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Family, demographic and illness-related determinants of HRQL in children with brain tumours in the first year after diagnosis

Aims To evaluate the relationship between parent‐ and child‐report Health‐Related Quality of Life (HRQL) and demographic, tumour and family variables in children with a brain tumour in the first year after diagnosis and to identify determinants of HRQL at 12 months. Procedure Longitudinal prospectiv...

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Published in:Pediatric blood & cancer 2009-12, Vol.53 (6), p.1092-1099
Main Authors: Penn, Anthony, Lowis, Stephen P., Stevens, Michael C.G., Hunt, Linda P., Shortman, Robert I., McCarter, Renee J., Pauldhas, Darwin, Curran, Andrew L., Sharples, Peta M.
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cited_by cdi_FETCH-LOGICAL-c3947-dd6023bdc3aa6b95ec637202c8773d9ccbfb1308d98fbf663232bdc996e8bf963
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container_end_page 1099
container_issue 6
container_start_page 1092
container_title Pediatric blood & cancer
container_volume 53
creator Penn, Anthony
Lowis, Stephen P.
Stevens, Michael C.G.
Hunt, Linda P.
Shortman, Robert I.
McCarter, Renee J.
Pauldhas, Darwin
Curran, Andrew L.
Sharples, Peta M.
description Aims To evaluate the relationship between parent‐ and child‐report Health‐Related Quality of Life (HRQL) and demographic, tumour and family variables in children with a brain tumour in the first year after diagnosis and to identify determinants of HRQL at 12 months. Procedure Longitudinal prospective study: Semi‐structured interviews took place approximately 1, 6 and 12 months after diagnosis. HRQL was measured using the self‐ and parent‐report PedsQL 4.0 Total Scale Score. Tumour and treatment variables considered included tumour site and grade, hydrocephalus at diagnosis, chemotherapy and radiotherapy. Family variables included measures of family function, family support and family stress, the primary carer's coping strategies and symptoms of depression and anxiety. Univariate analyses were used at all three time points, and to identify potential early predictors of HRQL at 1 year. Regression analysis was then used to identify the most important determinants of HRQL at 1 year. Results Thirty‐five patients completed the 12‐month interviews. There were consistent significant negative correlations between concurrent family impact of illness and parent and self‐report HRQL, and positive correlations between concurrent family support and parent‐report HRQL. Treatment with radio‐ or chemotherapy correlated with child‐report HRQL only at some time points. Multivariate analysis showed infratentorial tumour site, and poor HRQL at 1 month best predicted poor self‐ and parent‐report HRQL at 12 months. Conclusion Children with infratentorial tumours and poor HRQL early after diagnosis tend to have poor HRQL at 1 year. While family factors are important modulators of concurrent HRQL, they do not appear important in predicting HRQL. Pediatr Blood Cancer 2009;53:1092–1099. © 2009 Wiley‐Liss, Inc.
doi_str_mv 10.1002/pbc.22157
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Procedure Longitudinal prospective study: Semi‐structured interviews took place approximately 1, 6 and 12 months after diagnosis. HRQL was measured using the self‐ and parent‐report PedsQL 4.0 Total Scale Score. Tumour and treatment variables considered included tumour site and grade, hydrocephalus at diagnosis, chemotherapy and radiotherapy. Family variables included measures of family function, family support and family stress, the primary carer's coping strategies and symptoms of depression and anxiety. Univariate analyses were used at all three time points, and to identify potential early predictors of HRQL at 1 year. Regression analysis was then used to identify the most important determinants of HRQL at 1 year. Results Thirty‐five patients completed the 12‐month interviews. There were consistent significant negative correlations between concurrent family impact of illness and parent and self‐report HRQL, and positive correlations between concurrent family support and parent‐report HRQL. Treatment with radio‐ or chemotherapy correlated with child‐report HRQL only at some time points. Multivariate analysis showed infratentorial tumour site, and poor HRQL at 1 month best predicted poor self‐ and parent‐report HRQL at 12 months. Conclusion Children with infratentorial tumours and poor HRQL early after diagnosis tend to have poor HRQL at 1 year. While family factors are important modulators of concurrent HRQL, they do not appear important in predicting HRQL. Pediatr Blood Cancer 2009;53:1092–1099. © 2009 Wiley‐Liss, Inc.