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Volume 155, Issue 6, Pages 315-319 (June 2010)


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Shortened activated partial thromboplastin time, a hemostatic marker for hypercoagulable state during acute coronary event

Wan Zaidah AbdullahaCorresponding Author Informationemail address, Shaimaa K. Moufaka, Zurkurnai Yusofb, Mohd Sapawi Mohamadb, I.M. Kamarulc

Received 13 September 2009; received in revised form 7 February 2010; accepted 9 February 2010. published online 08 March 2010.

Various factors may contribute to a hypercoagulable state and acute vascular thrombosis. A prospective study was conducted involving 165 coronary heart disease (CHD) patients from the Cardiology Unit, Hospital Universiti Sains Malaysia. The purpose of this study was to investigate the relationship among factor VIII (FVIII), prothrombin time (PT), activated partial thromboplastin time (APTT), and activated protein C resistance (APC-R) state among CHD patients and to look for potential clinical applications from these laboratory findings. There were 110 cases diagnosed as acute coronary syndrome (ACS), whereas another 55 were stable coronary artery disease (SCAD) patients. PT, APTT, FVIII, and APC-R assays were performed on all subjects. There was a significant difference between the FVIII level and the APTT results (P value < 0.0001). A negative relationship was found between the FVIII level and the APTT from linear regression analysis (R2 = 10%, P value < 0.0001). For each 1% increase in the FVIII level, the APTT was reduced by 0.013 s (95% confidence interval (CI) between –0.019 and –0.007). Interestingly, none of the SCAD patients had abnormally short APTT. Approximately 68.4% of cases with a positive APC-R assay were found to have a high FVIII level. In conclusion, the APTT test is a potential hemostatic marker for hypercoagulable state including in arterial thrombosis.

a Haematology Department, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kelantan, Malaysia

b Cardiology Unit, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kelantan, Malaysia

c Department of Community Medicine, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kelantan, Malaysia

Corresponding Author InformationReprint requests: Dr. Wan Zaidah Abdullah, Haematology Department, School of Medical Sciences, Health Campus, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia

 Supported by Grant 1001/PPSP/812004 from the Universiti Sains Malaysia (USM)

PII: S1931-5244(10)00032-0

doi:10.1016/j.trsl.2010.02.001


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