Variability in clinical laboratory practice in testing for disorders of platelet function - Results of two surveys of the North American Specialized Coagulation Laboratory Association

被引:95
作者
Moffat, KA
Ledford-Kraemer, MR
Nichols, WL
Hayward, CPM
机构
[1] McMaster Univ, Hamilton, ON L8N 3Z5, Canada
[2] Hamilton Reg Lab Med Program, Hamilton, ON L8N 3Z5, Canada
[3] CLOT ED Inc, Islamorada, FL USA
[4] Univ Miami, Sch Med, Miami, FL USA
[5] Mayo Clin, Rochester, MN USA
关键词
platelet disorders; platelet function testing; platelet secretion;
D O I
10.1160/TH04-10-0670
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Disorders of platelet function are important causes of abnormal bleeding that require laboratory tests for diagnosis. Currently there are limited guidelines on how to perform clinical testing for these disorders. The goal of our study was to obtain information on how disorders of platelet function are currently evaluated in clinical laboratories. Two patterns-of-practice surveys were distributed to laboratories of the North American Specialized Coagulation Laboratory Association (NASCOLA). The information collected was analyzed to determine practices and common problems. Forty-seven NASCOLA laboratories participated and 54% completed both surveys. The majority of the laboratories that responded performed more than 50 aggregation tests per year, mainly using platelet rich plasma based methodologies. A minority performed testing for platelet secretion and dense granule abnormalities. While platelet aggregation results were reviewed in various ways, laboratories most commonly issued a combined report containing quantitative values (% aggregation and/or slope) and a qualitative interpretation. Although laboratories used similar agonists for aggregation testing, the final agonist concentrations varied widely. Several approaches were also used to obtain reference intervals. Comments offered by the participants indicated that performing, and interpreting platelet function tests were challenging for many clinical laboratories. Although common practices have evolved, there is considerable variability in the diagnostic test procedures used by clinical laboratories to evaluate disorders of platelet function. These patterns-of-practice surveys illustrate a need for guidelines and recommendations for clinical laboratories performing tests of platelet function.
引用
收藏
页码:549 / 553
页数:5
相关论文
共 24 条
[1]  
CARRANEO M, 2002, PLATELETS THROMBOTIC, P655
[2]   Inherited platelet-based bleeding disorders [J].
Cattaneo, M .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (07) :1628-1636
[3]   Platelets from a patient heterozygous for the defect of P2CYC receptors for ADP have a secretion defect despite normal thromboxane A2 production and normal granule stores -: Further evidence that some cases of platelet 'primary secretion defect' are heterozygous for a defect of P2CYC receptors [J].
Cattaneo, M ;
Lecchi, A ;
Lombardi, R ;
Gachet, C ;
Zighetti, ML .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (11) :E101-E106
[4]  
DAVIDSON JF, 1988, J CLIN PATHOL, V41, P1322
[5]   Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects [J].
Fontana, P ;
Dupont, A ;
Gandrille, S ;
Bachelot-Loza, C ;
Reny, JL ;
Aiach, M ;
Gaussem, P .
CIRCULATION, 2003, 108 (08) :989-995
[6]  
Fuse I, 1996, THROMB HAEMOSTASIS, V76, P1080
[7]   Inherited platelet disorders [J].
Hayward, CPM .
CURRENT OPINION IN HEMATOLOGY, 2003, 10 (05) :362-368
[8]   An autosomal dominant, qualitative platelet disorder associated with multimerin deficiency, abnormalities in platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen and an epinephrine aggregation defect [J].
Hayward, CPM ;
Rivard, GE ;
Kane, WH ;
Drouin, J ;
Zheng, SL ;
Moore, JC ;
Kelton, JG .
BLOOD, 1996, 87 (12) :4967-4978
[9]   Prevalence of impaired responsiveness to epinephrine in platelets among Japanese [J].
Kambayashi, JI ;
Shinoki, N ;
Nakamura, T ;
Ariyoshi, H ;
Kawasaki, T ;
Sakon, M ;
Monden, M .
THROMBOSIS RESEARCH, 1996, 81 (01) :85-90
[10]   The diagnosis of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctors' Organization [J].
Laffan, M ;
Brown, SA ;
Collins, PW ;
Cumming, AM ;
Hill, FGH ;
Keeling, D ;
Peake, IR ;
Pasi, KJ .
HAEMOPHILIA, 2004, 10 (03) :199-217