Characterization of Factors Influencing the Occurrence of Cognitive Decline in Patients With Coronary Artery Disease and Undergoing Cardiac Surgery and Coronary Angioplasty
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Coronary Artery Disease
- Sponsor
- University Hospital, Lille
- Enrollment
- 155
- Locations
- 1
- Primary Endpoint
- Compare cognitive disorders using the scale Dementia rating scale (DRS) of Mattis in 2 groups
- Status
- Completed
- Last Updated
- 9 years ago
Overview
Brief Summary
The real impact of cardiac surgery and coronary angioplasty remains to be clarified and, where appropriate, the influencing factors in a way beneficial or deleterious remain to be identified.
The identification of such factors could make even faster screening, prevention and therefore open therapeutic prospects for those patients.
The objective of the study is to constitute a prospective cohort to assess the occurrence of cognitive decline after cardiac surgery (200 patients) and coronary angioplasty (200 patients) using the scale Dementia rating scale (DRS) of Mattis. In addition, the investigators will identify factors that influence positively or negatively, the occurrence of such a cognitive decline. The study based on a systematic monitoring of clinical, biological, imaging and pharmacological factors and, to correlate the respective influence of these factors on the incidence of cognitive decline.
Detailed Description
Cardiovascular invasive interventions (surgery and angioplasty) save thousands of lives every year, but questions remain about the neurological complications and in particular cognitive deficit. Indeed, cardiac surgery has been associated with cognitive decline in 50 to 70% of patients in the first postoperative week and in 20 to 40% of patients 6 months to one year after surgery. The study will be based on a prospective monitoring during 1 year of a cohort of 400 patients who will receive either a cardiac surgery or coronary angioplasty. At inclusion, will be collected medical history, risk factors, treatment history, clinical and etiological data (imaging, cardiac and vascular balance). The results of routine tests performed complementary to hospitalization will be recorded (echo-doppler vessels of the neck, cardiac ultrasound trans-thoracic and/or transesophageal a holter cardiac). In recruiting, we will apply a method of matching based on age (on 5 years) between 2 groups in order to compare 2 homogeneous groups.
Investigators
Eligibility Criteria
Inclusion Criteria
- •aged more than 18 years,
- •candidate to cardiac surgery or patients candidate to coronary angioplasty.
Exclusion Criteria
- •presenting a psychiatric illness that can interfere with the mental state and with scores provided in this study (explored in a systematic manner by the Mini International Neuropsychiatric Interview DSM 4).
Outcomes
Primary Outcomes
Compare cognitive disorders using the scale Dementia rating scale (DRS) of Mattis in 2 groups
Time Frame: Before intervention and 12 month after intervention
Secondary Outcomes
- Blood biomarkers: inflammation, coagulation, protein(Before intervention, 3 weeks (no biology), 6 months (no MRI and biology) and 12 month after intervention (no biology))
- Imaging parameters (MRI): abnormalities of white matter, ischemic lesions, hippocampus volume(Before intervention, 3 weeks (no biology), 6 months (no MRI and biology) and 12 month after intervention (no biology))
- Neuropsychological evaluation: global cognitive function using MMSE, memory, attention(Before intervention, 3 weeks (no biology), 6 months (no MRI and biology) and 12 month after intervention (no biology))