An evidence-based score to detect prevalent peripheral artery disease (PAD)
Detection of peripheral artery disease (PAD) typically entails collection of medical history, physical examination, and noninvasive imaging, but whether a risk factor-based model has clinical utility in population screening is unclear. Our objective was to derive and validate a new score for estimat...
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Veröffentlicht in: | Vascular Medicine 2012-10, Vol.17 (5), p.342-351 |
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creator | Duval, Sue Massaro, Joseph M Jaff, Michael R Boden, William E Alberts, Mark J Califf, Robert M Eagle, Kim A D’Agostino, Ralph B Pedley, Alison Fonarow, Gregg C Murabito, Joanne M Steg, P Gabriel Bhatt, Deepak L Hirsch, Alan T |
description | Detection of peripheral artery disease (PAD) typically entails collection of medical history, physical examination, and noninvasive imaging, but whether a risk factor-based model has clinical utility in population screening is unclear. Our objective was to derive and validate a new score for estimating PAD probability in individuals or populations. PAD presence was determined by a history of previous or current intermittent claudication associated with an ankle–brachial index (ABI) of < 0.9 or previous lower extremity arterial intervention. Multivariable stepwise logistic regression identified cross-sectional correlates of PAD from demographic, clinical, and laboratory variables. Analyses were derived from 18,049 US REACH (REduction of Atherothrombosis for Continued Health) Registry outpatients with a complete baseline risk factor profile (enrolled from December 2003 to June 2004). Model performance was assessed internally using 10-fold cross validation, and effect estimates were used to generate the score. The model was externally validated using the Framingham Offspring Study. Age, sex, smoking, diabetes mellitus, body mass index, hypertension stage, and history of heart failure, coronary artery disease, and cerebrovascular disease were predictive of PAD prevalence. The model had reasonable discrimination on derivation and internal validation (c-statistic = 0.61 and 0.60, respectively) and external validation (c-statistic = 0.63 [ABI < 0.9] or 0.64 [clinical PAD]). The model-estimated PAD prevalence varied more than threefold from lowest to highest decile (range, 4.5–16.7) and corresponded closely with actual PAD prevalence in each population. In conclusion, this new tool uses clinical variables to estimate PAD prevalence. While predictive power may be limited, it may improve PAD detection in vulnerable, at-risk populations. |
doi_str_mv | 10.1177/1358863X12445102 |
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Our objective was to derive and validate a new score for estimating PAD probability in individuals or populations. PAD presence was determined by a history of previous or current intermittent claudication associated with an ankle–brachial index (ABI) of < 0.9 or previous lower extremity arterial intervention. Multivariable stepwise logistic regression identified cross-sectional correlates of PAD from demographic, clinical, and laboratory variables. Analyses were derived from 18,049 US REACH (REduction of Atherothrombosis for Continued Health) Registry outpatients with a complete baseline risk factor profile (enrolled from December 2003 to June 2004). Model performance was assessed internally using 10-fold cross validation, and effect estimates were used to generate the score. The model was externally validated using the Framingham Offspring Study. Age, sex, smoking, diabetes mellitus, body mass index, hypertension stage, and history of heart failure, coronary artery disease, and cerebrovascular disease were predictive of PAD prevalence. The model had reasonable discrimination on derivation and internal validation (c-statistic = 0.61 and 0.60, respectively) and external validation (c-statistic = 0.63 [ABI < 0.9] or 0.64 [clinical PAD]). The model-estimated PAD prevalence varied more than threefold from lowest to highest decile (range, 4.5–16.7) and corresponded closely with actual PAD prevalence in each population. In conclusion, this new tool uses clinical variables to estimate PAD prevalence. While predictive power may be limited, it may improve PAD detection in vulnerable, at-risk populations.