Circulation, Vol 83, 170-175, Copyright © 1991 by American Heart Association
DC Sane, DC Stump, EJ Topol, KN Sigmon, WK Clair, DJ Kereiakes, BS George, MF Stoddard, ER Bates and RS Stack
To determine whether there are differences in responses to thrombolytic
therapy in certain populations, the data for the Thrombolysis and
Angioplasty in Myocardial Infarction (phase 1) study were analyzed for
black and white patients. Baseline variables including risk factors and
extent of coronary artery disease were similar in the 352 white and 24
black patients. The time from onset of chest pain to recombinant tissue-
type plasminogen activator (rt-PA) therapy and rt-PA dosing regimens were
the same in the two groups. The patency rate of the infarct- related artery
at 90 minutes was 91% for blacks and was 72% for whites (p = 0.051). Blacks
displayed significantly lower nadir fibrinogen levels (0.57 +/- 0.62 versus
1.3 +/- 0.76 g/l, p less than 0.0001), greater delta fibrinogen
(baseline-nadir) (2.7 +/- 1.1 versus 1.7 +/- 1.1 g/l, p less than 0.0001),
and increased peak levels of fibrin(ogen) degradation products (837 +/- 865
versus 245 +/- 475 micrograms/ml, p less than 0.0001). rt-PA antigen levels
tended to be higher in blacks than in whites (2.8 +/- 2.2 versus 2.2 +/-
3.2 micrograms/ml [p = 0.10] at the peak and 1.6 +/- 1.3 versus 0.99 +/-
1.4 micrograms/ml [p = 0.06] at the end of the maintenance infusion). Major
clinical outcomes including survival until time of hospital discharge (92%
black versus 93% white, p = 0.68) were not significantly different.
However, despite undergoing fewer angioplasty procedures (25% versus 46.3%,
p = 0.047), blacks received more transfusions (58.8% versus 19.5% were
administered greater than or equal to 2 units packed erythrocytes, p =
0.001).(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Racial differences in responses to thrombolytic therapy with recombinant tissue-type plasminogen activator. Increased fibrin(ogen)olysis in blacks. The Thrombolysis and Angioplasty in Myocardial Infarction Study Group
Department of Medicine, Duke University, Durham, N.C.
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