Characteristics of sudden arrhythmic death in a diverse, urban community

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• 作者：Daniel A.  ; Steinhaus MD^a ; Eric  ; Vittinghoff PhD ; MPH^b ; Ellen  ; Moffatt MD^c ; Amy P.  ; Hart MD^c ; Philip  ; Ursell MD^d ; Zian H.  ; Tseng MD ; MAS^e ;   ; ^{zhtseng@medicine.ucsf.edu}
• 刊名：American Heart Journal
• 出版年：2012
• 出版时间：January 2012
• 年：2012
• 卷：163
• 期：1
• 页码：125-131
• 全文大小：306 K

文摘

<h4 class=""h4"">Backgroundh4>Sudden cardiac death (SCD) remains a major public health problem; however, its true burden remains unknown with widely variable estimates of its incidence. We aimed to examine the contemporary epidemiology and autopsy characteristics of SCD in an ethnically diverse community.<h4 class=""h4"">Methodsh4>

Three physicians reviewed all deaths of individuals aged ?0 years reported to the San Francisco medical examiner in 2007 for presentations fitting World Health Organization (WHO) SCD criteria¡ªwithin 1 hour of symptom onset (witnessed) or within 24 hours of being observed alive and symptom free (unwitnessed). After comprehensive review of medical examiner investigation, WHO SCDs were classified as sudden arrhythmic death (SAD) or nonarrhythmic death. Coronary artery disease (CAD) and cardiac mass were evaluated in all SADs undergoing autopsy and compared with demographically similar accidental trauma control deaths.<h4 class=""h4"">Resultsh4>

We identified 252 WHO SCDs; 145 were SADs. Men had a 2.2-fold higher SAD rate (P < .0005). Blacks had a 3.15-fold higher SAD rate compared with whites (P = .003). Significant CAD was present in 38.9 % of SADs and associated with higher SAD risk compared with control deaths (OR 2.58, 95 % CI 1.12-5.97, P = .026). Mean cardiac mass was linearly associated with risk for SAD in cases without significant CAD (OR 2.06 per 100 g, 95 % CI 1.43-2.98, P < .0005).<h4 class=""h4"">Conclusionsh4>

In a diverse, urban population, SAD incidence varied substantially by gender and race. Significant CAD accounted for far fewer SADs than previous studies but remained associated with a 2.6-fold higher risk as compared with control deaths. These findings may reflect the evolving contemporary epidemiology of SCD.