</description><identifier>ISSN: 1545-5009</identifier><identifier>ISSN: 1545-5017</identifier><identifier>EISSN: 1545-5017</identifier><identifier>DOI: 10.1002/pbc.22157</identifier><identifier>PMID: 19743518</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Brain Neoplasms - diagnosis ; Brain Neoplasms - psychology ; Brain Neoplasms - rehabilitation ; brain tumour ; Child ; CNS tumour ; Family ; Family Health ; health-related quality of life ; HRQL ; Humans ; Infratentorial Neoplasms ; Longitudinal Studies ; Multivariate Analysis ; paediatric ; Parent-Child Relations ; Prognosis ; Quality of Life ; Surveys and Questionnaires</subject><ispartof>Pediatric blood &amp; cancer, 2009-12, Vol.53 (6), p.1092-1099</ispartof><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3947-dd6023bdc3aa6b95ec637202c8773d9ccbfb1308d98fbf663232bdc996e8bf963</citedby><cites>FETCH-LOGICAL-c3947-dd6023bdc3aa6b95ec637202c8773d9ccbfb1308d98fbf663232bdc996e8bf963</cites></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/19743518$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Penn, Anthony</creatorcontrib><creatorcontrib>Lowis, Stephen P.</creatorcontrib><creatorcontrib>Stevens, Michael C.G.</creatorcontrib><creatorcontrib>Hunt, Linda P.</creatorcontrib><creatorcontrib>Shortman, Robert I.</creatorcontrib><creatorcontrib>McCarter, Renee J.</creatorcontrib><creatorcontrib>Pauldhas, Darwin</creatorcontrib><creatorcontrib>Curran, Andrew L.</creatorcontrib><creatorcontrib>Sharples, Peta M.</creatorcontrib><title>Family, demographic and illness-related determinants of HRQL in children with brain tumours in the first year after diagnosis</title><title>Pediatric blood &amp; cancer</title><addtitle>Pediatr. Blood Cancer</addtitle><description>Aims To evaluate the relationship between parent‐ and child‐report Health‐Related Quality of Life (HRQL) and demographic, tumour and family variables in children with a brain tumour in the first year after diagnosis and to identify determinants of HRQL at 12 months. Procedure Longitudinal prospective study: Semi‐structured interviews took place approximately 1, 6 and 12 months after diagnosis. HRQL was measured using the self‐ and parent‐report PedsQL 4.0 Total Scale Score. Tumour and treatment variables considered included tumour site and grade, hydrocephalus at diagnosis, chemotherapy and radiotherapy. Family variables included measures of family function, family support and family stress, the primary carer's coping strategies and symptoms of depression and anxiety. Univariate analyses were used at all three time points, and to identify potential early predictors of HRQL at 1 year. Regression analysis was then used to identify the most important determinants of HRQL at 1 year. Results Thirty‐five patients completed the 12‐month interviews. There were consistent significant negative correlations between concurrent family impact of illness and parent and self‐report HRQL, and positive correlations between concurrent family support and parent‐report HRQL. Treatment with radio‐ or chemotherapy correlated with child‐report HRQL only at some time points. Multivariate analysis showed infratentorial tumour site, and poor HRQL at 1 month best predicted poor self‐ and parent‐report HRQL at 12 months. Conclusion Children with infratentorial tumours and poor HRQL early after diagnosis tend to have poor HRQL at 1 year. While family factors are important modulators of concurrent HRQL, they do not appear important in predicting HRQL. Pediatr Blood Cancer 2009;53:1092–1099. © 2009 Wiley‐Liss, Inc.</description><subject>Brain Neoplasms - diagnosis</subject><subject>Brain Neoplasms - psychology</subject><subject>Brain Neoplasms - rehabilitation</subject><subject>brain tumour</subject><subject>Child</subject><subject>CNS tumour</subject><subject>Family</subject><subject>Family Health</subject><subject>health-related quality of life</subject><subject>HRQL</subject><subject>Humans</subject><subject>Infratentorial Neoplasms</subject><subject>Longitudinal Studies</subject><subject>Multivariate Analysis</subject><subject>paediatric</subject><subject>Parent-Child Relations</subject><subject>Prognosis</subject><subject>Quality of Life</subject><subject>Surveys and Questionnaires</subject><issn>1545-5009</issn><issn>1545-5017</issn><issn>1545-5017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp90UtrVDEYBuAgiq3VhX9AshIFT5vLSXKytEMvwuClKIqbkGsnei7TJIc6C_-7aWdaV7pKyPd8L4QXgOcYHWKEyNHa2ENCMBMPwD5mLWsYwuLh_R3JPfAk5x-VcsS6x2APS9FShrt98PtUD7HfvIHOD9Nl0utVtFCPDsa-H33OTfK9Lt7VefFpiKMeS4ZTgOcXn5YwjtCuYu-SH-F1LCtokq5vZR6mOeWbcVl5GGLKBW68TlCHmgJd1JfjlGN-Ch4F3Wf_bHcegC-nJ58X583yw9m7xdtlY6lsReMcR4QaZ6nW3EjmLaeCIGI7IaiT1ppgMEWdk10wgXNKKKlaSu47EySnB-DlNnedpqvZ56KGmK3vez36ac6KC85YS2iFr_4LMeWi7UjLUaWvt9SmKefkg1qnOOi0URipm1pUrUXd1lLti13sbAbv_spdDxUcbcF17P3m30nq4_HiLrLZbsRc_K_7DZ1-1t9QwdTX92fqmFAhvpML9Y3-ATzNpx4</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Penn, Anthony</creator><creator>Lowis, Stephen P.</creator><creator>Stevens, Michael C.G.</creator><creator>Hunt, Linda P.</creator><creator>Shortman, Robert I.</creator><creator>McCarter, Renee J.</creator><creator>Pauldhas, Darwin</creator><creator>Curran, Andrew L.</creator><creator>Sharples, Peta M.