Endothelial Dysfunction Clinical Trial
— DYVAOfficial title:
Evaluation of the Association Between Pre-existing Endothelial Dysfunction and the Onset of Vasoplegia During Cardiac Surgery With Cardiopulmonary Bypass
Cardiac surgery patients have many risk factors for endothelial dysfunction (hypertension,
atherosclerosis, dyslipidemia, chronic renal failure ...).
It is likely that a significant number of patients suffering from a preexisting endothelial
dysfunction. This endothelial dysfunction can be assessed by a molecular approach
(determination of NO, ICAM1, VCAM1, IL8, endothelial microparticles ...). Extracorporeal
circulation with ischemia-reperfusion causes a breach of particularly important glycocalyx as
ischemia-reperfusion injury is. No studies have evaluated the time course of the
infringement, and its association with the immediate post-operative complications (SIRS,
coagulopathy, vasoplegic syndrome, renal failure). Only one study has regained an association
between endothelial dysfunction during cardiac bypass surgery and postoperative cardiac
surgery vasoplegic syndrome. A study in noncardiac surgery has regained an association
between endothelial dysfunction (assessed by a vasoplegia test) and postoperative acute renal
failure. Thus there is some data in the literature to suggest that the occurrence of
postoperative complications (SIRS, coagulopathy, capillary leak syndrome, acute circulatory
failure vasoplegic and acute renal failure) may result from the interaction between a
pre-existing endothelial dysfunction and "operative" aggression (extracorporeal circulation).
The onset of complications result from an interaction that depends on the importance of
endothelial dysfunction at baseline.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | November 2018 |
Est. primary completion date | September 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Patients = 18 years. - Patient operated on for cardiac surgical myocardial revascularization (CABG) or surgical correction of aortic valve. - Consent signed. Exclusion Criteria: - Standing arrhythmia. - Pregnant woman. - curative anticoagulation (warfarin, NANCO, heparin). - Patient under guardianship. - Patient Refused to participate. - Cardiac surgery without CPB. - bicuspid aortic valve. - Participation in another study. - preoperative sepsis. - Minor or major, under guardianship or trusteeship (art L1121-5, L1121-8 and L1122 1-2) |
Country | Name | City | State |
---|---|---|---|
France | CHU De Caen | Caen |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire, Amiens |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The primary endpoint was the occurrence of vasoplegic syndrome | The primary endpoint was the occurrence of vasoplegic syndrome correlate with markers of endothelial function following: IL8, P-selectin, von Willebrand factor precursor. | 6 months | |
Secondary | Occurrence of vasoplegic syndrome | Occurrence of vasoplegic syndrome correlate with markers of endothelial function following: endothelial microparticles, Von Willebrand factor, VCAM1. | 6 months | |
Secondary | Marker of degradation glycocalyx: | Marker of degradation glycocalyx: syndecan, heparan sulfate. | 6 months | |
Secondary | Inflammatory markers: | Inflammatory markers: leukocytes, CRP, procalcitonin, albumin, TNF alpha, IL-10, IL-6, IL1beta | 6 months | |
Secondary | Markers of blood coagulation | Markers of blood coagulation: Platelet count, PT, APTT, fibrinogen, D dimers, soluble complexes. | 6 months | |
Secondary | Complications | Complications: cardiovascular (vasoplegic syndrome), kidney (KDIGO). | 6 months | |
Secondary | Death | Death | 6 months |
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