Pulmonic Valve
Anupama Rao
High-Yield Findings
Pulmonic stenosis (PS) is usually found in conjunction with congenital heart disease
PS may occur at the valvular, subvalvular, or supravalvular levels
Carcinoid disease is a common cause of acquired pulmonic valve disease and can cause both stenosis and regurgitation
Severe pulmonic regurgitation (PR) is most often seen in the setting of pulmonary hypertension or in patients with repaired tetralogy of Fallot
With severe PR, CW Doppler shows rapid deceleration of the PR jet. Presystolic forward flow can be seen with severe PR due to premature opening of PV due to high RVEDP
Key Views
TTE
PLAX and PSAX views tilted toward RV outflow tract (RVOT)
Subcostal view
TEE
High esophageal view at 0 to 20 degrees
Mid esophageal level at 50 to 90 degrees (RV inflow/outflow view)
Deep transgastric view 110 to 140 degrees
Anatomy
The pulmonic valve is a semi-lunar valve regulating flow between the right ventricle and the pulmonary artery. It consists of three leaflets projecting into the pulmonary artery, namely the anterior, right, and left cusps. The leaflets are attached at their base to the valve annulus, a scalloped ring of fibrous tissue.
Physiology
The pulmonic valve opens in ventricular systole when pressure in the right ventricle exceeds that of the pulmonary artery. The valve closes at the end of systole when the pressure in the pulmonary artery is greater than in the right ventricle. Closure of the pulmonic valve produces the P2 component of the second heart sound.
Pulmonic Stenosis
Pulmonic stenosis involves fixed or dynamic obstruction of blood flow from the right ventricle to the pulmonary vasculature. It is mostly seen in the setting of congenital heart disease.
Etiology
Congenital heart disease (most common) |
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Other causes (rare) |
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Obstruction can arise from the subvalvular, valvular, or supravalvular regions.
Valvular: Dysplastic, bicuspid, or unicuspid valves
Subvalvular: Narrowing of infundibulum/RVOT, which can be seen in tetralogy of Fallot or double-chambered right ventricle, congenital VSD, severe right ventricular hypertrophy, external compression by mass or tumor
Supravalvular: Obstruction at the level of the main pulmonary artery or its more distal branches (e.g., Noonan’s syndrome and Williams syndrome) (see Fig. 11-3)
2D Findings
Right ventricular hypertrophy (normal thickness of the RV is <5 mm at end-diastole) (Fig. 11-1A)
Right ventricular enlargement (Fig. 11-1B and C)
Thickened pulmonic valve leaflets with systolic doming
Post-stenotic dilatation of pulmonary artery
M-Mode
Exaggerated “a” wave of PV during diastole (due to increased force of right atrial contraction against stenotic valve)Stay updated, free articles. Join our Telegram channel
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