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Updated: Jul 11, 2026

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Measurement of Factor V Activity in Human Plasma Using a Microplate Coagulation Assay
Published on: September 9, 2012
Hypercoagulable state in five thalassemia intermedia patients.
Maitreyee Bhattacharyya1, Meganathan Kannan, Ved P Chaudhry
1Department of Hematology, All India Institute of Medical Sciences, New Delhi, India.
Summary
Patients with beta thalassemia intermedia exhibit a chronic hypercoagulable state, increasing thrombosis risk. Red blood cell abnormalities likely drive these coagulation and platelet issues.
Area of Science:
- Hematology
- Thrombosis Research
- Coagulation Disorders
Background:
- Thalassemia intermedia patients face increased risks beyond anemia.
- Understanding hypercoagulable states is crucial for managing complications.
Observation:
- Thrombotic episodes occurred in 9.4% of patients.
- Abnormalities in platelet aggregation and coagulation inhibitors were noted.
- Lower antithrombin III levels correlated with hepatic dysfunction.
Findings:
- A chronic hypercoagulable state exists in beta thalassemia intermedia.
- Procoagulant red blood cell surface expression is a potential cause.
- Alterations are independent of iron overload or hepatic dysfunction.
Implications:
- This research highlights a need for proactive thrombosis management in thalassemia intermedia.
- Identifying underlying mechanisms can lead to targeted therapies.
- Further research into red blood cell surface properties is warranted.
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