Pregnancy-associated spontaneous coronary artery dissection accounted for 43% of myocardial infarctions in pregnant women.
This AHA scientific statement establishes SCAD as a distinct, underdiagnosed cause of ACS that predominantly affects women and requires tailored diagnostic and therapeutic strategies.
Effect estimate: null (95% CI null)
p-value: p=null
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.
Hayes et al. (Thu,) conducted a other in Spontaneous Coronary Artery Dissection (SCAD). SCAD management vs. Atherosclerotic myocardial infarction management was evaluated on Prevalence of SCAD as a cause of acute coronary syndrome (ACS) (null, 95% CI null, p=null). Pregnancy-associated spontaneous coronary artery dissection accounted for 43% of myocardial infarctions in pregnant women.
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