scholarly journals Outcome of Patients having Congenital Anomalies of the Kidney and Urinary Tract Associated with Congenital Heart Diseases in Pediatric Cardiac ICU.

GEGET ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. 34-48
Author(s):  
Amr Salem ◽  
Sonia El-Saiedi ◽  
Nevine Soliman ◽  
Ahmed Badr ◽  
Ahmed Hassan ◽  
...  
Keyword(s):  
Urinary Tract ◽  
Congenital Anomalies ◽  
Congenital Heart ◽  
Heart Diseases ◽  
Congenital Heart Diseases

Repairing the tricuspid valve in congenital heart diseases other than Ebstein’s

2014 ◽  
Vol 24 (6) ◽  
pp. 1077-1087
Author(s):  
Ali Dodge-Khatami ◽  
Constantine D. Mavroudis ◽  
Jennifer Frost ◽  
Jeffrey P. Jacobs ◽  
Constantine Mavroudis
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Tricuspid Valve ◽  
Congenital Anomalies ◽  
Congenital Heart ◽  
Heart Diseases ◽  
Surgical Techniques ◽  
Congenital Heart Diseases ◽  
Right Heart ◽  
The Right

AbstractThe tricuspid valve is being increasingly recognised as an important safeguard to the heart with congenital heart disease. Both structural anomalies of the valve and functional burdens from other malformations of the right heart can lead to major haemodynamic consequences both upstream and downstream. The indications to surgically intervene on the tricuspid valve are evolving and vary depending on the malformation. The extant surgical techniques and their applications to corresponding frequent congenital anomalies of the tricuspid valve are reviewed.

scholarly journals Congenital Heart Diseases Associated with Congenital Anomalies of the Gastrointestinal Tract

2015 ◽  
Vol 31 (4) ◽  
pp. 192-198
Author(s):  
Tomohiro Nawa ◽  
Masato Yokozawa ◽  
Tsutomu Wada ◽  
Keiji Haseyama ◽  
Motoki Takamuro
Keyword(s):  
Gastrointestinal Tract ◽  
Congenital Anomalies ◽  
Congenital Heart ◽  
Heart Diseases ◽  
Congenital Heart Diseases

scholarly journals Ascertaining and classifying cases of congenital anomalies in the ALSPAC birth cohort

2021 ◽  
Vol 5 ◽  
pp. 231
Author(s):  
Kurt Taylor ◽  
Richard Thomas ◽  
Mark Mumme ◽  
Jean Golding ◽  
Andy Boyd ◽  
...  
Keyword(s):  
Longitudinal Study ◽  
Congenital Anomalies ◽  
Congenital Heart ◽  
Heart Diseases ◽  
Congenital Heart Diseases ◽  
Functional Disorders ◽  
Multiple Sources ◽  
Health Records ◽  
Parents And Children ◽  
Avon Longitudinal Study

Congenital anomalies (CAs) are structural or functional disorders that occur during intrauterine life. Longitudinal cohort studies provide unique opportunities to investigate potential causes and consequences of these disorders. In this data note, we describe how we identified cases of major CAs, with a specific focus on congenital heart diseases (CHDs), in the Avon Longitudinal Study of Parents and Children (ALSPAC). We demonstrate that combining multiple sources of data including data from antenatal, delivery, primary and secondary health records, and parent-reported information can improve case ascertainment. Our approach identified 590 participants with a CA according to the European Surveillance of Congenital Anomalies (EUROCAT) guidelines, 127 of whom had a CHD. We describe the methods that identified these cases and provide statistics on subtypes of anomalies. The data note contains details on the processes required for researchers to access these data.

scholarly journals Ascertaining and classifying cases of congenital anomalies in the ALSPAC birth cohort

2020 ◽  
Vol 5 ◽  
pp. 231
Author(s):  
Kurt Taylor ◽  
Richard Thomas ◽  
Mark Mumme ◽  
Jean Golding ◽  
Andy Boyd ◽  
...  
Keyword(s):  
Longitudinal Study ◽  
Congenital Anomalies ◽  
Congenital Heart ◽  
Heart Diseases ◽  
Congenital Heart Diseases ◽  
Functional Disorders ◽  
Multiple Sources ◽  
Health Records ◽  
Parents And Children ◽  
Avon Longitudinal Study

Congenital anomalies (CAs) are structural or functional disorders that occur during intrauterine life. Longitudinal cohort studies provide unique opportunities to investigate potential causes and consequences of these disorders. In this data note, we describe how we identified cases of major CAs, with a specific focus on congenital heart diseases (CHDs), in the Avon Longitudinal Study of Parents and Children (ALSPAC). We demonstrate that combining multiple sources of data including data from antenatal, delivery, primary and secondary health records, and parent-reported information can improve case ascertainment. Our approach identified 590 participants with a CA according to the Euro Registers of Congenital Anomalies (EUROCAT) guidelines, 127 of whom had a CHD. We describe the methods that identified these cases and provide statistics on subtypes of anomalies. The data note contains details on the processes required for researchers to access these data.

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