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Spontaneous coronary artery dissection: one entity with several therapeutic options
Julien Wain-Hobson1, Vincent Roule, Ziad Dahdouh
1Department of Cardiology, University Hospital of Caen, 14033 Caen Cedex, France.
Insights
Spontaneous coronary artery dissection (SCAD) is a rare cause of heart attack. This study presents four cases, highlighting varied treatments from medication to surgery, emphasizing the need for prompt recognition and management.
Area of Science:
- Cardiology
- Vascular Medicine
Background:
- Spontaneous coronary artery dissection (SCAD) is an uncommon cause of acute coronary syndrome (ACS) and sudden cardiac death.
- Predisposing factors are numerous, yet specific treatment guidelines remain underdeveloped.
- Early identification is critical for effective patient management.
Observation:
- This report details four cases of SCAD presenting with ST-elevation.
- Three cases involved women in the postpartum period.
- One case was associated with Marfan syndrome.
Findings:
- The cases illustrate a spectrum of clinical presentations and outcomes.
- Therapeutic interventions ranged from conservative medical management to revascularization procedures.
- Treatment options included medical therapy, percutaneous coronary intervention (stenting), and coronary artery bypass graft surgery.
Implications:
- The findings underscore the importance of considering SCAD in patients with ACS, particularly in specific demographics like postpartum women or those with connective tissue disorders.
- The diverse treatment approaches highlight the lack of standardized protocols and the need for further research.
- Further investigation into optimal management strategies for SCAD is warranted to improve patient outcomes.
Abstract:
Spontaneous coronary artery dissection is an unusual and a rare cause of acute coronary syndrome and sudden death with multiple predisposing factors. Prompt recognition is crucial for appropriate patient management, but specific guidelines for optimal treatment are lacking. We report four cases of women with spontaneous coronary artery dissection revealed by ST-segment elevation, three in women during postpartum and one case associated with a Marfan syndrome. Our cases span the different therapeutic options from medical treatment, stenting, to coronary artery bypass graft surgery.
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