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French Observatory of Acute Heart Failure

Completed
Conditions
Acute Heart Failure
Registration Number
NCT01080937
Lead Sponsor
French Cardiology Society
Brief Summary

During the last decade, progress has been made in the management of heart failure. However, the changing characteristics of patients and practices in the "real world" and their impact on the prognosis of patients admitted for acute heart failure remain poorly studied.

2000 consecutive patients recruited in a single day in hospitals volunteered to participate in the cohort during a day dedicated.

Detailed Description

The total duration of recruitment is one day (date to be set soon by the Executive Committee): all patients hospitalized, and whatever their date of admission with the diagnosis of heart failure will be selected for the study.

Information on each hospital stay will be obtained at baseline and at the end of the hospitalization by the hospital teams.

A telephone follow-up will be conducted at 3 months among survivors and / or their doctor by CRAs dedicated to the French Society of Cardiology.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1818
Inclusion Criteria
  1. Male or female age (e) over 18 years

  2. Inpatient, whatever the mode of initial admission with acute heart failure (de novo heart failure or decompensation of chronic heart failure) regardless of severity, corresponding to one of the following clinical situations (clinical criteria in Appendix 1):

    • Pulmonary edema, hypertensive or not
    • congestive heart failure (pulmonary congestion and peripheral edema)
    • cardiogenic shock
    • Insufficient high output cardiac
  3. Patients who agreed to participate in the study

  4. Isolated right heart failure

Exclusion Criteria
  1. expressed refusal to participate in the study
  2. Hospitalization scheduled for review
  3. Background surgery (immediate postoperative period)
  4. Diagnosis of acute heart failure reversed in favor of an alternative diagnosis before discharge from hospital

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Survival at 3 months3 months

Analyze survival 3 months after the end of initial hospitalization

Secondary Outcome Measures
NameTimeMethod
Co-morbidities3 months

Analyze the co-morbidities and their impact on care and survival

Drug treatments3 months

Analyze the evolution of drug treatment between the output and monitoring to 3 months

Hospital Methods3 months

Compare methods of care based on clinical characteristics and hospital structures.

Resources specific diagnostic3 months

Analyze the use of resources specific diagnostic: measurement of BNP or NTproBNP, conducting echocardiogram, coronary angiography, Holter-ECG, Cardiac MRI, Cardiac CT

During of stay3 months

Analyze the duration of stay according to clinical characteristics.

Patterns of admission3 months

Analyze patterns of admission and discharge of patients, depending on their characteristics

Therapeutic resources3 months

Analyze the use of therapeutic resources based on specific clinical features: intensive care, ventilation, inotropes, ultrafiltration, introduction of beta-blockers, stimulation, implantable cardioverter defibrillator, circulatory support, graft

Trial Locations

Locations (1)

Lariboisiere Hospital

🇫🇷

Paris, France

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