Journal of Hematology & Thromboembolic Diseases
Open Access

Amal Hayati H

Publications

• Research Article
  The Level of Natural Anticoagulants in Transfusion Dependent Thalassemia Patients in Kelantan, Northeastern Malaysia
  Author(s): Rosnah B, Noor Halina MN, Shafini Y, Marini R, Rosline H, Amal Hayati HRosnah B, Noor Halina MN, Shafini Y, Marini R, Rosline H, Amal Hayati H
  
  The association of the severe form of thalassemia with complications of blood transfusion, iron overload, bony deformity and gall stone is well described. Currently, due to improvement in the way of managing thalassemia, most of thalassemia patients survive longer. However more new complications had been observed. Increased incidence of thromboembolism among thalassemia patients had triggered various studies done to determine hypercoagulable state among thalassemia patients. Several factors for the hypercoagulable state had been identified such as RBC membrane disruption, chronic platelet activation and defect in coagulation pathway. This study was carried out to determine the level of Protein C, protein S, free protein S and antithrombin among thalassemia patients and to compare the level of Protein C, protein S, free Protein S and antithrombin level between thalassemia patients and .. View More»
  DOI: 10.4172/2329-8790.1000140

  Abstract PDF

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