</description><identifier>ISSN: 1358-863X</identifier><identifier>EISSN: 1477-0377</identifier><identifier>DOI: 10.1177/1358863X12445102</identifier><identifier>PMID: 22711750</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Aged ; Aged, 80 and over ; Ankle Brachial Index ; Chi-Square Distribution ; Comorbidity ; Discriminant Analysis ; Evidence-Based Medicine ; Female ; Humans ; Intermittent Claudication - diagnosis ; Intermittent Claudication - epidemiology ; Logistic Models ; Male ; Mass Screening - methods ; Middle Aged ; Multivariate Analysis ; Nomograms ; Peripheral Arterial Disease - diagnosis ; Peripheral Arterial Disease - epidemiology ; Predictive Value of Tests ; Prevalence ; Probability ; Prognosis ; Prospective Studies ; Registries ; Reproducibility of Results ; Risk Assessment ; Risk Factors ; United States - epidemiology</subject><ispartof>Vascular Medicine, 2012-10, Vol.17 (5), p.342-351</ispartof><rights>The Author(s) 2012</rights><rights>SAGE Publications © Oct 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-73cf53db43f2fa07223cd6312fa6512b63a35fccfc2c1ab2086da3b95b4659c53</citedby><cites>FETCH-LOGICAL-c365t-73cf53db43f2fa07223cd6312fa6512b63a35fccfc2c1ab2086da3b95b4659c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1358863X12445102$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1358863X12445102$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>313,314,778,782,790,21806,27909,27911,27912,43608,43609</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22711750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Duval, Sue</creatorcontrib><creatorcontrib>Massaro, Joseph M</creatorcontrib><creatorcontrib>Jaff, Michael R</creatorcontrib><creatorcontrib>Boden, William E</creatorcontrib><creatorcontrib>Alberts, Mark J</creatorcontrib><creatorcontrib>Califf, Robert M</creatorcontrib><creatorcontrib>Eagle, Kim A</creatorcontrib><creatorcontrib>D’Agostino, Ralph B</creatorcontrib><creatorcontrib>Pedley, Alison</creatorcontrib><creatorcontrib>Fonarow, Gregg C</creatorcontrib><creatorcontrib>Murabito, Joanne M</creatorcontrib><creatorcontrib>Steg, P Gabriel</creatorcontrib><creatorcontrib>Bhatt, Deepak L</creatorcontrib><creatorcontrib>Hirsch, Alan T</creatorcontrib><creatorcontrib>REACH Registry Investigators</creatorcontrib><creatorcontrib>on behalf of the REACH Registry Investigators</creatorcontrib><title>An evidence-based score to detect prevalent peripheral artery disease (PAD)</title><title>Vascular Medicine</title><addtitle>Vasc Med</addtitle><description>Detection of peripheral artery disease (PAD) typically entails collection of medical history, physical examination, and noninvasive imaging, but whether a risk factor-based model has clinical utility in population screening is unclear. Our objective was to derive and validate a new score for estimating PAD probability in individuals or populations. PAD presence was determined by a history of previous or current intermittent claudication associated with an ankle–brachial index (ABI) of < 0.9 or previous lower extremity arterial intervention. Multivariable stepwise logistic regression identified cross-sectional correlates of PAD from demographic, clinical, and laboratory variables. Analyses were derived from 18,049 US REACH (REduction of Atherothrombosis for Continued Health) Registry outpatients with a complete baseline risk factor profile (enrolled from December 2003 to June 2004). Model performance was assessed internally using 10-fold cross validation, and effect estimates were used to generate the score. The model was externally validated using the Framingham Offspring Study. Age, sex, smoking, diabetes mellitus, body mass index, hypertension stage, and history of heart failure, coronary artery disease, and cerebrovascular disease were predictive of PAD prevalence. The model had reasonable discrimination on derivation and internal validation (c-statistic = 0.61 and 0.60, respectively) and external validation (c-statistic = 0.63 [ABI < 0.9] or 0.64 [clinical PAD]). The model-estimated PAD prevalence varied more than threefold from lowest to highest decile (range, 4.5–16.7) and corresponded closely with actual PAD prevalence in each population. In conclusion, this new tool uses clinical variables to estimate PAD prevalence. While predictive power may be limited, it may improve PAD detection in vulnerable, at-risk populations.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Ankle Brachial Index</subject><subject>Chi-Square Distribution</subject><subject>Comorbidity</subject><subject>Discriminant Analysis</subject><subject>Evidence-Based Medicine</subject><subject>Female</subject><subject>Humans</subject><subject>Intermittent Claudication - diagnosis</subject><subject>Intermittent Claudication - epidemiology</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Mass Screening - methods</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Nomograms</subject><subject>Peripheral Arterial Disease - diagnosis</subject><subject>Peripheral Arterial Disease - epidemiology</subject><subject>Predictive Value of Tests</subject><subject>Prevalence</subject><subject>Probability</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Registries</subject><subject>Reproducibility of Results</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>United States - 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diagnosis</topic><topic>Intermittent Claudication - epidemiology</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Mass