The Potential of Survivorship Care Plans in Primary Care Follow-up of Minority Breast Cancer Patients
Identifieur interne : 003573 ( Pmc/Checkpoint ); précédent : 003572; suivant : 003574The Potential of Survivorship Care Plans in Primary Care Follow-up of Minority Breast Cancer Patients
Auteurs : Mary Ann Burg [États-Unis] ; Ellen D. S. Lopez [États-Unis] ; Amy Dailey [États-Unis] ; Mary Elspeth Keller [États-Unis] ; Brendan Prendergast [États-Unis]Source :
- Journal of General Internal Medicine [ 0884-8734 ] ; 2009.
Abstract
When the clinical care of minority breast cancer survivors is transferred from oncology settings to primary care, quality of care may be compromised if their primary care providers do not have adequate cancer treatment records and follow-up care guidelines. Survivorship care plans (SCPs) given to survivors before they transition to primary care settings are designed to improve the transfer of this information. This study examined these issues in a sample of minority breast cancer survivors.
During four focus groups with minority breast cancer survivors, data were collected about the types of information survivors remember receiving from their oncologists about follow-up health care needs. Survivors were also asked their opinions on the value and content of a survivorship care plan.
Minority breast cancer survivors received variable amounts of information about their cancer treatments. They were dissatisfied with the amount of information they received on cancer-related side-effects, including race-specific information. The American Society of Clinical Oncology’s breast cancer survivorship care plan was viewed as important, but too highly technical and limited in information on side-effects and self-care approaches.
Survivorship care plans may help increase information transfer from oncologists to patients and primary care providers, but the content of care plans needs to be adapted to minority patients’ concerns. Primary care physicians may be challenged by survivors to explain recommended surveillance guidelines and to respond to untreated physical and psychosocial problems.
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DOI: 10.1007/s11606-009-1012-y
PubMed: 19838852
PubMed Central: 2763149
Affiliations:
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<front><div type="abstract" xml:lang="en"><title>ABSTRACT</title>
<sec><title>BACKGROUND</title>
<p>When the clinical care of minority breast cancer survivors is transferred from oncology settings to primary care, quality of care may be compromised if their primary care providers do not have adequate cancer treatment records and follow-up care guidelines. Survivorship care plans (SCPs) given to survivors before they transition to primary care settings are designed to improve the transfer of this information. This study examined these issues in a sample of minority breast cancer survivors.</p>
</sec>
<sec><title>DESIGN</title>
<p>During four focus groups with minority breast cancer survivors, data were collected about the types of information survivors remember receiving from their oncologists about follow-up health care needs. Survivors were also asked their opinions on the value and content of a survivorship care plan.</p>
</sec>
<sec><title>RESULTS</title>
<p>Minority breast cancer survivors received variable amounts of information about their cancer treatments. They were dissatisfied with the amount of information they received on cancer-related side-effects, including race-specific information. The American Society of Clinical Oncology’s breast cancer survivorship care plan was viewed as important, but too highly technical and limited in information on side-effects and self-care approaches.</p>
</sec>
<sec><title>CONCLUSIONS</title>
<p>Survivorship care plans may help increase information transfer from oncologists to patients and primary care providers, but the content of care plans needs to be adapted to minority patients’ concerns. Primary care physicians may be challenged by survivors to explain recommended surveillance guidelines and to respond to untreated physical and psychosocial problems.</p>
</sec>
</div>
</front>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Gen Intern Med</journal-id>
<journal-title>Journal of General Internal Medicine</journal-title>
<issn pub-type="ppub">0884-8734</issn>
<issn pub-type="epub">1525-1497</issn>
<publisher><publisher-name>Springer-Verlag</publisher-name>
<publisher-loc>New York</publisher-loc>
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<contrib-group><contrib contrib-type="author" corresp="yes"><name name-style="western"><surname>Burg</surname>
<given-names>Mary Ann</given-names>
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<xref ref-type="aff" rid="Aff1">1</xref>
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<contrib contrib-type="author"><name name-style="western"><surname>Lopez</surname>
<given-names>Ellen D. S.</given-names>
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<degrees>PhD</degrees>
<xref ref-type="aff" rid="Aff2">2</xref>
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<contrib contrib-type="author"><name name-style="western"><surname>Dailey</surname>
<given-names>Amy</given-names>
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<degrees>PhD</degrees>
<xref ref-type="aff" rid="Aff3">3</xref>
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<contrib contrib-type="author"><name name-style="western"><surname>Keller</surname>
<given-names>Mary Elspeth</given-names>
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<contrib contrib-type="author"><name name-style="western"><surname>Prendergast</surname>
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<aff id="Aff1"><label>1</label>
Department of Community Health & Family Medicine, University of Florida, P.O. Box 100237, Gainesville, FL 32610-0237 USA</aff>
<aff id="Aff2"><label>2</label>
Department of Behavioral Science and Community Health, University of Florida, Gainesville, FL USA</aff>
<aff id="Aff3"><label>3</label>
Department of Epidemiology and Biostatistics, University of Florida, Gainesville, FL USA</aff>
<aff id="Aff4"><label>4</label>
Colorado Health Foundation, Denver, CO USA</aff>
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<pub-date pub-type="epub"><day>18</day>
<month>10</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="ppub"><month>11</month>
<year>2009</year>
</pub-date>
<volume>24</volume>
<issue>Suppl 2</issue>
<fpage>467</fpage>
<lpage>471</lpage>
<permissions><copyright-statement>© Society of General Internal Medicine 2009</copyright-statement>
</permissions>
<abstract xml:lang="EN"><title>ABSTRACT</title>
<sec><title>BACKGROUND</title>
<p>When the clinical care of minority breast cancer survivors is transferred from oncology settings to primary care, quality of care may be compromised if their primary care providers do not have adequate cancer treatment records and follow-up care guidelines. Survivorship care plans (SCPs) given to survivors before they transition to primary care settings are designed to improve the transfer of this information. This study examined these issues in a sample of minority breast cancer survivors.</p>
</sec>
<sec><title>DESIGN</title>
<p>During four focus groups with minority breast cancer survivors, data were collected about the types of information survivors remember receiving from their oncologists about follow-up health care needs. Survivors were also asked their opinions on the value and content of a survivorship care plan.</p>
</sec>
<sec><title>RESULTS</title>
<p>Minority breast cancer survivors received variable amounts of information about their cancer treatments. They were dissatisfied with the amount of information they received on cancer-related side-effects, including race-specific information. The American Society of Clinical Oncology’s breast cancer survivorship care plan was viewed as important, but too highly technical and limited in information on side-effects and self-care approaches.</p>
</sec>
<sec><title>CONCLUSIONS</title>
<p>Survivorship care plans may help increase information transfer from oncologists to patients and primary care providers, but the content of care plans needs to be adapted to minority patients’ concerns. Primary care physicians may be challenged by survivors to explain recommended surveillance guidelines and to respond to untreated physical and psychosocial problems.</p>
</sec>
</abstract>
<kwd-group><title>KEY WORDS</title>
<kwd>breast cancer</kwd>
<kwd>primary care</kwd>
<kwd>minority</kwd>
<kwd>survivorship</kwd>
</kwd-group>
<custom-meta-wrap><custom-meta><meta-name>issue-copyright-statement</meta-name>
<meta-value>© Society of General Internal Medicine 2009</meta-value>
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<name sortKey="Lopez, Ellen D S" sort="Lopez, Ellen D S" uniqKey="Lopez E" first="Ellen D. S." last="Lopez">Ellen D. S. Lopez</name>
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