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| http://dx.doi.org/10.11909/j.issn.1671-5411.2018.01.009 | DOI Listing |
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Leveraging artificial intelligence for predicting spontaneous closure of perimembranous ventricular septal defect in children: a multicentre, retrospective study in China.
Lancet Digit Health
January 2025
Department of Pediatric Cardiology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Engineering Research Center of Techniques and Instruments for Diagnosis and Treatment of Congenital Heart Disease, Ministry of Education, Shanghai, China. Electronic address:
Background: Perimembranous ventricular septal defect (PMVSD) is a prevalent congenital heart disease, presenting challenges in predicting spontaneous closure, which is crucial for therapeutic decisions. Existing models mainly rely on structured echocardiographic parameters or restricted data. This study introduces an artificial intelligence (AI)-based model, which uses natural language processing (NLP) and machine learning with the aim of improving spontaneous closure predictability in PMVSD.
View Article and Find Full Text PDFRight-sided infective endocarditis complicated with aortic pseudoaneurysms and systemic embolism in a 27-year-old female with ventricular septal defect: a case report.
Pan Afr Med J
December 2024
Department of Cardiology B, Hospital University Center Ibn Sina, Mohamed V University, Rabat, Morocco.
Article Synopsis
- Infective endocarditis (IE) can occur in adults with ventricular septal defects (VSD), and this case reports a rare instance involving systemic embolisms and aortic pseudoaneurysms.
- A 27-year-old woman with a previously asymptomatic VSD presented with prolonged fever and was found to have staphylococcus infection, heart murmurs, and serious complications like mycotic aneurysms and embolisms.
- The patient received targeted antibiotics and underwent urgent heart surgery, emphasizing the importance of checking for systemic embolism in right ventricle IE and noting that congenital VSD can lead to serious complications from bacteremia.
Spontaneously Corrected Hypoplastic Left Heart: A Case Report and Exceptional Opportunity to Discuss Etiology with Novel Therapeutic Vision.
Arch Iran Med
September 2024
Department of Pediatric Cardiology, Besat Hospital, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Hypoplastic left heart syndrome (HLHS) is a relatively prevalent fetal echocardiography finding in complex congenital heart diseases. Current studies indicate that intrinsic and extrinsic mechanisms could be involved in the development of left heart hypoplasia. Left ventricular inflow or outflow disorders may cause left heart hypoplasia.
View Article and Find Full Text PDFVentricular septal defect associated with aortic regurgitation and ascending aortic aneurysm: a case report.
J Med Case Rep
October 2023
Clinic of Cardiology, University Clinical Centre of Kosova, Rrethi i Spitalit, pn., 10000, Prishtina, Republic of Kosovo.
Introduction: Ventricular septal defect (VSD) is one of the most common congenital cardiac anomalies. Patients with perimembranous VSD may have aortic regurgitation (AR) secondary to prolapse of the aortic cusp.
Case Presentation: We present a case of 23-year-old White man with VSD, AR and ascending aortic aneurysm.
Laubry-Pezzi syndrome: three case reports and review of the literature.
Ann Med Surg (Lond)
May 2023
Cardiology Department, CHU IBN Rochd, B.P, Casablanca, Morocco.
Unlabelled: Laubry-Pezzi syndrome is a rare congenital heart disease characterized by the association of ventricular defect septal to aortic cusp prolapse responsible for aortic regurgitation (AR).
Case Presentation: We reported three cases of Laubry-Pezzi syndrome diagnosed in our department of cardiology on a cohort of more than 3000 cases of congenital heart disease. A 13-year-old patient presented a Laubry-Pezzi syndrome with severe AR and significant volumetric left ventricle overload and was operated on in time to allow a good evolution of his condition.
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