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20091201</creationdate><title>Family, demographic and illness-related determinants of HRQL in children with brain tumours in the first year after diagnosis</title><author>Penn, Anthony ; Lowis, Stephen P. ; Stevens, Michael C.G. ; Hunt, Linda P. ; Shortman, Robert I. ; McCarter, Renee J. ; Pauldhas, Darwin ; Curran, Andrew L. ; Sharples, Peta M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3947-dd6023bdc3aa6b95ec637202c8773d9ccbfb1308d98fbf663232bdc996e8bf963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Brain Neoplasms - diagnosis</topic><topic>Brain Neoplasms - psychology</topic><topic>Brain Neoplasms - rehabilitation</topic><topic>brain tumour</topic><topic>Child</topic><topic>CNS tumour</topic><topic>Family</topic><topic>Family Health</topic><topic>health-related quality of life</topic><topic>HRQL</topic><topic>Humans</topic><topic>Infratentorial Neoplasms</topic><topic>Longitudinal Studies</topic><topic>Multivariate Analysis</topic><topic>paediatric</topic><topic>Parent-Child Relations</topic><topic>Prognosis</topic><topic>Quality of Life</topic><topic>Surveys and Questionnaires</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Penn, Anthony</creatorcontrib><creatorcontrib>Lowis, Stephen P.</creatorcontrib><creatorcontrib>Stevens, Michael C.G.</creatorcontrib><creatorcontrib>Hunt, Linda P.</creatorcontrib><creatorcontrib>Shortman, Robert I.</creatorcontrib><creatorcontrib>McCarter, Renee J.</creatorcontrib><creatorcontrib>Pauldhas, Darwin</creatorcontrib><creatorcontrib>Curran, Andrew L.</creatorcontrib><creatorcontrib>Sharples, Peta M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric blood &amp; cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Penn, Anthony</au><au>Lowis, Stephen P.</au><au>Stevens, Michael C.G.</au><au>Hunt, Linda P.</au><au>Shortman, Robert I.</au><au>McCarter, Renee J.</au><au>Pauldhas, Darwin</au><au>Curran, Andrew L.</au><au>Sharples, Peta M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Family, demographic and illness-related determinants of HRQL in children with brain tumours in the first year after diagnosis</atitle><jtitle>Pediatric blood &amp; cancer</jtitle><addtitle>Pediatr. Blood Cancer</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>53</volume><issue>6</issue><spage>1092</spage><epage>1099</epage><pages>1092-1099</pages><issn>1545-5009</issn><issn>1545-5017</issn><eissn>1545-5017</eissn><abstract>Aims To evaluate the relationship between parent‐ and child‐report Health‐Related Quality of Life (HRQL) and demographic, tumour and family variables in children with a brain tumour in the first year after diagnosis and to identify determinants of HRQL at 12 months. Procedure Longitudinal prospective study: Semi‐structured interviews took place approximately 1, 6 and 12 months after diagnosis. HRQL was measured using the self‐ and parent‐report PedsQL 4.0 Total Scale Score. Tumour and treatment variables considered included tumour site and grade, hydrocephalus at diagnosis, chemotherapy and radiotherapy. Family variables included measures of family function, family support and family stress, the primary carer's coping strategies and symptoms of depression and anxiety. Univariate analyses were used at all three time points, and to identify potential early predictors of HRQL at 1 year. Regression analysis was then used to identify the most important determinants of HRQL at 1 year. Results Thirty‐five patients completed the 12‐month interviews. There were consistent significant negative correlations between concurrent family impact of illness and parent and self‐report HRQL, and positive correlations between concurrent family support and parent‐report HRQL. Treatment with radio‐ or chemotherapy correlated with child‐report HRQL only at some time points. Multivariate analysis showed infratentorial tumour site, and poor HRQL at 1 month best predicted poor self‐ and parent‐report HRQL at 12 months. Conclusion Children with infratentorial tumours and poor HRQL early after diagnosis tend to have poor HRQL at 1 year. While family factors are important modulators of concurrent HRQL, they do not appear important in predicting HRQL. Pediatr Blood Cancer 2009;53:1092–1099. © 2009 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19743518</pmid><doi>10.1002/pbc.22157</doi><tpages>8</tpages></addata></record>
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subjects Brain Neoplasms - diagnosis
Brain Neoplasms - psychology
Brain Neoplasms - rehabilitation
brain tumour
Child
CNS tumour
Family
Family Health
health-related quality of life
HRQL
Humans
Infratentorial Neoplasms
Longitudinal Studies
Multivariate Analysis
paediatric
Parent-Child Relations
Prognosis
Quality of Life
Surveys and Questionnaires
title Family, demographic and illness-related determinants of HRQL in children with brain tumours in the first year after diagnosis
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