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Novel and Innovative Hybrid Technique for Type A Aortic Dissection
Published on: March 28, 2025
Aortic Dissection in Pregnancy: Management Strategy and Outcomes
Jun-Ming Zhu1, Wei-Guo Ma2, Sven Peterss3
1Department of Cardiovascular Surgery, Beijing Anzhen Hospital of Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, and Beijing Engineering Research Center of Vascular Prostheses, Beijing, China; Fu Wai Hospital and Cardiovascular Institute, Chinese Academy of Medical Sciences, Beijing, China.
Aortic dissection in pregnancy, often linked to Marfan syndrome, requires tailored management. For Type A dissections after 28 weeks, delivery then repair offers good outcomes; before 28 weeks, prioritize maternal survival. Type B dissections benefit from nonsurgical approaches.
Area of Science:
- Cardiology
- Obstetrics
- Vascular Surgery
Background:
- Aortic dissection during pregnancy is a rare but life-threatening condition with limited clinical data.
- This study focuses on the etiology, management, and outcomes of aortic dissection in a cohort of pregnant patients.
Purpose of the Study:
- To analyze the clinical characteristics, treatment strategies, and survival rates of pregnant women experiencing aortic dissection.
- To provide evidence-based recommendations for managing aortic dissection in pregnancy based on dissection type and gestational age.
Main Methods:
- A retrospective review of 25 pregnant patients with aortic dissection between June 1998 and February 2015.
- Classified dissections into Type A (TAAD) and Type B (TBAD), noting the high prevalence of Marfan syndrome (68%).
- Management strategies were determined by dissection type and gestational weeks (GWs).
Main Results:
- TAAD (80%) was predominantly managed surgically. Maternal mortality varied by management strategy (14.3% to 100%), with fetal survival rates also differing significantly.
- TBAD (20%) saw 60% surgical management, with no maternal deaths but 100% fetal mortality in the surgical group.
- Overall 5-year maternal survival was 68.6% in the TAAD group, with late follow-up revealing additional maternal and fetal deaths.
Conclusions:
- Marfan syndrome is a key risk factor for aortic dissection in pregnancy.
- For TAAD after 28 GWs, a "delivery first" approach followed by surgical repair optimizes maternal and fetal survival.
- For TAAD before 28 GWs, prioritizing maternal survival is crucial; nonsurgical management is preferred for TBAD in pregnancy.
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