G89 Individual Risk Assessment Tool for Asthma Prediction at School Age in a UK Birth Cohort

Background Commonly used Asthma Predictive Index (API; Castro-Rodriguez 2000) has good negative but poor positive predictive value (PPV) which reduces its clinical usefulness. We aimed to develop, within a population-based cohort, an asthma risk prediction tool (ARPT) better suited for clinical use....

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Veröffentlicht in:Archives of disease in childhood 2014-04, Vol.99 (Suppl 1), p.A38-A38
Hauptverfasser: Wang, R, Custovic, A, Simpson, A, Belgrave, D, Murray, CS
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container_end_page A38
container_issue Suppl 1
container_start_page A38
container_title Archives of disease in childhood
container_volume 99
creator Wang, R
Custovic, A
Simpson, A
Belgrave, D
Murray, CS
description Background Commonly used Asthma Predictive Index (API; Castro-Rodriguez 2000) has good negative but poor positive predictive value (PPV) which reduces its clinical usefulness. We aimed to develop, within a population-based cohort, an asthma risk prediction tool (ARPT) better suited for clinical use. Method Children from a UK birth cohort attended follow-up at age 3, 8 and 11 years. Parents completed validated questionnaires. Children were skin prick tested (SPT) to common inhalant and food allergens. GP records were transcribed to collect information on physician-confirmed wheeze. An ARPT was developed using backwards logistic regression of data collected at age 3 years. We assessed its predictive performance using area under the receiver operating characteristic curve (AUROC). Repeated internal validation was performed. Results Of 829 children were included in the analysis, 132(17.8%) had asthma at school-age (year 8 or 11). The ARPT was found to include 4 predictors at age 3 years yielding a total score of 5: wheeze ever (1), wheeze causing shortness of breath (1), wheeze after exercise (2) and eczema (1). In the whole population, children with a score of >4 had a significantly increased risk of having asthma at school-age odds ratio [OR] 25.3, 95% CI [11.8–54.1], p < 0.0001; PPV 80%; sensitivity 28%). API, when applied to our cohort, yielded an OR for asthma at school-age of 7.4 (95% CI [4.5–12.2], p < 0.0001; PPV 54%; sensitivity 31%). We then applied our ARPT amongst children who presented to their GP with wheeze within the first 3 years of life; those with ARTP score of ≥4 had a significantly increased risk of asthma at school-age (OR 15.6, 95% CI [6.1–39.9] p < 0.0001; PPV 82%; sensitivity 35%). API, when applied in this population, had OR of 4.7 (95% CI [2.53–8.60], p < 0.0001; PPV 57%, Sensitivity 44%). Internal validation showed good agreement (AUCpredicting 0.78 vs. AUCobserved 0.77). Conclusion APRT is a simple tool based mainly on clinical history which could easily be applied in primary/secondary care to risk stratify children with wheeze symptoms in early childhood and predict asthma by school-age with a good positive predictive value.
doi_str_mv 10.1136/archdischild-2014-306237.89
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We aimed to develop, within a population-based cohort, an asthma risk prediction tool (ARPT) better suited for clinical use. Method Children from a UK birth cohort attended follow-up at age 3, 8 and 11 years. Parents completed validated questionnaires. Children were skin prick tested (SPT) to common inhalant and food allergens. GP records were transcribed to collect information on physician-confirmed wheeze. An ARPT was developed using backwards logistic regression of data collected at age 3 years. We assessed its predictive performance using area under the receiver operating characteristic curve (AUROC). Repeated internal validation was performed. Results Of 829 children were included in the analysis, 132(17.8%) had asthma at school-age (year 8 or 11). The ARPT was found to include 4 predictors at age 3 years yielding a total score of 5: wheeze ever (1), wheeze causing shortness of breath (1), wheeze after exercise (2) and eczema (1). In the whole population, children with a score of &gt;4 had a significantly increased risk of having asthma at school-age odds ratio [OR] 25.3, 95% CI [11.8–54.1], p &lt; 0.0001; PPV 80%; sensitivity 28%). API, when applied to our cohort, yielded an OR for asthma at