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Published on: February 20, 2017
Juxtaposition of the Atrial Appendages: A Large Echocardiographic Series
Katherine Dalldorf1, Ira Parness2, David Ezon3
1Mount Sinai Hospital, 1 Gustave L Levy Place, New York, NY, 10029, USA.
Insights
Juxtaposition of atrial appendages, a rare congenital heart variant, is analyzed in this large echocardiographic study. Findings detail its prevalence and associations with specific heart defects, crucial for surgical planning.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Juxtaposition of atrial appendages is a rare congenital heart anomaly.
- Its prevalence and associated cardiac anomalies require further investigation.
- Accurate identification is critical for surgical interventions like balloon atrial septostomy.
Purpose of the Study:
- To determine the prevalence of juxtaposed atrial appendages.
- To identify associated intracardiac and extracardiac anomalies.
- To analyze the association of juxtaposed atrial appendages with specific congenital heart lesions.
Main Methods:
- Retrospective analysis of the Mt. Sinai echocardiogram database (EchoLAN) from 1992-2019.
- Review of 49 patients with juxtaposed atrial appendages for associated anomalies.
- Calculation of prevalence and statistical analysis (Fisher's exact test) for associations.
Main Results:
- Forty-nine patients (1.2/1000) had juxtaposed atrial appendages: 38 with left juxtaposed right atrial appendage (LJRAA) and 11 with right juxtaposed left atrial appendage (RJLAA).
- LJRAA was associated with tricuspid atresia (22%), d-TGA (6%), l-TGA (1%), and DORV (5%).
- Associated anomalies included dextrocardia, transposition, and tricuspid atresia for LJRAA; bicuspid aortic valve and LV hypoplasia for RJLAA.
Conclusions:
- This study provides the largest echocardiographic data on juxtaposed atrial appendages.
- It confirms the prevalence and highlights significant associations with specific congenital heart diseases.
- Understanding these associations is vital for improved diagnosis and surgical management.
Abstract:
Juxtaposition of the atrial appendages is known to occur in specific congenital heart lesions. Recognition of these variants is critical in balloon atrial septostomy and atrial switch operations. There remains little clinical data on the prevalence and associations of these lesions. This is the largest echocardiographic study of juxtaposition of the atrial appendages. This is a retrospective study using the Mt. Sinai echocardiogram database (EchoLAN), which contains echocardiogram reports performed or reviewed at Mt. Sinai Hospital (New York, NY) between 1992 and 2019. Each report was reviewed for associated intracardiac and extracardiac anomalies and the prevalence of juxtaposed atrial appendage among specific diagnosis, including tricuspid atresia, transposition of the great arteries, and double outlet right ventricle, was calculated. Descriptive and analytical statistics were performed as applicable, including Fisher's exact test, with p value < 0.05 considered statistically significant. Forty-nine patients had juxtaposed atrial appendages (1.2/1000 patients): Thirty-eight had LJRAA (0.9 per 1000 patients) and eleven had RJLAA (0.3 per 1000 patients). LJRAA was seen in 22% of tricuspid atresia, 6% of d-TGA, 1% of l-TGA, and 5% of DORV. RJLAA was seen in 2% of DORV, and none of the other lesions. Of associated lesions, dextrocardia, mesocardia, transposition, tricuspid atresia, double inlet left ventricle, and pulmonary valve stenosis were more likely to be present in LJRAA, while bicuspid aortic valve and left ventricular hypoplasia were more likely to be present in RJLAA. This study reaffirms our understanding of juxtaposition of the atrial appendages, its prevalence, and clinical importance.
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