Cardiopulmonary Exercise Testing in the Prediction of Post-operative Complications in Patients Undergoing Coronary Artery Bypass Graft Surgery

Status: Recruiting
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Cardiopulmonary exercise testing (CPET) is considered to be a gold standard in pre-operative risk assessment and stratification of high risk patients scheduled for major surgery. Surprisingly, only a limited number of studies examined the prognostic role of CPET in cardiothoracic surgery. This is in contrast with rather poor discriminating quality of cardiovascular surgery risk scores and predominantly elderly cardiovascular surgery patients, with significant comorbidity and high degree of frailty. Recently, CPET was shown feasible in coronary artery bypass grafting surgery candidates. Additionally, the rest parameter, which is the partial pressure of end-tidal carbon dioxide (PETCO2) and a submaximal exercise parameter (the VE/VCO2 slope) with good prognostic utility across multiple respiratory exchange ratio values), has been shown to predict mortality and post-operative complications. Whether these rest and submaximal exercise parameters can be used to predict postoperative complications in cardiovascular surgery patients is yet to be determined.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• patients scheduled for coronary artery bypass graft surgery

Contact Information
Primary
Ivan Cundrle, prof., M.D.
Ivan.Cundrle@fnusa.cz
00420 543182553
Backup
Marek Lukes, M.D.
marek.lukes@cktch.cz
00 420 543 182 484
Time Frame
Start Date: 2024-12-01
Estimated Completion Date: 2028-04-01
Participants
Target number of participants: 130
Treatments
coronary artery bypass graft candidates
patients scheduled for CABG surgery will undergo pre-operative cardiopulmonary exercise testing and post-operative complications monitoring
Sponsors
Leads: St. Anne's University Hospital Brno, Czech Republic
Collaborators: Centre of Cardiovascular and Transplantation Surgery, Czech Republic

This content was sourced from clinicaltrials.gov