A prospective, observational cohort study designed to identify clinical phenotypes and evaluate predictors \& outcomes of functional mitral and tricuspid valve regurgitation in patients with atrial fibrillation. Participant will under go: * Baseline echocardiography * Cpex Echocardiography * Blood test: BNP * 1 year follow up Echocardiography Participants will be stratified into three subgroups: * Atrial Functional MR * Atrial Functional TR * Mixed MR \& TR
Rationale The natural history and risk factors for atrial valve disease are poorly understood and characterised. This study will examine differences between atrial mitral and atrial tricuspid disease and help us understand the natural history of these pathologies. Study objectives Primary objective * Identify \& characterise phenotypes in functional mitral and tricuspid valve regurgitation * Identify risk factors for progression of disease and outcome. Secondary objective Compare the three groups: atrial functional MR, atrial functional TR, and mixed disease, and identify any differences/similarities. Primary endpoint Effective Regurgitant Orifice Area at 1 year Secondary endpoint * Progression of valve disease defined as worsening of mitral or tricuspid regurgitation \> 1 grade at 1 year. * Functional: New York Heart Association Class, Predicted VO2max (\<84%). * Heart Failure admission within 1 year of recruitment. * Mortality. Recruitment will take place from the out-patient clinics \& echocardiography laboratory at St Bartholomew's Hospital
Study Type
OBSERVATIONAL
Enrollment
141
Ultrasound scan of the heart
St Bartholomew's Hospital
London, United Kingdom
RECRUITINGEffective Regurgitant Orifice Area at 1 year
Measure the EROA by echocardiography after 1 year
Time frame: 1 year
Progression of valve disease defined as worsening of mitral or tricuspid regurgitation > 1 grade at 1 year.
Measure the change in regurgitation severity
Time frame: 1 year
Functional: New York Heart Association Class, Predicted VO2max (<84%).
Evaluate participants' physical abilities and endurance, focusing on two key measures: The New York Heart Association (NYHA) Functional Classification and the predicted maximum oxygen uptake (VO2max)
Time frame: 1 year
Heart Failure admission within 1 year of recruitment.
incidence of heart failure admissions within a one-year period following the recruitment of participants.
Time frame: 1 year
Mortality
Document and analyze the mortality rates among participants
Time frame: 1 year
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