school-age of 7.4 (95% CI [4.5–12.2], p &lt; 0.0001; PPV 54%; sensitivity 31%). We then applied our ARPT amongst children who presented to their GP with wheeze within the first 3 years of life; those with ARTP score of ≥4 had a significantly increased risk of asthma at school-age (OR 15.6, 95% CI [6.1–39.9] p &lt; 0.0001; PPV 82%; sensitivity 35%). API, when applied in this population, had OR of 4.7 (95% CI [2.53–8.60], p &lt; 0.0001; PPV 57%, Sensitivity 44%). Internal validation showed good agreement (AUCpredicting 0.78 vs. AUCobserved 0.77). Conclusion APRT is a simple tool based mainly on clinical history which could easily be applied in primary/secondary care to risk stratify children with wheeze symptoms in early childhood and predict asthma by school-age with a good positive predictive value.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2014-306237.89</identifier><identifier>CODEN: ADCHAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Asthma ; Health risks ; Risk assessment ; Skin diseases ; Young Children</subject><ispartof>Archives of disease in childhood, 2014-04, Vol.99 (Suppl 1), p.A38-A38</ispartof><rights>2014, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2014 (c) 2014, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://adc.bmj.com/content/99/Suppl_1/A38.1.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://adc.bmj.com/content/99/Suppl_1/A38.1.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77342,77373</link.rule.ids></links><search><creatorcontrib>Wang, R</creatorcontrib><creatorcontrib>Custovic, A</creatorcontrib><creatorcontrib>Simpson, A</creatorcontrib><creatorcontrib>Belgrave, D</creatorcontrib><creatorcontrib>Murray, CS</creatorcontrib><title>G89 Individual Risk Assessment Tool for Asthma Prediction at School Age in a UK Birth Cohort</title><title>Archives of disease in childhood</title><description>Background Commonly used Asthma Predictive Index (API; Castro-Rodriguez 2000) has good negative but poor positive predictive value (PPV) which reduces its clinical usefulness. We aimed to develop, within a population-based cohort, an asthma risk prediction tool (ARPT) better suited for clinical use. Method Children from a UK birth cohort attended follow-up at age 3, 8 and 11 years. Parents completed validated questionnaires. Children were skin prick tested (SPT) to common inhalant and food allergens. GP records were transcribed to collect information on physician-confirmed wheeze. An ARPT was developed using backwards logistic regression of data collected at age 3 years. We assessed its predictive performance using area under the receiver operating characteristic curve (AUROC). Repeated internal validation was performed. Results Of 829 children were included in the analysis, 132(17.8%) had asthma at school-age (year 8 or 11). The ARPT was found to include 4 predictors at age 3 years yielding a total score of 5: wheeze ever (1), wheeze causing shortness of breath (1), wheeze after exercise (2) and eczema (1). In the whole population, children with a score of &gt;4 had a significantly increased risk of having asthma at school-age odds ratio [OR] 25.3, 95% CI [11.8–54.1], p &lt; 0.0001; PPV 80%; sensitivity 28%). API, when applied to our cohort, yielded an OR for asthma at school-age of 7.4 (95% CI [4.5–12.2], p &lt; 0.0001; PPV 54%; sensitivity 31%). We then applied our ARPT amongst children who presented to their GP with wheeze within the first 3 years of life; those with ARTP score of ≥4 had a significantly increased risk of asthma at school-age (OR 15.6, 95% CI [6.1–39.9] p &lt; 0.0001; PPV 82%; sensitivity 35%). API, when applied in this population, had OR of 4.7 (95% CI [2.53–8.60], p &lt; 0.0001; PPV 57%, Sensitivity 44%). Internal validation showed good agreement (AUCpredicting 0.78 vs. AUCobserved 0.77). Conclusion APRT is a simple tool based mainly on clinical history which could easily be applied in primary/secondary care to risk stratify children with wheeze symptoms in early childhood and predict asthma by school-age with a good positive predictive value.