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Rationale and design of the Karolinska‐Rennes (KaRen) prospective study of dyssynchrony in heart failure with preserved ejection fraction

Identifieur interne : 003906 ( Main/Exploration ); précédent : 003905; suivant : 003907

Rationale and design of the Karolinska‐Rennes (KaRen) prospective study of dyssynchrony in heart failure with preserved ejection fraction

Auteurs : Erwan Donal [France] ; Lars H. Lund [Suède] ; Cecilia Linde [Suède] ; Magnus Edner [Suède] ; Stéphane Lafitte [France] ; Hans Persson [Suède] ; Fabrice Bauer [France] ; John Öhrvik [Suède] ; Pierre-Vladimir Ennezat [France] ; Camilla Hage [Suède] ; Ida Löfman [Suède] ; Yves Juilliere [France] ; Damien Logeart [France] ; Geneviève Derumeaux [France] ; Pascal Gueret [France] ; Jean-Claude Daubert [France]

Source :

RBID : ISTEX:3E5C7880FCEF730F22DC27A5C866DA8FC37482F7

English descriptors

Abstract

Heart failure with preserved ejection fraction (HFPEF) is common but not well understood. Electrical dyssynchrony in systolic heart failure is harmful. Little is known about the prevalence and the prognostic impact of dyssynchrony in HFPEF.
We have designed a prospective, multicenter, international, observational study to characterize HFPEF and to determine whether electrical or mechanical dyssynchrony affects prognosis. Patients presenting with acute heart failure (HF) will be screened so as to identify 400 patients with HFPEF. Inclusion criteria will be: acute presentation with Framingham criteria for HF, left ventricular ejection fraction ≥ 45%, brain natriuretic peptide (BNP) > 100 pg/mL or NT‐proBNP > 300 pg/mL. Once stabilized, 4–8 weeks after the index presentation, patients will return and undergo questionnaires, serology, ECG, and Doppler echocardiography. Thereafter, patients will be followed for mortality and HF hospitalization every 6 months for at least 18 months. Sub‐studies will focus on echocardiographic changes from the acute presentation to the stable condition and on exercise echocardiography, cardiopulmonary exercise testing, and serological markers.
KaRen aims to characterize electrical and mechanical dyssynchrony and to assess its prognostic impact in HFPEF. The results might improve our understanding of HFPEF and generate answers to the question whether dyssynchrony could be a target for therapy in HFPEF.

Url:
DOI: 10.1093/eurjhf/hfn025


Affiliations:


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Le document en format XML

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<div type="abstract">Heart failure with preserved ejection fraction (HFPEF) is common but not well understood. Electrical dyssynchrony in systolic heart failure is harmful. Little is known about the prevalence and the prognostic impact of dyssynchrony in HFPEF.</div>
<div type="abstract">We have designed a prospective, multicenter, international, observational study to characterize HFPEF and to determine whether electrical or mechanical dyssynchrony affects prognosis. Patients presenting with acute heart failure (HF) will be screened so as to identify 400 patients with HFPEF. Inclusion criteria will be: acute presentation with Framingham criteria for HF, left ventricular ejection fraction ≥ 45%, brain natriuretic peptide (BNP) > 100 pg/mL or NT‐proBNP > 300 pg/mL. Once stabilized, 4–8 weeks after the index presentation, patients will return and undergo questionnaires, serology, ECG, and Doppler echocardiography. Thereafter, patients will be followed for mortality and HF hospitalization every 6 months for at least 18 months. Sub‐studies will focus on echocardiographic changes from the acute presentation to the stable condition and on exercise echocardiography, cardiopulmonary exercise testing, and serological markers.</div>
<div type="abstract">KaRen aims to characterize electrical and mechanical dyssynchrony and to assess its prognostic impact in HFPEF. The results might improve our understanding of HFPEF and generate answers to the question whether dyssynchrony could be a target for therapy in HFPEF.</div>
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