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Pulmonary valve stenosis in the adult patient: pathophysiology, diagnosis and management

Heart, 2018
### Learning objectives The most common form of right ventricular outflow tract (RVOT) obstruction is pulmonary valve stenosis. Pulmonary stenosis (PS) occurs in isolation in 8%–10% of congenital heart disease but is often associated with other ...
E. Ruckdeschel, Yuli Y. Kim
semanticscholar   +1 more source

Pulmonary Valve Stenosis

2021
Echocardiography has an important role both in diagnosis and follow up of patients with pulmonary stenosis (PS), Dome shape opening, post stenotic dilation, and right ventricular hyprtrophy are two dimensional echocardiographic (2D) findings of pulmonary stenosis and should be completed by color and Doppler echocardiographic evidences.
Shamsi Ghaffari, Maryam Moradian
openaire   +1 more source

Pulmonary Valve Stenosis

2014
Pulmonary valvular stenosis is one of the most common congenital heart defects. In this defect, the pulmonary valve opening from the right ventricle is restricted. It may interfere with the growth and development of the lung and cause pressure overload on the right heart.
Tingliang Liu, Wei Gao
openaire   +2 more sources

The Genetics of Canine Pulmonary Valve Stenosis

Veterinary Clinics of North America: Small Animal Practice, 2023
There have been recent advancements in understanding the genetic contribution to pulmonary valve stenosis (PS) in brachycephalic breeds such as the French Bulldog and Bulldog. The associated genes are transcriptions factors involved in cardiac development, which is comparable to the genes that cause PS in humans.
Samantha, Kovacs   +2 more
openaire   +2 more sources

Pulmonary Valve Stenosis

1983
Severe pulmonary valve stenosis causing symptoms of cardiac failure in the first months of life can be accurately diagnosed by non-invasive techniques. Auscultation reveals a harsh systolic ejection murmur at the left parasternal area. In the presence of cardiac failure this murmur may be absent and there may a high-pitched murmur caused by secondary ...
G. J. van Mill   +2 more
openaire   +1 more source

Pulmonary Hypertension in Patients With Severe Aortic Stenosis: Prognostic Impact After Transcatheter Aortic Valve Replacement: Pulmonary Hypertension in Patients Undergoing TAVR.

JACC Cardiovascular Imaging, 2019
OBJECTIVES The authors investigated the development of pulmonary hypertension (PH), predictors of PH regression, and its prognostic impact on short, mid-, and long-term outcomes in patients undergoing transcatheter aortic valve replacement (TAVR) for ...
B. Alushi   +12 more
semanticscholar   +1 more source

Pulmonary atresia and aortic valve stenosis

International Journal of Cardiology, 1987
A case is described of pulmonary atresia with ventricular septal defect and severe aortic valve stenosis. The aortic valve gradient measured at the time of insertion of an aortic to pulmonary arterial shunt was only 5 mm Hg and aortic valvotomy was deferred. Post-operative low output cardiac failure resulted in the death of the patient. The severity of
R P, Martin   +2 more
openaire   +2 more sources

Pulmonary valve disease: Pulmonary valve stenosis

2015
Introduction Transcatheter therapy of valvar pulmonary stenosis is one of the rst, if not the rst, catheter intervention that has facilitated the application of this technology for children so that many of them can benet by less invasive treatment for structural congenital heart defects.
openaire   +1 more source

Dysplastic Pulmonary Valve Stenosis

2014
Hypoplasia of the pulmonary valve (PV) ring and dysplastic PV may exist in rare patients. PV dysplasia is described by thickened and nodular valvular leaflets with no or minimal commissural fusion, hypoplasia of the valve ring, and absence of poststenotic dilation of the pulmonary artery (PA).
Azin Alizadehasl, Majid Kyavar
openaire   +1 more source

Pulmonary valve stenosis associated with hypertrophic cardiomyopathy

Pediatric Cardiology, 1987
The association of pulmonic stenosis with hypertrophic cardiomyopathy is rare in infancy. Presented here is an infant with atypical picture of pulmonic stenosis and echocardiographic evidence of hypertrophic cardiomyopathy. At eight months of age, she had a successful percutaneous balloon valvuloplasty and has subsequently been managed with propranolol.
M, Heydarian, S B, Yeager
openaire   +2 more sources

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