Autor: |
Hobbach, Hans-Peter, Gibson, C., Giugliano, Robert, Hundertmark, Julia, Schaeffer, Christel, Tscherleniak, Wassillij, Schuster, Peter |
Zdroj: |
Journal of Thrombosis & Thrombolysis; Dec2003, Vol. 16 Issue 3, p167-174, 8p |
Abstrakt: |
Background: Previous studies have demonstrated that impaired renal function is associated with unfavourable outcomes in patients with acute coronary syndromes and following percutaneous coronary intervention. Methods: We hypothesized that serum creatinine (Cr) on admission is a useful predictor of mortality in fibrinolytic-eligible patients with ST-elevation myocardial infarction (MI). Data were collected from 352 patients with ST-elevation MI, 89% of patients underwent early invasive management. Results: 30-day and 6-month mortality were increased among patients with mild to moderate (Cr > 1.2–2.8 mg/dl) renal dysfunction compared to patients with normal (Cr ≤ 1.2 mg/dl) renal function (3.4% vs. 16.1%, p < 0.001 and 4.5% vs. 19.5%, p < 0.001). After adjustment for previously identified correlates of mortality in a multiple logistic regression model, higher Cr on admission remained independently associated with increased mortality (30-day, OR 4.78, 95%CI 1.55–14.73, p = 0.006; 6-month, 3.82 (1.45–10.11), p = 0.007). The incidence of mortality was reduced among those patients with renal dysfunction that also underwent acute percutaneous coronary intervention [30-day, OR 0.13, 95%CI 0.02–1.06, p < 0.03; 6-month, 0.23 (0.05–1.07), p < 0.05]. Conclusion: Cr on admission is a strong and independent predictor of mortality in patients with ST-elevation MI. This association does not appear to be mediated by reduced fibrinolytic efficacy, or by higher reinfarction rates among patients with renal dysfunction. Cr on admission is a rapid and widely available marker to identify high-risk patients with ST-elevation MI that have additional improvements in survival when treated with percutaneous coronary intervention. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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