×
About 1,304 results

ALLMedicine™ Atrioventricular Septal Defect Center

Research & Reviews  647 results

Outcomes of single ventricle palliation in infants with heterotaxy syndrome.
https://doi.org/10.1093/ejcts/ezab141
European Journal of Cardio-thoracic Surgery : Official Jo... Vodiskar J, Kido T et. al.

Mar 30th, 2021 - Heterotaxy is a known risk factor for morbidity and mortality in single ventricle palliation. In this study, we examined our experience with this challenging group of patients. Records of patients born between 2001 and 2019 with heterotaxy, who ne...

Commentary: Early repair of complete atrioventricular septal defect is the forward move.
https://doi.org/10.1016/j.jtcvs.2020.08.053
The Journal of Thoracic and Cardiovascular Surgery; Clark JB

Feb 24th, 2021 - Commentary: Early repair of complete atrioventricular septal defect is the forward move.|2021|Clark JB,|

Characteristics of the pulmonary circulation in infants with complete atrioventricular ...
https://doi.org/10.1017/S1047951120004424
Cardiology in the Young; Doi H, Muneuchi J et. al.

Dec 11th, 2020 - Infants with complete atrioventricular septal defect occasionally accompany pulmonary hypertension; however, the pulmonary circulation can be altered by pulmonary vascular conditions as well as the left heart lesions. This study aimed to explore w...

Unique foetal diagnosis of aorto-pulmonary collaterals in right atrial isomerism.
https://doi.org/10.1017/S1047951120003649
Cardiology in the Young; Mawad W, Dutil N et. al.

Nov 26th, 2020 - Right atrial isomerism is associated with complex cardiac malformations, particularly single-ventricle lesions; right atrial isomerism is rarely associated with aorto-pulmonary collateral arteries. We report a foetal diagnosis of right atrial isom...

see more →

Clinicaltrials.gov  653 results

Outcomes of single ventricle palliation in infants with heterotaxy syndrome.
https://doi.org/10.1093/ejcts/ezab141
European Journal of Cardio-thoracic Surgery : Official Jo... Vodiskar J, Kido T et. al.

Mar 30th, 2021 - Heterotaxy is a known risk factor for morbidity and mortality in single ventricle palliation. In this study, we examined our experience with this challenging group of patients. Records of patients born between 2001 and 2019 with heterotaxy, who ne...

Commentary: Early repair of complete atrioventricular septal defect is the forward move.
https://doi.org/10.1016/j.jtcvs.2020.08.053
The Journal of Thoracic and Cardiovascular Surgery; Clark JB

Feb 24th, 2021 - Commentary: Early repair of complete atrioventricular septal defect is the forward move.|2021|Clark JB,|

First Trimester Use of Macrolide Antibiotics and Risk of Congenital Anomaly
https://www.medscape.com/viewarticle/944995

Feb 1st, 2021 - Takeaway First trimester use of macrolide antibiotics (mainly erythromycin, spiramycin, clarithromycin and azithromycin) was not associated with an increased risk of congenital heart defects (CHDs) as a whole. Erythromycin, clarithromycin and azit...

Characteristics of the pulmonary circulation in infants with complete atrioventricular ...
https://doi.org/10.1017/S1047951120004424
Cardiology in the Young; Doi H, Muneuchi J et. al.

Dec 11th, 2020 - Infants with complete atrioventricular septal defect occasionally accompany pulmonary hypertension; however, the pulmonary circulation can be altered by pulmonary vascular conditions as well as the left heart lesions. This study aimed to explore w...

see more →

News  2 results

First Trimester Use of Macrolide Antibiotics and Risk of Congenital Anomaly
https://www.medscape.com/viewarticle/944995

Feb 1st, 2021 - Takeaway First trimester use of macrolide antibiotics (mainly erythromycin, spiramycin, clarithromycin and azithromycin) was not associated with an increased risk of congenital heart defects (CHDs) as a whole. Erythromycin, clarithromycin and azit...

Congenital Heart Disease Risk Assessment
https://www.mdedge.com/obgyn/article/50932/congenital-heart-disease-risk-assessment/page/0/1

Jan 1st, 2011 - One study done in the United Kingdom, for instance, identified 727 adults with surgically modified major heart defects and their 393 live offspring. Of these infants, 16 were born with cardiac malformations, representing a total recurrence risk of.

see more →

Patient Education  2 results see all →