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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Perceptions of survivorship care among South Asian female breast cancer survivors</title>
<author><name sortKey="Singh Arlson, S" sort="Singh Arlson, S" uniqKey="Singh Arlson S" first="S." last="Singh Arlson">S. Singh Arlson</name>
<affiliation><nlm:aff id="af1-conc-20-e80">School of Nursing, California State University–Long Beach, Long Beach, CA, U.S.A.</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Nguyen, S K A" sort="Nguyen, S K A" uniqKey="Nguyen S" first="S. K. A." last="Nguyen">S. K. A. Nguyen</name>
<affiliation><nlm:aff id="af2-conc-20-e80">BC Cancer Agency–Fraser Valley Centre, Surrey, BC.</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Wong, F" sort="Wong, F" uniqKey="Wong F" first="F." last="Wong">F. Wong</name>
<affiliation><nlm:aff id="af2-conc-20-e80">BC Cancer Agency–Fraser Valley Centre, Surrey, BC.</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">23559889</idno>
<idno type="pmc">3615874</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615874</idno>
<idno type="RBID">PMC:3615874</idno>
<idno type="doi">10.3747/co.20.1205</idno>
<date when="2013">2013</date>
<idno type="wicri:Area/Pmc/Corpus">002D68</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">002D68</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Perceptions of survivorship care among South Asian female breast cancer survivors</title>
<author><name sortKey="Singh Arlson, S" sort="Singh Arlson, S" uniqKey="Singh Arlson S" first="S." last="Singh Arlson">S. Singh Arlson</name>
<affiliation><nlm:aff id="af1-conc-20-e80">School of Nursing, California State University–Long Beach, Long Beach, CA, U.S.A.</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Nguyen, S K A" sort="Nguyen, S K A" uniqKey="Nguyen S" first="S. K. A." last="Nguyen">S. K. A. Nguyen</name>
<affiliation><nlm:aff id="af2-conc-20-e80">BC Cancer Agency–Fraser Valley Centre, Surrey, BC.</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Wong, F" sort="Wong, F" uniqKey="Wong F" first="F." last="Wong">F. Wong</name>
<affiliation><nlm:aff id="af2-conc-20-e80">BC Cancer Agency–Fraser Valley Centre, Surrey, BC.</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="2013">2013</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><sec><title>Background and Objectives</title>
<p>To explore the perceptions of South Asian (<sc>sa</sc>
) breast cancer survivors concerning their follow-up care, and to determine the optimal content and format of a survivorship care plan (<sc>scp</sc>
) for this population, according to various life stages.</p>
</sec>
<sec><title>Methods</title>
<p>A survey was mailed to 259 <sc>sa</sc>
women with a diagnosis of nonmetastatic breast cancer who were 18–85 years of age, 3–60 months post-discharge, and not on active treatment. Descriptive statistics and content analysis were applied to the responses. The data were cross-tabulated by age: group A (<44 years), group B (45–54 years), group C (55–64 years), and group D (>64 years).</p>
</sec>
<sec><title>Results</title>
<p>We received 64 completed surveys. The compliance rate for adjuvant hormonal therapy was high (86.3%). Most of the respondents (<italic>n</italic>
= 61, 95.4%) had visited their family doctor within several months (0.5–24 months) after discharge. Their main physical effects concern was fatigue, and anxiety concerning health was the main psychosocial impact. Groups A and B were more concerned about physical appearance, depression, and the impact of cancer on family members. Women in the older groups were concerned about family obligations and work issues. Several women (<italic>n</italic>
= 9, 14.1%) described strain on their marriage and on their relationships with family and friends as significant issues. Slightly more than one third (<italic>n</italic>
= 24, 37.5%) experienced a deepening of faith, and almost as many (<italic>n</italic>
= 23, 35.9%) felt that their illness was something that was meant to happen.</p>
</sec>
<sec><title>Conclusions</title>
<p>Many of the impacts of breast cancer treatment are shared by women of all ethnic backgrounds. Others—such as high levels of compliance, little reported strain on spousal and family relationships, and the importance of faith—reflect specific cultural variations. These universal and culture-specific themes should all be kept in mind when developing a <sc>scp</sc>
tailored to <sc>sa</sc>
