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Factors associated with disagreement between clinician app‐based ultra‐brief Confusion Assessment Method and reference standard delirium assessments

Background Recently, the Ultra‐Brief Confusion Assessment Method (UB‐CAM), designed to help physicians and nurses to recognize delirium, showed high, but imperfect, accuracy compared with Research Reference Standard Delirium Assessments (RRSDAs). The aim of this study is to identify factors associat...

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Published in:Journal of the American Geriatrics Society (JAGS) 2024-03, Vol.72 (3), p.828-836
Main Authors: Dhliwayo, Rejoice, Trivedi, Shrunjal, Ngo, Long, Fick, Donna M., Inouye, Sharon K., Boltz, Marie, Leslie, Douglas, Husser, Erica, Shrestha, Priyanka, Marcantonio, Edward R.
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container_end_page 836
container_issue 3
container_start_page 828
container_title Journal of the American Geriatrics Society (JAGS)
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creator Dhliwayo, Rejoice
Trivedi, Shrunjal
Ngo, Long
Fick, Donna M.
Inouye, Sharon K.
Boltz, Marie
Leslie, Douglas
Husser, Erica
Shrestha, Priyanka
Marcantonio, Edward R.
description Background Recently, the Ultra‐Brief Confusion Assessment Method (UB‐CAM), designed to help physicians and nurses to recognize delirium, showed high, but imperfect, accuracy compared with Research Reference Standard Delirium Assessments (RRSDAs). The aim of this study is to identify factors associated with disagreement between clinicians' app‐based UB‐CAM assessments and RRSDAs. Methods This is a secondary analysis of a prospective diagnostic test study. The study was conducted at two hospitals and included 527 inpatients (≥70 years old) and 289 clinicians (53 physicians, 236 nurses). Trained research associates performed RRSDAs and determined delirium presence using the CAM. Clinicians administered the UB‐CAM using an iPad app. Disagreement factors considered were clinician, patient, and delirium characteristics. We report odds ratios and 95% confidence intervals. Results One thousand seven hundred and ninety‐five clinician UB‐CAM assessments paired with RRSDAs were administered. The prevalence of delirium was 17%. The rate of disagreement between clinician UB‐CAM assessments and RRSDAs was 12%. Significant factors associated with disagreement between clinician UB‐CAM assessments and RRSDAs (OR [95% CI]) included: presence of dementia (2.7 [1.8–4.1]), patient education high school or less (1.9 [1.3–2.9]), psychomotor retardation (2.5 [1.4–4.2]), and the presence of mild delirium or subsyndromal delirium (5.5 [3.5–8.7]). Significant risk factors for false negatives were patient age less than 80 (2.2 [1.1–4.3]) and mild delirium (3.5 [1.6–7.4]). Significant risk factors for false positives were presence of dementia (4.0 [2.3–7.0]), subsyndromal delirium (5.1 [2.9–9.1]), and patient education high school or less (2.0 [1.2–3.6]). Clinician characteristics were not significantly associated with disagreement. Conclusions The strongest factors associated with disagreement between clinician UB‐CAM screens and RRSDAs were the presence of dementia and subsyndromal delirium as risk factors for false positives, and mild delirium and younger age as a risk factor for false negatives. These disagreement factors contrast with previous studies of risk factors for incorrect clinician delirium screening, and better align screening results with patient outcomes.
doi_str_mv 10.1111/jgs.18690
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The aim of this study is to identify factors associated with disagreement between clinicians' app‐based UB‐CAM assessments and RRSDAs. Methods This is a secondary analysis of a prospective diagnostic test study. The study was conducted at two hospitals and included 527 inpatients (≥70 years old) and 289 clinicians (53 physicians, 236 nurses). Trained research associates performed RRSDAs and determined delirium presence using the CAM. Clinicians administered the UB‐CAM using an iPad app. Disagreement factors considered were clinician, patient, and delirium characteristics. We report odds ratios and 95% confidence intervals. Results One thousand seven hundred and ninety‐five clinician UB‐CAM assessments paired with RRSDAs were administered. The prevalence of delirium was 17%. The rate of disagreement between clinician UB‐CAM assessments and RRSDAs was 12%. Significant factors associated with disagreement between clinician UB‐CAM assessments and RRSDAs (OR [95% CI]) included: presence of dementia (2.7 [1.8–4.1]), patient education high school or less (1.9 [1.3–2.9]), psychomotor retardation (2.5 [1.4–4.2]), and the presence of mild delirium or subsyndromal delirium (5.5 [3.5–8.7]). Significant risk factors for false negatives were patient age less than 80 (2.2 [1.1–4.3]) and mild delirium (3.5 [1.6–7.4]). Significant risk factors for false positives were presence of dementia (4.0 [2.3–7.0]), subsyndromal delirium (5.1 [2.9–9.1]), and patient education high school or less (2.0 [1.2–3.6]). Clinician characteristics were not significantly associated with disagreement. Conclusions The strongest factors associated with disagreement between clinician UB‐CAM screens and RRSDAs were the presence of dementia and subsyndromal delirium as risk factors for false positives, and mild delirium and younger age as a risk factor for false negatives. These disagreement factors contrast with previous studies of risk factors for incorrect clinician delirium screening, and better align screening results with patient outcomes.