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Abstract
Coronary artery anomalies (CAAs) are a diverse group of congenital disorders whose
manifestations and pathophysiological mechanisms are highly variable. The subject
of CAAs is undergoing profound evolutionary changes related to the definition, morphogenesis,
clinical presentation, diagnostic workup, prognosis, and treatment of these anomalies.
To understand the clinical impact of CAAs, the fundamental challenge is the firm establishment,
for a particular type of CAA, of a mechanism capable of interference with the coronary
artery's function, which is to provide adequate blood flow to the dependent myocardium.
The present review focuses on anomalous origination of a coronary artery from the
opposite sinus--the subgroup of CAAs that has the most potential for clinical repercussions,
specifically sudden death in the young. For this subgroup, solid diagnostic screening
protocols should be established, especially for athletes and other young individuals
subjected to extreme exertion. Intravascular ultrasonography is the preferred means
to evaluate the mechanisms responsible for ischemia in anomalous origination of a
coronary artery from the opposite sinus and other potentially significant CAAs. Patients
symptomatic of anomalous origination of a coronary artery from the opposite sinus
may undergo medical treatment/observation, coronary angioplasty with stent deployment,
or surgical repair. To be competent to advise CAA carriers, especially in the context
of sporting or military activities, cardiologists should undergo specific training
in these disorders. Only multicenter collaboration on protocols dedicated to CAAs
can give rise to the large-scale studies needed to define the prognosis and optimal
treatment of these disorders.
Congenital coronary anomalies are associated with sudden death and exercise-related death. Clarification of the risk and mechanisms of sudden death in patients with coronary anomalies may aid in decisions on intervention. The clinicopathologic records of 242 patients with isolated coronary artery anomalies were reviewed for information on mode of death and abnormalities of the initial segment (acute angle takeoff, valvelike ridges or aortic intramural segments) and course of the anomalous coronary artery. Cardiac death occurred in 142 patients (59%); 78 (32%) of these deaths occurred suddenly. Of sudden deaths, 45% occurred with exercise. Sudden death (28 of 49, 57%) and exercise-related death (18 of 28, 64%) were most common with origin of the left main coronary artery from the right coronary sinus. Anomalous origin of the right coronary artery from the left coronary sinus was also commonly associated with exercise-related sudden death (6 of 13 sudden deaths, 46%). High risk anatomy involved abnormalities of the initial coronary artery segment or coursing of the anomalous artery between the pulmonary artery and aorta. Younger patients (less than or equal to 30 years old) were significantly more likely than older patients (greater than or equal to 30 years old) to die suddenly (62% vs. 12%, p = 0.0001) or during exercise (40% vs. 2%, p = 0.00001) despite their low frequency of significant atherosclerotic coronary artery disease (1% vs. 40%, p = 0.00001). Younger patients (less than or equal to 30 years old) with an isolated coronary artery anomaly are at risk of dying suddenly and with exercise. Therefore, greater effort for early detection and surgical repair of these lesions is warranted.
Coronary arteries anomalies may be part of complex congenital malformations of the heart or be an isolated defect. In our anatomic collection of congenital heart disease, an isolated anomalous origin of coronary arteries was observed in 27 of 1,200 specimens (2.2%): left coronary artery from pulmonary trunk in five, origin from the wrong aortic sinus in 12 (both right and left coronary artery from the right sinus in four and from the left sinus in seven, left coronary artery from the posterior sinus in one), left circumflex branch from right aortic sinus or from very proximal right coronary artery in three, high takeoff of right coronary artery in three, stenosis of the coronary ostia attributable to valvelike ridge in four. In 16 (59%) patients (12 males and 4 females, age ranging from 2 months to 53 years; median, 14), the final outcome was sudden death; it occurred in all cases of left coronary artery origin from right aortic sinus, in 43% of right coronary artery origin from left aortic sinus, and in 40% of the left coronary artery from the pulmonary trunk. Sudden death was precipitated by effort in eight (50%) and was the first manifestation of the disease in eight (50%); previous symptoms consisted of recurrent syncope in four, palpitations in three, and chest pain in one. Five patients who died suddenly during effort were athletes. In conclusion, (1) more than half of our postmortem cases with anomalous origin of coronary arteries died suddenly, (2) all but two patients with sudden death had anomalous coronary artery origin from the aorta itself, (3) the fatal event was frequently precipitated by effort, (4) palpitations, syncope, and ventricular arrhythmias were the only prodromic symptoms and signs. Recognition during life of these coronary anomalies, by the use of noninvasive procedures, is mandatory to prevent the risk of sudden death and to plan surgical correction if clinically indicated.
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