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Methodist Debakey Cardiovasc J ; 20(2): 51-58, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38495666

RESUMO

Thoracic aortic disease (TAD) poses substantial risks during pregnancy, particularly for women with genetic conditions such as Marfan syndrome, Loeys-Dietz syndrome, and vascular Ehlers-Danlos syndrome. This review examines the epidemiology, risk assessment, and management of TAD in pregnancy. Preconception counseling is vital considering the hereditary nature of TAD and potential pregnancy-related complications. Genetic testing and imaging surveillance aid in risk assessment. Medical management, including beta-blockade and strict blood pressure control, is essential throughout pregnancy. Surgical interventions may be necessary in certain cases. A multidisciplinary approach involving cardiologists, obstetricians, cardiac surgeons, anesthesiologists, and other specialists with expertise in cardio-obstetrics is essential for optimal outcomes. Patient education and shared decision-making play vital roles in navigating the complexities of TAD in pregnancy and improving maternal and neonatal outcomes.


Assuntos
Doenças da Aorta , Síndrome de Loeys-Dietz , Síndrome de Marfan , Gravidez , Recém-Nascido , Humanos , Feminino , Aorta , Síndrome de Loeys-Dietz/complicações , Síndrome de Marfan/diagnóstico , Síndrome de Marfan/epidemiologia , Síndrome de Marfan/terapia , Medição de Risco
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