Validity of the RAI-MDS for ascertaining diabetes and comorbid conditions in long-term care facility residents

This study assessed the validity of the Resident Assessment Instrument Minimum Data Set (RAI-MDS) Version 2.0 for diagnoses of diabetes and comorbid conditions in residents of long-term care facilities (LTCFs). Hospital inpatient, outpatient physician billing, RAI-MDS, and population registry data f...

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Veröffentlicht in:BMC health services research 2014-01, Vol.14 (1), p.17-17, Article 17
Hauptverfasser: Lix, Lisa M, Yan, Lin, Blackburn, David, Hu, Nianping, Schneider-Lindner, Verena, Teare, Gary F
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creator Lix, Lisa M
Yan, Lin
Blackburn, David
Hu, Nianping
Schneider-Lindner, Verena
Teare, Gary F
description This study assessed the validity of the Resident Assessment Instrument Minimum Data Set (RAI-MDS) Version 2.0 for diagnoses of diabetes and comorbid conditions in residents of long-term care facilities (LTCFs). Hospital inpatient, outpatient physician billing, RAI-MDS, and population registry data for 1997 to 2011 from Saskatchewan, Canada were used to ascertain cases of diabetes and 12 comorbid conditions. Prevalence estimates were calculated for both RAI-MDS and administrative health data. Sensitivity, specificity, and positive and negative predictive values (PPV and NPV) were calculated using population-based administrative health data as the validation data source. Cohen's κ was used to estimate agreement between the two data sources. 23,217 LTCF residents were in the diabetes case ascertainment cohort. Diabetes prevalence was 25.3% in administrative health data and 21.9% in RAI-MDS data. Overall sensitivity of a RAI-MDS diabetes diagnoses was 0.79 (95% CI: 0.79, 0.80) and the PPV was 0.92 (95% CI: 0.91, 0.92), when compared to administrative health data. Sensitivity of the RAI-MDS for ascertaining comorbid conditions ranged from 0.21 for osteoporosis to 0.92 for multiple sclerosis; specificity was high for most conditions. RAI-MDS clinical assessment data are sensitive to ascertain diabetes cases in LTCF populations when compared to administrative health data. For many comorbid conditions, RAI-MDS data have low validity when compared to administrative data. Risk-adjustment measures based on these comorbidities might not produce consistent results for RAI-MDS and administrative health data, which could affect the conclusions of studies about health outcomes and quality of care across facilities.
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Hospital inpatient, outpatient physician billing, RAI-MDS, and population registry data for 1997 to 2011 from Saskatchewan, Canada were used to ascertain cases of diabetes and 12 comorbid conditions. Prevalence estimates were calculated for both RAI-MDS and administrative health data. Sensitivity, specificity, and positive and negative predictive values (PPV and NPV) were calculated using population-based administrative health data as the validation data source. Cohen's κ was used to estimate agreement between the two data sources. 23,217 LTCF residents were in the diabetes case ascertainment cohort. Diabetes prevalence was 25.3% in administrative health data and 21.9% in RAI-MDS data. Overall sensitivity of a RAI-MDS diabetes diagnoses was 0.79 (95% CI: 0.79, 0.80) and the PPV was 0.92 (95% CI: 0.91, 0.92), when compared to administrative health data. Sensitivity of the RAI-MDS for ascertaining comorbid conditions ranged from 0.21 for osteoporosis to 0.92 for multiple sclerosis; specificity was high for most conditions. RAI-MDS clinical assessment data are sensitive to ascertain diabetes cases in LTCF populations when compared to administrative health data. For many comorbid conditions, RAI-MDS data have low validity when compared to administrative data. Risk-adjustment measures based on these comorbidities might not produce consistent results for RAI-MDS and administrative health data, which could affect the conclusions of studies about health outcomes and quality of care across facilities.</description><identifier>ISSN: 1472-6963</identifier><identifier>EISSN: 1472-6963</identifier><identifier>DOI: 10.1186/1472-6963-14-17</identifier><identifier>PMID: 24423071</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Activities of daily living ; Aged ; Aged, 80 and over ; Alzheimer's disease ; Biomedical research ; Care and treatment ; Chronic diseases ; Chronic illnesses ; Comorbidity ; Decision Support Techniques ; Diabetes ; Diabetes Mellitus - diagnosis ; Diabetes Mellitus - epidemiology ; Diagnosis ; Female ; Fiscal years ; Health insurance ; Heart attacks ; Hospitals ; Humans ; Insurance coverage ; Long term health care ; Long-Term Care - methods ; Long-Term Care - statistics &amp; numerical data ; Male ; Medical care ; Medical research ; Medicine, Experimental ; Mortality ; Multiple sclerosis ; Nursing Homes - statistics &amp; numerical data ; Personal health ; Population ; Prevalence ; Quality management ; Reproducibility of Results ; Retrospective Studies ; Saskatchewan - epidemiology ; Sensitivity and Specificity ; Studies ; Technology application ; Validity</subject><ispartof>BMC health services research, 2014-01, Vol.14 (1), p.17-17, Article 17</ispartof><rights>COPYRIGHT 2014 BioMed Central Ltd.