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How to approach clinically discordant FT4 results when changing testing platforms: real-world evidence
PURPOSE: Measurement of thyroid-stimulating hormone (TSH) and free thyroxine (FT4) is important for assessing thyroid dysfunction. After changing assay manufacturer, high FT4 versus TSH levels were reported at Ente Ospedaliero Cantonale (EOC; Bellinzona, Switzerland). METHODS: Exploratory analysis u...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325840/ https://www.ncbi.nlm.nih.gov/pubmed/35689789 http://dx.doi.org/10.1007/s12020-022-03098-5 |
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author | Giovanella, Luca Duntas, Leonidas D’Aurizio, Federica Kurka, Hedwig Ammer, Tatjana Rank, Christopher M. Visser, W. Edward van den Berg, Sjoerd A. A. |
author_facet | Giovanella, Luca Duntas, Leonidas D’Aurizio, Federica Kurka, Hedwig Ammer, Tatjana Rank, Christopher M. Visser, W. Edward van den Berg, Sjoerd A. A. |
author_sort | Giovanella, Luca |
collection | PubMed |
description | PURPOSE: Measurement of thyroid-stimulating hormone (TSH) and free thyroxine (FT4) is important for assessing thyroid dysfunction. After changing assay manufacturer, high FT4 versus TSH levels were reported at Ente Ospedaliero Cantonale (EOC; Bellinzona, Switzerland). METHODS: Exploratory analysis used existing TSH and FT4 measurements taken at EOC during routine clinical practice (February 2018–April 2020) using Elecsys® TSH and Elecsys FT4 III immunoassays on cobas® 6000 and cobas 8000 analyzers (Roche Diagnostics). Reference intervals (RIs) were estimated using both direct and indirect (refineR algorithm) methods. RESULTS: In samples with normal TSH levels, 90.9% of FT4 measurements were within the normal range provided by Roche (12–22 pmol/L). For FT4 measurements, confidence intervals (CIs) for the lower end of the RI obtained using direct and indirect methods were lower than estimated values in the method sheet; the estimated value of the upper end of the RI (UEoRI) in the method sheet was within the CI for the UEoRI using the direct method but not the indirect method. CIs for the direct and indirect methods overlapped at both ends of the RI. The most common cause of increased FT4 with normal TSH was identified in a subset of patients as use of thyroxine therapy (72.6%). CONCLUSIONS: It is important to verify RIs for FT4 in the laboratory population when changing testing platforms; indirect methods may constitute a convenient tool for this. Applying specific RIs for selected subpopulations should be considered to avoid misinterpretations and inappropriate clinical actions. |
format | Online Article Text |
id | pubmed-9325840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-93258402022-07-28 How to approach clinically discordant FT4 results when changing testing platforms: real-world evidence Giovanella, Luca Duntas, Leonidas D’Aurizio, Federica Kurka, Hedwig Ammer, Tatjana Rank, Christopher M. Visser, W. Edward van den Berg, Sjoerd A. A. Endocrine Original Article PURPOSE: Measurement of thyroid-stimulating hormone (TSH) and free thyroxine (FT4) is important for assessing thyroid dysfunction. After changing assay manufacturer, high FT4 versus TSH levels were reported at Ente Ospedaliero Cantonale (EOC; Bellinzona, Switzerland). METHODS: Exploratory analysis used existing TSH and FT4 measurements taken at EOC during routine clinical practice (February 2018–April 2020) using Elecsys® TSH and Elecsys FT4 III immunoassays on cobas® 6000 and cobas 8000 analyzers (Roche Diagnostics). Reference intervals (RIs) were estimated using both direct and indirect (refineR algorithm) methods. RESULTS: In samples with normal TSH levels, 90.9% of FT4 measurements were within the normal range provided by Roche (12–22 pmol/L). For FT4 measurements, confidence intervals (CIs) for the lower end of the RI obtained using direct and indirect methods were lower than estimated values in the method sheet; the estimated value of the upper end of the RI (UEoRI) in the method sheet was within the CI for the UEoRI using the direct method but not the indirect method. CIs for the direct and indirect methods overlapped at both ends of the RI. The most common cause of increased FT4 with normal TSH was identified in a subset of patients as use of thyroxine therapy (72.6%). CONCLUSIONS: It is important to verify RIs for FT4 in the laboratory population when changing testing platforms; indirect methods may constitute a convenient tool for this. Applying specific RIs for selected subpopulations should be considered to avoid misinterpretations and inappropriate clinical actions. Springer US 2022-06-11 2022 /pmc/articles/PMC9325840/ /pubmed/35689789 http://dx.doi.org/10.1007/s12020-022-03098-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Giovanella, Luca Duntas, Leonidas D’Aurizio, Federica Kurka, Hedwig Ammer, Tatjana Rank, Christopher M. Visser, W. Edward van den Berg, Sjoerd A. A. How to approach clinically discordant FT4 results when changing testing platforms: real-world evidence |
title | How to approach clinically discordant FT4 results when changing testing platforms: real-world evidence |
title_full | How to approach clinically discordant FT4 results when changing testing platforms: real-world evidence |
title_fullStr | How to approach clinically discordant FT4 results when changing testing platforms: real-world evidence |
title_full_unstemmed | How to approach clinically discordant FT4 results when changing testing platforms: real-world evidence |
title_short | How to approach clinically discordant FT4 results when changing testing platforms: real-world evidence |
title_sort | how to approach clinically discordant ft4 results when changing testing platforms: real-world evidence |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325840/ https://www.ncbi.nlm.nih.gov/pubmed/35689789 http://dx.doi.org/10.1007/s12020-022-03098-5 |
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