Development and Internal Validation of a Prediction Model to Risk Stratify Children With Suspected Community-Acquired Pneumonia

Abstract Background Although community-acquired pneumonia (CAP) is one of the most common infections in children, no tools exist to risk stratify children with suspected CAP. We developed and validated a prediction model to risk stratify and inform hospitalization decisions in children with suspecte...

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Veröffentlicht in:Clinical infectious diseases 2021-11, Vol.73 (9), p.e2713-e2721
Hauptverfasser: Florin, Todd A, Ambroggio, Lilliam, Lorenz, Douglas, Kachelmeyer, Andrea, Ruddy, Richard M, Kuppermann, Nathan, Shah, Samir S
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container_end_page e2721
container_issue 9
container_start_page e2713
container_title Clinical infectious diseases
container_volume 73
creator Florin, Todd A
Ambroggio, Lilliam
Lorenz, Douglas
Kachelmeyer, Andrea
Ruddy, Richard M
Kuppermann, Nathan
Shah, Samir S
description Abstract Background Although community-acquired pneumonia (CAP) is one of the most common infections in children, no tools exist to risk stratify children with suspected CAP. We developed and validated a prediction model to risk stratify and inform hospitalization decisions in children with suspected CAP. Methods We performed a prospective cohort study of children aged 3 months to 18 years with suspected CAP in a pediatric emergency department. Primary outcome was disease severity, defined as mild (discharge home or hospitalization for 24 hours, septic shock, vasoactive agents, positive-pressure ventilation, chest drainage, extracorporeal membrane oxygenation, or death). Ordinal logistic regression and bootstrapped backwards selection were used to derive and internally validate our model. Results Of 1128 children, 371 (32.9%) developed moderate disease and 48 (4.3%) severe disease. Severity models demonstrated excellent discrimination (optimism-corrected c-indices of 0.81) and outstanding calibration. Severity predictors in the final model included respiratory rate, systolic blood pressure, oxygenation, retractions, capillary refill, atelectasis or pneumonia on chest radiograph, and pleural effusion. Conclusions We derived and internally validated a score that accurately predicts disease severity in children with suspected CAP. Once externally validated, this score has potential to facilitate management decisions by providing individualized risk estimates that can be used in conjunction with clinical judgment to improve the care of children with suspected CAP. In this prospective study of 1128 children with suspected CAP, we developed a well-calibrated severity score of 7 variables (respiratory rate, blood pressure, oxygenation, retractions, capillary refill, radiographic findings, pleural effusion) with excellent discriminatory ability for moderate or severe disease.
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We developed and validated a prediction model to risk stratify and inform hospitalization decisions in children with suspected CAP. Methods We performed a prospective cohort study of children aged 3 months to 18 years with suspected CAP in a pediatric emergency department. Primary outcome was disease severity, defined as mild (discharge home or hospitalization for &lt;24 hours with no oxygen or intravenous [IV] fluids), moderate (hospitalization &lt;24 hours with oxygen or IV fluids, or hospitalization &gt;24 hours), or severe (intensive care unit stay for &gt;24 hours, septic shock, vasoactive agents, positive-pressure ventilation, chest drainage, extracorporeal membrane oxygenation, or death). Ordinal logistic regression and bootstrapped backwards selection were used to derive and internally validate our model. Results Of 1128 children, 371 (32.9%) developed moderate disease and 48 (4.3%) severe disease. Severity models demonstrated excellent discrimination (optimism-corrected c-indices of 0.81) and outstanding calibration. Severity predictors in the final model included respiratory rate, systolic blood pressure, oxygenation, retractions, capillary refill, atelectasis or pneumonia on chest radiograph, and pleural effusion. Conclusions We derived and internally validated a score that accurately predicts disease severity in children with suspected CAP. Once externally validated, this score has potential to facilitate management decisions by providing individualized risk estimates that can be used in conjunction with clinical judgment to improve the care of children with suspected CAP. In this prospective study of 1128 children with suspected CAP, we developed a well-calibrated severity score of 7 variables (respiratory rate, blood pressure, oxygenation, retractions, capillary refill, radiographic findings, pleural effusion) with excellent discriminatory ability for moderate or severe disease.