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Characteristics of hospitalized COVID-19 patients with other respiratory pathogens identified by rapid diagnostic test
Rapid diagnostic tests (RDTs) significantly impact disease treatment strategy. In Japan, information on the use of RDTs for patients with COVID-19 is limited. Here, we aimed to investigate the RDT implementation rate, pathogen detection rate, and clinical characteristics of patients positive for oth...
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Published in: | Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 2023-05, Vol.29 (5), p.539-545 |
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container_title | Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy |
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creator | Suzuki, Michiyo Hayakawa, Kayoko Asai, Yusuke Terada, Mari Kitajima, Koji Tsuzuki, Shinya Moriya, Ataru Moriya, Kyoji Uchiyama-Nakamura, Fukumi Ohmagari, Norio |
description | Rapid diagnostic tests (RDTs) significantly impact disease treatment strategy. In Japan, information on the use of RDTs for patients with COVID-19 is limited. Here, we aimed to investigate the RDT implementation rate, pathogen detection rate, and clinical characteristics of patients positive for other pathogens by using COVIREGI-JP, a national registry of hospitalized patients with COVID-19.
A total of 42,309 COVID-19 patients were included. For immunochromatographic testing, influenza was the most common (n = 2881 [6.8%]), followed by Mycoplasma pneumoniae (n = 2129 [5%]) and group A streptococcus (GAS) (n = 372 [0.9%]). Urine antigen testing was performed for 5524 (13.1%) patients for S. pneumoniae and for 5326 patients (12.6%) for L. pneumophila.
The completion rate of M. pneumonia loop-mediated isothermal amplification (LAMP) testing was low (n = 97 [0.2%]). FilmArray RP was performed in 372 (0.9%) patients; 1.2% (36/2881) of patients were positive for influenza, 0.9% (2/223) for the respiratory syncytial virus (RSV), 9.6% (205/2129) for M. pneumoniae, and 7.3% (27/372) for GAS. The positivity rate for urine antigen testing was 3.3% (183/5524) for S. pneumoniae and 0.2% (13/5326) for L. pneumophila. The positivity rate for LAMP test was 5.2% (5/97) for M. pneumoniae. Five of 372 patients (1.3%) had positive FilmArray RP, with human enterovirus being the most frequently detected (1.3%, 5/372).
The characteristics of patients with and without RDTs submission and positive and negative results differed for each pathogen. RDTs remain an important diagnostic tool in patients with COVID-19 in whom coinfection with other pathogens needs to be tested based on clinical evaluation. |
doi_str_mv | 10.1016/j.jiac.2023.02.006 |
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A total of 42,309 COVID-19 patients were included. For immunochromatographic testing, influenza was the most common (n = 2881 [6.8%]), followed by Mycoplasma pneumoniae (n = 2129 [5%]) and group A streptococcus (GAS) (n = 372 [0.9%]). Urine antigen testing was performed for 5524 (13.1%) patients for S. pneumoniae and for 5326 patients (12.6%) for L. pneumophila.
The completion rate of M. pneumonia loop-mediated isothermal amplification (LAMP) testing was low (n = 97 [0.2%]). FilmArray RP was performed in 372 (0.9%) patients; 1.2% (36/2881) of patients were positive for influenza, 0.9% (2/223) for the respiratory syncytial virus (RSV), 9.6% (205/2129) for M. pneumoniae, and 7.3% (27/372) for GAS. The positivity rate for urine antigen testing was 3.3% (183/5524) for S. pneumoniae and 0.2% (13/5326) for L. pneumophila. The positivity rate for LAMP test was 5.2% (5/97) for M. pneumoniae. Five of 372 patients (1.3%) had positive FilmArray RP, with human enterovirus being the most frequently detected (1.3%, 5/372).