women. The developmental life stage of a woman affects how she views the cancer diagnosis, especially with respect to family, reproduction, and work issues.</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">23559889</article-id>
<article-id pub-id-type="pmc">3615874</article-id>
<article-id pub-id-type="doi">10.3747/co.20.1205</article-id>
<article-id pub-id-type="publisher-id">conc-20-e80</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>Perceptions of survivorship care among South Asian female breast cancer survivors</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Singh–Carlson</surname>
<given-names>S.</given-names>
</name>
<degrees>BSN APHN PhD</degrees>
<xref ref-type="aff" rid="af1-conc-20-e80"><sup>*</sup>
</xref>
<xref ref-type="corresp" rid="c1-conc-20-e80"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Nguyen</surname>
<given-names>S.K.A.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="af2-conc-20-e80"><sup>†</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Wong</surname>
<given-names>F.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="af2-conc-20-e80"><sup>†</sup>
</xref>
</contrib>
</contrib-group>
<aff id="af1-conc-20-e80"><label>*</label>
School of Nursing, California State University–Long Beach, Long Beach, CA, U.S.A.</aff>
<aff id="af2-conc-20-e80"><label>†</label>
BC Cancer Agency–Fraser Valley Centre, Surrey, BC.</aff>
<author-notes><corresp id="c1-conc-20-e80">Correspondence to: Savitri W. Singh–Carlson, California State University–Long Beach, School of Nursing, Long Beach, California, U.S.A. E-mail: <email>savitri.singh-carlson@csulb.edu</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub"><month>4</month>
<year>2013</year>
</pub-date>
<volume>20</volume>
<issue>2</issue>
<fpage>e80</fpage>
<lpage>e89</lpage>
<permissions><copyright-statement>2013 Multimed Inc.</copyright-statement>
<copyright-year>2013</copyright-year>
</permissions>
<abstract><sec><title>Background and Objectives</title>
<p>To explore the perceptions of South Asian (<sc>sa</sc>
) breast cancer survivors concerning their follow-up care, and to determine the optimal content and format of a survivorship care plan (<sc>scp</sc>
) for this population, according to various life stages.</p>
</sec>
<sec><title>Methods</title>
<p>A survey was mailed to 259 <sc>sa</sc>
women with a diagnosis of nonmetastatic breast cancer who were 18–85 years of age, 3–60 months post-discharge, and not on active treatment. Descriptive statistics and content analysis were applied to the responses. The data were cross-tabulated by age: group A (<44 years), group B (45–54 years), group C (55–64 years), and group D (>64 years).</p>
</sec>
<sec><title>Results</title>
<p>We received 64 completed surveys. The compliance rate for adjuvant hormonal therapy was high (86.3%). Most of the respondents (<italic>n</italic>
= 61, 95.4%) had visited their family doctor within several months (0.5–24 months) after discharge. Their main physical effects concern was fatigue, and anxiety concerning health was the main psychosocial impact. Groups A and B were more concerned about physical appearance, depression, and the impact of cancer on family members. Women in the older groups were concerned about family obligations and work issues. Several women (<italic>n</italic>
= 9, 14.1%) described strain on their marriage and on their relationships with family and friends as significant issues. Slightly more than one third (<italic>n</italic>
= 24, 37.5%) experienced a deepening of faith, and almost as many (<italic>n</italic>
= 23, 35.9%) felt that their illness was something that was meant to happen.</p>
</sec>
<sec><title>Conclusions</title>
<p>Many of the impacts of breast cancer treatment are shared by women of all ethnic backgrounds. Others—such as high levels of compliance, little reported strain on spousal and family relationships, and the importance of faith—reflect specific cultural variations. These universal and culture-specific themes should all be kept in mind when developing a <sc>scp</sc>
tailored to <sc>sa</sc>
women. The developmental life stage of a woman affects how she views the cancer diagnosis, especially with respect to family, reproduction, and work issues.</p>
</sec>
</abstract>
<kwd-group><kwd>Breast cancer survivors</kwd>
<kwd>survivorship care plans</kwd>
<kwd>follow-up cancer care</kwd>
<kwd>South Asian</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>
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