Diagnostic Assessment of Platelet Disorders: What Are the Challenges to Standardization?

被引:35
作者
Pai, Menaka
Hayward, Catherine P. M. [1 ,2 ,3 ]
机构
[1] McMaster Univ, Hlth Sci Ctr, Dept Med, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada
[3] Hamilton Reg Lab Med Program, Hamilton, ON, Canada
关键词
Platelet disorders; bleeding scores; platelet function tests; laboratory diagnosis; UROKINASE PLASMINOGEN-ACTIVATOR; VON-WILLEBRAND-DISEASE; CHILDREN; QUESTIONNAIRE; AGGREGOMETRY; AGGREGATION; VARIABILITY; MECHANISMS; EXPRESSION; PHENOTYPE;
D O I
10.1055/s-0029-1220321
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The platelet disorders are a group of heterogeneous, congenital and acquired bleeding disorders associated with impaired platelet function. There is a growing interest in standardizing the assessment of these disorders, but this is challenged by their heterogeneity, the absence of widely accepted diagnostic criteria, and inconsistency in laboratory testing practices for platelet disorders. Symptoms commonly associated with platelet disorders include rapid-onset bleeding with hemostatic challenges, peripartum bleeding, menorrhagia, epistaxis, gingival bleeding, and increased bruising. Attempts have been made to standardize the assessment of these symptoms, using clinical tools and bleeding scores. However, there are currently no standardized tools available with proven utility for the assessment of platelet disorders, apart from a too] specifically designed to assess Quebec platelet disorder. There have been several efforts to improve and standardize the laboratory assessment of platelet disorders. These efforts Include guidelines from the International Society on Thrombosis and Haemostasis and the Clinical and Laboratory Standards Institute. Recent research indicates that the application of standardized laboratory tests for the assessment of platelet disorders in individuals referred for bleeding problems has valuable diagnostic utility. This has provided further incentive to standardize clinical and laboratory approaches to improve the diagnostic evaluation of platelet disorders worldwide.
引用
收藏
页码:131 / 138
页数:8
相关论文
共 53 条
[1]   MYH9-Related Platelet Disorders [J].
Althaus, Karina ;
Greinacher, Andreas .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2009, 35 (02) :189-203
[2]  
[Anonymous], 1988, J Clin Pathol, V41, P1322
[3]  
[Anonymous], 2008, CLIN LAB STANDARDS I
[4]   Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study [J].
Castaman, G. ;
Rodeghiero, F. ;
Tosetto, A. ;
Cappelletti, A. ;
Baudo, F. ;
Eikenboom, J. C. J. ;
Federici, A. B. ;
Lethagen, S. ;
Linari, S. ;
Lusher, J. ;
Nishino, M. ;
Petrini, P. ;
Srivastava, A. ;
Ungerstedt, J. S. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (10) :2164-2169
[5]   Light Transmission Aggregometry and ATP Release for the Diagnostic Assessment of Platelet Function [J].
Cattaneo, Marco .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2009, 35 (02) :158-167
[6]   Role of Platelet Electron Microscopy in the Diagnosis of Platelet Disorders [J].
Clauser, Sylvain ;
Cramer-Borde, Elisabeth .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2009, 35 (02) :213-223
[7]   Quebec platelet disorder: features, pathogenesis and treatment [J].
Diamandis, Maria ;
Veljkovic, D. Kika ;
Maurer-Spurej, Elisabeth ;
Rivard, Georges E. ;
Hayward, Catherine P. M. .
BLOOD COAGULATION & FIBRINOLYSIS, 2008, 19 (02) :109-119
[8]   Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes [J].
Diamandis, Maria ;
Paterson, Andrew D. ;
Rommens, Johanna M. ;
Veljkovic, D. Kika ;
Blavignac, Jessica ;
Bulman, Dennis E. ;
Waye, John S. ;
Derome, Francine ;
Rivard, Georges E. ;
Hayward, Catherine P. M. .
BLOOD, 2009, 113 (07) :1543-1546
[9]  
DUNCAN EM, 2008, INT J LAB HEMAT 0321
[10]   Internal Quality Control and External Quality Assurance of Platelet Function Tests [J].
Favaloro, Emmanuel J. .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2009, 35 (02) :139-149