Comparison of Immunological and Functional Assays for Measurement of Soluble Fibrin

C E Dempfle; S A Pfitzner; M Dollman; K Huck; G Stehle; D L Heene

doi:10.1055/s-0038-1649796

Thrombosis and Haemostasis, Inhaltsverzeichnis

Thromb Haemost 1995; 74(02): 673-679
DOI: 10.1055/s-0038-1649796

Original Article

Coagulation

Schattauer GmbH Stuttgart

Comparison of Immunological and Functional Assays for Measurement of Soluble Fibrin

C E Dempfle

The University of Heidelberg, Klinikum Mannheim, Ist Dept. of Medicine, Mannheim, Germany

,

S A Pfitzner

The University of Heidelberg, Klinikum Mannheim, Ist Dept. of Medicine, Mannheim, Germany

,

M Dollman

The University of Heidelberg, Klinikum Mannheim, Ist Dept. of Medicine, Mannheim, Germany

,

K Huck

^*The University of Heidelberg, Klinikum Mannheim, IInd Dept. of Medicine, Mannheim, Germany

,

G Stehle

The University of Heidelberg, Klinikum Mannheim, Ist Dept. of Medicine, Mannheim, Germany

,

D L Heene

The University of Heidelberg, Klinikum Mannheim, Ist Dept. of Medicine, Mannheim, Germany

› Institutsangaben

Abstract

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Summary

Various assays have been developed for quantitation of soluble fibrin or fibrin monomer in clinical plasma samples, since this parameter directly reflects in vivo thrombin action on fibrinogen. Using plasma samples from healthy blood donors, patients with cerebral ischemic insult, patients with septicemia, and patients with venous thrombosis, we compared two immunologic tests using monoclonal antibodies against fibrin-specific neo-epitopes, and two functional tests based on the cofactor activity of soluble fibrin complexes in tPA-induced plasminogen activation. Test A (Enzymun^®-Test FM) showed the best discriminating power among normal range and pathological samples. Test B (Fibrinostika^® soluble fibrin) clearly separated normal range from pathological samples, but failed to discriminate among samples from patients with low grade coagulation activation in septicemia, and massive activation in venous thrombosis. Functional test C (Fibrin monomer test Behring) displayed good discriminating power between normal and pathological range samples, and correlated with test A (r = 0.61), whereas assay D (Coa-Set^® Fibrin monomer) showed little discriminating power at values below 10 μg/ml and little correlation with other assays. Standardization of assays will require further characterization of analytes detected.

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Referenzen

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