South Of France Cardiac Assist Registry

Methods:

It's a prospective multicentric observational study realised on 3 University Hospital in France: Bordeaux, Montpellier and Toulouse.

Population:

All patients undergoing implantation of a long-term LVAD support whatever the brand and type, on one of the 3 participating centers (Montpellier, Toulouse or Bordeaux) during the 3 years period, after approval of informed consent.

Patients were followed up at 1 and 6 months, and 1 year as part of their routine management of their disease.

Patients should have agreed to participate in the observatory, knowing that participation or refusal to participate will not alter the therapeutic attitude of the team responsible for the patient.

Aim:

Main aim is 1 year mortality of LVAD recipients

Secondary aim are:

• Descriptive epidemiology of LVAD implantation: prevalence, etiology, affected populations
• Description of the state of practice: indications, against-indications, preimplantation data, intraoperative data, postoperative data, tracking data
• Rating prognosis of patients under LVAD support
• In-hospital, 30 days, 6 months, and 1 year survival
• Number of transplanted and assisted patients at 1 year
• Evaluation of complications (infections, bleeding, thromboembolism, equipment failures, ...)
• Analyses in subgroups according to age, sex, initial indication (including ischemic heart disease vs nonischemic), assistance used and year of implantation
• Research of prognostic factors for postoperative and chronic right ventricular failure, prognostic factors of cardiovascular and all causes death.

Feasibility:

Based on historical data of the concerned centers (CHU Montpellier, Bordeaux and Toulouse) and recent predictions of french health authority HAS ("Haute Autorité de Santé"), 200 patients are provided in the observatory register, rhythm about 20-30 patients per year per center for a 3-year recruitment period Monitoring will be carried out by the referring physician for each patient at 1 and 6 months, and at 1 year in the usual care of pathology in each center with the possibility to adapt the follow-up date to +/- 1 month.

For patients who have moved and have therefore changed of referral center, an evaluation at one year will be made by mail or phone contact with the physician and / or patient.

Collect and circulation of patients' data:

Data will be collected under the patient's referring physician's responsibility in each center. Data will be entered directly into the electronic database (e-CRF) developed University of Montpellier.

Patient will be identified by the number of the center (1 = Bordeaux, 2 = Montpellier 3 = Toulouse) followed by the first letter of the name and the first initial and the center of the patient number in question (automatic chronological number according to the entry on the e-CRF - data coding is integrated into the e-CRF) Monitoring at 1 month, 6 months and 1 year, will be completed by the middle of referring physicians and entered directly into the electronic database.

There will be no traffic data on paper for these two steps.

In case of lost sight, follow-up at 1 year will be carried out by the centers, by phone or mail from the municipality of birth, the attending physician or cardiologist and patient, which requires knowledge of the date full birth patients to avoid confusion.

For the analysis, data will be anonymized (as shown above).

Members of the scientific committee, persons responsible for logistics and coordination statistics will have access to all of the identified data.

Research data is entered via an electronic case report forms (e-CRF) developed from the Capture System software (CLINSIGHT company), enabling quality control of data in real time. To meet regulatory requirements, this software complies with the FDA's recommendations on Computerized Systems for Managing Clinical Trials and electronic signature and standards (CDISC, ICH, GCP 2001/20 / EC ...). The connection is via a password and a unique identifier specific to each user that will give access only to his patients himself. An audit function is integrated allowing traceability of data as well as changes. The encrypted data will then be transmitted to the responsible center of the data-management via a secure internet connection.

The e-CRF must be composed of all the information required by the protocol.

Information and Consent of participants:

Prior to the completion of this research, the free, writing and informed consent of patients must be collected after information by the investigator during a consultation, and after a sufficient period of reflection.

Participants information for research should be written simply, in language understandable by the patient. After having read the participant and the investigator will have dated and signed the consent form (original archived by the investigator and an original will be given to research participants).