Does pain affect executive function in sickle cell disease?

Aims Research in populations with sickle cell anaemia (SCA) has consistently found differences from healthy controls on tests of executive function (EF), attributed to the elevated stroke risk. In older adults without SCA there is an association between pain and mental flexibility. The aims of this...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Archives of disease in childhood 2012-05, Vol.97 (Suppl 1), p.A83
Hauptverfasser: Seymour, EL, Hollocks, M, Roberts-Harewood, M, Robins, A, Wilkey, O, Morgan, MA, Kirkham, FJ
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue Suppl 1
container_start_page A83
container_title Archives of disease in childhood
container_volume 97
creator Seymour, EL
Hollocks, M
Roberts-Harewood, M
Robins, A
Wilkey, O
Morgan, MA
Kirkham, FJ
description Aims Research in populations with sickle cell anaemia (SCA) has consistently found differences from healthy controls on tests of executive function (EF), attributed to the elevated stroke risk. In older adults without SCA there is an association between pain and mental flexibility. The aims of this study were to investigate the executive function performance of a group of SCA children across a single test battery and the possibility that chronic pain impacts upon these skills. Methods Patients with SCA were recruited via their consultants at outpatients clinics. Sibling controls and other ethnically matched children were recruited via the community. The Weschler Abbreviated Scales of Intelligence (WASI): two-sub-test version was administered together with five of the nine available sub-tests of the Delis Kaplan Executive Function System (D-KEFS), representing a range of different skills: the trail-making, the design fluency, colour-word interference, sorting and tower tests. Composite scores were created for each of the DKEFS sub-tests. Current pain was measured using the Faces Pain Scale-Revised (FPS-R). Frequency of pain was measured via self-report of the number of pain episodes over the past year. A number of t-tests, followed by correlations, were then employed to compare performance across the two groups. Results Eight controls (3 male), mean age 11 y 3 m (9 y 8 m-14 y 8 m) and 14 (11 male) children with SCA, mean age 13 y 4 m (10 y 7 m-17 y 6 m) were recruited. There was a significant difference between the frequency of pain episodes in the SCA and control groups, t (20)=−2.56, p=0.019. T-tests showed no significant differences at the 95% confidence interval in FPS-R scores, any of the DKEFS sub-tests, or FSIQ. No significant correlations were found between either frequency of pain episodes or current pain, and any of the composite EF sub-test scores. Discussion We found no evidence of impaired performance by the SCA group on any of the EF sub-tests. The SCA group reported significantly more frequent pain episodes, and a wider range of pain levels on the day of testing but there was no association between current pain, or pain frequency, and EF test performance, perhaps explained by the subjective nature of pain, and differences in pain perception. Abstract G151 Table 1 Transfusion Strategy Mean DE rate (95% CI) Number of babies exposed to >1 donor No. of babies exposed to >2 donors SP wastage (Rounded) 4-SP 2.47 (2.03,2.88) 20 (86.9%) 8 (34.7%) 5 6
doi_str_mv 10.1136/archdischild-2012-301885.201
format Article
fullrecord <record><control><sourceid>proquest_istex</sourceid><recordid>TN_cdi_proquest_journals_1828841127</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4214720781</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1147-c043baf2c76fcb7582a167de54f2a0a9b23399bf4614e474ea5c371c1907deea3</originalsourceid><addsrcrecordid>eNpNkG9LwzAQh4MoOKffoaBvO3NJ2qT4QmQ6J_gHQX0b0uzCsnXtbFqZ396Mivjqftw93HEPIRdAJwA8vzStXS58sEtfLVJGgaWcglLZJOYDMgKRq9gW4pCMKKU8LZRSx-QkhBWNsFJ8RK5uGwzJ1vg6Mc6h7RLcoe07_4WJ62vb-aZO4jB4u64wsVhVSTyJJuD1KTlypgp49lvH5H129zadp48v9w_Tm8e0BBAytVTw0jhmZe5sKTPFDORygZlwzFBTlIzzoiidyEGgkAJNZrkECwWNFBo-JufD3m3bfPYYOr1q-raOJzWo-IYAYDJS6UD50OFOb1u_Me23Nu1a55LLTD9_TPUrexIim821iLwc-HKz-qOB6r1Z_d-s3pvVg9l95j_7vm4O</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1828841127</pqid></control><display><type>article</type><title>Does pain affect executive function in sickle cell disease?