Abstract
Spontaneous aortic dissection (AoD) is a rare, life-threatening disease, yet it is the most common catastrophe of the aorta with a high mortality rate of 22–24% (Januzzi et al., J Am Coll Cardiol 43:665–669, 2004). Nontraumatic rupture of an aortic dissection can occur in patients without risk factors. However, there is a higher prevalence in patient populations with risk factors such as dilation of the aorta, connective tissue disorders, vasculitides, and other systemic conditions affecting the aorta. Patients under 40 years of age have a unique set of risk factors for aortic dissection compared to older patients: Marfan syndrome, bicuspid aortic valve, and larger aortic dimensions (Januzzi et al., J Am Coll Cardiol 43:665–669, 2004). The mortality in the younger group of patients is similar to that of the older group. A dramatic improvement has been observed in survival rates of patients with aortic dissections due to increased awareness, improved diagnostic modalities, and advances in operative repair and postoperative surveillance.
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Domnina, Y.A., Gardner, M.M., Morell, V.O. (2020). Aortic Dissection. In: Munoz, R., Morell, V., da Cruz, E., Vetterly, C., da Silva, J. (eds) Critical Care of Children with Heart Disease . Springer, Cham. https://doi.org/10.1007/978-3-030-21870-6_41
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