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Diagnostic accuracy of four different D-dimer assays: A post-hoc analysis of the YEARS study.
Hamer, Henrike M; Stroobants, An K; Bavalia, Roisin; Ponjee, Gabrielle A E; Klok, Frederikus A; van der Hulle, Tom; Huisman, Menno V; Hendriks, Henriët A; Middeldorp, Saskia.
Affiliation
  • Hamer HM; Department of Clinical Chemistry, Amsterdam UMC, Amsterdam, the Netherlands. Electronic address: h.hamer@amsteramumc.nl.
  • Stroobants AK; Department of Clinical Chemistry, Amsterdam UMC, Amsterdam, the Netherlands.
  • Bavalia R; Department of Vascular Medicine, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
  • Ponjee GAE; Department of Clinical Chemistry and Hematology, MCH, The Hague, the Netherlands.
  • Klok FA; Department of Thrombosis and Hemostasis, LUMC, Leiden, the Netherlands.
  • van der Hulle T; Department of Thrombosis and Hemostasis, LUMC, Leiden, the Netherlands.
  • Huisman MV; Department of Thrombosis and Hemostasis, LUMC, Leiden, the Netherlands.
  • Hendriks HA; OLVG Lab bv, Amsterdam, the Netherlands.
  • Middeldorp S; Department of Vascular Medicine, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands; Department of Internal Medicine & Radboud Institute of Health Sciences (RIHS), Radboud University Medical Center, Nijmegen, the Netherlands.
Thromb Res ; 201: 18-22, 2021 05.
Article in En | MEDLINE | ID: mdl-33626463
ABSTRACT

INTRODUCTION:

For exclusion of pulmonary embolism (PE) clinical decision rules in combination with a D-dimer assay are applied. Currently available D-dimer assays are not standardized and it is unknown whether these differences have an impact on diagnostic management of suspected PE. Therefore, the aim is to explore differences between D-dimer assays and their impact on diagnostic outcome.

METHODS:

Data from all patients included in the YEARS study were collected. The YEARS study is a prospective, multicentre, cohort outcome study evaluating 3462 patients with suspected PE in which four different D-dimer assays were applied (Liatest, Innovance, Tinaquant, Vidas). Median D-dimer concentrations were calculated for each D-dimer assay. Sensitivity, specificity, PPV and NPV for detection of PE of all four assays were determined in patients without YEARS items and in those with ≥1 YEARS items (i.e. symptomatic deep vein thrombosis, haemoptysis, and whether PE is the most likely diagnosis).

RESULTS:

A total of 1323, 1100, 768 and 271 D-dimer concentrations were collected using the Liatest Innovance, Tinaquant and Vidas assay, respectively. Median D-dimer concentrations differed significantly between assays, with lowest values in the Tinaquant assay. In patients without YEARS items using a cutoff level of 1000 ng/mL, the NPV varied from 99,5 to 100%. In patients with ≥1 YEARS items using a 500 ng/mL cutoff, the NPV varied from 97,0 to 100% depending on the assay.

CONCLUSIONS:

The overall high NPV for all assays demonstrates the clinical value of the D-dimer assay. However, these results confirm differences between D-dimer assays, which have an impact on follow-up imaging. This emphasizes the need for standardization of D-dimer assays.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pulmonary Embolism / Venous Thrombosis Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Thromb Res Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pulmonary Embolism / Venous Thrombosis Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Thromb Res Year: 2021 Document type: Article
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