardiography.Timepoint: Before Elective Surgery | — |
Countries
India
Contacts
Public ContactDr Deepak Borde
Ozone Anesthesia Group
Outcome results
None listed