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Pregnancy outcome in thoracic aortic disease data from the Registry Of Pregnancy And Cardiac disease
Laurence Campens1, Lucia Baris2, Nandita S Scott3
1Department of Cardiology, Ghent University Hospital, Gent, Belgium.
Insights
Pregnancy in women with thoracic aortic disease, including Marfan syndrome, generally has good outcomes when managed with current guidelines. Acute aortic dissection during pregnancy did not result in maternal or fetal mortality in this study.
Area of Science:
- Cardiology
- Genetics
- Obstetrics
Background:
- Cardiovascular disease is a leading cause of pregnancy-related death, with thoracic aortic dissection being a significant factor.
- Thoracic aortic disease is often linked to hereditary conditions and congenital heart defects like bicuspid aortic valve (BAV).
- Pregnancy poses a high risk for women with pre-existing aortopathy.
Purpose of the Study:
- To investigate maternal and fetal outcomes in pregnant women with thoracic aortic disease.
- To analyze data from the prospective global ESC EORP Registry Of Pregnancy And Cardiac disease (ROPAC) registry.
- To assess the safety and risks associated with thoracic aortic disease during pregnancy.
Main Methods:
- Analysis of data from the ROPAC registry, which prospectively enrolled 5739 women with cardiac disease.
- Focus on a subgroup of 189 women diagnosed with thoracic aortic disease.
- Review of maternal and fetal outcomes, including aortic dissection events and birth weights.
Main Results:
- Thoracic aortic disease was present in 3.3% of women, with Marfan syndrome (50%) and BAV (26%) being common causes.
- Aortic dilatation affected 58% of patients; 6% had a history of aortic dissection.
- Four cases of acute aortic dissection occurred (three Type A, one Type B) without maternal or fetal mortality. Beta-blocker use did not significantly impact fetal birth weight.
Conclusions:
- This study represents the largest prospective review of pregnancy risks in women with thoracic aortic disease.
- Overall pregnancy outcomes for women with thoracic aortic disease are favorable when managed according to current guidelines.
- Adherence to established guidelines ensures good outcomes for both mother and fetus in this high-risk population.
Background:
Cardiovascular disease is the leading cause of death during pregnancy with thoracic aortic dissection being one of the main causes. Thoracic aortic disease is commonly related to hereditary disorders and congenital heart malformations such as bicuspid aortic valve (BAV). Pregnancy is considered a high risk period in women with underlying aortopathy.
Methods:
The ESC EORP Registry Of Pregnancy And Cardiac disease (ROPAC) is a prospective global registry that enrolled 5739 women with pre-existing cardiac disease. With this analysis, we aim to study the maternal and fetal outcome of pregnancy in women with thoracic aortic disease.
Results:
Thoracic aortic disease was reported in 189 women (3.3%). Half of them were patients with Marfan syndrome (MFS), 26% had a BAV, 8% Turner syndrome, 2% vascular Ehlers-Danlos syndrome and 11% had no underlying genetic defect or associated congenital heart defect. Aortic dilatation was reported in 58% of patients and 6% had a history of aortic dissection. Four patients, of whom three were patients with MFS, had an acute aortic dissection (three type A and one type B aortic dissection) without maternal or fetal mortality. No complications occurred in women with a history of aortic dissection. There was no significant difference in median fetal birth weight if treated with a beta-blocker or not (2960 g (2358-3390 g) vs 3270 g (2750-3570 g), p value 0.25).
Conclusion:
This ancillary analysis provides the largest prospective data review on pregnancy risk for patients with thoracic aortic disease. Overall pregnancy outcomes in women with thoracic aortic disease followed according to current guidelines are good.
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