Results 71 to 80 of about 165,950,521 (230)
The Evolving Landscape of CHD Genetics: A Contemporary Guide to Genetic Testing and Management
ABSTRACT Congenital heart disease (CHD) is the most common birth defect, affecting an estimated 9.4/1000 infants globally. The genetics of CHD is complex, with most cases thought to have multifactorial aetiology, implicating both genetic and environmental factors.
Bridget R. O'Malley +3 more
wiley +1 more source
Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects
ABSTRACT Cases with congenital heart defects (CHD) often have other associated anomalies. The aim of this investigation was to assess the prevalence and the types of co‐occurring anomalies in CHD in a well‐defined population. The anomalies co‐occurring with CHD were ascertained in all live births, stillbirths and terminations of pregnancy for fetal ...
Claude Stoll +2 more
wiley +1 more source
Abstract Aim Besides registries, healthcare databases can provide useful information for assessing the frequency of major congenital malformations (MCMs) and investigating their risk factors, particularly medication exposures. This study aimed to assess the validity of MCMs identification based on French national, comprehensive healthcare databases ...
Tom Duchemin +7 more
wiley +1 more source
Pregnancy with Tetralogy of Fallot
Introduction: Tetralogy of Fallot is a congenital heart defect that is present at birth. It features four problems: a ventricular septal defect, pulmonary stenosis, a right ventricular hypertrophy and an overriding aorta.
Koleva, Denica +4 more
core +1 more source
Neighborhood Economic Deprivation, Hispanic Ethnic Enclaves, and Congenital Anomalies in Texas
ABSTRACT Background Congenital anomalies are common, costly, and potentially life‐threatening. The impacts of structural determinants of health on risk for these conditions have scarcely been studied. We evaluated associations between residence in economically disadvantaged neighborhoods or Hispanic/Latino enclaves and congenital anomalies.
Jeremy M. Schraw +6 more
wiley +1 more source
Natural and unnatural history of tetralogy of Fallot repaired during adolescence and adulthood
Surgical repair of tetralogy of Fallot (TOF) in countries with sound medical care systems is seldom delayed until adolescence. This study investigated the clinical profile and the surgical outcomes in such a population from Taiwan. Between 1970 and 2009,
Yang, Ming-Chun;Chiu, Shuenn-Nan;Wang, Jou-Kou;Lu, Chun-Wei;Lin, Ming-Tai;Chen, Chun-An;Chang, Chung-I;Chen, Yih-Sharng;Chiu, Ing-Sh;Wu, Mei-Hwan +1 more
core +1 more source
Methodological framework among international observers to understand clinical decision‐making and interobserver agreement in TPVR planning. ABSTRACT Background Transcatheter pulmonary valve replacement (TPVR) requires selecting the optimal device type, size, and position. Variability in anatomical shape may affect procedural planning.
Camilo E. Pérez‐Cualtán +10 more
wiley +1 more source
Arrhythmic burdens in patients with tetralogy of Fallot: A national database study
BACKGROUND Tetralogy of Fallot (TOF) is a common cyanotic congenital heart disease with increasingly recognized late morbidity. ;OBJECTIVE The purpose of this study was to explore the long-term outcome by using a national database of Taiwan, a country ...
Wu, Mei-Hwan;Lu, Chun-Wei;Chen, Hui-Chi;Chiu, Sheunn-Nan;Kao, Feng-Yu;Huang, San-Kuei +1 more
core +1 more source
ABSTRACT Background Pulmonary valve replacement is frequently required in adults with congenital heart disease (CHD). Comparative real‐world outcomes between percutaneous transcatheter pulmonary valve implantation (TPVR) and surgical pulmonary valve replacement (SPVR) remain incompletely characterized. We evaluated outcomes and resource utilization for
Adam Bolad +4 more
wiley +1 more source

