Introduction
Speaker: Sophie Offin, cardiologist, PhD candidate on tricuspid valve disease at Royal Prince Alfred Hospital.
Main focus: Tricuspid and pulmonary valves, including anatomy, clinical features, investigations, and management aspects.
Anatomy
Heart valve overview:
Pulmonary Valve:
Tri-leaflet semilunar valve with three cusps and fibrous annulus.
Separation of right ventricular outflow tract from pulmonary trunk.
No fibrous continuity between pulmonary valve and tricuspid valve.
Tricuspid Valve:
Largest heart valve, three leaflets:
Anterior leaflet (largest).
Septal leaflet (smallest).
Posterior leaflet.
Fibrous annulus around it, with the right coronary artery coursing around.
Leaflets attached via chordae tendineae to papillary muscles (less defined than mitral valve).
Tricuspid Regurgitation
Classification
Primary Causes: Intrinsic valve abnormalities, includes:
Congenital abnormalities (e.g., Ebstein's anomaly: apical displacement of septal and posterior leaflets).
Iatrogenic causes (e.g., pacemaker or defibrillator leads perforating leaflets).
Rheumatic valvular causes, carcinoid, infective causes (e.g., endocarditis).
Secondary Causes (Functional Regurgitation):
Normal leaflets with:
Annular dilatation and caudal retraction/stretch.
Volume overload from conditions like right ventricular infarction, pulmonary hypertension, or left ventricle dysfunction.
Isolated Tricuspid Regurgitation (Atrial Functional):
Due to severe right atrial dilatation leading to annular dilatation, often in chronic atrial fibrillation.
Symptoms and Clinical Presentation
Symptoms typically present late due to relative asymptomatic periods.
Consequences of tricuspid regurgitation:
Regurgitant flow leads to elevation in right atrial pressures and systemic venous congestion:
Dependent edema.
Early satiety.
Right ventricular failure:
Inadequate forward flow resulting in breathlessness, exercise intolerance, and fatigue.
Clinical examination findings:
Pathognomonic pansystolic murmur (can be soft/absent in severe cases due to equalization of pressures).
Right ventricular heave due to dilatation.
Jugular venous distension with elevation and ‘v’ waves due to systolic regurgitation.
Systemic symptoms: hepatomegaly, ascites, peripheral edema.
Investigations
Primary Investigation: Echocardiography (transthoracic and transesophageal):
Transthoracic echo is often preferable due to the anterior location of the tricuspid valve.
Assessing etiology and severity of tricuspid regurgitation:
Determine if intrinsic (primary) or secondary (normal leaflets).
Severity assessment using:
2D Doppler and color Doppler.
Vena contracta width to measure regurgitant jet width.
Consequences visible in echocardiography:
Annular, right ventricular, and right atrial dilatation, as well as right ventricular dysfunction.
Other imaging options:
Cardiac CT for assessing annular size and evaluating annularity before interventions.
Cardiac MRI for advanced assessment of right ventricular function and volumes.
Prognosis and Management
Tricuspid regurgitation previously thought of as benign but now recognized for its poor prognosis:
Stepwise progression of worsening prognosis with increasing severity (from none to severe) independent of ventricular functions.
Surgical interventions:
Surgery for isolated tricuspid valve regurgitation is infrequent with high mortality rates.
Challenges include diverse etiologies and patients often remaining asymptomatic until late stages.
Management Approaches:
Diuretics for severe tricuspid regurgitation and right heart failure to treat volume overload.
Surgical guidelines advocate for tricuspid valve repair during left-sided valve surgeries for functional tricuspid regurgitation if annular dilatation >40 mm.
Emerging transcatheter interventions for high-risk surgical patients despite limited evidence.
Surgical Options
Repair: Preferred where possible, particularly for secondary (functional) tricuspid regurgitation:
Annuloplasty devices for cinching the dilated annulus, potentially with leaflet repair.
Replacement: More common in primary regurgitation with abnormal leaflets:
Usually involves bioprosthetic valves.
Transcatheter Options: Includes:
Transcatheter tricuspid valve replacement, valve-in-valve techniques, ring annuloplasty, coaptation devices (based on Alfieri repair).
Early trials show promise for symptom improvement and reduced hospitalization, but more extensive studies needed.
Tricuspid Stenosis
Etiology: Rare and often presents with tricuspid regurgitation, commonly rheumatic in nature.
Symptoms result from elevated right atrial pressure and limited forward flow causing:
Breathlessness on exertion, fatigue.
Echocardiographic assessment for valuation:
Features of stenosis visible via Doppler showing elevated gradients and reduced valve area.
Pulmonary Valve Disease
Incidence and Etiology:
Congenital pulmonary valve disease more common than acquired.
Can present as isolated or as part of multi-system heart diseases.
Conditions:
Pulmonary stenosis:
Usually treated in childhood via balloon valvotomy or surgery, excellent prognosis.
Can present as suvalvular or supravalvular stenosis, significant in conditions like tetralogy of Fallot.
Pulmonary regurgitation (primary and secondary):
Severe pulmonary regurgitation leads to right ventricular volume overload and dysfunction, often associated with congenital heart disease.
Secondary can arise from severe pulmonary hypertension or post-repair of stenosis.
Treatment Options:
Melody valve as a percutaneous option for previously operated patients requiring repeated surgeries.