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The impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: A multi‐center retrospective study

The aim of this study was to evaluate the role of viral polymerase chain reaction (PCR) testing in patients with aseptic meningitis and identify opportunities for improvement in clinical management. All cerebrospinal fluid samples collected in 1 year from four teaching hospitals in Sydney, Australia...

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Autores principales: Kim, Myong Gyu, Gulholm, Trine, Lennard, Kate, Mirdad, Feras, Overton, Kristen, Maley, Michael, Konecny, Pamela, Andresen, David, Post, Jeffrey John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092443/
https://www.ncbi.nlm.nih.gov/pubmed/36207770
http://dx.doi.org/10.1002/jmv.28198
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author Kim, Myong Gyu
Gulholm, Trine
Lennard, Kate
Mirdad, Feras
Overton, Kristen
Maley, Michael
Konecny, Pamela
Andresen, David
Post, Jeffrey John
author_facet Kim, Myong Gyu
Gulholm, Trine
Lennard, Kate
Mirdad, Feras
Overton, Kristen
Maley, Michael
Konecny, Pamela
Andresen, David
Post, Jeffrey John
author_sort Kim, Myong Gyu
collection PubMed
description The aim of this study was to evaluate the role of viral polymerase chain reaction (PCR) testing in patients with aseptic meningitis and identify opportunities for improvement in clinical management. All cerebrospinal fluid samples collected in 1 year from four teaching hospitals in Sydney, Australia, were reviewed. Patients with aseptic meningitis were selected, and clinical and diagnostic features, hospital length of stay (LOS), and treatment were analyzed. Identifying a cause by viral PCR did not reduce hospital LOS (median 3 days) or antibiotic use (median 2 days), but the turnaround time of the PCR test correlated with LOS (Rs = 0.3822, p = 0.0003). Forty‐one percent of patients received intravenous acyclovir treatment, which was more frequent in patients admitted under neurologists than infectious diseases physicians (56% vs. 24%; p = 0.013). The majority of patients did not have investigations for alternative causes of aseptic meningitis such as human immunodeficiency virus and syphilis if the viral PCR panel was negative. The benefit of PCR testing in aseptic meningitis in adults in reducing LOS and antibiotic use is unclear. The reasons for unnecessary aciclovir use in meningitis syndromes require further assessment.
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spelling pubmed-100924432023-04-13 The impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: A multi‐center retrospective study Kim, Myong Gyu Gulholm, Trine Lennard, Kate Mirdad, Feras Overton, Kristen Maley, Michael Konecny, Pamela Andresen, David Post, Jeffrey John J Med Virol Research Articles The aim of this study was to evaluate the role of viral polymerase chain reaction (PCR) testing in patients with aseptic meningitis and identify opportunities for improvement in clinical management. All cerebrospinal fluid samples collected in 1 year from four teaching hospitals in Sydney, Australia, were reviewed. Patients with aseptic meningitis were selected, and clinical and diagnostic features, hospital length of stay (LOS), and treatment were analyzed. Identifying a cause by viral PCR did not reduce hospital LOS (median 3 days) or antibiotic use (median 2 days), but the turnaround time of the PCR test correlated with LOS (Rs = 0.3822, p = 0.0003). Forty‐one percent of patients received intravenous acyclovir treatment, which was more frequent in patients admitted under neurologists than infectious diseases physicians (56% vs. 24%; p = 0.013). The majority of patients did not have investigations for alternative causes of aseptic meningitis such as human immunodeficiency virus and syphilis if the viral PCR panel was negative. The benefit of PCR testing in aseptic meningitis in adults in reducing LOS and antibiotic use is unclear. The reasons for unnecessary aciclovir use in meningitis syndromes require further assessment. John Wiley and Sons Inc. 2022-10-13 2023-01 /pmc/articles/PMC10092443/ /pubmed/36207770 http://dx.doi.org/10.1002/jmv.28198 Text en © 2022 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Kim, Myong Gyu
Gulholm, Trine
Lennard, Kate
Mirdad, Feras
Overton, Kristen
Maley, Michael
Konecny, Pamela
Andresen, David
Post, Jeffrey John
The impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: A multi‐center retrospective study
title The impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: A multi‐center retrospective study
title_full The impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: A multi‐center retrospective study
title_fullStr The impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: A multi‐center retrospective study
title_full_unstemmed The impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: A multi‐center retrospective study
title_short The impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: A multi‐center retrospective study
title_sort impact of cerebrospinal fluid viral polymerase chain reaction testing on the management of adults with viral meningitis: a multi‐center retrospective study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092443/
https://www.ncbi.nlm.nih.gov/pubmed/36207770
http://dx.doi.org/10.1002/jmv.28198
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