Non-invasive risk stratification within 48 h of hospital admission in patients with unstable coronary disease.

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Abstract
In this study we evaluated the prognostic value of three methods of early risk estimation in patients with unstable coronary disease. The methods evaluated were: clinical risk estimation at hospital admission, continuous ST analysis with computerized vectorcardiography for 24 h and serial measurements of creatinine kinase-MB for 48 h. Twenty-seven (14%) of the 195 patients died or had a non-fatal infarction within one year. Clinical risk evaluation correctly identified a subgroup of patients with low risk but did not otherwise predict outcome. Fifty-six (29%) patients had ST vector magnitude episodes on vectorcardiography, 70 (38%) had three or more episodes of ST change vector magnitude and 74 (38%) had a peak creatinine kinase-MB value of 6 μg. 1−1 or more. The even rate for patients with ST vector magnitude episodes (23%) was significantly higher than for those without (10%; PP−1 the event rate was 23% and 8% respectively (P<0·01). The positive predictive value of having none, either one or both of the ST or creatinine kinase-MB markers positive was incremental. Continuous vectorcardiographic monitoring of ischaemia in combination with serial creatinine kinase-MB measurement considerably improves risk stratification in unstable coronary disease.

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