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/ciaa1690</identifier><identifier>PMID: 33159514</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Online only</subject><ispartof>Clinical infectious diseases, 2021-11, Vol.73 (9), p.e2713-e2721</ispartof><rights>The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2020</rights><rights>The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-623cf2491c0beeec5500368b3d744426cb89bf4e5ae35bfc1bfc0ccdf6d671ca3</citedby><cites>FETCH-LOGICAL-c416t-623cf2491c0beeec5500368b3d744426cb89bf4e5ae35bfc1bfc0ccdf6d671ca3</cites><orcidid>0000-0002-4387-2605</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,1579,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33159514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Florin, Todd A</creatorcontrib><creatorcontrib>Ambroggio, Lilliam</creatorcontrib><creatorcontrib>Lorenz, Douglas</creatorcontrib><creatorcontrib>Kachelmeyer, Andrea</creatorcontrib><creatorcontrib>Ruddy, Richard M</creatorcontrib><creatorcontrib>Kuppermann, Nathan</creatorcontrib><creatorcontrib>Shah, Samir S</creatorcontrib><title>Development and Internal Validation of a Prediction Model to Risk Stratify Children With Suspected Community-Acquired Pneumonia</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Abstract Background Although community-acquired pneumonia (CAP) is one of the most common infections in children, no tools exist to risk stratify children with suspected CAP. We developed and validated a prediction model to risk stratify and inform hospitalization decisions in children with suspected CAP. Methods We performed a prospective cohort study of children aged 3 months to 18 years with suspected CAP in a pediatric emergency department. Primary outcome was disease severity, defined as mild (discharge home or hospitalization for &lt;24 hours with no oxygen or intravenous [IV] fluids), moderate (hospitalization &lt;24 hours with oxygen or IV fluids, or hospitalization &gt;24 hours), or severe (intensive care unit stay for &gt;24 hours, septic shock, vasoactive agents, positive-pressure ventilation, chest drainage, extracorporeal membrane oxygenation, or death). Ordinal logistic regression and bootstrapped backwards selection were used to derive and internally validate our model. Results Of 1128 children, 371 (32.9%) developed moderate disease and 48 (4.3%) severe disease. Severity models demonstrated excellent discrimination (optimism-corrected c-indices of 0.81) and outstanding calibration. Severity predictors in the final model included respiratory rate, systolic blood pressure, oxygenation, retractions, capillary refill, atelectasis or pneumonia on chest radiograph, and pleural effusion. Conclusions We derived and internally validated a score that accurately predicts disease severity in children with suspected CAP. Once externally validated, this score has potential to facilitate management decisions by providing individualized risk estimates that can be used in conjunction with clinical judgment to improve the care of children with suspected CAP. In this prospective study of 1128 children with suspected CAP, we developed a well-calibrated severity score of 7 variables (respiratory rate, blood pressure, oxygenation, retractions, capillary refill, radiographic findings, pleural effusion) with excellent discriminatory ability for moderate or severe disease.