What does a high LY30 value on a Thromboelastography (TEG) report indicate?

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High LY30 on TEG Indicates Hyperfibrinolysis

A high LY30 value on TEG indicates hyperfibrinolysis—excessive breakdown of blood clots—which is associated with increased risk of massive transfusion requirements and mortality. 1

What LY30 Measures

  • LY30 represents the percentage of clot degradation occurring 30 minutes after the clot reaches its maximum strength (MA), providing a real-time assessment of how rapidly the body is breaking down formed clots 1
  • This measurement captures fibrinolytic activity in whole blood, reflecting the balance between clot formation and clot breakdown 1

Critical Threshold Values

LY30 ≥3% defines clinically significant hyperfibrinolysis and represents a critical indication for antifibrinolytic therapy. 2

  • Patients with LY30 ≥3% have a 90.9% risk of requiring massive transfusion compared to only 30.5% in those with LY30 <3% 2
  • Mortality from hemorrhage increases dramatically to 45.5% when LY30 ≥3% versus only 4.8% when LY30 <3% 2
  • The traditional upper limit of normal (7.5%) is inappropriate in severe trauma, as mortality risk rises at much lower levels of clot lysis 2
  • LY30 >7.5% indicates severe hyperfibrinolysis according to guideline societies 3

Immediate Management Algorithm

When LY30 ≥3%, activate massive transfusion protocol immediately with 1:1:1 ratio of packed RBCs, FFP, and platelets. 1

For LY30 ≥10% (on TEG 6s), administer tranexamic acid (TXA) 1g IV over 10 minutes, followed by 1g infusion over 8 hours—this intervention may be life-saving. 1

  • Repeat TEG 15-30 minutes after any intervention to assess response to antifibrinolytic therapy 1
  • Goal-directed therapy using TEG parameters improves survival compared to conventional coagulation test-guided therapy 4

Molecular Pathophysiology

  • Patients with high LY30 demonstrate elevated tissue plasminogen activator and plasmin-antiplasmin levels upon hospital arrival, confirming true fibrinolytic activation 5
  • Hyperfibrinolysis is the most clinically significant form of traumatic fibrinolytic dysfunction and is associated with worse outcomes 5
  • High LY30 is associated with increased 24-hour and 30-day mortality 5

Special Population Considerations

  • Patients with antiphospholipid syndrome or persistent antiphospholipid antibodies demonstrate significantly increased LY30 compared to controls, reflecting enhanced fibrinolysis 1
  • In pregnancy, baseline fibrinolysis is typically suppressed (LY30 near 0%), so any elevation is particularly concerning and indicates severe pathology in obstetric hemorrhage 4

Critical Pitfall: Distinguishing True Fibrinolysis from Clot Retraction

In postpartum hemorrhage specifically, an elevated kaolin TEG LY30 may represent platelet-mediated clot retraction rather than true fibrinolysis. 6

  • To distinguish between these two mechanisms, obtain a functional fibrinogen TEG (which contains a platelet inhibitor) 6
  • True fibrinolysis shows a nonzero functional fibrinogen TEG LY30, while platelet-mediated clot retraction shows zero functional fibrinogen TEG LY30 6
  • In one study of postpartum hemorrhage, none of the patients with kaolin TEG LY30 ≥3% had detectable clot lysis on functional fibrinogen TEG, suggesting clot retraction rather than fibrinolysis 6

Device-Specific Considerations

  • Results are not interchangeable between TEG and ROTEM devices—use device-specific reference ranges 1
  • TEG is performed at 37°C and cannot assess effects of hypothermia on coagulation 3

References

Guideline

High LY30 on TEG Indicates Hyperfibrinolysis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Interpreting Thromboelastography (TEG) Parameters and Clinical Applications

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Critical Interpretation of Progressive Coagulopathy with Severe Hyperfibrinolysis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Hyperfibrinolysis: a crucial phenotypic abnormality of posttraumatic fibrinolytic dysfunction.

Research and practice in thrombosis and haemostasis, 2024

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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