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Determining a sampling regime for PCR detection of respiratory tract viral infection at coronial post-mortem examinations

Death due to respiratory infection is commonly encountered at autopsy. With only one opportunity to obtain samples for identification of a causative agent, it is important to ensure that sampling regimes are optimized to provide the greatest detection, without the expense and redundancy that can ari...

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Autores principales: Gilsenan-Reed, Caitlin, Higgins, Geoff, Langlois, Neil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308444/
https://www.ncbi.nlm.nih.gov/pubmed/32578131
http://dx.doi.org/10.1007/s12024-020-00273-w
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author Gilsenan-Reed, Caitlin
Higgins, Geoff
Langlois, Neil
author_facet Gilsenan-Reed, Caitlin
Higgins, Geoff
Langlois, Neil
author_sort Gilsenan-Reed, Caitlin
collection PubMed
description Death due to respiratory infection is commonly encountered at autopsy. With only one opportunity to obtain samples for identification of a causative agent, it is important to ensure that sampling regimes are optimized to provide the greatest detection, without the expense and redundancy that can arise from over-sampling. This study was performed retrospectively using data from Coronial autopsies over the period 2012–2019 from which swabs from the nasopharyngeal region, trachea and lung parenchyma, in addition to samples of lung tissue, had been submitted for multiplex PCR detection of respiratory pathogens. From 97 cases with all four samples, there were 24 with at least one positive result for viral infection. Some cases had multiple positive results and a total of 27 respiratory tract viruses were identified, of which rhinovirus, influenza A virus and respiratory syncytial virus were the most common. Seventeen of the 27 viral infections (63%) were identified in all four samples. However, in nearly all cases (96%) the nasopharyngeal swab detected the infective agent when the multiplex PCR panel had detected infection in any of the four sample types. A nasopharyngeal swab is considered to be an optimal sample for detection of respiratory tract viral infection. As the samples analyzed were acquired before the appearance of the COVID-19 virus, the applicability of this finding for COVID-19 screening is not established.
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spelling pubmed-73084442020-06-23 Determining a sampling regime for PCR detection of respiratory tract viral infection at coronial post-mortem examinations Gilsenan-Reed, Caitlin Higgins, Geoff Langlois, Neil Forensic Sci Med Pathol Original Article Death due to respiratory infection is commonly encountered at autopsy. With only one opportunity to obtain samples for identification of a causative agent, it is important to ensure that sampling regimes are optimized to provide the greatest detection, without the expense and redundancy that can arise from over-sampling. This study was performed retrospectively using data from Coronial autopsies over the period 2012–2019 from which swabs from the nasopharyngeal region, trachea and lung parenchyma, in addition to samples of lung tissue, had been submitted for multiplex PCR detection of respiratory pathogens. From 97 cases with all four samples, there were 24 with at least one positive result for viral infection. Some cases had multiple positive results and a total of 27 respiratory tract viruses were identified, of which rhinovirus, influenza A virus and respiratory syncytial virus were the most common. Seventeen of the 27 viral infections (63%) were identified in all four samples. However, in nearly all cases (96%) the nasopharyngeal swab detected the infective agent when the multiplex PCR panel had detected infection in any of the four sample types. A nasopharyngeal swab is considered to be an optimal sample for detection of respiratory tract viral infection. As the samples analyzed were acquired before the appearance of the COVID-19 virus, the applicability of this finding for COVID-19 screening is not established. Springer US 2020-06-23 2020 /pmc/articles/PMC7308444/ /pubmed/32578131 http://dx.doi.org/10.1007/s12024-020-00273-w Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Gilsenan-Reed, Caitlin
Higgins, Geoff
Langlois, Neil
Determining a sampling regime for PCR detection of respiratory tract viral infection at coronial post-mortem examinations
title Determining a sampling regime for PCR detection of respiratory tract viral infection at coronial post-mortem examinations
title_full Determining a sampling regime for PCR detection of respiratory tract viral infection at coronial post-mortem examinations
title_fullStr Determining a sampling regime for PCR detection of respiratory tract viral infection at coronial post-mortem examinations
title_full_unstemmed Determining a sampling regime for PCR detection of respiratory tract viral infection at coronial post-mortem examinations
title_short Determining a sampling regime for PCR detection of respiratory tract viral infection at coronial post-mortem examinations
title_sort determining a sampling regime for pcr detection of respiratory tract viral infection at coronial post-mortem examinations
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308444/
https://www.ncbi.nlm.nih.gov/pubmed/32578131
http://dx.doi.org/10.1007/s12024-020-00273-w
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