Detailed methods have been published earlier (6 (link), 11 (link)). Briefly, the ongoing Oregon Sudden Unexpected Death Study (Ore-SUDS) prospectively identified all cases of SCD that occurred among residents of the Portland, OR metropolitan area (pop. approx. 1,000,000) during Feb 2002-Jan 2005 from the emergency medical response system, the Medical Examiner’s office, and local hospitals. During Feb 2005-Jan 2006, identification was limited to the majority subset identified by first responders or investigated by the medical examiner. SCD was defined as a sudden unexpected pulseless condition of likely cardiac etiology. If un-witnessed, SCDs were those in which patients were found dead within 24 hours of having last been seen alive and in normal state of health. Subjects with likely SCD were assigned a diagnosis of SCD after a review of available medical records and the circumstances of arrest; survivors of SCD were included. Subjects with chronic terminal illnesses (e.g. cancer), known non-cardiac causes of sudden death (e.g. pulmonary embolism, CVA), traumatic deaths and overdoses were excluded. Cases were also required to have documented significant CAD or if aged ≥50 years were assumed to have CAD (based on 95% likelihood of CAD in SCD cases aged≥50 years) (12 (link), 13 ). CAD was defined as ≥50% stenosis of a major coronary artery or history of myocardial infarction, coronary artery bypass grafting or percutaneous coronary intervention.
During the same time period a control group of subjects from the same geographic region were identified who had CAD, but no history of SCD. They had either been transported by the Emergency Medical Response system for complaints suggestive of ongoing coronary ischemia, recruited from clinics of participating health systems, or received a coronary angiogram revealing significant CAD. After consent was obtained, medical records for each potential control subject were reviewed; those with documented CAD (as defined above) were enrolled.
During the same time period a control group of subjects from the same geographic region were identified who had CAD, but no history of SCD. They had either been transported by the Emergency Medical Response system for complaints suggestive of ongoing coronary ischemia, recruited from clinics of participating health systems, or received a coronary angiogram revealing significant CAD. After consent was obtained, medical records for each potential control subject were reviewed; those with documented CAD (as defined above) were enrolled.