Screening - methods</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Nomograms</topic><topic>Peripheral Arterial Disease - diagnosis</topic><topic>Peripheral Arterial Disease - epidemiology</topic><topic>Predictive Value of Tests</topic><topic>Prevalence</topic><topic>Probability</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Registries</topic><topic>Reproducibility of Results</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>United States - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duval, Sue</creatorcontrib><creatorcontrib>Massaro, Joseph M</creatorcontrib><creatorcontrib>Jaff, Michael R</creatorcontrib><creatorcontrib>Boden, William E</creatorcontrib><creatorcontrib>Alberts, Mark J</creatorcontrib><creatorcontrib>Califf, Robert M</creatorcontrib><creatorcontrib>Eagle, Kim A</creatorcontrib><creatorcontrib>D’Agostino, Ralph B</creatorcontrib><creatorcontrib>Pedley, Alison</creatorcontrib><creatorcontrib>Fonarow, Gregg C</creatorcontrib><creatorcontrib>Murabito, Joanne M</creatorcontrib><creatorcontrib>Steg, P Gabriel</creatorcontrib><creatorcontrib>Bhatt, Deepak L</creatorcontrib><creatorcontrib>Hirsch, Alan T</creatorcontrib><creatorcontrib>REACH Registry Investigators</creatorcontrib><creatorcontrib>on behalf of the REACH Registry Investigators</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Vascular Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duval, Sue</au><au>Massaro, Joseph M</au><au>Jaff, Michael R</au><au>Boden, William E</au><au>Alberts, Mark J</au><au>Califf, Robert M</au><au>Eagle, Kim A</au><au>D’Agostino, Ralph B</au><au>Pedley, Alison</au><au>Fonarow, Gregg C</au><au>Murabito, Joanne M</au><au>Steg, P Gabriel</au><au>Bhatt, Deepak L</au><au>Hirsch, Alan T</au><aucorp>REACH Registry Investigators</aucorp><aucorp>on behalf of the REACH Registry Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An evidence-based score to detect prevalent peripheral artery disease (PAD)</atitle><jtitle>Vascular Medicine</jtitle><addtitle>Vasc Med</addtitle><date>2012-10</date><risdate>2012</risdate><volume>17</volume><issue>5</issue><spage>342</spage><epage>351</epage><pages>342-351</pages><issn>1358-863X</issn><eissn>1477-0377</eissn><abstract>Detection of peripheral artery disease (PAD) typically entails collection of medical history, physical examination, and noninvasive imaging, but whether a risk factor-based model has clinical utility in population screening is unclear. Our objective was to derive and validate a new score for estimating PAD probability in individuals or populations. PAD presence was determined by a history of previous or current intermittent claudication associated with an ankle–brachial index (ABI) of < 0.9 or previous lower extremity arterial intervention. Multivariable stepwise logistic regression identified cross-sectional correlates of PAD from demographic, clinical, and laboratory variables. Analyses were derived from 18,049 US REACH (REduction of Atherothrombosis for Continued Health) Registry outpatients with a complete baseline risk factor profile (enrolled from December 2003 to June 2004). Model performance was assessed internally using 10-fold cross validation, and effect estimates were used to generate the score. The model was externally validated using the Framingham Offspring Study. Age, sex, smoking, diabetes mellitus, body mass index, hypertension stage, and history of heart failure, coronary artery disease, and cerebrovascular disease were predictive of PAD prevalence. The model had reasonable discrimination on derivation and internal validation (c-statistic = 0.61 and 0.60, respectively) and external validation (c-statistic = 0.63 [ABI < 0.9] or 0.64 [clinical PAD]). The model-estimated PAD prevalence varied more than threefold from lowest to highest decile (range, 4.5–16.7) and corresponded closely with actual PAD prevalence in each population. In conclusion, this new tool uses clinical variables to estimate PAD prevalence. While predictive power may be limited, it may improve PAD detection in vulnerable, at-risk populations.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>22711750</pmid><doi>10.1177/1358863X12445102</doi><tpages>10</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Ankle Brachial Index Chi-Square Distribution Comorbidity Discriminant Analysis Evidence-Based Medicine Female Humans Intermittent Claudication - diagnosis Intermittent Claudication - epidemiology Logistic Models Male Mass Screening - methods Middle Aged Multivariate Analysis Nomograms Peripheral Arterial Disease - diagnosis Peripheral Arterial Disease - epidemiology Predictive Value of Tests Prevalence Probability Prognosis Prospective Studies Registries Reproducibility of Results Risk Assessment Risk Factors United States - epidemiology |
title | An evidence-based score to detect prevalent peripheral artery disease (PAD) |
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