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Prospective Study of Heart Failure With Preserved Left Ventricular Ejection Fraction (KaRen)

F

French Cardiology Society

Status

Completed

Conditions

Heart Failure With Preserved Ejection Fraction
Left Ventricular Ejection Fraction
Congestive Heart Failure

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to examine electrical and echocardiographic characteristics and prognosis of consecutive patients admitted with acute heart failure and diagnosed to have heart failure with preserved ejection fraction (HFPEF).

Full description

  • Time 0: Patients will be screened at the time of presentation to the hospital at participating centres
  • Usually patients will be hospitalised for an acute dyspnea in relation with a pulmonary congestion. This congestion does not necessarily justify a hospitalization and for part of the patients a consultation and a dedicated treatment would be good enough to cure the symptoms.
  • Thus, patients seen in emergency for a congestion and diagnosed or known to have a preserved left ventricular ejection fraction (LV EF > 45%) will be proposed to participate to the study.
  • Patients meeting inclusion criteria will be invited back to the clinic in stable condition, approximately 4-8 weeks after the initial hospitalization.
  • Time 4-8 weeks after initial hospitalisation (NOT after discharge): Comprehensive history-taking and examinations.
  • Any information necessary for the study will be collected by the principal investigator in each participating center in a dedicated, secure, e-CRF. The access to the e-CRF will be restrictive to the only principal investigator of each center. The lonely other persons able to take look to the e-CRF are the study monitors.
  • Time 6, 12, and 18 months: Follow up by phone call or review of charts or other records such as death registries. This part of the study will be performed by the CRAs in the French Society of Cardiology

Enrollment

362 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patient presenting to the hospital with congestive heart failure, defined as:

    1. Clinical signs of heart failure

      Major criteria

      • Paroxysmal nocturnal dyspnea
      • Orthopnea
      • Jugular venous distension
      • Pulmonary crackling rales
      • 3rd heart sound
      • Cardiothoracic ratio > 0.5 on X-ray
      • Pulmonary oedema on X-ray

      Minor Criteria

      • peripheral oedema
      • nocturnal cough
      • dyspnoea at exercise
      • hepatomegaly
      • pleural effusion
      • tachycardia (defined as ≥ 100 beats per minute)

      Heart failure if: presence of 2 major criteria or 1 major + 2 minor criteria

    2. LVEF ≥ 45% by echocardiography within 72h

    3. BNP > 100 ng/L or NT-proBNP > 300 ng/L

      Exclusion Criteria:

  • Evidence of primary hypertrophic or restrictive cardiomyopathy or systemic illness known to be associated with infiltrative heart disease

  • Known cause of right heart failure not related to left ventricular dysfunction

  • Pericardial constriction

  • Clinically significant pulmonary disease, as evidenced by requirement of home oxygen.

  • End-stage renal disease requiring dialysis

  • Bi-ventricular pacemaker (CRT)

Trial design

362 participants in 1 patient group

Patients with HF
Description:
Each patient seen in hospital emergency or for congestive heart failure and with an ejection fraction above 45%

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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