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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Views of breast and colorectal cancer survivors on their routine follow-up care</title><author><name sortKey="Urquhart, R" sort="Urquhart, R" uniqKey="Urquhart R" first="R." last="Urquhart">R. Urquhart</name><affiliation><nlm:aff id="af1-conc-19-294"> Cancer Outcomes Research Program, Cancer Care Nova Scotia, Halifax, NS.</nlm:aff></affiliation></author><author><name sortKey="Folkes, A" sort="Folkes, A" uniqKey="Folkes A" first="A." last="Folkes">A. Folkes</name><affiliation><nlm:aff id="af2-conc-19-294"> Prevention and Early Detection, Cancer Care Nova Scotia, Halifax, NS.</nlm:aff></affiliation></author><author><name sortKey="Babineau, J" sort="Babineau, J" uniqKey="Babineau J" first="J." last="Babineau">J. Babineau</name><affiliation><nlm:aff id="af1-conc-19-294"> Cancer Outcomes Research Program, Cancer Care Nova Scotia, Halifax, NS.</nlm:aff></affiliation></author><author><name sortKey="Grunfeld, E" sort="Grunfeld, E" uniqKey="Grunfeld E" first="E." last="Grunfeld">E. Grunfeld</name><affiliation><nlm:aff id="af3-conc-19-294"> Ontario Institute for Cancer Research, Toronto, ON.</nlm:aff></affiliation><affiliation><nlm:aff id="af4-conc-19-294"> Department of Family and Community Medicine, University of Toronto, Toronto, ON.</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">23300354</idno><idno type="pmc">3503661</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503661</idno><idno type="RBID">PMC:3503661</idno><idno type="doi">10.3747/co.19.1051</idno><date when="2012">2012</date><idno type="wicri:Area/Pmc/Corpus">002D67</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">002D67</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Views of breast and colorectal cancer survivors on their routine follow-up care</title><author><name sortKey="Urquhart, R" sort="Urquhart, R" uniqKey="Urquhart R" first="R." last="Urquhart">R. Urquhart</name><affiliation><nlm:aff id="af1-conc-19-294"> Cancer Outcomes Research Program, Cancer Care Nova Scotia, Halifax, NS.</nlm:aff></affiliation></author><author><name sortKey="Folkes, A" sort="Folkes, A" uniqKey="Folkes A" first="A." last="Folkes">A. Folkes</name><affiliation><nlm:aff id="af2-conc-19-294"> Prevention and Early Detection, Cancer Care Nova Scotia, Halifax, NS.</nlm:aff></affiliation></author><author><name sortKey="Babineau, J" sort="Babineau, J" uniqKey="Babineau J" first="J." last="Babineau">J. Babineau</name><affiliation><nlm:aff id="af1-conc-19-294"> Cancer Outcomes Research Program, Cancer Care Nova Scotia, Halifax, NS.</nlm:aff></affiliation></author><author><name sortKey="Grunfeld, E" sort="Grunfeld, E" uniqKey="Grunfeld E" first="E." last="Grunfeld">E. Grunfeld</name><affiliation><nlm:aff id="af3-conc-19-294"> Ontario Institute for Cancer Research, Toronto, ON.</nlm:aff></affiliation><affiliation><nlm:aff id="af4-conc-19-294"> Department of Family and Community Medicine, University of Toronto, Toronto, ON.</nlm:aff></affiliation></author></analytic><series><title level="j">Current Oncology</title><idno type="ISSN">1198-0052</idno><idno type="eISSN">1718-7729</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Objective</title><p>Our understanding of optimum health care delivery for cancer survivors is limited by the lack of a patient-centred perspective. The objectives of the present study were to explore the views of breast and colorectal cancer survivors on their routine follow-up care, with respect to needs, preferences, and quality of follow-up, and their views on cancer specialist– compared with family physician (<sc>fp</sc>)–led follow-up care.</p></sec><sec><title>Methods</title><p>In Nova Scotia, Canada, 23 cancer survivors (13 breast, 10 colorectal) participated in either a focus group or a one-on-one interview. Participants were asked to reflect upon their lives as cancer survivors and on the type and quality of care and support they received during the follow-up period. Each focus group or interview was transcribed verbatim, and the transcripts were audited and subjected to a thematic analysis.</p></sec><sec><title>Results</title><p>Six themes were identified:
<list list-type="bullet"><list-item><p>My care is my responsibility</p></list-item><list-item><p>How I receive information on follow-up care</p></list-item><list-item><p>I have many care needs</p></list-item><list-item><p>I want to be prepared and informed</p></list-item><list-item><p>The role of my <sc>fp</sc> in my cancer experience and follow-up care</p></list-item><list-item><p>The role of media</p></list-item></list></p><p>Survivors often characterized the post–primary treatment experience as lacking in information and preparation for follow-up and providing inadequate support to address many of the care needs prevalent in survivor populations. Despite valuing <sc>fp</sc> participation in follow-up care, many survivors continued to receive comfort and reassurance from specialist care.</p></sec><sec><title>Conclusions</title><p>Our findings point to the need to implement strategies that better prepare breast cancer and colorectal cancer survivors for post-treatment care and that reassure survivors of the ability of their <sc>fp</sc> to provide quality care during this period.