</title><source>BMJ Journals - NESLi2</source><creator>Seymour, EL ; Hollocks, M ; Roberts-Harewood, M ; Robins, A ; Wilkey, O ; Morgan, MA ; Kirkham, FJ</creator><creatorcontrib>Seymour, EL ; Hollocks, M ; Roberts-Harewood, M ; Robins, A ; Wilkey, O ; Morgan, MA ; Kirkham, FJ</creatorcontrib><description>Aims Research in populations with sickle cell anaemia (SCA) has consistently found differences from healthy controls on tests of executive function (EF), attributed to the elevated stroke risk. In older adults without SCA there is an association between pain and mental flexibility. The aims of this study were to investigate the executive function performance of a group of SCA children across a single test battery and the possibility that chronic pain impacts upon these skills. Methods Patients with SCA were recruited via their consultants at outpatients clinics. Sibling controls and other ethnically matched children were recruited via the community. The Weschler Abbreviated Scales of Intelligence (WASI): two-sub-test version was administered together with five of the nine available sub-tests of the Delis Kaplan Executive Function System (D-KEFS), representing a range of different skills: the trail-making, the design fluency, colour-word interference, sorting and tower tests. Composite scores were created for each of the DKEFS sub-tests. Current pain was measured using the Faces Pain Scale-Revised (FPS-R). Frequency of pain was measured via self-report of the number of pain episodes over the past year. A number of t-tests, followed by correlations, were then employed to compare performance across the two groups. Results Eight controls (3 male), mean age 11 y 3 m (9 y 8 m-14 y 8 m) and 14 (11 male) children with SCA, mean age 13 y 4 m (10 y 7 m-17 y 6 m) were recruited. There was a significant difference between the frequency of pain episodes in the SCA and control groups, t (20)=−2.56, p=0.019. T-tests showed no significant differences at the 95% confidence interval in FPS-R scores, any of the DKEFS sub-tests, or FSIQ. No significant correlations were found between either frequency of pain episodes or current pain, and any of the composite EF sub-test scores. Discussion We found no evidence of impaired performance by the SCA group on any of the EF sub-tests. The SCA group reported significantly more frequent pain episodes, and a wider range of pain levels on the day of testing but there was no association between current pain, or pain frequency, and EF test performance, perhaps explained by the subjective nature of pain, and differences in pain perception. Abstract G151 Table 1 Transfusion Strategy Mean DE rate (95% CI) Number of babies exposed to &gt;1 donor No. of babies exposed to &gt;2 donors SP wastage (Rounded) 4-SP 2.47 (2.03,2.88) 20 (86.9%) 8 (34.7%) 5 6-SP 2.44 (1.98,2.88) 18 (78.2%) 8 (34.7%) 10 8-SP 2.44 (1.98,2.88) 18 (78.2%) 8 (34.7%) 15</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2012-301885.201</identifier><identifier>CODEN: ADCHAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><subject>Aging (Individuals) ; Control Groups ; Executive Function ; Health risks ; Older people ; Pain</subject><ispartof>Archives of disease in childhood, 2012-05, Vol.97 (Suppl 1), p.A83</ispartof><rights>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: 2012 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/97/Suppl_1/A83.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://adc.bmj.com/content/97/Suppl_1/A83.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,23570,27923,27924,77371,77402</link.rule.ids></links><search><creatorcontrib>Seymour, EL</creatorcontrib><creatorcontrib>Hollocks, M</creatorcontrib><creatorcontrib>Roberts-Harewood, M</creatorcontrib><creatorcontrib>Robins, A</creatorcontrib><creatorcontrib>Wilkey, O</creatorcontrib><creatorcontrib>Morgan, MA</creatorcontrib><creatorcontrib>Kirkham, FJ</creatorcontrib><title>Does pain affect executive function in sickle cell disease?