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Mechanism of benefit of combination thrombolytic therapy for acute myocardial infarction: a quantitative angiographic and hematologic study.

Publication ,  Journal Article
Popma, JJ; Califf, RM; Ellis, SG; George, BS; Kereiakes, DJ; Samaha, JK; Worley, SJ; Anderson, JL; Stump, D; Woodlief, L
Published in: J Am Coll Cardiol
November 15, 1992

OBJECTIVES: The goal of this study was to lend insight into the mechanisms responsible for the beneficial effects of combination thrombolytic therapy. BACKGROUND: Combination thrombolytic therapy for acute myocardial infarction has been associated with less reocclusion and fewer in-hospital clinical events than has monotherapy. METHODS: Infarct-related quantitative coronary dimensions and hemostatic protein levels were evaluated in 287 patients with acute myocardial infarction during the early (90-min) and convalescent (7-day) phases after administration of recombinant tissue-type plasminogen activator (rt-PA), urokinase or combination rt-PA and urokinase. RESULTS: Minimal lumen diameter was similar in the 90-min and 7-day phases after treatment with rt-PA, urokinase and combination rt-PA and urokinase (0.72 +/- 0.45 mm, 0.62 +/- 0.53 mm and 0.75 +/- 0.58 mm, respectively, at 90 min, p = 0.16; and 1.05 +/- 0.56 mm, 1.12 +/- 0.72 mm and 0.94 +/- 0.54 mm, respectively, at 7 days, p = 0.22). In-hospital clinical event and reocclusion rates were less frequent in patients receiving combination therapy than in those receiving monotherapy (25% vs. 38% and 32% for rt-PA and urokinase, respectively, p = 0.084; and 3% vs. 13% and 9% for rt-PA and urokinase, respectively, p = 0.03), but these events were unrelated to early or late coronary dimensions. Patients receiving combination therapy or urokinase monotherapy had significantly higher peak fibrin degradation products (1,307 +/- 860 and 1,285 +/- 898 micrograms/ml vs. 435 +/- 717 micrograms/ml, respectively, p < 0.0001) and lower nadir fibrinogen levels (0.85 +/- 1.00 and 0.75 +/- 0.53 g/liter vs. 1.90 +/- 0.86 g/liter, respectively, p < 0.0001) than did those receiving rt-PA monotherapy. Peak fibrinogen degradation products indirectly correlated (p = 0.004) and baseline (p = 0.026) and nadir (p = 0.089) fibrinogen levels directly correlated with reocclusion. CONCLUSIONS: Lower in-hospital clinical event and reocclusion rates observed with combination thrombolytic therapy may relate to systemic hematologic factors rather than to the residual lumen obstruction after thrombolysis.

Published In

J Am Coll Cardiol

DOI

ISSN

0735-1097

Publication Date

November 15, 1992

Volume

20

Issue

6

Start / End Page

1305 / 1312

Location

United States

Related Subject Headings

  • Ventricular Function, Left
  • Urokinase-Type Plasminogen Activator
  • Tissue Plasminogen Activator
  • Time Factors
  • Thrombolytic Therapy
  • Regression Analysis
  • Recombinant Proteins
  • Myocardial Infarction
  • Humans
  • Hemostasis
 

Citation

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Popma, J. J., Califf, R. M., Ellis, S. G., George, B. S., Kereiakes, D. J., Samaha, J. K., … Woodlief, L. (1992). Mechanism of benefit of combination thrombolytic therapy for acute myocardial infarction: a quantitative angiographic and hematologic study. J Am Coll Cardiol, 20(6), 1305–1312. https://doi.org/10.1016/0735-1097(92)90241-e
Popma, J. J., R. M. Califf, S. G. Ellis, B. S. George, D. J. Kereiakes, J. K. Samaha, S. J. Worley, J. L. Anderson, D. Stump, and L. Woodlief. “Mechanism of benefit of combination thrombolytic therapy for acute myocardial infarction: a quantitative angiographic and hematologic study.J Am Coll Cardiol 20, no. 6 (November 15, 1992): 1305–12. https://doi.org/10.1016/0735-1097(92)90241-e.
Popma JJ, Califf RM, Ellis SG, George BS, Kereiakes DJ, Samaha JK, et al. Mechanism of benefit of combination thrombolytic therapy for acute myocardial infarction: a quantitative angiographic and hematologic study. J Am Coll Cardiol. 1992 Nov 15;20(6):1305–12.
Popma, J. J., et al. “Mechanism of benefit of combination thrombolytic therapy for acute myocardial infarction: a quantitative angiographic and hematologic study.J Am Coll Cardiol, vol. 20, no. 6, Nov. 1992, pp. 1305–12. Pubmed, doi:10.1016/0735-1097(92)90241-e.
Popma JJ, Califf RM, Ellis SG, George BS, Kereiakes DJ, Samaha JK, Worley SJ, Anderson JL, Stump D, Woodlief L. Mechanism of benefit of combination thrombolytic therapy for acute myocardial infarction: a quantitative angiographic and hematologic study. J Am Coll Cardiol. 1992 Nov 15;20(6):1305–1312.
Journal cover image

Published In

J Am Coll Cardiol

DOI

ISSN

0735-1097

Publication Date

November 15, 1992

Volume

20

Issue

6

Start / End Page

1305 / 1312

Location

United States

Related Subject Headings

  • Ventricular Function, Left
  • Urokinase-Type Plasminogen Activator
  • Tissue Plasminogen Activator
  • Time Factors
  • Thrombolytic Therapy
  • Regression Analysis
  • Recombinant Proteins
  • Myocardial Infarction
  • Humans
  • Hemostasis