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Inflammatory biomarkers are not useful for predicting prognosis in nursing and healthcare-associated pneumonia: A prospective, cohort study
Whether inflammatory biomarkers including procalcitonin (PCT) and C-reactive protein (CRP) are useful for predicting prognosis in nursing and healthcare-associated pneumonia (NHCAP) is unknown. The aim of the present study was to investigate the utility of serial PCT and CRP measurements for predict...
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Published in: | Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 2022-05, Vol.28 (5), p.623-630 |
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description | Whether inflammatory biomarkers including procalcitonin (PCT) and C-reactive protein (CRP) are useful for predicting prognosis in nursing and healthcare-associated pneumonia (NHCAP) is unknown. The aim of the present study was to investigate the utility of serial PCT and CRP measurements for predicting prognosis and treatment efficacy for hospitalized NHCAP patients.
This prospective, observational, cohort study enrolled consecutive NHCAP patients hospitalized at Kurashiki Central Hospital from October 2010 to September 2017. PCT and CRP were measured twice, once on admission and again within 48–72 h after admission. The primary outcome was 30-day all-cause mortality, and the secondary outcome was initial treatment failure.
A total of 299 patients were included. The 30-day mortality rate was 8.4% (25/299), and the initial treatment failure rate was 15.4% (46/299). On multivariate analysis, performance status [odds ratio (OR) (95% confidence interval (CI)): 2.25 (1.34–3.77), P = 0.002], temperature [OR (95%CI): 0.53 (0.32–0.88), P = 0.02], heart rate [OR (95%CI): 1.03 (1.01–1.06), P = 0.007], albumin [OR (95%CI): 0.42 (0.18–0.95), P = 0.04], and blood urea nitrogen [OR (95%CI): 1.02 (1.00–1.05), P = 0.04] were significant prognostic factors, and CRP D3 [OR (95%CI): 1.07 (1.02–1.11), P = 0.003] and PSI [OR (95%CI): 1.01 (1.00–1.02), P = 0.01] were the predictors of initial treatment failure. Consecutive measurements of PCT and CRP were not significant predictors of 30-day mortality.
Inflammatory biomarkers including PCT and CRP were not useful for predicting prognosis and treatment efficacy in NHCAP patients. We should carefully evaluate the patients’ vital signs and comorbidities when managing NHCAP patients. |
doi_str_mv | 10.1016/j.jiac.2022.01.006 |
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This prospective, observational, cohort study enrolled consecutive NHCAP patients hospitalized at Kurashiki Central Hospital from October 2010 to September 2017. PCT and CRP were measured twice, once on admission and again within 48–72 h after admission. The primary outcome was 30-day all-cause mortality, and the secondary outcome was initial treatment failure.
A total of 299 patients were included. The 30-day mortality rate was 8.4% (25/299), and the initial treatment failure rate was 15.4% (46/299). On multivariate analysis, performance status [odds ratio (OR) (95% confidence interval (CI)): 2.25 (1.34–3.77), P = 0.002], temperature [OR (95%CI): 0.53 (0.32–0.88), P = 0.02], heart rate [OR (95%CI): 1.03 (1.01–1.06), P = 0.007], albumin [OR (95%CI): 0.42 (0.18–0.95), P = 0.04], and blood urea nitrogen [OR (95%CI): 1.02 (1.00–1.05), P = 0.04] were significant prognostic factors, and CRP D3 [OR (95%CI): 1.07 (1.02–1.11), P = 0.003] and PSI [OR (95%CI): 1.01 (1.00–1.02), P = 0.01] were the predictors of initial treatment failure. Consecutive measurements of PCT and CRP were not significant predictors of 30-day mortality.
