Circulation, Vol 81, 1818-1825, Copyright © 1990 by American Heart Association
B Brenner, CW Francis, S Totterman, CM Kessler, AK Rao, R Rubin, HC Kwaan, KR Gabriel and VJ Marder
Plasma cross-linked fibrin-degradation products were analyzed using a D-
dimer (DD) immunoassay in patients with deep vein thrombosis (DVT) or acute
myocardial infarction (MI) treated with fibrinolytic therapy, and the
results were correlated with clot lysis documented angiographically. In 13
patients with DVT, the mean DD concentration increased 10-fold (1,074 +/-
252 to 10,333 +/- 1,004 ng/ml) during therapy, but neither the peak level
nor the DD concentration integrated over the course of therapy correlated
with clot lysis. Since plasma DD can derive from degradation of soluble
plasma fibrin as well as from thrombi, the contribution of the former was
estimated by in vitro incubation of the pretreatment plasma with
plasminogen activator. Subtraction of this value from the measured
posttreatment DD concentration provided a "corrected" level that
represented DD originating from lysis of thrombi. This modification
resulted in improved correlation of DD levels with clot lysis. The mean
corrected peak DD was higher in patients with successful thrombolysis
(8,780 +/- 1,352 ng/ml) compared with patients without lysis (3,075 +/- 589
ng/ml, p less than 0.001). There was a moderate correlation between the
volume of clot lysed and the corrected peak DD (r = 0.62) and a higher
correlation with the corrected DD integrated over the course of treatment
(r = 0.97). By contrast, the corrected DD concentrations were near zero in
patients treated for MI with or without thrombolytic reperfusion,
suggesting that fibrin in small coronary thrombi did not contribute
significantly to total plasma DD during therapy.(ABSTRACT TRUNCATED AT 250
WORDS)
ARTICLES
Quantitation of venous clot lysis with the D-dimer immunoassay during fibrinolytic therapy requires correction for soluble fibrin degradation
Department of Medicine, University of Rochester School of Medicine, NY.
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