How is thromboelastography (TEG) interpreted in clinical practice?

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Thromboelastography (TEG) Interpretation in Clinical Practice

Thromboelastography (TEG) provides a comprehensive assessment of the entire coagulation process from initial clot formation through fibrinolysis, allowing for real-time evaluation of hemostatic function that should be interpreted with careful attention to specific parameters and clinical context. 1

Key TEG Parameters and Their Clinical Significance

Primary Parameters

  • R time (Reaction time)

    • Measures time from test start to initial fibrin formation (normal: 5-10 minutes)
    • Reflects coagulation factor activity in the intrinsic pathway
    • Prolonged in: factor deficiencies, anticoagulant effect (heparin, warfarin)
    • Shortened in: hypercoagulable states (pregnancy, malignancy)
  • K time (Kinetics)

    • Represents speed of clot formation (normal: 1-3 minutes)
    • Prolonged in: hypofibrinogenemia, thrombocytopenia
    • Shortened in: hypercoagulable states
  • Alpha angle (α)

    • Reflects fibrinogen function and platelet interaction (normal: 53-72°)
    • Decreased in: hypofibrinogenemia, platelet dysfunction
    • Increased in: hypercoagulability
  • MA (Maximum Amplitude)

    • Represents overall clot strength (normal: 50-70 mm)
    • Decreased in: thrombocytopenia, platelet dysfunction, hypofibrinogenemia
    • Increased in: hypercoagulable states
    • Note: Fibrinogen contributes 45% and platelets contribute 55% to overall clot strength 1
  • LY30/LY60 (Lysis at 30/60 minutes)

    • Reflects fibrinolytic activity (normal: 0-8%)
    • Increased values indicate hyperfibrinolysis

Common TEG Patterns and Clinical Correlations

  1. Hypercoagulable Pattern

    • Shortened R and K times
    • Increased α-angle and MA
    • Common in: pregnancy, malignancy, post-operative states 1
  2. Hypocoagulable Pattern

    • Prolonged R and K times
    • Decreased α-angle and MA
    • Common in: factor deficiencies, thrombocytopenia, hemodilution
  3. Hyperfibrinolytic Pattern

    • Normal initial parameters with declining amplitude after MA
    • Increased LY30/LY60
    • Common in: trauma with massive hemorrhage, liver disease
  4. Anticoagulant Effect

    • Prolonged R time
    • Can detect effects of DOACs with variable sensitivity
    • Heparinase TEG can differentiate heparin effect from coagulopathy 2

Specialized TEG Applications

  • Heparinase TEG (hTEG)

    • Contains heparinase to neutralize heparin effect
    • Useful for assessing coagulation in heparinized patients 1
  • Functional Fibrinogen TEG (FLEV-TEG)

    • Assesses relative contribution of platelets and fibrin to clot strength 1
  • TEG Platelet Mapping (TEG-PM)

    • Evaluates effects of antiplatelet agents 1
    • Note: Standard TEG has limited sensitivity for platelet dysfunction 3

Clinical Applications and Transfusion Guidance

  • Trauma and Massive Transfusion

    • Guides component therapy based on specific deficiencies
    • Helps identify hyperfibrinolysis requiring antifibrinolytic therapy
  • Liver Disease

    • TEG often reveals rebalanced hemostasis despite abnormal conventional tests
    • TEG-guided transfusion reduces unnecessary blood product use in cirrhotic patients with nonvariceal bleeding 4
  • Cardiac Surgery

    • Guides hemostatic management during and after cardiopulmonary bypass
    • Helps differentiate surgical from coagulopathic bleeding
  • Obstetrics

    • Can detect pregnancy-associated hypercoagulability
    • Limited sensitivity for detecting hyperfibrinolysis in pregnancy 2

Important Limitations and Pitfalls

  • Device Variability and Operator Dependency

    • High coefficients of variance (7.1% to 39.9%) reported for TEG parameters 2, 1
    • Requires proper training and quality control measures
  • Insensitivity to Platelet Dysfunction

    • Standard TEG cannot reliably detect platelet function disorders or effects of antiplatelet drugs 3
    • Should be supplemented with specific platelet function tests when needed
  • Limited Sensitivity for Hypofibrinolysis

    • May not detect subtle changes in fibrinolysis
    • British Society for Hematology advises that TXA should not be withheld based on normal TEG/ROTEM profile 2
  • Sample Processing Issues

    • Delayed analysis and improper collection technique can affect results 1, 5
    • Hemolysis can interfere with TEG results by shortening coagulation times 1
  • Interpretation Challenges

    • Results must be interpreted in device-specific context 2
    • Local reference ranges should be established as they are device and manufacturer-specific 2

Best Practices for TEG Implementation

  • Establish institution-specific reference ranges
  • Implement rigorous quality control measures
  • Ensure adequate training of personnel
  • Interpret results in clinical context
  • Use specialized TEG tests when appropriate (heparinase, functional fibrinogen)
  • Recognize that TEG and ROTEM results are not interchangeable due to different reagents and hardware 2

By understanding these parameters and their clinical significance, clinicians can effectively use TEG to guide hemostatic management and transfusion therapy, potentially reducing unnecessary blood product use while improving patient outcomes.

References

Guideline

Thromboelastography (TEG) Guideline Summary

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Value of thromboelastography in the assessment of platelet function.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis, 2003

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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