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Sökning: WFRF:(Federici A B) > (2010-2014) > Validation of a rap...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003840naa a2200505 4500
001oai:lup.lub.lu.se:3fc96eae-581d-4993-b2dc-ad9f8f73d70f
003SwePub
008160401s2010 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/16721002 URI
024a https://doi.org/10.1016/j.thromres.2010.06.0132 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Castaman, G.4 aut
2451 0a Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD
264 1b Elsevier BV,c 2010
520 a Background: Accurate measurement of von Willebrand factor (VWF) is a critical requirement for the diagnosis of von Willebrand disease (VWD). Aim of the study: To evaluate the diagnostic efficiency of a rapid quantitative test for the measurement of VWF antigen (VWF:Ag) in type 1 VWD. Patients and methods: VWF: Ag was measured with an ELISA in a robotic instrument, as a reference method, and with a fully automated latex-immunoassay (LIA) on an ACL 9000 analyser in 1,716 subjects enrolled within the Molecular and Clinical Markers for Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD) Study. Among these subjects, 1,049 were healthy controls, 281 healthy family members and 386 affected members from 127 European families with type 1 VWD. Results: The assay linearity range was 10-125 IU/dL for LIA (R-2 = 0.99) and 5-133 IU/dL for ELISA (R-2 = 0.99). The inter-assay CV for low VWF levels (similar to 30 IU/dL) was 2% for the LIA test and 8.7 % for ELISA. The sensitivity for detection of type 1 VWD affected members was 86% and the specificity 91% for LIA, 87% and 90% for ELISA. A receiver-operator (ROC) analysis disclosed only a marginal difference between the two tests, LIA having a slightly greater area under the curve (0.94 vs. 0.93, p = 0.03). Conclusion: VWF: Ag LIA compared well to standard ELISA in this large population of patients and controls, showing better CV. However the lower detection limit for the VWF: Ag LIA compared to the VWF: Ag ELISA means that the LIA assay is less good at discriminating between type 3 VWD and moderate type 1 VWD. (C) 2010 Elsevier Ltd. All rights reserved.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Kardiologi0 (SwePub)302062 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cardiac and Cardiovascular Systems0 (SwePub)302062 hsv//eng
653 a disorders
653 a Inherited bleeding
653 a von Willebrand factor
653 a von Willebrand disease
700a Tosetto, A.4 aut
700a Cappelletti, A.4 aut
700a Goodeve, A.4 aut
700a Federici, A. B.4 aut
700a Batlle, J.4 aut
700a Meyer, D.4 aut
700a Goudemand, J.4 aut
700a Eikenboom, J. C. J.4 aut
700a Schneppenheim, R.4 aut
700a Budde, U.4 aut
700a Ingerslev, J.4 aut
700a Lethagen, Stefanu Lund University,Lunds universitet,Institutionen för kliniska vetenskaper, Malmö,Medicinska fakulteten,Department of Clinical Sciences, Malmö,Faculty of Medicine4 aut0 (Swepub:lu)medf-sle
700a Hill, F.4 aut
700a Peake, I. R.4 aut
700a Rodeghiero, F.4 aut
710a Institutionen för kliniska vetenskaper, Malmöb Medicinska fakulteten4 org
773t Thrombosis Researchd : Elsevier BVg 126:3, s. 227-231q 126:3<227-231x 1879-2472x 0049-3848
856u http://dx.doi.org/10.1016/j.thromres.2010.06.013y FULLTEXT
8564 8u https://lup.lub.lu.se/record/1672100
8564 8u https://doi.org/10.1016/j.thromres.2010.06.013

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