</p></sec></div></front></TEI><pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Curr Oncol</journal-id><journal-id journal-id-type="iso-abbrev">Curr Oncol</journal-id><journal-id journal-id-type="publisher-id">CO</journal-id><journal-title-group><journal-title>Current Oncology</journal-title></journal-title-group><issn pub-type="ppub">1198-0052</issn><issn pub-type="epub">1718-7729</issn><publisher><publisher-name>Multimed Inc.</publisher-name><publisher-loc>66 Martin St. Milton, ON, Canada L9T 2R2</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">23300354</article-id><article-id pub-id-type="pmc">3503661</article-id><article-id pub-id-type="doi">10.3747/co.19.1051</article-id><article-id pub-id-type="publisher-id">conc-19-294</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Article</subject><subj-group><subject>Cancer Rehabilitation and Survivorship</subject></subj-group></subj-group></article-categories><title-group><article-title>Views of breast and colorectal cancer survivors on their routine follow-up care</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Urquhart</surname><given-names>R.</given-names></name><degrees>MSc</degrees><xref ref-type="aff" rid="af1-conc-19-294"><sup>*</sup></xref><xref ref-type="corresp" rid="c1-conc-19-294"></xref></contrib><contrib contrib-type="author"><name><surname>Folkes</surname><given-names>A.</given-names></name><degrees>MAHSR</degrees><xref ref-type="aff" rid="af2-conc-19-294"><sup>†</sup></xref></contrib><contrib contrib-type="author"><name><surname>Babineau</surname><given-names>J.</given-names></name><degrees>MLIS</degrees><xref ref-type="aff" rid="af1-conc-19-294"><sup>*</sup></xref></contrib><contrib contrib-type="author"><name><surname>Grunfeld</surname><given-names>E.</given-names></name><degrees>MD DPhil</degrees><xref ref-type="aff" rid="af3-conc-19-294"><sup>‡</sup></xref><xref ref-type="aff" rid="af4-conc-19-294"><sup>§</sup></xref></contrib></contrib-group><aff id="af1-conc-19-294"><label>*</label> Cancer Outcomes Research Program, Cancer Care Nova Scotia, Halifax, NS.</aff><aff id="af2-conc-19-294"><label>†</label> Prevention and Early Detection, Cancer Care Nova Scotia, Halifax, NS.</aff><aff id="af3-conc-19-294"><label>‡</label> Ontario Institute for Cancer Research, Toronto, ON.</aff><aff id="af4-conc-19-294"><label>§</label> Department of Family and Community Medicine, University of Toronto, Toronto, ON.</aff><author-notes><corresp id="c1-conc-19-294">Correspondence to: Robin Urquhart, Cancer Outcomes Research Program, 1276 South Park Street, Room 804, Victoria Building, Halifax, Nova Scotia B3H 2Y9., E-mail: <email>urquhartr@cdha.nshealth.ca</email></corresp></author-notes><pub-date pub-type="ppub"><month>12</month><year>2012</year></pub-date><volume>19</volume><issue>6</issue><fpage>294</fpage><lpage>301</lpage><permissions><copyright-statement>2012 Multimed Inc.</copyright-statement><copyright-year>2012</copyright-year></permissions><abstract><sec><title>Objective</title><p>Our understanding of optimum health care delivery for cancer survivors is limited by the lack of a patient-centred perspective. The objectives of the present study were to explore the views of breast and colorectal cancer survivors on their routine follow-up care, with respect to needs, preferences, and quality of follow-up, and their views on cancer specialist– compared with family physician (<sc>fp</sc>)–led follow-up care.</p></sec><sec><title>Methods</title><p>In Nova Scotia, Canada, 23 cancer survivors (13 breast, 10 colorectal) participated in either a focus group or a one-on-one interview. Participants were asked to reflect upon their lives as cancer survivors and on the type and quality of care and support they received during the follow-up period. Each focus group or interview was transcribed verbatim, and the transcripts were audited and subjected to a thematic analysis.</p></sec><sec><title>Results</title><p>Six themes were identified:
<list list-type="bullet"><list-item><p>My care is my responsibility</p></list-item><list-item><p>How I receive information on follow-up care</p></list-item><list-item><p>I have many care needs</p></list-item><list-item><p>I want to be prepared and informed</p></list-item><list-item><p>The role of my <sc>fp</sc> in my cancer experience and follow-up care</p></list-item><list-item><p>The role of media</p></list-item></list></p><p>Survivors often characterized the post–primary treatment experience as lacking in information and preparation for follow-up and providing inadequate support to address many of the care needs prevalent in survivor populations. Despite valuing <sc>fp</sc> participation in follow-up care, many survivors continued to receive comfort and reassurance from specialist care.</p></sec><sec><title>Conclusions</title><p>Our findings point to the need to implement strategies that better prepare breast cancer and colorectal cancer survivors for post-treatment care and that reassure survivors of the ability of their <sc>fp</sc> to provide quality care during this period.</p></sec></abstract><kwd-group><kwd>Breast cancer</kwd><kwd>colorectal cancer</kwd><kwd>oncology</kwd><kwd>follow-up care</kwd><kwd>survivorship</kwd></kwd-group></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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