Inflammatory biomarkers including PCT and CRP were not useful for predicting prognosis and treatment efficacy in NHCAP patients. We should carefully evaluate the patients’ vital signs and comorbidities when managing NHCAP patients.</description><identifier>ISSN: 1341-321X</identifier><identifier>EISSN: 1437-7780</identifier><identifier>DOI: 10.1016/j.jiac.2022.01.006</identifier><identifier>PMID: 35153137</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Biomarkers ; C-reactive protein ; C-Reactive Protein - analysis ; Cohort Studies ; Healthcare-Associated Pneumonia ; Humans ; Inflammatory biomarker ; Nursing and healthcare-associated pneumonia ; Procalcitonin ; Prognosis ; Prospective Studies</subject><ispartof>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2022-05, Vol.28 (5), p.623-630</ispartof><rights>2022 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases</rights><rights>Copyright © 2022 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c331t-4cb9763afbce08ef87b8208c986f1f456ff5fb90ba47c1e4bee2ac1bb26c37b3</cites><orcidid>0000-0002-7508-0442 ; 0000-0001-9628-9125</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35153137$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ito, Akihiro</creatorcontrib><creatorcontrib>Ishida, Tadashi</creatorcontrib><creatorcontrib>Nakanishi, Yosuke</creatorcontrib><creatorcontrib>Yamazaki, Akio</creatorcontrib><creatorcontrib>Washio, Yasuyoshi</creatorcontrib><title>Inflammatory biomarkers are not useful for predicting prognosis in nursing and healthcare-associated pneumonia: A prospective, cohort study</title><title>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</title><addtitle>J Infect Chemother</addtitle><description>Whether inflammatory biomarkers including procalcitonin (PCT) and C-reactive protein (CRP) are useful for predicting prognosis in nursing and healthcare-associated pneumonia (NHCAP) is unknown. The aim of the present study was to investigate the utility of serial PCT and CRP measurements for predicting prognosis and treatment efficacy for hospitalized NHCAP patients.
This prospective, observational, cohort study enrolled consecutive NHCAP patients hospitalized at Kurashiki Central Hospital from October 2010 to September 2017. PCT and CRP were measured twice, once on admission and again within 48–72 h after admission. The primary outcome was 30-day all-cause mortality, and the secondary outcome was initial treatment failure.
A total of 299 patients were included. The 30-day mortality rate was 8.4% (25/299), and the initial treatment failure rate was 15.4% (46/299). On multivariate analysis, performance status [odds ratio (OR) (95% confidence interval (CI)): 2.25 (1.34–3.77), P = 0.002], temperature [OR (95%CI): 0.53 (0.32–0.88), P = 0.02], heart rate [OR (95%CI): 1.03 (1.01–1.06), P = 0.007], albumin [OR (95%CI): 0.42 (0.18–0.95), P = 0.04], and blood urea nitrogen [OR (95%CI): 1.02 (1.00–1.05), P = 0.04] were significant prognostic factors, and CRP D3 [OR (95%CI): 1.07 (1.02–1.11), P = 0.003] and PSI [OR (95%CI): 1.01 (1.00–1.02), P = 0.01] were the predictors of initial treatment failure. Consecutive measurements of PCT and CRP were not significant predictors of 30-day mortality.
Inflammatory biomarkers including PCT and CRP were not useful for predicting prognosis and treatment efficacy in NHCAP patients. We should carefully evaluate the patients’ vital signs and comorbidities when managing NHCAP patients.</description><subject>Biomarkers</subject><subject>C-reactive protein</subject><subject>C-Reactive Protein - analysis</subject><subject>Cohort Studies</subject><subject>Healthcare-Associated Pneumonia</subject><subject>Humans</subject><subject>Inflammatory biomarker</subject><subject>Nursing and healthcare-associated pneumonia</subject><subject>Procalcitonin</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><issn>1341-321X</issn><issn>1437-7780</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9UctuFDEQtBCIPOAHOCAfOTATP2bGXsQlishDisQlB26W7WlnvczYi-2JtN-Qn8ajDRxz6lKrqtRdhdAnSlpK6HCxa3de25YRxlpCW0KGN-iUdlw0QkjytmLe0YYz-usEneW8I4SKXsr36IT3tOeUi1P0fBfcpOdZl5gO2Pg46_QbUsY6AQ6x4CWDWybsYsL7BKO3xYfHCuNjiNln7AMOS8rrUocRb0FPZWurutE5R-t1gRHvAyxzDF5_w5erNu-h-jzBV2zjNqaCc1nGwwf0zukpw8eXeY4ern88XN029z9v7q4u7xvLOS1NZ81GDFw7Y4FIcFIYyYi0Gzk46rp-cK53ZkOM7oSl0BkApi01hg2WC8PP0ZejbT3kzwK5qNlnC9OkA8QlKzYwOYiOc1mp7Ei19eacwKl98jWhg6JErR2onVo7UGsHilBVO6iizy_-i5lh_C_5F3olfD8SoD755CGpbD0EW9NNNRc1Rv-a_18e05yj</recordid><startdate>202205</startdate><enddate>202205</enddate><creator>Ito, Akihiro</creator><creator>Ishida, Tadashi</creator><creator>Nakanishi, Yosuke</creator><creator>Yamazaki, Akio</creator><creator>Washio, Yasuyoshi</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7508-0442</orcidid><orcidid>https://orcid.org/0000-0001-9628-9125</orcidid></search><sort><creationdate>202205</creationdate><title>Inflammatory