Diagnose angeborener störungen der Thrombozytenfunktion;Interdisziplinäre S2K-Leitlinie* der ständigen Kommission Pädiatrie der gesellschaft für thrombose- und hämostaseforschung e. V.

Hamostaseologie

Volumn 34, Issue 3, 2014, Pages 201-212

  Knofler R ^a   Eberl, W ^b   Schulze, H ^c   Bakchoul, T ^d   Bergmann, F ^e   Gehrisch, S ^f   Geisen, C ^g   Gottstein, S ^h   Halimeh, S ⁱ   Harbrecht, U ^j   Kappert, G ⁱ   Kirchmaier, C ^k   Kehrel, B ^l   Losche W ^m   Krause, M ^k   Mahnel, R ⁿ   Meyer, O ^o   Pilgrimm, A K ^k   Pillitteri, D ^k   Rott, H ⁱ   Santoso, S ^d   Siegemund, A ^p   Schambeck, C ^q   Scheer, M ^r   Schmugge, M ^s   Scholl, T ^k   Strauss, G ^c   Zieger, B ^t   Zotz, R ^u   Hermann, M ^v   Streif, W ^v   more..

^a UNIVERSITY HOSPITAL CARL GUSTAV CARUS   (Germany)

^b KLINIKUM BRAUNSCHWEIG   (Germany)

^c Lehrstuhl für Experimentelle Biomedizin   (Germany)

^d Institut für Klinische Immunologie und Transfusionsmedizin   (Germany)

^e MVZ Wagnerstibbe   (Germany)

^f DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^g Institut fur Transfusionsmedizin und Immunhamatologie   (Germany)

^h VIVANTES KLINIKUM IM FRIEDRICHSHAIN   (Germany)

ⁱ Gerinnungszentrum Rhein Ruhr   (Germany)

^j UNIVERSITY OF BONN   (Germany)

^k DEUTSCHE KLINIK FÜR DIAGNOSTIK   (Germany)

^l UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^m FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

ⁿ Hamostaseo logische Praxis und Labor zur Diagnostik und Therapie von Blutgerinnungsstorungen   (Germany)

^o Institut für Transfusionsmedizin Thrombozytenlabor Blutbank mit Immunhämatologie   (Germany)

^p MVZ Labor Dr Reising Ackermann und Kollegen   (Germany)

^q Hämostasikum München ^*  (Germany)

^r UNIVERSITY HOSPITAL ESSEN   (Germany)

^s UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^t UNIVERSITY OF FREIBURG   (Germany)

^u Centrum für Blutgerinnungsstörungen und Transfusionsmedizin Düsseldorf   (Germany)

^v INNSBRUCK MEDICAL UNIVERSITY   (Austria)

more..

Author keywords

Guideline; Platelet disorders; Platelets

Indexed keywords

ALGORITHM; ARTICLE; BERNARD SOULIER DISEASE; BLEEDING; BLOOD CLOTTING DISORDER; CONGENITAL DISORDER; DISEASE CLASSIFICATION; FLOW CYTOMETRY; GLANZMANN DISEASE; HUMAN; MEDICAL HISTORY; MOLECULAR GENETICS; SCREENING; THROMBOCYTE ANOMALY; THROMBOCYTE COUNT; THROMBOCYTE DISORDER; THROMBOCYTE FUNCTION; THROMBOCYTE FUNCTION ANALYZER; THROMBOCYTE STRUCTURE; THROMBOCYTE VOLUME; VON WILLEBRAND DISEASE; BLOOD; BLOOD CLOTTING PARAMETERS; BLOOD PLATELET DISORDERS; GENETIC SCREENING; GENETICS; GERMANY; HEMATOLOGY; MOLECULAR DIAGNOSIS; PEDIATRICS; PRACTICE GUIDELINE; STANDARDS;

BLOOD PLATELET DISORDERS; GENETIC TESTING; GERMANY; HEMATOLOGY; HUMANS; MOLECULAR DIAGNOSTIC TECHNIQUES; PEDIATRICS; PLATELET FUNCTION TESTS; PRACTICE GUIDELINES AS TOPIC;

EID: 84907242217     PISSN: 07209355     EISSN: None     Source Type: Journal    
DOI: 10.5482/HAMO-13-04-0024     Document Type: Article

References (25)

