Diagnosing Disseminated Intravascular Coagulation (DIC)?

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Last updated: February 9, 2025View editorial policy

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From the Guidelines

Diagnosing Disseminated Intravascular Coagulation (DIC) is best done using the International Society on Thrombosis and Haemostasis (ISTH) overt DIC criteria or the Sepsis-Induced Coagulopathy (SIC) scoring system.

Key Diagnostic Criteria

  • The ISTH overt DIC criteria include platelet count, fibrin-related markers (D-dimer or FDP), prothrombin time (PT) ratio, and fibrinogen 1.
  • The SIC scoring system, introduced in 2019, is designed to detect the compensated phase of DIC in sepsis and includes platelet count, prothrombin time (PT) ratio, SOFA score, and fibrinogen is not included 1.

Diagnostic Approach

  • Both the ISTH overt DIC and SIC scoring systems can be used to diagnose sepsis-associated coagulopathy, with the SIC scoring system being more suitable for early and rapid diagnosis 1.
  • The SIC scoring system has been shown to identify patients with sepsis who are at risk of developing overt DIC and may benefit from anticoagulant therapy 1.

Limitations and Future Perspectives

  • The SIC scoring system has limitations, including low specificity and adaptivity, but it can be modified to include additional markers, such as thrombin-related markers or antithrombin activity, to improve its performance 1.
  • Future studies are needed to evaluate the effectiveness of anticoagulant therapies in patients with sepsis-induced coagulopathy and DIC, using the SIC scoring system as a diagnostic tool 1.

From the Research

Diagnosing Disseminated Intravascular Coagulation (DIC)

Diagnosing DIC involves a combination of clinical and laboratory assessments. The International Society on Thrombosis and Haemostasis (ISTH) established a DIC diagnostic scoring system consisting of global haemostatic test parameters 2. This scoring system has been validated in diverse clinical settings.

Laboratory Tests for DIC

Several laboratory tests can be used to diagnose DIC, including:

  • Prothrombin time (PT) and partial thromboplastin time (PTT) 3
  • Fibrinogen/fibrin degradation products (FDP) and D-dimer 3
  • Platelet count and fibrinogen levels 4, 3
  • Soluble fibrin monomer (FM) and fibrin(ogen) split products (FSP) 5

Diagnostic Efficiency of Laboratory Tests

The combination of FDP and D-dimer has been shown to have the highest diagnostic efficiency for DIC, with a sensitivity of 91% and specificity of 94% 3. Other tests, such as PT, PTT, and platelet count, have lower sensitivity and specificity.

Clinical Assessment

Clinical assessment is also crucial in diagnosing DIC. The ISTH scoring system takes into account clinical observations, such as bleeding or thrombosis, in addition to laboratory results 2, 6. The diagnosis of DIC should be based on a combination of clinical and laboratory findings.

Monitoring and Management

Once DIC is diagnosed, it is essential to monitor the patient's condition closely and adjust treatment accordingly. The cornerstone of treatment is to address the underlying condition that triggered DIC 2, 6, 5. Transfusion of platelets or plasma may be necessary in some cases, and anticoagulant therapy may be considered in patients with thrombosis 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Disseminated intravascular coagulation.

Nature reviews. Disease primers, 2016

Research

Diagnosis and treatment of disseminated intravascular coagulation.

International journal of laboratory hematology, 2014

Research

Disseminated intravascular coagulation (DIC).

Clinical laboratory science : journal of the American Society for Medical Technology, 2000

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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