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Evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis
INTRODUCTION: The high diagnostic accuracy of plasma metanephrines (PMets) in the diagnosis of Phaeochromocytoma/Paraganglioma (PPGL) is well established. Considerable controversy exists regarding optimum sampling conditions for PMets. The use of reference intervals that do not compromise diagnostic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574516/ https://www.ncbi.nlm.nih.gov/pubmed/28856203 http://dx.doi.org/10.1016/j.plabm.2016.05.001 |
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author | Griffin, T.P. Casey, R. Wall, D. Bell, M. O'Shea, P.M. |
author_facet | Griffin, T.P. Casey, R. Wall, D. Bell, M. O'Shea, P.M. |
author_sort | Griffin, T.P. |
collection | PubMed |
description | INTRODUCTION: The high diagnostic accuracy of plasma metanephrines (PMets) in the diagnosis of Phaeochromocytoma/Paraganglioma (PPGL) is well established. Considerable controversy exists regarding optimum sampling conditions for PMets. The use of reference intervals that do not compromise diagnostic sensitivity is recommended. However, the optimum rest period prior to sampling has yet to be clearly established. The aim of this study was to evaluate PMets concentrations in paired blood samples collected following 30 and 40 min seated-rest prior to sampling, in patients in whom it was clinically reasonable to suspect that PPGL may be present. DESIGN AND METHODS: A retrospective cross-sectional study design was used. PMets results from paired blood samples collected after 30 and 40 min seated-rest between January 2009 and June 2015 were recorded. Results were interpreted using reference intervals established in subjects seated and supine. RESULTS: A total of 410 patient results were eligible for analysis. There was no statistical difference between plasma normetanephrine (NMN) or metanephrine (MN) concentrations in samples collected following 30 and 40 min seated-rest in subjects with PPGL (n=11), post-resection of PPGL (n=20) or in whom PPGL was excluded (n=379). Using reference intervals established in the seated position, diagnostic sensitivity was 100% at 30 min and 90.9% at 40 min. Diagnostic specificity was approximately 95% at both time points. When supine reference intervals were used, diagnostic sensitivity was 100% and diagnostic specificity was reduced by ≈22% at both time points. CONCLUSION: Based on these data, we recommend at most 30 min continuous rest prior to sampling for PMets measurement. |
format | Online Article Text |
id | pubmed-5574516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-55745162017-08-30 Evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis Griffin, T.P. Casey, R. Wall, D. Bell, M. O'Shea, P.M. Pract Lab Med Article INTRODUCTION: The high diagnostic accuracy of plasma metanephrines (PMets) in the diagnosis of Phaeochromocytoma/Paraganglioma (PPGL) is well established. Considerable controversy exists regarding optimum sampling conditions for PMets. The use of reference intervals that do not compromise diagnostic sensitivity is recommended. However, the optimum rest period prior to sampling has yet to be clearly established. The aim of this study was to evaluate PMets concentrations in paired blood samples collected following 30 and 40 min seated-rest prior to sampling, in patients in whom it was clinically reasonable to suspect that PPGL may be present. DESIGN AND METHODS: A retrospective cross-sectional study design was used. PMets results from paired blood samples collected after 30 and 40 min seated-rest between January 2009 and June 2015 were recorded. Results were interpreted using reference intervals established in subjects seated and supine. RESULTS: A total of 410 patient results were eligible for analysis. There was no statistical difference between plasma normetanephrine (NMN) or metanephrine (MN) concentrations in samples collected following 30 and 40 min seated-rest in subjects with PPGL (n=11), post-resection of PPGL (n=20) or in whom PPGL was excluded (n=379). Using reference intervals established in the seated position, diagnostic sensitivity was 100% at 30 min and 90.9% at 40 min. Diagnostic specificity was approximately 95% at both time points. When supine reference intervals were used, diagnostic sensitivity was 100% and diagnostic specificity was reduced by ≈22% at both time points. CONCLUSION: Based on these data, we recommend at most 30 min continuous rest prior to sampling for PMets measurement. Elsevier 2016-05-07 /pmc/articles/PMC5574516/ /pubmed/28856203 http://dx.doi.org/10.1016/j.plabm.2016.05.001 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Griffin, T.P. Casey, R. Wall, D. Bell, M. O'Shea, P.M. Evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis |
title | Evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis |
title_full | Evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis |
title_fullStr | Evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis |
title_full_unstemmed | Evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis |
title_short | Evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis |
title_sort | evaluating the optimum rest period prior to blood collection for fractionated plasma free metanephrines analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574516/ https://www.ncbi.nlm.nih.gov/pubmed/28856203 http://dx.doi.org/10.1016/j.plabm.2016.05.001 |
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