</description><identifier>ISSN: 0002-8614</identifier><identifier>EISSN: 1532-5415</identifier><identifier>DOI: 10.1111/jgs.18690</identifier><identifier>PMID: 38014821</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>accuracy ; Delirium ; Dementia ; Dementia disorders ; Intellectual disabilities ; Older people ; Patient education ; Risk factors ; screening</subject><ispartof>Journal of the American Geriatrics Society (JAGS), 2024-03, Vol.72 (3), p.828-836</ispartof><rights>2023 The American Geriatrics Society.</rights><rights>2024 American Geriatrics Society and Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3130-9d72649cc6002ec49fd442186198d7fee000f1787b38276c136905ec759d369a3</cites><orcidid>0000-0002-6777-1913 ; 0000-0002-0799-5122 ; 0000-0003-3817-747X ; 0000-0003-1822-9906 ; 0000-0003-1133-2249 ; 0000-0002-2911-4250</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/38014821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dhliwayo, Rejoice</creatorcontrib><creatorcontrib>Trivedi, Shrunjal</creatorcontrib><creatorcontrib>Ngo, Long</creatorcontrib><creatorcontrib>Fick, Donna M.</creatorcontrib><creatorcontrib>Inouye, Sharon K.</creatorcontrib><creatorcontrib>Boltz, Marie</creatorcontrib><creatorcontrib>Leslie, Douglas</creatorcontrib><creatorcontrib>Husser, Erica</creatorcontrib><creatorcontrib>Shrestha, Priyanka</creatorcontrib><creatorcontrib>Marcantonio, Edward R.</creatorcontrib><title>Factors associated with disagreement between clinician app‐based ultra‐brief Confusion Assessment Method and reference standard delirium assessments</title><title>Journal of the American Geriatrics Society (JAGS)</title><addtitle>J Am Geriatr Soc</addtitle><description>Background Recently, the Ultra‐Brief Confusion Assessment Method (UB‐CAM), designed to help physicians and nurses to recognize delirium, showed high, but imperfect, accuracy compared with Research Reference Standard Delirium Assessments (RRSDAs). The aim of this study is to identify factors associated with disagreement between clinicians' app‐based UB‐CAM assessments and RRSDAs. Methods This is a secondary analysis of a prospective diagnostic test study. The study was conducted at two hospitals and included 527 inpatients (≥70 years old) and 289 clinicians (53 physicians, 236 nurses). Trained research associates performed RRSDAs and determined delirium presence using the CAM. Clinicians administered the UB‐CAM using an iPad app. Disagreement factors considered were clinician, patient, and delirium characteristics. We report odds ratios and 95% confidence intervals. Results One thousand seven hundred and ninety‐five clinician UB‐CAM assessments paired with RRSDAs were administered. The prevalence of delirium was 17%. The rate of disagreement between clinician UB‐CAM assessments and RRSDAs was 12%. Significant factors associated with disagreement between clinician UB‐CAM assessments and RRSDAs (OR [95% CI]) included: presence of dementia (2.7 [1.8–4.1]), patient education high school or less (1.9 [1.3–2.9]), psychomotor retardation (2.5 [1.4–4.2]), and the presence of mild delirium or subsyndromal delirium (5.5 [3.5–8.7]). Significant risk factors for false negatives were patient age less than 80 (2.2 [1.1–4.3]) and mild delirium (3.5 [1.6–7.4]). Significant risk factors for false positives were presence of dementia (4.0 [2.3–7.0]), subsyndromal delirium (5.1 [2.9–9.1]), and patient education high school or less (2.0 [1.2–3.6]). Clinician characteristics were not significantly associated with disagreement. Conclusions The strongest factors associated with disagreement between clinician UB‐CAM screens and RRSDAs were the presence of dementia and subsyndromal delirium as risk factors for false positives, and mild delirium and younger age as a risk factor for false negatives. These disagreement factors contrast with previous studies of risk factors for incorrect clinician delirium screening, and better align screening results with patient outcomes.