Differential clinical features and long-term prognosis of acute aortic syndrome according to disease entity

Jung-Min Ahn1, Hoyun Kim1, Osung Kwon1

  • 1Division of Cardiology, Heart Institute, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Republic of Korea.

Insights

Acute aortic syndrome (AAS) prognosis depends on disease type, not just location. Intramural hematoma (IMH) offers better survival than aortic dissection (AD) in both acute and long-term outcomes.

Area of Science:

  • Cardiovascular Medicine
  • Thoracic Surgery
  • Vascular Surgery

Background:

  • Acute aortic syndrome (AAS) encompasses intramural hematoma (IMH) and aortic dissection (AD).
  • Prognosis in AAS is influenced by disease entity and anatomical location (Type A vs. Type B).

Purpose of the Study:

  • To evaluate the acute and long-term prognosis of AAS based on disease entity (IMH vs. AD) and anatomical location (Type A vs. Type B).

Main Methods:

  • A total of 1012 patients with AAS were analyzed retrospectively between 1993 and 2015.
  • Patients were categorized by disease entity (AD or IMH) and anatomical location (Type A or Type B).
  • In-hospital and long-term mortality (aortic death) were assessed using survival analysis and hazard ratios.

Main Results:

  • IMH patients were older, more frequently female, and had more distal aorta involvement compared to AD patients.
  • Overall in-hospital mortality was 8.6%. Type A AD had the highest mortality (15.0%), followed by Type A IMH (8.0%), Type B AD (5.0%), and Type B IMH (1.5%).
  • During long-term follow-up, AD and Type A location were associated with higher aortic death risk. After 90 days, disease entity, not location, remained an independent predictor of aortic death.

Conclusions:

  • Clinical features and outcomes differ significantly between IMH and AD patients.
  • Both early and long-term survival are better for IMH compared to AD.
  • Disease entity is an independent prognostic factor for both acute and long-term mortality in AAS, alongside anatomical location.
Abstract

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