Primary and secondary aortopathy associated with adult congenital heart disease - retrospective study
Ingrid Schusterova1, Alžbeta Banovcinova2, Marianna Vachalcova1
11th Department of Cardiology, East Slovak Institute of Cardiovascular Diseases, Faculty of Medicine, Pavol Jozef Safarik University in Kosice, Kosice, Slovakia.
Insights
Adults with congenital heart disease and aortopathy, particularly secondary aortopathy, show significantly larger aortic diameters. Regular monitoring of aortic size is crucial for these patients.
Area of Science:
- Cardiovascular Medicine
- Adult Congenital Heart Disease
- Aortopathy
Background:
- Aortopathy is a common complication in adult patients with congenital heart disease (CHD).
- Understanding the incidence and characteristics of primary and secondary aortopathy in this population is essential.
Purpose of the Study:
- To investigate the incidence and clinical features of primary and secondary aortopathy in adult CHD patients.
- To compare aortic dimensions between patients with and without aortopathy, and between primary and secondary aortopathy groups.
Main Methods:
- Retrospective analysis of adult CHD patients from a specialized registry.
- Inclusion of 35 patients with primary aortopathy, 12 with secondary aortopathy, and 64 controls with non-aortopathy CHD.
- Comparison of aortic root and ascending aorta diameters using follow-up data.
Main Results:
- Patients with primary and secondary aortopathy exhibited significantly larger ascending aorta and aortic root diameters compared to controls.
- Secondary aortopathy patients demonstrated statistically larger ascending aorta diameters than primary aortopathy patients.
- Aortic root and ascending aorta operations were infrequent during follow-up.
Conclusions:
- Secondary aortopathy in adult CHD patients is associated with more pronounced dilation of the ascending aorta and aortic root.
- Routine surveillance of aortic diameters is recommended for adult CHD patients with aortopathy.
Background:
Primary and secondary aortopathy are frequently encountered in patients with congenital heart disease. The aim of this study is to present our experience and the incidence of primary and secondary adult CHD-associated aortopathy.
Methods:
The cohort is comprised of adult patients with congenital heart disease from the registry of the Eastern Slovakia Institute of Cardiovascular Diseases. Data from the last follow-up examinations are included in this study. In the primary and secondary aortopathy groups were 35 and 12 patients respectively. As a control group were selected 64 patients with non aortopathy associated congenital heart disease (atrial and ventricular septal defect).
Results:
Patients with primary and secondary aortopathy had larger ascending aorta/aortic root diameters than the control group (36.28 (26-49) mm vs 30.25 (21-41) mm p = 0.000113, 33.82 27-49) mm vs 29.03 (19-38)mm p = 0.000366 and 42.1 (30-50) mm vs 30.25 (21-41) mm, p = 0.000106, 35.67 (27-48) mm vs 29.03 (19-38) mm, p = 0.000119 respectively). Moreover, patients with secondary aortopathy had statistically significant larger ascending aorta diameter compared to the patients with primary aortopathy (42.1 (30-50) mm vs 36.28 (26-49) mm p = 0.030). During the follow-up period, were performed only in 2 patients (one from each group) operations on the aortic root and the ascending aorta due to aortic root or ascending aorta dilatation.
Conclusion:
More patients with secondary aortopathy had dilated ascending aorta/ aortic root, as well as larger aortic diameters compare to the patients with primary aortopathy. Routine follow-up of these patients with attention to aortic diameter is necessary.
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