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Assessment of Right Ventricular Structure and Function in Mouse Model of Pulmonary Artery Constriction by Transthoracic Echocardiography
Published on: February 3, 2014
[Echocardiographic diagnosis of the aorto-pulmonary window]
C Apitz1, R Kaulitz, L Sieverding
1Abteilung Kinderheilkunde II (Kardiologie, Intensivmedizin, Pulmologie), Universitätsklinikum Tübingen. christian.apitz@med.uni-tuebingen.de
Insights
Echocardiography effectively diagnoses aortopulmonary windows, revealing characteristic left heart dilation and shunting. Careful assessment is crucial due to frequent associated cardiac anomalies.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Medical Imaging
Background:
- Aortopulmonary window is a rare congenital cardiac malformation.
- It involves a connection between the ascending aorta and the main pulmonary artery.
- Associated cardiovascular malformations are common.
Purpose of the Study:
- To report the echocardiographic features of aortopulmonary window.
- To assess the diagnostic limitations of echocardiography for this condition.
- To highlight the importance of identifying associated anomalies.
Main Methods:
- Retrospective analysis of 5 consecutive patients treated between 7/2000 and 11/2005.
- Utilized 2D-echocardiography, pulsed-wave Doppler, and continuous-wave Doppler.
- Echocardiography was used to visualize the window and assess associated defects.
Main Results:
- Characteristic echocardiographic feature: dilation of the left atrium and ventricle due to left-to-right shunt.
- The aortopulmonary window was visualized in all patients via 2D-echocardiography.
- Doppler findings included diastolic negative flow in the descending aorta and systemic arteries.
- All patients had significant associated cardiovascular malformations accurately diagnosed by echocardiography.
- Coronary anomalies were noninvasively excluded in all cases.
Conclusions:
- Echocardiography is the primary diagnostic method for aortopulmonary window.
- Systematic investigation is essential due to frequent, significant associated cardiac anomalies.
- Cardiac catheterization is reserved for cases with unclear coronary anatomy or pulmonary hypertension in older patients.
Unlabelled:
PURPOSE/MATERIALS AND METHODS: The aorto-pulmonary window is a rare congenital cardiac malformation consisting of a connection between the ascending aorta and the main pulmonary artery. Based on 5 consecutive patients who were treated in our tertiary referral centre between 7/2000 and 11/2005, we report the echocardiographic features as well the limitations of this diagnostic method in the assessment of this rare malformation.
Results:
Dilation of the left atrium and ventricle due to the large left-to-right-shunt was the characteristic echocardiographic feature in all patients with aorto-pulmonary window. In all patients we were able to visualise the window by 2D-echocardiography. Pulsed- and continuous-wave Doppler showed diastolic negative flow in the descending aorta and in systemic arteries due to left-to-right shunting in diastole via the aorto-pulmonary window. All 5 patients had significant associated cardiovascular malformations. They were accurately diagnosed by echocardiography. Coronary anomalies could be excluded noninvasively in all patients.
Conclusion:
Echocardiography is the method of choice for diagnosis of aortopulmonary window. Detection of aortopulmonary window, however, requires a systematic and careful investigation of all cardiovascular anatomic details, since this anomaly is frequently associated with substantial additional cardiac anomalies, which would by themselves be sufficient to explain the haemodynamic abnormalities of the patient. Cardiac catheterisation is required only in cases with inadequate information about coronary artery anatomy or in older patients with pulmonary hypertension, to determine the patient's suitability for surgical correction.
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