</title><title>Archives of disease in childhood</title><addtitle>Arch Dis Child</addtitle><description>Aims Research in populations with sickle cell anaemia (SCA) has consistently found differences from healthy controls on tests of executive function (EF), attributed to the elevated stroke risk. In older adults without SCA there is an association between pain and mental flexibility. The aims of this study were to investigate the executive function performance of a group of SCA children across a single test battery and the possibility that chronic pain impacts upon these skills. Methods Patients with SCA were recruited via their consultants at outpatients clinics. Sibling controls and other ethnically matched children were recruited via the community. The Weschler Abbreviated Scales of Intelligence (WASI): two-sub-test version was administered together with five of the nine available sub-tests of the Delis Kaplan Executive Function System (D-KEFS), representing a range of different skills: the trail-making, the design fluency, colour-word interference, sorting and tower tests. Composite scores were created for each of the DKEFS sub-tests. Current pain was measured using the Faces Pain Scale-Revised (FPS-R). Frequency of pain was measured via self-report of the number of pain episodes over the past year. A number of t-tests, followed by correlations, were then employed to compare performance across the two groups. Results Eight controls (3 male), mean age 11 y 3 m (9 y 8 m-14 y 8 m) and 14 (11 male) children with SCA, mean age 13 y 4 m (10 y 7 m-17 y 6 m) were recruited. There was a significant difference between the frequency of pain episodes in the SCA and control groups, t (20)=−2.56, p=0.019. T-tests showed no significant differences at the 95% confidence interval in FPS-R scores, any of the DKEFS sub-tests, or FSIQ. No significant correlations were found between either frequency of pain episodes or current pain, and any of the composite EF sub-test scores. Discussion We found no evidence of impaired performance by the SCA group on any of the EF sub-tests. The SCA group reported significantly more frequent pain episodes, and a wider range of pain levels on the day of testing but there was no association between current pain, or pain frequency, and EF test performance, perhaps explained by the subjective nature of pain, and differences in pain perception. Abstract G151 Table 1 Transfusion Strategy Mean DE rate (95% CI) Number of babies exposed to &gt;1 donor No. of babies exposed to &gt;2 donors SP wastage (Rounded) 4-SP 2.47 (2.03,2.88) 20 (86.9%) 8 (34.7%) 5 6-SP 2.44 (1.98,2.88) 18 (78.2%) 8 (34.7%) 10 8-SP 2.44 (1.98,2.88) 18 (78.2%) 8 (34.7%) 15</description><subject>Aging (Individuals)</subject><subject>Control Groups</subject><subject>Executive Function</subject><subject>Health risks</subject><subject>Older people</subject><subject>Pain</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpNkG9LwzAQh4MoOKffoaBvO3NJ2qT4QmQ6J_gHQX0b0uzCsnXtbFqZ396Mivjqftw93HEPIRdAJwA8vzStXS58sEtfLVJGgaWcglLZJOYDMgKRq9gW4pCMKKU8LZRSx-QkhBWNsFJ8RK5uGwzJ1vg6Mc6h7RLcoe07_4WJ62vb-aZO4jB4u64wsVhVSTyJJuD1KTlypgp49lvH5H129zadp48v9w_Tm8e0BBAytVTw0jhmZe5sKTPFDORygZlwzFBTlIzzoiidyEGgkAJNZrkECwWNFBo-JufD3m3bfPYYOr1q-raOJzWo-IYAYDJS6UD50OFOb1u_Me23Nu1a55LLTD9_TPUrexIim821iLwc-HKz-qOB6r1Z_d-s3pvVg9l95j_7vm4O</recordid><startdate>201205</startdate><enddate>201205</enddate><creator>Seymour, EL</creator><creator>Hollocks, M</creator><creator>Roberts-Harewood, M</creator><creator>Robins, A</creator><creator>Wilkey, O</creator><creator>Morgan, MA</creator><creator>Kirkham, FJ</creator><general>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</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>201205</creationdate><title>Does pain affect executive function in sickle cell disease?</title><author>Seymour, EL ; Hollocks, M ; Roberts-Harewood, M ; Robins, A ; Wilkey, O ; Morgan, MA ; Kirkham, FJ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1147-c043baf2c76fcb7582a167de54f2a0a9b23399bf4614e474ea5c371c1907deea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aging (Individuals)</topic><topic>Control Groups</topic><topic>Executive Function</topic><topic>Health risks</topic><topic>Older people</topic><topic>Pain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seymour, EL</creatorcontrib><creatorcontrib>Hollocks, M</creatorcontrib><creatorcontrib>Roberts-Harewood, M</creatorcontrib><creatorcontrib>Robins, A</creatorcontrib><creatorcontrib>Wilkey, O</creatorcontrib><creatorcontrib>Morgan, MA</creatorcontrib><creatorcontrib>Kirkham, FJ</creatorcontrib><collection>Istex</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Education Collection</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Education Database</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</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>Seymour, EL</au><au>Hollocks, M</au><au>Roberts-Harewood, M</au><au>Robins, A</au><au>Wilkey, O</au><au>Morgan, MA</au><au>Kirkham, FJ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does pain affect executive function in sickle cell disease?