1. Cox K, Price V, Kahr WH. Inherited platelet disorders: a clinical approach to diagnosis and management. Expert Rev Hematol 2011; 4: 455-472.
2. Streif W, Olivieri M, Weickardt S et al. Testing for inherited platelet defects in clinical laboratories in Germany, Austria and Switzerland. Platelets 2010; 21: 470-478.
3. Guidelines on platelet function testing. The British Society for Haematology BCSH Haemostasis and Thrombosis Task Force. J Clin Pathol 1988; 41: 1322-1330.
4. Christie JD, Avari T, Carrington RL et al. H58-A - Platelet Function Testing by Aggregometry; Approved Guideline. Clinical And Laboratory Standards Institute (CLSI) 2008.
5. Schambeck CM. Blutungsneigung: Diagnostische Strategie zur Abklärung einer Thrombozytendysfunktion. Consensus-Papier der DGKL-Arbeitsgruppe “Hämostaseologische Labordiagnostik“. J Lab Med 2004; 28: 453-462.
6. Cattaneo M, Hayward CP, Moffat KA et al. Results of a worldwide survey on the assessment of platelet function by light transmission aggregometry: a report from the platelet physiology subcommittee of the SSC of the ISTH. J Thromb Haemost 2009; 7: 1029.
7. Duncan EM, Bonar R, Rodgers SE et al. Methodology and outcomes of platelet aggregation testing in Australia, New Zealand and the Asia-Pacific region. Int J Lab Hematol 2009; 31: 398-406.
8. Harrison P, Mackie I, Mumford A et al. Guidelines for the laboratory investigation of heritable disorders of platelet function. Br J Haematol 2011; 155: 30-44.
9. Hayward CP, Moffat KA, Plumhoff E, Van Cott EM. Approaches to investigating common bleeding disorders: an evaluation of North American coagulation laboratory practices. Am J Hematol 2012; 87 (Suppl 1): S45-S50.
10. Rodgers RP. Bleeding time tables. A tabular summary of pertinent literature. Semin Thromb Hemost 1990; 16: 21-138.
11. Hayward CP, Harrison P, Cattaneo M et al. Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function. J Thromb Haemost 2006; 4: 312-319.
12. Halimeh S, Angelis G, Sander A et al. Multiplate whole blood impedance point of care aggregometry: preliminary reference values in healthy infants, children and adolescents. Klin Pädiatr 2010; 222: 158-163.
13. Favaloro EJ. Clinical utility of the PFA-100. Semin Thromb Hemost 2008; 34: 709-733.
14. Born GV. Aggregation of blood platelets by adenosine diphosphate and its reversal. Nature 1962; 194: 927-929.
15. Cardinal DC, Flower RJ. The electronic aggregometer: a novel device for assessing platelet behavior in blood. J Pharmacol Methods 1980; 3: 135-158.
16. Bonduel M, Frontroth JP, Hepner M et al. Platelet aggregation and adenosine triphosphate release values in children and adults. J Thromb Haemost 2007; 5: 1782-1783.
17. Knöfler R, Weissbach G, Kuhlisch E. Platelet function tests in childhood. Measuring aggregation and release reaction in whole blood. Semin Thromb Hemost 1998; 24: 513-521.
18. Lundin A, Richardsson A, Thore A. Continuous monitoring of ATP-converting reactions by purified firefly luciferase. Anal Biochem 1976; 75: 611-620.
19. George JN, Shattil SJ. The clinical importance of acquired abnormalities of platelet function. N Engl J Med 1991; 324: 27-39.
20. Schmitz G, Rothe G, Ruf A et al. European Working Group on Clinical Cell Analysis: Consensus protocol for the flow cytometric characterisation of platelet function. Thromb Haemost 1998; 79: 885-896.
21. Michelson AD. Evaluation of platelet function by flow cytometry. Pathophysiol Haemost Thromb 2006; 35: 67-82.
22. Wall JE, Buijs-Wilts M, Arnold JT et al. A flow cytometric assay using mepacrine for study of uptake and release of platelet dense granule contents. Br J Haematol 1995; 89: 380-385.
23. Israels SJ, Kahr WH, Blanchette VS et al. Platelet disorders in children: A diagnostic approach. Pediatr Blood Cancer 2011; 56: 975-983.
24. Balduini CL, Cattaneo M, Fabris F et al. Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle Piastrine. Haematologica 2003; 88: 582-592.
25. Nurden A, Nurden P. Advances in our understanding of the molecular basis of disorders of platelet function. J Thromb Haemost 2011; 9 (Suppl 1): 76-91.