We developed a logistic regression model with data from the GUSTO-I trial to predict mortality rate differences in individual patients who received accelerated tissue plasminogen activator (TPA) versus streptokinase treatment for acute myocardial infarction. A nomogram was developed from a reduced version of this model that approximated the underlying risk of patients treated with streptokinase, and thus the benefit of TPA. The 30-day mortality rate with accelerated TPA was 0.063 versus 0.073 with streptokinase and subcutaneously administered heparin and 0.074 with streptokinase and intravenously administered heparin. No baseline patient characteristics were significantly associated with a different relative effect of TPA. Older patients and those with anterior infarction, higher Killip classification (except Killip class IV), lower blood pressure, and increased heart rate had the greatest absolute benefit with accelerated TPA. Patients with acute myocardial infarction who had more high-risk characteristics derived a greater absolute benefit from treatment with accelerated TPA versus streptokinase.

, , , , , , , , , , , , , , , , , , , , , , , , , , , ,
hdl.handle.net/1765/5550
American Heart Journal
Erasmus MC: University Medical Center Rotterdam

Califf, R., Woodlief, L., Harrell, F., Lee, K., White, H., Guerci, A., … Topol, E. (1997). Selection of thrombolytic therapy for individual patients: development of a clinical model. American Heart Journal, 133, 630–639. Retrieved from http://hdl.handle.net/1765/5550