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Patient Care Management Strategies for Severe Heart Failure in Rhône-Alpes, France. (EFFICARD)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Completed

Conditions

Severe Heart Failure

Treatments

Other: PRETICARD patient care management
Other: "As usual " patient care management

Study type

Interventional

Funder types

Other

Identifiers

NCT02763670
2013.838

Details and patient eligibility

About

The heart failure is a chronic pathology with prevalence from 2 to 3% of general population, a death rate of 50% at 6 months for patients with stage IV, and a probability of death or hospitalization or emergency consultation of 40% at 3 years. The care of patients is heterogeneous, especially in light of the organization of therapeutic education offered to patients and patient monitoring modalities.

The aim of this study is to investigate the management strategies for patients with chronic heart failure stage III or IV NYHA, and heart failure patients with stage II NYHA with previous hospitalization for heart failure.

This is a longitudinal observational multicenter study comparing a management strategy including patient education and monitoring as part of a hospital dedicated organization and an organization of care as usually done in France.

The primary endpoint was a composite endpoint of morbidity and mortality involving deaths, unplanned readmissions and emergency visits for heart failure.

The expected number of patients is 720 patients (360 per strategy). The follow-up duration of 24 months.

Enrollment

186 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic heart failure patient with left ventricular ejection fraction (LVEF) defined by an impaired LVEF less than or equal to 40%.
  • Heart failure stage III or IV NYHA, or heart failure patients with stage II NYHA with previous hospitalization for heart failure.
  • Patient who has received a written or oral information of the study
  • Patient affiliated with French health Insurance

Exclusion criteria

  • Patient refusal to participate in the study
  • Progressive neoplastic pathology.
  • Patient with impaired cognitive functions known.
  • Patient subject to a measure of socio-legal protection.
  • Heart failure secondary to curable causes (an arrhythmia, valvular dysfunction, myocardial infarction, bypass surgery scheduled, aortic stenosis, breaking rope...)
  • Dyspnea pulmonary origin: pulmonary arterial hypertension pre-capillary origin catheterization, defined by a Pcap ≤15 mmHg.
  • Patient who underwent ventricular mechanical assistance.
  • Patient with acute breathlessness is explained by: a severe lung infection (CPT <60% of predicted, ventricular ejection fraction <60% predicted) or pulmonary embolism or respiratory failure with ambient air PaO2 (arterial oxygen pressure) below 60 mmHg or oxygen therapy.
  • Dialysis patient

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

186 participants in 2 patient groups

Interventional
Other group
Description:
PRETICARD patient care management
Treatment:
Other: PRETICARD patient care management
Control
Other group
Description:
Heterogenous "as usual" patient care management.
Treatment:
Other: "As usual " patient care management

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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