</description><subject>Online only</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kctvFSEUh4mxsbW6c23Y2YVjYXjcmY1Jc301aWNjfSwJA2e8KANTYJrcVf910ds2unFxAuR8-Q4nP4SeUfKKkp4dG2draU1lTx6gAyrYqpGipw_rnYiu4R3r9tHjnH8QQmlHxCO0zxgVvaD8AN28gWvwcZ4gFKyDxaehQAra46_aO6uLiwHHEWt8kcA68-d9Hi14XCL-5PJPfFlSxcYtXm-ctwkC_ubKBl8ueQZTwOJ1nKYluLJtTszV4qoHXwRYphicfoL2Ru0zPL09D9GXd28_rz80Zx_fn65PzhrDqSyNbJkZW95TQwYAMEIQwmQ3MLvinLfSDF0_jByEBiaG0dBaxBg7SitX1Gh2iF7vvPMyTGBNXTdpr-bkJp22Kmqn_u0Et1Hf47XqhGQtlVVwdCtI8WqBXNTksgHvdYC4ZNVy0a3atme0oi93qEkx5wTj_RhK1O_MVM1M3WVW8ed_f-0evgupAi92QFzm_6t-AQVdpMY</recordid><startdate>20211102</startdate><enddate>20211102</enddate><creator>Florin, Todd A</creator><creator>Ambroggio, Lilliam</creator><creator>Lorenz, Douglas</creator><creator>Kachelmeyer, Andrea</creator><creator>Ruddy, Richard M</creator><creator>Kuppermann, Nathan</creator><creator>Shah, Samir S</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4387-2605</orcidid></search><sort><creationdate>20211102</creationdate><title>Development and Internal Validation of a Prediction Model to Risk Stratify Children With Suspected Community-Acquired Pneumonia</title><author>Florin, Todd A ; Ambroggio, Lilliam ; Lorenz, Douglas ; Kachelmeyer, Andrea ; Ruddy, Richard M ; Kuppermann, Nathan ; Shah, Samir S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-623cf2491c0beeec5500368b3d744426cb89bf4e5ae35bfc1bfc0ccdf6d671ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Online only</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Florin, Todd A</creatorcontrib><creatorcontrib>Ambroggio, Lilliam</creatorcontrib><creatorcontrib>Lorenz, Douglas</creatorcontrib><creatorcontrib>Kachelmeyer, Andrea</creatorcontrib><creatorcontrib>Ruddy, Richard M</creatorcontrib><creatorcontrib>Kuppermann, Nathan</creatorcontrib><creatorcontrib>Shah, Samir S</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Florin, Todd A</au><au>Ambroggio, Lilliam</au><au>Lorenz, Douglas</au><au>Kachelmeyer, Andrea</au><au>Ruddy, Richard M</au><au>Kuppermann, Nathan</au><au>Shah, Samir S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and Internal Validation of a Prediction Model to Risk Stratify Children With Suspected Community-Acquired Pneumonia</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2021-11-02</date><risdate>2021</risdate><volume>73</volume><issue>9</issue><spage>e2713</spage><epage>e2721</epage><pages>e2713-e2721</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>Abstract Background Although community-acquired pneumonia (CAP) is one of the most common infections in children, no tools exist to risk stratify children with suspected CAP. We developed and validated a prediction model to risk stratify and inform hospitalization decisions in children with suspected CAP. Methods We performed a prospective cohort study of children aged 3 months to 18 years with suspected CAP in a pediatric emergency department. Primary outcome was disease severity, defined as mild (discharge home or hospitalization for &lt;24 hours with no oxygen or intravenous [IV] fluids), moderate (hospitalization &lt;24 hours with oxygen or IV fluids, or hospitalization &gt;24 hours), or severe (intensive care unit stay for &gt;24 hours, septic shock, vasoactive agents, positive-pressure ventilation, chest drainage, extracorporeal membrane oxygenation, or death). Ordinal logistic regression and bootstrapped backwards selection were used to derive and internally validate our model. Results Of 1128 children, 371 (32.9%) developed moderate disease and 48 (4.3%) severe disease. Severity models demonstrated excellent discrimination (optimism-corrected c-indices of 0.81) and outstanding calibration. Severity predictors in the final model included respiratory rate, systolic blood pressure, oxygenation, retractions, capillary refill, atelectasis or pneumonia on chest radiograph, and pleural effusion. Conclusions We derived and internally validated a score that accurately predicts disease severity in children with suspected CAP. Once externally validated, this score has potential to facilitate management decisions by providing individualized risk estimates that can be used in conjunction with clinical judgment to improve the care of children with suspected CAP. In this prospective study of 1128 children with suspected CAP, we developed a well-calibrated severity score of 7 variables (respiratory rate, blood pressure, oxygenation, retractions, capillary refill, radiographic findings, pleural effusion) with excellent discriminatory ability for moderate or severe disease.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>33159514</pmid><doi>10.1093/cid/ciaa1690</doi><orcidid>https://orcid.org/0000-0002-4387-2605</orcidid><oa>free_for_read</oa></addata></record>
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title Development and Internal Validation of a Prediction Model to Risk Stratify Children With Suspected Community-Acquired Pneumonia
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