</description><subject>Asthma</subject><subject>Health risks</subject><subject>Risk assessment</subject><subject>Skin diseases</subject><subject>Young Children</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqVkE1OwzAQhS0EEqVwB0tdp_gviS1WpYJSUQkE7RbLcWzi0sRgp0js2HBRTkKisGDLakZv3pvRfABMMJpiTLNzFXRVuqgrtysTgjBLKMoIzadcHIARZhnvVMYOwQghRBPBOT8GJzFuEcKEczoCTwsuvj-_lk3p3l25Vzv44OILnMVoYqxN08K19ztofei0tqoVvA-mdLp1voGqhY-66uezZwNdJ8DNLbx0oa3g3Fc-tKfgyKpdNGe_dQw211fr-U2yulss57NVUmCS84SVyCqjCs1KxTOb8kxgYgtmhdKYpMTmyuA0FRTlxnClrBB9rxkvFFcE0zGYDHtfg3_bm9jKrd-HpjspMe8-FTTNeee6GFw6-BiDsfI1uFqFD4mR7IHKv0BlD1QOQGW3YQyyIV3U238FfwCzHX8h</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Wang, R</creator><creator>Custovic, A</creator><creator>Simpson, A</creator><creator>Belgrave, D</creator><creator>Murray, CS</creator><general>BMJ Publishing Group LTD</general><scope>AAYXX</scope><scope>CITATION</scope><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8A4</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>201404</creationdate><title>G89 Individual Risk Assessment Tool for Asthma Prediction at School Age in a UK Birth Cohort</title><author>Wang, R ; 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Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Education Database</collection><collection>Family Health Database (Proquest)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>ProQuest One Education</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 Basic</collection><jtitle>Archives of disease in childhood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, R</au><au>Custovic, A</au><au>Simpson, A</au><au>Belgrave, D</au><au>Murray, CS</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>G89 Individual Risk Assessment Tool for Asthma Prediction at School Age in a UK Birth Cohort</atitle><jtitle>Archives of disease in childhood</jtitle><date>2014-04</date><risdate>2014</risdate><volume>99</volume><issue>Suppl 1</issue><spage>A38</spage><epage>A38</epage><pages>A38-A38</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><coden>ADCHAK</coden><abstract>Background Commonly used Asthma Predictive Index (API; Castro-Rodriguez 2000) has good negative but poor positive predictive value (PPV) which reduces its clinical usefulness. We aimed to develop, within a population-based cohort, an asthma risk prediction tool (ARPT) better suited for clinical use. Method Children from a UK birth cohort attended follow-up at age 3, 8 and 11 years. Parents completed validated questionnaires. Children were skin prick tested (SPT) to common inhalant and food allergens. GP records were transcribed to collect information on physician-confirmed wheeze. An ARPT was developed using backwards logistic regression of data collected at age 3 years. We assessed its predictive performance using area under the receiver operating characteristic curve (AUROC). Repeated internal validation was performed. Results Of 829 children were included in the analysis, 132(17.8%) had asthma at school-age (year 8 or 11). The ARPT was found to include 4 predictors at age 3 years yielding a total score of 5: wheeze ever (1), wheeze causing shortness of breath (1), wheeze after exercise (2) and eczema (1). In the whole population, children with a score of &gt;4 had a significantly increased risk of having asthma at school-age odds ratio [OR] 25.3, 95% CI [11.8–54.1], p &lt; 0.0001; PPV 80%; sensitivity 28%). API, when applied to our cohort, yielded an OR for asthma at school-age of 7.4 (95% CI [4.5–12.2], p &lt; 0.0001; PPV 54%; sensitivity 31%). We then applied our ARPT amongst children who presented to their GP with wheeze within the first 3 years of life; those with ARTP score of ≥4 had a significantly increased risk of asthma at school-age (OR 15.6, 95% CI [6.1–39.9] p &lt; 0.0001; PPV 82%; sensitivity 35%). API, when applied in this population, had OR of 4.7 (95% CI [2.53–8.60], p &lt; 0.0001; PPV 57%, Sensitivity 44%). Internal validation showed good agreement (AUCpredicting 0.78 vs. AUCobserved 0.77). Conclusion APRT is a simple tool based mainly on clinical history which could easily be applied in primary/secondary care to risk stratify children with wheeze symptoms in early childhood and predict asthma by school-age with a good positive predictive value.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/archdischild-2014-306237.89</doi></addata></record>
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subjects Asthma
Health risks
Risk assessment
Skin diseases
Young Children
title G89 Individual Risk Assessment Tool for Asthma Prediction at School Age in a UK Birth Cohort
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