biomarkers are not useful for predicting prognosis in nursing and healthcare-associated pneumonia: A prospective, cohort study</title><author>Ito, Akihiro ; Ishida, Tadashi ; Nakanishi, Yosuke ; Yamazaki, Akio ; Washio, Yasuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c331t-4cb9763afbce08ef87b8208c986f1f456ff5fb90ba47c1e4bee2ac1bb26c37b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biomarkers</topic><topic>C-reactive protein</topic><topic>C-Reactive Protein - analysis</topic><topic>Cohort Studies</topic><topic>Healthcare-Associated Pneumonia</topic><topic>Humans</topic><topic>Inflammatory biomarker</topic><topic>Nursing and healthcare-associated pneumonia</topic><topic>Procalcitonin</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ito, Akihiro</creatorcontrib><creatorcontrib>Ishida, Tadashi</creatorcontrib><creatorcontrib>Nakanishi, Yosuke</creatorcontrib><creatorcontrib>Yamazaki, Akio</creatorcontrib><creatorcontrib>Washio, Yasuyoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ito, Akihiro</au><au>Ishida, Tadashi</au><au>Nakanishi, Yosuke</au><au>Yamazaki, Akio</au><au>Washio, Yasuyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inflammatory biomarkers are not useful for predicting prognosis in nursing and healthcare-associated pneumonia: A prospective, cohort study</atitle><jtitle>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</jtitle><addtitle>J Infect Chemother</addtitle><date>2022-05</date><risdate>2022</risdate><volume>28</volume><issue>5</issue><spage>623</spage><epage>630</epage><pages>623-630</pages><issn>1341-321X</issn><eissn>1437-7780</eissn><abstract>Whether inflammatory biomarkers including procalcitonin (PCT) and C-reactive protein (CRP) are useful for predicting prognosis in nursing and healthcare-associated pneumonia (NHCAP) is unknown. The aim of the present study was to investigate the utility of serial PCT and CRP measurements for predicting prognosis and treatment efficacy for hospitalized NHCAP patients.
This prospective, observational, cohort study enrolled consecutive NHCAP patients hospitalized at Kurashiki Central Hospital from October 2010 to September 2017. PCT and CRP were measured twice, once on admission and again within 48–72 h after admission. The primary outcome was 30-day all-cause mortality, and the secondary outcome was initial treatment failure.
A total of 299 patients were included. The 30-day mortality rate was 8.4% (25/299), and the initial treatment failure rate was 15.4% (46/299). On multivariate analysis, performance status [odds ratio (OR) (95% confidence interval (CI)): 2.25 (1.34–3.77), P = 0.002], temperature [OR (95%CI): 0.53 (0.32–0.88), P = 0.02], heart rate [OR (95%CI): 1.03 (1.01–1.06), P = 0.007], albumin [OR (95%CI): 0.42 (0.18–0.95), P = 0.04], and blood urea nitrogen [OR (95%CI): 1.02 (1.00–1.05), P = 0.04] were significant prognostic factors, and CRP D3 [OR (95%CI): 1.07 (1.02–1.11), P = 0.003] and PSI [OR (95%CI): 1.01 (1.00–1.02), P = 0.01] were the predictors of initial treatment failure. Consecutive measurements of PCT and CRP were not significant predictors of 30-day mortality.
Inflammatory biomarkers including PCT and CRP were not useful for predicting prognosis and treatment efficacy in NHCAP patients. We should carefully evaluate the patients’ vital signs and comorbidities when managing NHCAP patients.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>35153137</pmid><doi>10.1016/j.jiac.2022.01.006</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-7508-0442</orcidid><orcidid>https://orcid.org/0000-0001-9628-9125</orcidid></addata></record> |
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subjects | Biomarkers C-reactive protein C-Reactive Protein - analysis Cohort Studies Healthcare-Associated Pneumonia Humans Inflammatory biomarker Nursing and healthcare-associated pneumonia Procalcitonin Prognosis Prospective Studies |
title | Inflammatory biomarkers are not useful for predicting prognosis in nursing and healthcare-associated pneumonia: A prospective, cohort study |
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