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Comparison of methods for detecting soluble fibrin in plasma. An in vitro study

S Halvorsen1, O H Skjønsberg, R Ruyter

  • 1Haematological Research Laboratory, Ullevål Hospital, University of Oslo, Norway.

Thrombosis Research
|February 15, 1990
PubMed

Insights

The COA-SET Fibrin monomer (FM) test detects soluble fibrin but is less sensitive than fibrinopeptide A (FPA) assays. Discrepancies suggest fibrinogen may interfere with the COA-SET FM test

Area of Science:

  • Coagulation and Hemostasis Research
  • Biochemical Assays and Diagnostics
  • Thrombosis and Fibrinolysis Studies

Background:

  • Soluble fibrin is a marker in thrombotic disorders.
  • Accurate detection of soluble fibrin is crucial for clinical diagnostics.
  • Existing assays for soluble fibrin have varying sensitivities and specificities.

Purpose of the Study:

  • To evaluate the diagnostic performance of the COA-SET Fibrin monomer (FM) test for soluble fibrin detection.
  • To compare the COA-SET FM test with fibrinopeptide A (FPA) assays and other semiquantitative tests.
  • To investigate potential interferences affecting the COA-SET FM test.

Main Methods:

  • Plasma and whole blood samples were incubated with thrombin.
  • Soluble fibrin was measured using the COA-SET FM test.
  • Fibrinopeptide A (FPA) levels were determined.
  • Two semiquantitative tests, the erythrocytes-agglutination test (FM-test) and ethanol gelation test (EGT), were also employed.

Main Results:

  • The COA-SET FM test showed lower sensitivity compared to the FPA assay.
  • A strong correlation was observed between COA-SET FM and FPA results (r=0.86), but weaker at low soluble fibrin levels (r=0.59).
  • FPA levels were 2-25 times higher than fibrin monomer levels, indicating a discrepancy potentially due to fibrinogen interference.

Conclusions:

  • The COA-SET FM test is less sensitive than FPA assays for soluble fibrin detection.
  • Fibrinogen may interfere with the COA-SET FM test's principle, affecting its accuracy.
  • Further research is needed to optimize soluble fibrin detection methods.

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