131 patients with EDTA-K2 Analysis of platelet aggregation induced by.docVIP

131 patients with EDTA-K2 Analysis of platelet aggregation induced by.doc

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131 patients with EDTA-K2 Analysis of platelet aggregation induced by

 PAGE \* MERGEFORMAT 8 131 patients with EDTA-K2 Analysis of platelet aggregation induced by [Abstract] Objective: To investigate the induction of platelet aggregation in EDTA-K2 reasons. Methods: Sysmex KX-21 hematology analyzer and manual microscopy, were instrumental method detected 131 cases of platelet aggregation occurred alarm specimens of hospitalized patients, and two those results were compared. Results: The blood platelet aggregation alarm of some diseases (iron deficiency anemia, aplastic anemia, idiopathic thrombocytopenic purpura and platelet count with coronary heart disease instrument method difference between the statistical microscope significance (P lt;0.05, while the difference between two methods of other diseases, no significant (Pgt; 0.05. Conclusion: The correct and rational use of EDTA-K2 anticoagulant to do a complete blood count, platelet aggregation alarm in case of specimens to be Law review with a microscope, can play a complementary role, but also help to improve test quality and avoid the occurrence of pseudo-thrombocytopenia. [Keywords:] EDTA-K2, induced platelet aggregation Complete blood count (CBC is the most conventional basic clinical examination items, the accuracy of the platelet count problem has been widespread concern and discussion, particularly ethylenediaminetetraacetic acid (EDTA anticoagulant induced platelet aggregation led to false thrombocytopenia (EDTA-PTCT more relevant reports, but the mechanism remains to be further studied. Some experts believe that the accuracy of platelet count may be obtained with the EDTA anticoagulant antibodies in the presence of lead to platelet aggregation [1]. We are in the application hematology analyzer process, the platelet count appeared together specimens of the alarm in different ways were compared, the results reported below. 1 Subjects and methods 1.1 The test subjects were from August 2006 to April 2007 the Department of our hospital treatment to patients w

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