Evidence map›Paper›PMID 38840662›Full record

ArticleResearch and practice in thrombosis and haemostasis2024

Evaluation of an automated von Willebrand factor glycoprotein IbM activity assay compared with 3 alternative von Willebrand factor activity assays.

Kenneth D Friedman, Martina Böhm-Weigert, Nicole DeSimone, Dennis J Dietzen, Charles Eby, Cynthia Flickinger, Walter Hoyer, Mareike Kahl, Kandice Kottke-Marchant, Thomas L Ortel and 5 more

Abstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Kenneth D FriedmanMedical Science Institute, Versiti Blood Center of Wisconsin, Milwaukee, Wisconsin, USA.
Martina Böhm-WeigertDepartment of Medical Affairs, Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany.
Nicole DeSimonePathology and Internal Medicine (Hematology/Oncology), University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Dennis J DietzenDepartment of Pathology and Immunology, Washington University, St. Louis, Missouri, USA.
Charles EbyDepartment of Pathology and Immunology, Washington University, St. Louis, Missouri, USA.
Cynthia FlickingerDepartment of Clinical Evaluation, Siemens Healthcare Diagnostics Inc, Glasgow, Delaware, USA.
Walter HoyerDepartment of Medical Affairs, Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany.
Mareike KahlDepartment of Medical Affairs, Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany.
Kandice Kottke-MarchantPathology and Laboratory Medicine Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
Thomas L OrtelDepartment of Medicine, Duke University, Durham, North Carolina, USA.
Jürgen PatzkeDepartment of Assay Development, Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany.
Steven W PipeDepartments of Pediatrics and Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Morgan StuartDepartments of Pediatrics and Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Ayse Anil TimurPathology and Laboratory Medicine Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
Ravindra SarodePathology and Internal Medicine (Hematology/Oncology), University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: To overcome deficiencies of the traditional von Willebrand factor (VWF) ristocetin cofactor activity assay (VWF:RCo), several automated assays for VWF platelet-binding activity have been developed. Information on the performance of these assays and their diagnostic utility remains limited. Objectives: To validate the VWF:glycoprotein IbM assay INNOVANCE VWF Ac and compare it with an automated VWF:RCo assay as well as with an automated assay and a manual VWF:Ab assay and to generate reference ranges and analyze reproducibility of the VWF:glycoprotein IbM assay. Methods: Clinical sites enrolled healthy subjects and patients representing the intended use population; VWF activity assays were performed, and results were analyzed. The performance of the INNOVANCE VWF Ac assay was also compared between the BCS XP System and the CS-2500 and CS-5100 analyzers. Results: The INNOVANCE VWF Ac assay correlated well with the VWF:RCo assay and the automated HemosIL VWF:Ab assay, with Pearson coefficients of >.9 and a predicted bias of ≤5.0 IU/dL at VWF levels of 30 IU/dL and ≤5.8 IU/dL at the levels of 50 IU/dL, but correlation and bias were not as good when compared with the REAADS manual VWF:Ab assay. Reference ranges observed for healthy subjects correlated well with previously published findings. Reproducibility of the INNOVANCE VWF Ac assay on the BCS XP System and the CS analyzers was excellent, as was correlation among devices. Conclusion: The characteristics of the INNOVANCE VWF Ac assay regarding comparability with other VWF activity assays, reference ranges, and precision support the use of this assay for evaluation of patients with concern for von Willebrand disease.

Indexed as

diagnosisreference rangereproducibility of resultsristocetin cofactorvon Willebrand diseasevon Willebrand factor

Identifiers

PMID38840662
PMCPMC11152683

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