Spontaneous coronary artery dissection (SCAD) has emerged as an important
cause of acute coronary syndrome, myocardial infarction, and sudden death,
particularly among young women and individuals with few conventional
atherosclerotic risk factors. Patient-initiated research has spurred increased
awareness of SCAD, and improved diagnostic capabilities and findings from large
case series have led to changes in approaches to initial and long-term
management and increasing evidence that SCAD not only is more common than
previously believed but also must be evaluated and treated differently from
atherosclerotic myocardial infarction. High rates of recurrent SCAD; its
association with female sex, pregnancy, and physical and emotional stress
triggers; and concurrent systemic arteriopathies, particularly fibromuscular
dysplasia, highlight the differences in clinical characteristics of SCAD
compared with atherosclerotic disease. Recent insights into the causes of,
clinical course of, treatment options for, outcomes of, and associated
conditions of SCAD and the many persistent knowledge gaps are presented.