Congenital Heart Defects
Mostrando 13-24 de 171 artigos, teses e dissertações.
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13. The study of copy number variations in the regions of PRKAB2 and PPM1K among congenital heart defects patients
RESUMO OBJETIVO: Este estudo teve como objetivo avaliar a associação genética do número de cópias em dois genes (PRKAB2 e PPM1K) localizados em duas regiões (tetralogia de Fallot e comunicação interventricular) em uma população chinesa da etnia Han. METODOLOGIA: Um total de 200 pacientes com doença cardíaca congênita (100 pacientes com tetralo
Rev. Assoc. Med. Bras.. Publicado em: 22/07/2019
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14. Ectopia Cordis Associated with Pentalogy of Cantrell-A Case Report
Resumo A pentalogia de Cantrell (PC) é uma rara anomalia congênita caracterizada por alterações nas estruturas medianas mesodérmicas e doenças cardíacas congênitas, cursando muitas vezes com um mau prognóstico. Em 1958, Cantrell et al2 definiram o espectro completo da síndrome com as seguintes anomalias: defeitos do diafragma anterior, da parte inf
Rev. Bras. Ginecol. Obstet.. Publicado em: 27/06/2019
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15. INSTRUCTIONAL DESIGN FOR NURSING CARE TO NEONATES WITH CONGENITAL HEART DEFECTS
RESUMO Objetivo: desenvolver e validar design instrucional para o cuidado clínico de Enfermagem aos neonatos com cardiopatias congênitas em maternidades, por meio de educação a distância. Método: pesquisa metodológica, aplicada, constituindo-se de cursoon-line, para enfermeiros de unidades neonatais. No desenvolvimento do design instrucional efetivo
Texto contexto - enferm.. Publicado em: 10/06/2019
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16. Surgical Treatment for Congenital Heart Defects in Down Syndrome Patients
Abstract Objective: To analyze data related to surgical treatment in patients with congenital heart defects (CHD) and Down syndrome (DS) based on information from International Quality Improvement Collaborative Database for Congenital Heart Disease (IQIC). Methods: Between July 1, 2010 and December 31, 2017, 139 patients with CHD and DS underwent surgery a
Braz. J. Cardiovasc. Surg.. Publicado em: 2019-02
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17. FUNCTIONAL CAPACITY IN CHILDREN AND ADOLESCENTS WITH CONGENITAL HEART DISEASE
RESUMO Objetivo: Avaliar o nível de atividade física e a capacidade funcional de crianças e adolescentes com cardiopatia congênita, além de descrever correlações entre funcionalidade, achados cirúrgicos e ecocardiográficos, perfil metabólico e inflamatório e diferenças entre cardiopatias congênitas acianótica e cianótica. Métodos: Estudo
Rev. paul. pediatr.. Publicado em: 07/01/2019
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18. Repair of Double Orifice Left AV Valve (DOLAVV) with Endocardial Cushion Defect in Adult
Abstract Double orifice left atrioventricular valve (DOLAVV) or double orifice mitral valve (DOMV) is a rare congenital cardiac anomaly manifesting either as an isolated lesion (mitral stenosis or mitral insufficiency) or in association with other congenital cardiac defects. Signs of mitral valve disease are usually present along with the symptoms of associa
Braz. J. Cardiovasc. Surg.. Publicado em: 2017-08
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19. Collaborative Quality Improvement in the Congenital Heart Defects: Development of the ASSIST Consortium and a Preliminary Surgical Outcomes Report
Abstract Objective: ASSIST is the first Brazilian initiative in building a collaborative quality improvement program in pediatric cardiology and congenital heart disease. The purposes of this manuscript are: (a) to describe the development of the ASSIST project, including the historical, philosophical, organizational, and infrastructural components that wil
Braz. J. Cardiovasc. Surg.. Publicado em: 2017-08
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20. Modified Hybrid Procedure in Hypoplastic Left Heart Syndrome: Initial Experience of a Center in Northeastern Brazil
Abstract Introduction: Although it only corresponds to 2.5% of congenital heart defects, hypoplastic left heart syndrome (HLHS) is responsible for more than 25% of cardiac deaths in the first week of life. Palliative surgery performed after the second week of life is considered an important risk factor in the treatment of HLHS. Objective: The aim of this s
Braz. J. Cardiovasc. Surg.. Publicado em: 2017-06
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21. Quadricuspid Aortic Valve: A Comprehensive Review
Abstract Quadricuspid aortic valve (QAV) is a rare congenital heart disease. The functional status of QAV is predominantly a pure aortic regurgitation. Clinical manifestations of patients with a QAV depend on the functional status of the QAV and the associated disorders. Significant valvular regurgitation and (or) stenosis is often present with subsequent op
Braz. J. Cardiovasc. Surg.. Publicado em: 2016-12
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22. Analysis of Surgical Mortality for Congenital Heart Defects Using RACHS-1 Risk Score in a Brazilian Single Center
ABSTRACT Introduction: Risk Adjustment for Congenital Heart Surgery 1 (RACHS-1) score is a simple model that can be easily applied and has been widely used for mortality comparison among pediatric cardiovascular services. It is based on the categorization of several surgical palliative or corrective procedures, which have similar mortality in the treatment
Braz. J. Cardiovasc. Surg.. Publicado em: 2016-06
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23. Proposal of an Integrated Health Care Network System for Patients with Congenital Heart Defects
ABSTRACT The perspective of the integrated health system has a network of care with multiple integration dimensions among subsystems as nuclear representation, relating the clinical aspects and governance to the representations and collective values. The normative integration aims to ensure coherence between the system of representations and values of societ
Braz. J. Cardiovasc. Surg.. Publicado em: 2016-06
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24. Transposition of Great Arteries with Intramural Coronary Artery: Experience with a Modified Surgical Technique
Abstract Objective: Transposition of the great arteries is a common congenital heart disease. Arterial switch is the gold standard operation for this complex heart disease. Arterial switch operation in the presence of intramural coronary artery is surgically the most demanding even for the most experienced hands. We are presenting our experience with a modi
Braz. J. Cardiovasc. Surg.. Publicado em: 2016-02