Post-operative Cardiac Outcome of Non-cardiac Surgery Predicted by INVOS
- Conditions
- Peri-operativeCardiac OutcomeInvos
- Registration Number
- NCT02079454
- Lead Sponsor
- Cliniques universitaires Saint-Luc- Université Catholique de Louvain
- Brief Summary
Research aimed to find a correlation with an invos drop and cardiac events in the peri-operative period of non cardiac surgery.
The investigators postulate that a drop in the Invos numbers (with or without significant drop in BP) is associated with a variable degree of cardiac suffering.
The idea is to prevent per and foremostpost-operative myocardial necrosis complications by acting as soon as we have an INVOS drop during anesthesia.
The "cardiac events" will be monitored and defined according to the EHA (european heart association) guidelines.
(Changes of the EKG and/or troponin I values above the threshold). Patient will be monitored per and post operatively.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 34
- Male and female
- Age minimum 18 years old
- Chronic renal failure
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A composite measurement of major vascular events in the post-operative period 96 hours post-operative Myocardial infarction (measured by positivation of troponin I assay above the defined threshold) associated with clinical data (pain, dyspnea,...) or ST modification on the EKG or apparition of a new LBBB, or new wall abnormalities on the TTE.
Or new TIAs or CVAs
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
cliniques universitaires St Luc
🇧🇪Brussels, Brabant, Belgium