Consultation at 8 Days to Reduce Hospitalisations in Heart Failure Patient (CHIC)

Assistance Publique - Hôpitaux de Paris

Status: Completed

Conditions: Acute Heart Failure

Treatments: Other: Follow-up

Study type: Interventional

Funder types: Other

Identifiers

NCT01834833

P110601 - PHRQ1104

Details and patient eligibility

About

Evaluate the benefit of systematic appointment with a cardiologist a week after hospitalisation for acute heart failure. Randomised, endpoint: number of day alive out of hospital during 6 months

Full description

Background: the risk for rehospitalisation is very high after hospitalisation for acute heart failure. Aim: evaluate the benefit of a consultation with a cardiologist, including echocardiography and education of the patient, between 7 and 15 days after discharge, in high risk patients, identified with BNP or incomplete therapy. Parallel randomised study. The main endpoint is the number of day alive out of hospital during the 6 months post discharge; statistics intention to treat comparison of the number of days alive out of hospital in the group with consultation compared with the group without consultation. Recruitment 3 years and 4 months, follow-up 6 months. Patients included have been hospitalised in hospital BICHAT 75018 Paris, France. Financing is by the ministry of health (PHRQHOS)

Enrollment: 326 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Criteria of inclusion :

• Patient with decompensated heart failure hospitalized in the hospital BICHAT,
• For whom is planned a return at home,
• Valid (being able to return for a consultation to the hospital)
• Having Nt-ProBNP of exit ≥ 3500 ng /l and/or a non optimized treatment of exit - according to the doctor who has it the responsibility,
• Having signed the consent form by participation in the study.

Criteria of not inclusion :

• Age < 18 years,
• Not membership in a national insurance scheme or in the Universal Health
• Coverage (CMU)(FREE UNIVERSAL HEALTH CARE)(A patient benefiting from the Medical aid of the State (AME) cannot be included)
• Participation to another protocol of research,
• Not being reachable by telephone in 6 months.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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326 participants in 2 patient groups

Control

No Intervention group

Description:

usual care without systematic cardiology evaluation between 1 and 2 weeks

Follow-up

Experimental group

Description:

Evaluation by a cardiologist using echocardiography, completed by education of the patient if necessary

Treatment:

Other: Follow-up