Exploration of Dyspnea at Non-high Brain Natriuretic Peptide (BNP)
- Conditions
- Heart Failure With Preserved Ejection Fraction
- Registration Number
- NCT03550235
- Lead Sponsor
- Assistance Publique - Hôpitaux de Paris
- Brief Summary
Patients with unexplained stress dyspnea ( ≥ stage 2 NYHA), no significant underlying lung disease, with an ejection fraction \> 50%, normal resting filling pressures, NTproBNP \< 220 pg/ml in \< 75 years, and \< 450 pg/ml in ≥ 75 years will be studied with stress echocardiography and cardiometabolic stress test (VO2). These patients may have abnormal adaptation during exercise, suggesting that chronic symptoms may be related to a heart failure with preserved ejection fraction (HFPEF). More accurate and earlier diagnosis of HFPEF using stress echocardiography and VO2 may better manage stress dyspnea in patients and prevent progression of HFPEF.
A clinical assessment will be offered to people with unexplained stress dyspnea. The procedures and products used in this study are usually used as part of HFpEF's diagnostic strategy. During this assessment, carried out on an outpatient basis, an anamnesis collection, a cardiovascular clinical examination, an evaluation of dyspnea by the NYHA functional class and by 2 questionnaires, an electrocardiogram will be carried out, a 6-minute walk test, a biological blood test, a trans thoracic rest and stress cardiac ultrasound, respiratory functional tests (with diffusion capacity of lung for carbon monoxide (DLCO) and blood gas), and a metabolic stress test. A follow-up at 1 and 2 years is planned (visit, sampling and resting echocardiography).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 100
- Patient over 40 years of age, and under 80 years of age with unexplained effort dyspnea, able to pedal.
- Echocardiographic ejection fraction > 50%
- NTproBNP < 220 pg/ml in < 75 years, and < 450 pg/ml in ≥ 75 years
- Patient with coronary, valve, hypertrophic, hypertensive, infiltrative, constrictive, or rhythmic, significant and/or progressive heart disease.
BMI > 35 kg/m².
- Unstable patient (systolic blood pressure < 90 mmHg, resting pulse > 100 BPM) or clinically congested (edema of the lower limbs, crackling in the lungs).
- Patient with Pulmonary function testing (EFR) showing significant respiratory disease (FEV1/ vital capacity (CV) max < 0.7, total lung capacities (CPT)< LIN)
- Chronic renal failure with creatinine clearance < 30 ml/min (MDRD) or dialysis
- Patient with anemia (Hb < 12 g/dl)
- Patient with hypo or hyperthyroidism on thyreostimulating hormone (TSH) value
- Patient under justice safeguard measure or guardianship
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Occurence of HFpEF during the 2 years of follow-up HFpEF diagnosis will be made in attendance of following symptoms:
* heart failure
* NTproBNP\>125pg/ml
* preservation of ejection fraction with Left Ventricular Ejection Fraction (LVEF)\>50%
* structural heart disease with expansion of left ventricular mass (VM) (men: VM≥115 g/m² or women ≥ 95 g/m² and an E/e' ratio≥13dyspnea on exertion during the 2 years of follow-up NTproBNP levels at rest during the 2 years of follow-up
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (4)
CCM RANGUEIL - LARREY CHU toulouse
🇫🇷Toulouse, France
CHU Pontchaillou
🇫🇷Rennes, France
Hopital Bicêtre
🇫🇷Le Kremlin-Bicêtre, France
Polyclinique de Poitiers
🇫🇷Poitiers, France