Best management in isolated right ventricular hypoplasia with septal defects in adults.
Zahra KhajaliMaedeh ArabianMaryam AliramezanyPublished in: Journal of cardiovascular and thoracic research (2020)
Hypoplastic right ventricle is a rare congenital disease usually associated with pulmonary atresia or tricuspid atresia. Isolated right ventricular hypoplasia is a rare anomaly without important valvular abnormalities. It is associated with inter atrial septal defects leading to the right-to-left shunting of blood. Patients with isolated right ventricular hypoplasia usually have different and variable courses. In some patients, it is recognized in the perinatal period and necessitates prompt intervention; nonetheless, there are some reports of this anomaly in old age with no significant symptoms. In this report, we describe the clinical data and management of 6 adult cases with isolated right ventricular hypoplasia treated medically or surgically based on the severity of the disease and symptoms and then offer an in-depth discussion regarding this rare anomaly.
Keyphrases
- atrial fibrillation
- newly diagnosed
- pulmonary hypertension
- end stage renal disease
- ejection fraction
- aortic valve
- randomized controlled trial
- mitral valve
- pregnant women
- hypertrophic cardiomyopathy
- heart failure
- optical coherence tomography
- aortic stenosis
- big data
- prognostic factors
- peritoneal dialysis
- emergency department
- patient reported outcomes
- young adults
- coronary artery disease
- machine learning
- sleep quality
- transcatheter aortic valve replacement
- adverse drug
- left atrial
- left ventricular
- deep learning
- drug induced
- patient reported
- congenital heart disease