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Thromboelastography Detects Possible Coagulation Disturbance in Pediatric Patients with Portal Cavernoma
Linfeng Wu1,2, Gaofu Zhang3,2, Chunbao Guo1,3,4
1Chongqing Medical University, Chongqing, China.
Insights
Thromboelastography reveals portal cavernoma patients have a hypercoagulable state, despite thrombocytopenia. This finding suggests potential improvements in current treatment strategies for portal cavernoma syndrome.
Area of Science:
- Hematology
- Gastroenterology
- Vascular Medicine
Background:
- Thromboelastography (TEG) offers dynamic clot assessment but its role in portal cavernoma (PC) requires further definition.
- Understanding coagulation in PC patients is crucial for managing potential thrombotic or bleeding risks.
Purpose of the Study:
- To define the coagulation profile of patients with portal cavernoma (PC) using thromboelastography (TEG).
- To assess the hypercoagulable state in PC patients and the influence of thrombocytopenia.
Main Methods:
- Retrospective analysis of consecutive PC patients (excluding malignancy/cirrhosis) from July 2006 to June 2016.
- Coagulation assessment included conventional tests, factor levels, and TEG analysis.
Main Results:
- PC patients exhibited reduced procoagulant and anticoagulant factors, with elevated Factor VIII.
- TEG indicated a hypercoagulable state in PC patients (higher α-angle and MA), despite thrombocytopenia.
- Elevated D-dimer and LY30 in PC patients suggested in vivo coagulation and fibrinolysis activation.
Conclusions:
- TEG analysis demonstrated a hypercoagulable state in PC patients.
- Thrombocytopenia secondary to splenomegaly may mask the hypercoagulable state.
- Findings suggest opportunities to optimize prophylaxis and therapy regimens for PC.
Background:
Thromboelastography (TEG) allows a dynamic assessment of clot formation and dissolution that might be useful for assessing the relative contribution of the coagulation components to overall clot formation and dissolution, but it has not been fully defined in patients with portal cavernoma (PC).
Methods:
We retrospectively recruited consecutive patients with PC between July 2006 and June 2016 who had no abdominal malignancy or liver cirrhosis. Blood samples were drawn on admission and were subjected to coagulation parameter assessment, including conventional coagulation tests, measurement of the circulating levels of procoagulant and anticoagulant factors, and TEG assessment.
Results:
Compared with controls, patients with PC showed significant reductions in the serum levels of procoagulant factors and anticoagulants factors, whereas factor VIII was slightly elevated. TEG showed clot formation (α-angle), and the maximal clot strength (MA) was higher in patients with PC than in controls, indicating a hypercoagulable state. Thrombocytopenia decreased both clot formation (α-angle) and the maximal clot strength (MA) but was still significantly higher than the control. Furthermore, patients with PC had a higher level of D-dimer and LY30 than did controls, indicating the in vivo activation of coagulation and fibrinolysis.
Conclusion:
TEG analysis showed that patients with PC were in a hypercoagulable state that could be partially masked by thrombocytopenia secondary to splenomegaly and hypersplenism in these patients, which indicates that our current prophylaxis and therapy regimen could be improved.
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