Cardiac magnetic resonance left ventricular filling pressure is linked to symptoms, signs and prognosis in heart failure

Author:

Grafton‐Clarke Ciaran12ORCID,Garg Pankaj123ORCID,Swift Andrew J.34,Alabed Samer3,Thomson Ross56,Aung Nay56,Chambers Bradley7,Klassen Joel7,Levelt Eylem7,Farley Jonathan7,Greenwood John P.7,Plein Sven7,Swoboda Peter P.7

Affiliation:

1. Norwich Medical School University of East Anglia Norwich Research Park Norwich NR4 7UQ UK

2. Norfolk and Norwich University Hospitals NHS Foundation Trust Norfolk UK

3. Department of Infection, Immunity and Cardiovascular Disease University of Sheffield Medical School and Sheffield Teaching Hospitals NHS Trust Sheffield UK

4. Department of Clinical Radiology Sheffield Teaching Hospitals NHS Foundation Trust Sheffield UK

5. William Harvey Research Institute, NIHR Barts Biomedical Research Centre Queen Mary University of London London UK

6. Barts Heart Centre St Bartholomew's Hospital, Barts NHS Trust London UK

7. Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds Leeds UK

Abstract

AbstractAimsLeft ventricular filling pressure (LVFP) can be estimated from cardiovascular magnetic resonance (CMR). We aimed to investigate whether CMR‐derived LVFP is associated with signs, symptoms, and prognosis in patients with recently diagnosed heart failure (HF).Methods and resultsThis study recruited 454 patients diagnosed with HF who underwent same‐day CMR and clinical assessment between February 2018 and January 2020. CMR‐derived LVFP was calculated, as previously, from long‐ and short‐axis cines. CMR‐derived LVFP association with symptoms and signs of HF was investigated. Patients were followed for median 2.9 years (interquartile range 1.5–3.6 years) for major adverse cardiovascular events (MACE), defined as the composite of cardiovascular death, HF hospitalization, non‐fatal stroke, and non‐fatal myocardial infarction. The mean age was 62 ± 13 years, 36% were female (n = 163), and 30% (n = 135) had raised LVFP. Forty‐seven per cent of patients had an ejection fraction < 40% during CMR assessment. Patients with raised LVFP were more likely to have pleural effusions [hazard ratio (HR) 3.2, P = 0.003], orthopnoea (HR 2.0, P = 0.008), lower limb oedema (HR 1.7, P = 0.04), and breathlessness (HR 1.7, P = 0.01). Raised CMR‐derived LVFP was associated with a four‐fold risk of HF hospitalization (HR 4.0, P < 0.0001) and a three‐fold risk of MACE (HR 3.1, P < 0.0001). In the multivariable model, raised CMR‐derived LVFP was independently associated with HF hospitalization (adjusted HR 3.8, P = 0.0001) and MACE (adjusted HR 3.0, P = 0.0001).ConclusionsRaised CMR‐derived LVFP is strongly associated with symptoms and signs of HF. In addition, raised CMR‐derived LVFP is independently associated with subsequent HF hospitalization and MACE.

Funder

British Heart Foundation

National Institute for Health and Care Research

Wellcome Trust

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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