The characteristics of patients with and without RDTs submission and positive and negative results differed for each pathogen. RDTs remain an important diagnostic tool in patients with COVID-19 in whom coinfection with other pathogens needs to be tested based on clinical evaluation.</description><identifier>ISSN: 1341-321X</identifier><identifier>EISSN: 1437-7780</identifier><identifier>DOI: 10.1016/j.jiac.2023.02.006</identifier><identifier>PMID: 36813162</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Co-detection ; COVID-19 - diagnosis ; COVID-19 Testing ; Hospitalization ; Humans ; Influenza ; Influenza, Human - diagnosis ; Mycoplasma pneumoniae - genetics ; Rapid Diagnostic Tests ; Respiratory Syncytial Virus, Human ; SARS-CoV-2</subject><ispartof>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2023-05, Vol.29 (5), p.539-545</ispartof><rights>2023 Japanese Society of Chemotherapy, Japanese Association for Infectious Diseases, and Japanese Society for Infection Prevention and Control</rights><rights>Copyright © 2023 Japanese Society of Chemotherapy, Japanese Association for Infectious Diseases, and Japanese Society for Infection Prevention and Control. Published by Elsevier Ltd. All rights reserved.</rights><rights>2023 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved. 2023 Japanese Society of Chemotherapy, Japanese Association for Infectious Diseases, and Japanese Society for Infection Prevention and Control</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-543adcfd8684dc6f06deb48e57ad181fdf216c6086d8d6f0427d11219a68293</citedby><cites>FETCH-LOGICAL-c479t-543adcfd8684dc6f06deb48e57ad181fdf216c6086d8d6f0427d11219a68293</cites><orcidid>0000-0002-8504-1244 ; 0000-0002-9730-8532 ; 0000-0002-5171-1828 ; 0000-0003-2979-3449</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36813162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suzuki, Michiyo</creatorcontrib><creatorcontrib>Hayakawa, Kayoko</creatorcontrib><creatorcontrib>Asai, Yusuke</creatorcontrib><creatorcontrib>Terada, Mari</creatorcontrib><creatorcontrib>Kitajima, Koji</creatorcontrib><creatorcontrib>Tsuzuki, Shinya</creatorcontrib><creatorcontrib>Moriya, Ataru</creatorcontrib><creatorcontrib>Moriya, Kyoji</creatorcontrib><creatorcontrib>Uchiyama-Nakamura, Fukumi</creatorcontrib><creatorcontrib>Ohmagari, Norio</creatorcontrib><title>Characteristics of hospitalized COVID-19 patients with other respiratory pathogens identified by rapid diagnostic test</title><title>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</title><addtitle>J Infect Chemother</addtitle><description>Rapid diagnostic tests (RDTs) significantly impact disease treatment strategy. In Japan, information on the use of RDTs for patients with COVID-19 is limited. Here, we aimed to investigate the RDT implementation rate, pathogen detection rate, and clinical characteristics of patients positive for other pathogens by using COVIREGI-JP, a national registry of hospitalized patients with COVID-19.
A total of 42,309 COVID-19 patients were included. For immunochromatographic testing, influenza was the most common (n = 2881 [6.8%]), followed by Mycoplasma pneumoniae (n = 2129 [5%]) and group A streptococcus (GAS) (n = 372 [0.9%]). Urine antigen testing was performed for 5524 (13.1%) patients for S. pneumoniae and for 5326 patients (12.6%) for L. pneumophila.
The completion rate of M. pneumonia loop-mediated isothermal amplification (LAMP) testing was low (n = 97 [0.2%]). FilmArray RP was performed in 372 (0.9%) patients; 1.2% (36/2881) of patients were positive for influenza, 0.9% (2/223) for the respiratory syncytial virus (RSV), 9.6% (205/2129) for M. pneumoniae, and 7.3% (27/372) for GAS. The positivity rate for urine antigen testing was 3.3% (183/5524) for S. pneumoniae and 0.2% (13/5326) for L. pneumophila. The positivity rate for LAMP test was 5.2% (5/97) for M. pneumoniae. Five of 372 patients (1.3%) had positive FilmArray RP, with human enterovirus being the most frequently detected (1.3%, 5/372).
