Hypercoagulable state among thalassemia major patients
Increased incidence of thromboembolism among thalassemia patients had triggered various studies to determine hypercoagulable state among thalassemia patients. Several factors for the hypercoagulable state had been identified such as red blood cell membrane disruption, chronic platelet activation...
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| Main Author: | |
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| Format: | Thesis |
| Language: | English |
| Published: |
2013
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| Subjects: | |
| Online Access: | http://eprints.usm.my/60849/1/DR%20WAN%20AMAL%20HAYATI%20BINTI%20WAN%20HASSAN%20-%20e.pdf |
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| Summary: | Increased incidence of thromboembolism among thalassemia patients had triggered
various studies to determine hypercoagulable state among thalassemia patients. Several
factors for the hypercoagulable state had been identified such as red blood cell
membrane disruption, chronic platelet activation and defect in coagulation pathway.
The objectives of this study were to determine the level of Protein C, Protein S and
Antithrombin III among thalassemia major patients and to compare the level of these
natural anticoagulants between thalassemia major patients and healthy controls. For this
purpose, a case control study was conducted in Hospital Universiti Sains Malaysia
(HUSM). Thirty six thalassemia patients who came for regular blood transfusion and
twenty healthy blood donors for normal control were recruited. Blood samples were
collected and analysed for Protein C, Protein S, Free Protein S and Antithrombin III
using ACL Elite Pro coagulometer. The results showed mean Protein C, Protein S and Free Protein S levels were
significantly lower in thalassemia patients (54.54 ± 13.22,94.41 ± 18.73 and
70.09 ± 12.32 ; respectively ) compared to normal controls (94.14 ± 16.34 ,
105.12 ± 16.79 and 99.79 ± 17.33 ; respectively). Mean Antithrombin III showed no significant difference compared to normal controls
(116.09 ± 27.28 and 124.36 ± 12.49 respectively). There were no significant differences
of mean Protein C, Protein S, Free Protein S and Antithrombin III between splenectomised and non splenectomised patients. No thromboembolic events were
documented in this study. In conclusion, significantly decreased Protein C and Protein S in thalassemia patients
suggest hypercoagulable state in those patients. However further studies need to be done
to look for other parameters contributing to hypercoagulable state in thalassemia
patients. A normal antithrombin level could be due to protective effect of regular
transfusion, a further study need to be done to prove this hypothesis. Besides,
thromboembolic event can be subclinical, therefore a further study is needed to follow
up the patients and to detect subclinical thrombosis. |
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