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Diagnosis of disseminated intravascular coagulation by hemostatic molecular markers

H Wada1, E Gabazza, T Nakasaki

  • 1Second Department of Internal Medicine, Mie University School of Medicine, Tsu-city, Japan.

Insights

Diagnosing disseminated intravascular coagulation (DIC) can be improved by combining thrombin-antithrombin complex (TAT), plasmin-plasmin inhibitor complex (PPIC), and soluble fibrin monomer (sFM) markers. This combination offers a more accurate diagnostic approach for DIC and pre-DIC states.

Area of Science:

  • Hematology
  • Clinical Diagnostics
  • Biochemistry

Background:

  • Disseminated intravascular coagulation (DIC) is a complex hematological disorder.
  • Accurate and timely diagnosis of DIC is crucial for patient outcomes.
  • Existing diagnostic markers for DIC have limitations in sensitivity and specificity.

Purpose of the Study:

  • To evaluate the diagnostic utility of thrombin-antithrombin complex (TAT), plasmin-plasmin inhibitor complex (PPIC), soluble fibrin monomer (sFM), and D-dimer for DIC.
  • To compare the positive rates of these markers in patients with DIC, pre-DIC, and non-DIC states.
  • To assess the effectiveness of combining TAT, PPIC, and sFM for DIC diagnosis.

Main Methods:

  • Retrospective analysis of plasma samples from 307 DIC, 123 pre-DIC, and 121 non-DIC patients.
  • Measurement of plasma levels of TAT, PPIC, sFM, and D-dimer.
  • Calculation of positive rates and development of scoring systems based on marker positivity.

Main Results:

  • Plasma levels of TAT, PPIC, sFM, and D-dimer were significantly elevated in DIC and pre-DIC groups compared to non-DIC.
  • In DIC patients, sFM showed a high positive rate, while D-dimer had a low positive rate.
  • A scoring system combining TAT, PPIC, and sFM correctly identified 72% of DIC patients, 17.6% of pre-DIC patients, and 96.6% of non-DIC patients (≤2 points).

Conclusions:

  • The combination of TAT, PPIC, and sFM demonstrates significant utility in diagnosing DIC.
  • PPIC showed a higher positive rate in patients with hematopoietic malignancy.
  • The proposed scoring system using TAT, PPIC, and sFM offers a promising approach for improved DIC diagnosis.

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