The characteristics of patients with and without RDTs submission and positive and negative results differed for each pathogen. RDTs remain an important diagnostic tool in patients with COVID-19 in whom coinfection with other pathogens needs to be tested based on clinical evaluation.</description><subject>Co-detection</subject><subject>COVID-19 - diagnosis</subject><subject>COVID-19 Testing</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Influenza</subject><subject>Influenza, Human - diagnosis</subject><subject>Mycoplasma pneumoniae - genetics</subject><subject>Rapid Diagnostic Tests</subject><subject>Respiratory Syncytial Virus, Human</subject><subject>SARS-CoV-2</subject><issn>1341-321X</issn><issn>1437-7780</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kUuLFDEUhYMozjj6B1xIlm6qzKuTFIgg7WtgYBaKuAvpJNV1m-pKmaR7aH-9KXocdCNZJHC-e-4hB6GXlLSUUPlm1-7AupYRxlvCWkLkI3RJBVeNUpo8rm8uaMMZ_XGBnuW8I4SqldZP0QWXmnIq2SU6rgebrCshQS7gMo49HmKeodgRfgWP17ffrz80tMOzLRCmkvEdlAHHMoSEU6hksiWm06IPcRumjMFXDnqo05sTTnYGjz3Y7RSXFbiEXJ6jJ70dc3hxf1-hr58-flt_aW5uP1-v3980TqiuNCvBrXe911IL72RPpA8bocNKWU817X3PqHSSaOm1r7JgylPKaGelZh2_Qu_OrvNhsw_e1VjJjmZOsLfpZKIF868ywWC28Wi6jtdDqsHre4MUfx5qbrOH7MI42inEQzZMqY4LToSqKDujLsWcU-gf1lBilrrMzix1maUuQ5ipddWhV38HfBj5008F3p6BUD_pCCGZ7GoLLnhIwRXjI_zP_zesl6n0</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Suzuki, Michiyo</creator><creator>Hayakawa, Kayoko</creator><creator>Asai, Yusuke</creator><creator>Terada, Mari</creator><creator>Kitajima, Koji</creator><creator>Tsuzuki, Shinya</creator><creator>Moriya, Ataru</creator><creator>Moriya, Kyoji</creator><creator>Uchiyama-Nakamura, Fukumi</creator><creator>Ohmagari, Norio</creator><general>Elsevier Ltd</general><general>Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. 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In Japan, information on the use of RDTs for patients with COVID-19 is limited. Here, we aimed to investigate the RDT implementation rate, pathogen detection rate, and clinical characteristics of patients positive for other pathogens by using COVIREGI-JP, a national registry of hospitalized patients with COVID-19.
A total of 42,309 COVID-19 patients were included. For immunochromatographic testing, influenza was the most common (n = 2881 [6.8%]), followed by Mycoplasma pneumoniae (n = 2129 [5%]) and group A streptococcus (GAS) (n = 372 [0.9%]). Urine antigen testing was performed for 5524 (13.1%) patients for S. pneumoniae and for 5326 patients (12.6%) for L. pneumophila.
The completion rate of M. pneumonia loop-mediated isothermal amplification (LAMP) testing was low (n = 97 [0.2%]). FilmArray RP was performed in 372 (0.9%) patients; 1.2% (36/2881) of patients were positive for influenza, 0.9% (2/223) for the respiratory syncytial virus (RSV), 9.6% (205/2129) for M. pneumoniae, and 7.3% (27/372) for GAS. The positivity rate for urine antigen testing was 3.3% (183/5524) for S. pneumoniae and 0.2% (13/5326) for L. pneumophila. The positivity rate for LAMP test was 5.2% (5/97) for M. pneumoniae. Five of 372 patients (1.3%) had positive FilmArray RP, with human enterovirus being the most frequently detected (1.3%, 5/372).
The characteristics of patients with and without RDTs submission and positive and negative results differed for each pathogen. RDTs remain an important diagnostic tool in patients with COVID-19 in whom coinfection with other pathogens needs to be tested based on clinical evaluation.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>36813162</pmid><doi>10.1016/j.jiac.2023.02.006</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-8504-1244</orcidid><orcidid>https://orcid.org/0000-0002-9730-8532</orcidid><orcidid>https://orcid.org/0000-0002-5171-1828</orcidid><orcidid>https://orcid.org/0000-0003-2979-3449</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Co-detection COVID-19 - diagnosis COVID-19 Testing Hospitalization Humans Influenza Influenza, Human - diagnosis Mycoplasma pneumoniae - genetics Rapid Diagnostic Tests Respiratory Syncytial Virus, Human SARS-CoV-2 |
title | Characteristics of hospitalized COVID-19 patients with other respiratory pathogens identified by rapid diagnostic test |
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