</rights><rights>2014 Lix et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2014 Lix et al.; licensee BioMed Central Ltd. 2014 Lix et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-1e0d5f2e63bc9a93d1622811e737df5587a117cd21c8dcc2cd4acab02dad2fc53</citedby><cites>FETCH-LOGICAL-c521t-1e0d5f2e63bc9a93d1622811e737df5587a117cd21c8dcc2cd4acab02dad2fc53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898220/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898220/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24423071$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lix, Lisa M</creatorcontrib><creatorcontrib>Yan, Lin</creatorcontrib><creatorcontrib>Blackburn, David</creatorcontrib><creatorcontrib>Hu, Nianping</creatorcontrib><creatorcontrib>Schneider-Lindner, Verena</creatorcontrib><creatorcontrib>Teare, Gary F</creatorcontrib><title>Validity of the RAI-MDS for ascertaining diabetes and comorbid conditions in long-term care facility residents</title><title>BMC health services research</title><addtitle>BMC Health Serv Res</addtitle><description>This study assessed the validity of the Resident Assessment Instrument Minimum Data Set (RAI-MDS) Version 2.0 for diagnoses of diabetes and comorbid conditions in residents of long-term care facilities (LTCFs). Hospital inpatient, outpatient physician billing, RAI-MDS, and population registry data for 1997 to 2011 from Saskatchewan, Canada were used to ascertain cases of diabetes and 12 comorbid conditions. Prevalence estimates were calculated for both RAI-MDS and administrative health data. Sensitivity, specificity, and positive and negative predictive values (PPV and NPV) were calculated using population-based administrative health data as the validation data source. Cohen's κ was used to estimate agreement between the two data sources. 23,217 LTCF residents were in the diabetes case ascertainment cohort. Diabetes prevalence was 25.3% in administrative health data and 21.9% in RAI-MDS data. Overall sensitivity of a RAI-MDS diabetes diagnoses was 0.79 (95% CI: 0.79, 0.80) and the PPV was 0.92 (95% CI: 0.91, 0.92), when compared to administrative health data. 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Risk-adjustment measures based on these comorbidities might not produce consistent results for RAI-MDS and administrative health data, which could affect the conclusions of studies about health outcomes and quality of care across facilities.</description><subject>Activities of daily living</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer's disease</subject><subject>Biomedical research</subject><subject>Care and treatment</subject><subject>Chronic diseases</subject><subject>Chronic illnesses</subject><subject>Comorbidity</subject><subject>Decision Support Techniques</subject><subject>Diabetes</subject><subject>Diabetes Mellitus - diagnosis</subject><subject>Diabetes Mellitus - epidemiology</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Fiscal years</subject><subject>Health insurance</subject><subject>Heart attacks</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Insurance coverage</subject><subject>Long term health care</subject><subject>Long-Term Care - methods</subject><subject>Long-Term Care - statistics &amp; 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Hospital inpatient, outpatient physician billing, RAI-MDS, and population registry data for 1997 to 2011 from Saskatchewan, Canada were used to ascertain cases of diabetes and 12 comorbid conditions. Prevalence estimates were calculated for both RAI-MDS and administrative health data. Sensitivity, specificity, and positive and negative predictive values (PPV and NPV) were calculated using population-based administrative health data as the validation data source. Cohen's κ was used to estimate agreement between the two data sources. 23,217 LTCF residents were in the diabetes case ascertainment cohort. Diabetes prevalence was 25.3% in administrative health data and 21.9% in RAI-MDS data. Overall sensitivity of a RAI-MDS diabetes diagnoses was 0.79 (95% CI: 0.79, 0.80) and the PPV was 0.92 (95% CI: 0.91, 0.92), when compared to administrative health data. Sensitivity of the RAI-MDS for ascertaining comorbid conditions ranged from 0.21 for osteoporosis to 0.92 for multiple sclerosis; specificity was high for most conditions. RAI-MDS clinical assessment data are sensitive to ascertain diabetes cases in LTCF populations when compared to administrative health data. For many comorbid conditions, RAI-MDS data have low validity when compared to administrative data. Risk-adjustment measures based on these comorbidities might not produce consistent results for RAI-MDS and administrative health data, which could affect the conclusions of studies about health outcomes and quality of care across facilities.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24423071</pmid><doi>10.1186/1472-6963-14-17</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Activities of daily living
Aged
Aged, 80 and over
Alzheimer's disease
Biomedical research
Care and treatment
Chronic diseases
Chronic illnesses
Comorbidity
Decision Support Techniques
Diabetes
Diabetes Mellitus - diagnosis
Diabetes Mellitus - epidemiology
Diagnosis
Female
Fiscal years
Health insurance
Heart attacks
Hospitals
Humans
Insurance coverage
Long term health care
Long-Term Care - methods
Long-Term Care - statistics & numerical data
Male
Medical care
Medical research
Medicine, Experimental
Mortality
Multiple sclerosis
Nursing Homes - statistics & numerical data
Personal health
Population
Prevalence
Quality management
Reproducibility of Results
Retrospective Studies
Saskatchewan - epidemiology
Sensitivity and Specificity
Studies
Technology application
Validity
title Validity of the RAI-MDS for ascertaining diabetes and comorbid conditions in long-term care facility residents
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