Key result
Comprehensive review summarizes the pathogenesis, genetics, diagnosis, and management of SCAD.
Why the study?
Despite advances in understanding and diagnostic imaging improving outcomes in SCAD, knowledge gaps and management challenges remain.
This review provides a contemporary summary of the diagnosis, genetics, imaging, and management of spontaneous coronary artery dissection.
May aid SCAD recognition via imaging in young women; leaves open optimal management pending prospective data.
Spontaneous coronary artery dissection (SCAD) has emerged over the last decade as an increasingly recognised cause of myocardial infarction, especially among younger women. The advances in our understanding of SCAD and the evolution of coronary angiography and intracoronary imaging have led to improved diagnoses and outcomes; however, there are still knowledge gaps and challenges in the management of this condition. In this review, we summarise the pathogenesis, genetics, diagnosis and acute and chronic management of patients with SCAD. We also provide focused updates on the following: genetics of SCAD, the role of cardiac CT angiography and cardiac MRI, the use of intracoronary imaging, revascularisation techniques and the overlap between SCAD and Takotsubo syndrome.
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Yang et al. (2025) conducted a review in Spontaneous coronary artery dissection (SCAD). This review summarizes the pathogenesis, genetics, diagnosis, and acute and chronic management of spontaneous coronary artery dissection, including the role of cardiac imaging.
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