</description><subject>accuracy</subject><subject>Delirium</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Intellectual disabilities</subject><subject>Older people</subject><subject>Patient education</subject><subject>Risk factors</subject><subject>screening</subject><issn>0002-8614</issn><issn>1532-5415</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kc9u1DAQxi0EokvhwAsgS1zoIa3_JbGP1aotoFY9AGfLa09arxJn8SRa9cYjcOT5-iR4uwsHJHwZj_SbTzPfR8hbzk55eWfrOzzlujHsGVnwWoqqVrx-ThaMMVHphqsj8gpxzRgXTOuX5EhqxpUWfEF-XTo_jRmpQxx9dBMEuo3TPQ0R3V0GGCBNdAXTFiBR38cUC5Wo22wef_xcOSz83E_Z7bocoaPLMXUzxjHRc0RAfBK4gel-DNSlQDN0kCF5oDiV3uVAA_Qxx3nYLXGYwNfkRed6hDeHeky-XV58XX6srm-vPi3PrysvuWSVCa1olPG-KbeCV6YLSoliBjc6tB1A8aDjrW5XUou28VwWm2rwbW1C-Tp5TD7sdTd5_D4DTnaI6KHvXYJxRiu0Ua1QSrUFff8Puh7nnMp2Vpha80ZKIwt1sqd8HhHLtXaT4-Dyg-XM7uKyJS77FFdh3x0U59UA4S_5J58CnO2Bbezh4f9K9vPVl73kbzHQot0</recordid><startdate>202403</startdate><enddate>202403</enddate><creator>Dhliwayo, Rejoice</creator><creator>Trivedi, Shrunjal</creator><creator>Ngo, Long</creator><creator>Fick, Donna M.</creator><creator>Inouye, Sharon K.</creator><creator>Boltz, Marie</creator><creator>Leslie, Douglas</creator><creator>Husser, Erica</creator><creator>Shrestha, Priyanka</creator><creator>Marcantonio, Edward R.</creator><general>John Wiley &amp; 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Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Geriatrics Society (JAGS)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dhliwayo, Rejoice</au><au>Trivedi, Shrunjal</au><au>Ngo, Long</au><au>Fick, Donna M.</au><au>Inouye, Sharon K.</au><au>Boltz, Marie</au><au>Leslie, Douglas</au><au>Husser, Erica</au><au>Shrestha, Priyanka</au><au>Marcantonio, Edward R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Factors associated with disagreement between clinician app‐based ultra‐brief Confusion Assessment Method and reference standard delirium assessments</atitle><jtitle>Journal of the American Geriatrics Society (JAGS)</jtitle><addtitle>J Am Geriatr Soc</addtitle><date>2024-03</date><risdate>2024</risdate><volume>72</volume><issue>3</issue><spage>828</spage><epage>836</epage><pages>828-836</pages><issn>0002-8614</issn><eissn>1532-5415</eissn><abstract>Background Recently, the Ultra‐Brief Confusion Assessment Method (UB‐CAM), designed to help physicians and nurses to recognize delirium, showed high, but imperfect, accuracy compared with Research Reference Standard Delirium Assessments (RRSDAs). The aim of this study is to identify factors associated with disagreement between clinicians' app‐based UB‐CAM assessments and RRSDAs. Methods This is a secondary analysis of a prospective diagnostic test study. The study was conducted at two hospitals and included 527 inpatients (≥70 years old) and 289 clinicians (53 physicians, 236 nurses). Trained research associates performed RRSDAs and determined delirium presence using the CAM. Clinicians administered the UB‐CAM using an iPad app. Disagreement factors considered were clinician, patient, and delirium characteristics. We report odds ratios and 95% confidence intervals. Results One thousand seven hundred and ninety‐five clinician UB‐CAM assessments paired with RRSDAs were administered. The prevalence of delirium was 17%. The rate of disagreement between clinician UB‐CAM assessments and RRSDAs was 12%. Significant factors associated with disagreement between clinician UB‐CAM assessments and RRSDAs (OR [95% CI]) included: presence of dementia (2.7 [1.8–4.1]), patient education high school or less (1.9 [1.3–2.9]), psychomotor retardation (2.5 [1.4–4.2]), and the presence of mild delirium or subsyndromal delirium (5.5 [3.5–8.7]). Significant risk factors for false negatives were patient age less than 80 (2.2 [1.1–4.3]) and mild delirium (3.5 [1.6–7.4]). Significant risk factors for false positives were presence of dementia (4.0 [2.3–7.0]), subsyndromal delirium (5.1 [2.9–9.1]), and patient education high school or less (2.0 [1.2–3.6]). Clinician characteristics were not significantly associated with disagreement. Conclusions The strongest factors associated with disagreement between clinician UB‐CAM screens and RRSDAs were the presence of dementia and subsyndromal delirium as risk factors for false positives, and mild delirium and younger age as a risk factor for false negatives. These disagreement factors contrast with previous studies of risk factors for incorrect clinician delirium screening, and better align screening results with patient outcomes.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>38014821</pmid><doi>10.1111/jgs.18690</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6777-1913</orcidid><orcidid>https://orcid.org/0000-0002-0799-5122</orcidid><orcidid>https://orcid.org/0000-0003-3817-747X</orcidid><orcidid>https://orcid.org/0000-0003-1822-9906</orcidid><orcidid>https://orcid.org/0000-0003-1133-2249</orcidid><orcidid>https://orcid.org/0000-0002-2911-4250</orcidid></addata></record>
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subjects accuracy
Delirium
Dementia
Dementia disorders
Intellectual disabilities
Older people
Patient education
Risk factors
screening
title Factors associated with disagreement between clinician app‐based ultra‐brief Confusion Assessment Method and reference standard delirium assessments
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