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Implementation of the Ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome
BACKGROUND AND AIMS: Compiling evidence has emerged for the relevance of flow cytometric assessment as a valuable part of the diagnostic work‐up of myelodysplastic syndrome (MDS). This study aimed at evaluating the implementation of a simple flow cytometric scoring system (FCSS), the Ogata score, in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6242364/ https://www.ncbi.nlm.nih.gov/pubmed/30623045 http://dx.doi.org/10.1002/hsr2.90 |
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author | Matzen, Sara Maj Hyldig Raaschou‐Jensen, Klas Kræsten Kallenbach, Klaus |
author_facet | Matzen, Sara Maj Hyldig Raaschou‐Jensen, Klas Kræsten Kallenbach, Klaus |
author_sort | Matzen, Sara Maj Hyldig |
collection | PubMed |
description | BACKGROUND AND AIMS: Compiling evidence has emerged for the relevance of flow cytometric assessment as a valuable part of the diagnostic work‐up of myelodysplastic syndrome (MDS). This study aimed at evaluating the implementation of a simple flow cytometric scoring system (FCSS), the Ogata score, in a routine diagnostic laboratory. METHODS: A total of 35 patient samples with a clinical suspicion of MDS were retrospectively assessed using the FCSS. The accuracy of the FCSS was evaluated on the basis of the final diagnoses of the patients. RESULTS: The final diagnoses included 17 MDS, 4 other myeloid cancers, and 14 reactive changes. Thirty‐two of 35 (91%) were correctly scored by the FCSS. All 3 incorrect scores were from samples classified as “other myeloid cancers.” Of the initial pathological evaluation of the bone marrows, 20% were inconclusive or incorrect. All inconclusive samples were correctly scored using the FCSS. CONCLUSION: The FCSS evaluated here has high accuracy and low complexity. Cases with inconclusive pathological evaluation will especially potentially benefit from adding the Ogata score to the diagnostic work‐up. The system will be feasible to implement in most flow cytometry laboratories without the need for supplemental antibody panels. It should be emphasized that the FCSS, in our hands, provided poor discrimination between MDS and other myeloid clonal diseases. |
format | Online Article Text |
id | pubmed-6242364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62423642019-01-08 Implementation of the Ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome Matzen, Sara Maj Hyldig Raaschou‐Jensen, Klas Kræsten Kallenbach, Klaus Health Sci Rep Research Articles BACKGROUND AND AIMS: Compiling evidence has emerged for the relevance of flow cytometric assessment as a valuable part of the diagnostic work‐up of myelodysplastic syndrome (MDS). This study aimed at evaluating the implementation of a simple flow cytometric scoring system (FCSS), the Ogata score, in a routine diagnostic laboratory. METHODS: A total of 35 patient samples with a clinical suspicion of MDS were retrospectively assessed using the FCSS. The accuracy of the FCSS was evaluated on the basis of the final diagnoses of the patients. RESULTS: The final diagnoses included 17 MDS, 4 other myeloid cancers, and 14 reactive changes. Thirty‐two of 35 (91%) were correctly scored by the FCSS. All 3 incorrect scores were from samples classified as “other myeloid cancers.” Of the initial pathological evaluation of the bone marrows, 20% were inconclusive or incorrect. All inconclusive samples were correctly scored using the FCSS. CONCLUSION: The FCSS evaluated here has high accuracy and low complexity. Cases with inconclusive pathological evaluation will especially potentially benefit from adding the Ogata score to the diagnostic work‐up. The system will be feasible to implement in most flow cytometry laboratories without the need for supplemental antibody panels. It should be emphasized that the FCSS, in our hands, provided poor discrimination between MDS and other myeloid clonal diseases. John Wiley and Sons Inc. 2018-09-26 /pmc/articles/PMC6242364/ /pubmed/30623045 http://dx.doi.org/10.1002/hsr2.90 Text en © 2018 The Authors. Health Science Reports published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Matzen, Sara Maj Hyldig Raaschou‐Jensen, Klas Kræsten Kallenbach, Klaus Implementation of the Ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome |
title | Implementation of the Ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome |
title_full | Implementation of the Ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome |
title_fullStr | Implementation of the Ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome |
title_full_unstemmed | Implementation of the Ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome |
title_short | Implementation of the Ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome |
title_sort | implementation of the ogata flow cytometric scoring system in routine diagnostics of myelodysplastic syndrome |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6242364/ https://www.ncbi.nlm.nih.gov/pubmed/30623045 http://dx.doi.org/10.1002/hsr2.90 |
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