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Point of Care D-Dimer Testing in the Emergency Department: A Bioequivalence Study
BACKGROUND: D-dimer is used widely as a diagnostic aid in low- and moderate-risk patients with suspected venous thromboembolism (VTE). While our laboratory utilizes VIDAS D-dimer analyzer (bioMérieux SA, France), our emergency department (ED) recently procured a D-dimer analyzer AQT90 FLEX (Radiomet...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Laboratory Medicine
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535194/ https://www.ncbi.nlm.nih.gov/pubmed/23301220 http://dx.doi.org/10.3343/alm.2013.33.1.34 |
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author | Perveen, Shuhana Unwin, Danielle Shetty, Amith Loknath |
author_facet | Perveen, Shuhana Unwin, Danielle Shetty, Amith Loknath |
author_sort | Perveen, Shuhana |
collection | PubMed |
description | BACKGROUND: D-dimer is used widely as a diagnostic aid in low- and moderate-risk patients with suspected venous thromboembolism (VTE). While our laboratory utilizes VIDAS D-dimer analyzer (bioMérieux SA, France), our emergency department (ED) recently procured a D-dimer analyzer AQT90 FLEX (Radiometer Medical ApS, Denmark) for point of care testing (POCT) to facilitate patient management. We aimed to determine whether the time taken to receive D-dimer results using the 2 different analyzers differed significantly and to quantify the limits of agreement between the results of the 2 methods measured on the same patient. METHODS: Adult patients presenting to the ED and requiring diagnostic workup for suspected VTE were included in this prospective observational study. Patients underwent simultaneous D-dimer measurements using the 2 different analyzers. RESULTS: The paired results from 104 patients were analyzed. The median time for the D-dimer results from triage by VIDAS was 258 min (Inter-quartile range [IQR], 173-360) and by POCT was 146 min (IQR, 55-280.5); the median time difference was 101.5 min (IQR, 82-125.5). On an average, POCT D-dimer values were 15% lower on the same sample (limits of agreement, 34-213%). POCT predicted 83% of VIDAS positive results (sensitivity, 83.3% [95% confidence interval (CI), 70.4-91.3%]; specificity, 100% [95% CI, 93.6-100%]). All patients with positive imaging were identified correctly by both methods. CONCLUSIONS: POCT delivers D-dimer results in significantly shorter turnaround times than pathology services; however, poor bioequivalence between VIDAS and POCT raises the issue of acceptability for use in the ED. |
format | Online Article Text |
id | pubmed-3535194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Korean Society for Laboratory Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-35351942013-01-08 Point of Care D-Dimer Testing in the Emergency Department: A Bioequivalence Study Perveen, Shuhana Unwin, Danielle Shetty, Amith Loknath Ann Lab Med Original Article BACKGROUND: D-dimer is used widely as a diagnostic aid in low- and moderate-risk patients with suspected venous thromboembolism (VTE). While our laboratory utilizes VIDAS D-dimer analyzer (bioMérieux SA, France), our emergency department (ED) recently procured a D-dimer analyzer AQT90 FLEX (Radiometer Medical ApS, Denmark) for point of care testing (POCT) to facilitate patient management. We aimed to determine whether the time taken to receive D-dimer results using the 2 different analyzers differed significantly and to quantify the limits of agreement between the results of the 2 methods measured on the same patient. METHODS: Adult patients presenting to the ED and requiring diagnostic workup for suspected VTE were included in this prospective observational study. Patients underwent simultaneous D-dimer measurements using the 2 different analyzers. RESULTS: The paired results from 104 patients were analyzed. The median time for the D-dimer results from triage by VIDAS was 258 min (Inter-quartile range [IQR], 173-360) and by POCT was 146 min (IQR, 55-280.5); the median time difference was 101.5 min (IQR, 82-125.5). On an average, POCT D-dimer values were 15% lower on the same sample (limits of agreement, 34-213%). POCT predicted 83% of VIDAS positive results (sensitivity, 83.3% [95% confidence interval (CI), 70.4-91.3%]; specificity, 100% [95% CI, 93.6-100%]). All patients with positive imaging were identified correctly by both methods. CONCLUSIONS: POCT delivers D-dimer results in significantly shorter turnaround times than pathology services; however, poor bioequivalence between VIDAS and POCT raises the issue of acceptability for use in the ED. The Korean Society for Laboratory Medicine 2013-01 2012-12-17 /pmc/articles/PMC3535194/ /pubmed/23301220 http://dx.doi.org/10.3343/alm.2013.33.1.34 Text en © The Korean Society for Laboratory Medicine. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Perveen, Shuhana Unwin, Danielle Shetty, Amith Loknath Point of Care D-Dimer Testing in the Emergency Department: A Bioequivalence Study |
title | Point of Care D-Dimer Testing in the Emergency Department: A Bioequivalence Study |
title_full | Point of Care D-Dimer Testing in the Emergency Department: A Bioequivalence Study |
title_fullStr | Point of Care D-Dimer Testing in the Emergency Department: A Bioequivalence Study |
title_full_unstemmed | Point of Care D-Dimer Testing in the Emergency Department: A Bioequivalence Study |
title_short | Point of Care D-Dimer Testing in the Emergency Department: A Bioequivalence Study |
title_sort | point of care d-dimer testing in the emergency department: a bioequivalence study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535194/ https://www.ncbi.nlm.nih.gov/pubmed/23301220 http://dx.doi.org/10.3343/alm.2013.33.1.34 |
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