</atitle><jtitle>Archives of disease in childhood</jtitle><addtitle>Arch Dis Child</addtitle><date>2012-05</date><risdate>2012</risdate><volume>97</volume><issue>Suppl 1</issue><spage>A83</spage><pages>A83-</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><coden>ADCHAK</coden><abstract>Aims Research in populations with sickle cell anaemia (SCA) has consistently found differences from healthy controls on tests of executive function (EF), attributed to the elevated stroke risk. In older adults without SCA there is an association between pain and mental flexibility. The aims of this study were to investigate the executive function performance of a group of SCA children across a single test battery and the possibility that chronic pain impacts upon these skills. Methods Patients with SCA were recruited via their consultants at outpatients clinics. Sibling controls and other ethnically matched children were recruited via the community. The Weschler Abbreviated Scales of Intelligence (WASI): two-sub-test version was administered together with five of the nine available sub-tests of the Delis Kaplan Executive Function System (D-KEFS), representing a range of different skills: the trail-making, the design fluency, colour-word interference, sorting and tower tests. Composite scores were created for each of the DKEFS sub-tests. Current pain was measured using the Faces Pain Scale-Revised (FPS-R). Frequency of pain was measured via self-report of the number of pain episodes over the past year. A number of t-tests, followed by correlations, were then employed to compare performance across the two groups. Results Eight controls (3 male), mean age 11 y 3 m (9 y 8 m-14 y 8 m) and 14 (11 male) children with SCA, mean age 13 y 4 m (10 y 7 m-17 y 6 m) were recruited. There was a significant difference between the frequency of pain episodes in the SCA and control groups, t (20)=−2.56, p=0.019. T-tests showed no significant differences at the 95% confidence interval in FPS-R scores, any of the DKEFS sub-tests, or FSIQ. No significant correlations were found between either frequency of pain episodes or current pain, and any of the composite EF sub-test scores. Discussion We found no evidence of impaired performance by the SCA group on any of the EF sub-tests. The SCA group reported significantly more frequent pain episodes, and a wider range of pain levels on the day of testing but there was no association between current pain, or pain frequency, and EF test performance, perhaps explained by the subjective nature of pain, and differences in pain perception. Abstract G151 Table 1 Transfusion Strategy Mean DE rate (95% CI) Number of babies exposed to &gt;1 donor No. of babies exposed to &gt;2 donors SP wastage (Rounded) 4-SP 2.47 (2.03,2.88) 20 (86.9%) 8 (34.7%) 5 6-SP 2.44 (1.98,2.88) 18 (78.2%) 8 (34.7%) 10 8-SP 2.44 (1.98,2.88) 18 (78.2%) 8 (34.7%) 15</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</pub><doi>10.1136/archdischild-2012-301885.201</doi></addata></record>
fulltext fulltext
identifier ISSN: 0003-9888
ispartof Archives of disease in childhood, 2012-05, Vol.97 (Suppl 1), p.A83
issn 0003-9888
1468-2044
language eng
recordid cdi_proquest_journals_1828841127
source BMJ Journals - NESLi2
subjects Aging (Individuals)
Control Groups
Executive Function
Health risks
Older people
Pain
title Does pain affect executive function in sickle cell disease?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T16%3A13%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_istex&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Does%20pain%20affect%20executive%20function%20in%20sickle%20cell%20disease?&rft.jtitle=Archives%20of%20disease%20in%20childhood&rft.au=Seymour,%20EL&rft.date=2012-05&rft.volume=97&rft.issue=Suppl%201&rft.spage=A83&rft.pages=A83-&rft.issn=0003-9888&rft.eissn=1468-2044&rft.coden=ADCHAK&rft_id=info:doi/10.1136/archdischild-2012-301885.201&rft_dat=%3Cproquest_istex%3E4214720781%3C/proquest_istex%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1828841127&rft_id=info:pmid/&rfr_iscdi=true