Intraoperative complications
Conditions
Interventions
Study design and participants:
This is an observational, prospective and single-center study that will be performed in patients undergoing echocardiographic monitoring with myocardial Strain in cardia
E03.155.403
Sponsors
Universidade do Extremo Sul Catarinense
Universidade do Extremo Sul Catarinense
Eligibility
Inclusion criteria
Inclusion criteria: Patients undergoing cardiac surgery with extracorporeal circulation (ECC) and left ventricular ejection fraction (LVEF) = 50% who will undergo echocardiographic monitoring with myocardial strain.
Exclusion criteria
Exclusion criteria: Patients undergoing cardiac surgery without CPB, patients with LVEF < 50%, urgent and emergency surgery, patients with grade II or III diastolic dysfunction, use of intra-aortic balloon pump in the preoperative period and refusal to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of low cardiac output syndrome after cardiopulmonary bypass and within 24 hours after surgery, which will be analyzed by calculating cardiac output, systemic blood pressure and volume analysis. Defined as decreases in cardiac index to < 2.0 L/min/m2 and a systolic blood pressure of < 90 mmHg, together with signs of tissue hypoperfusion. | — |
Secondary
| Measure | Time frame |
|---|---|
| The following will be established: surgery time, cardiopulmonary bypass time, intubation time, length of stay in intensive care, hospital stay and the need to use inotropic agents in the postoperative period (24h). Will be evaluated: intraoperative mortality, hospital mortality and mortality within 30 days. | — |
Countries
Brazil
Contacts
Public ContactHospital José
Outcome results
None listed