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Survivorship Care Plan Information Needs: Perspectives of Safety-Net Breast Cancer Patients
by
Orenstein, Fern S.
, Napoles, Tessa M.
, Joseph, Galen
, Luce, Judith A.
, Banks, Priscilla J.
, Burke, Nancy J.
in
Access to information
/ Adult
/ African Americans
/ Aged
/ Biology and Life Sciences
/ Breast cancer
/ Breast Neoplasms - psychology
/ Cancer
/ Cancer patients
/ Care and treatment
/ Colorectal cancer
/ Communication
/ Community support
/ Continuity of Patient Care
/ Diagnosis
/ Female
/ Focus Groups
/ Health care
/ Health education
/ Health Knowledge, Attitudes, Practice
/ Health literacy
/ Hepatitis
/ Humans
/ Information dissemination
/ Internet
/ Literacy
/ Medical diagnosis
/ Medicine
/ Medicine and Health Sciences
/ Middle Aged
/ Oncology
/ Organizations
/ Patients
/ People and places
/ Primary care
/ Qualitative research
/ Safety
/ Safety and security measures
/ Social Sciences
/ Studies
/ Survival
/ Survival Rate
/ Survivor
/ Survivors - psychology
/ Symptom management
/ United States
2016
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Survivorship Care Plan Information Needs: Perspectives of Safety-Net Breast Cancer Patients
by
Orenstein, Fern S.
, Napoles, Tessa M.
, Joseph, Galen
, Luce, Judith A.
, Banks, Priscilla J.
, Burke, Nancy J.
in
Access to information
/ Adult
/ African Americans
/ Aged
/ Biology and Life Sciences
/ Breast cancer
/ Breast Neoplasms - psychology
/ Cancer
/ Cancer patients
/ Care and treatment
/ Colorectal cancer
/ Communication
/ Community support
/ Continuity of Patient Care
/ Diagnosis
/ Female
/ Focus Groups
/ Health care
/ Health education
/ Health Knowledge, Attitudes, Practice
/ Health literacy
/ Hepatitis
/ Humans
/ Information dissemination
/ Internet
/ Literacy
/ Medical diagnosis
/ Medicine
/ Medicine and Health Sciences
/ Middle Aged
/ Oncology
/ Organizations
/ Patients
/ People and places
/ Primary care
/ Qualitative research
/ Safety
/ Safety and security measures
/ Social Sciences
/ Studies
/ Survival
/ Survival Rate
/ Survivor
/ Survivors - psychology
/ Symptom management
/ United States
2016
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Survivorship Care Plan Information Needs: Perspectives of Safety-Net Breast Cancer Patients
by
Orenstein, Fern S.
, Napoles, Tessa M.
, Joseph, Galen
, Luce, Judith A.
, Banks, Priscilla J.
, Burke, Nancy J.
in
Access to information
/ Adult
/ African Americans
/ Aged
/ Biology and Life Sciences
/ Breast cancer
/ Breast Neoplasms - psychology
/ Cancer
/ Cancer patients
/ Care and treatment
/ Colorectal cancer
/ Communication
/ Community support
/ Continuity of Patient Care
/ Diagnosis
/ Female
/ Focus Groups
/ Health care
/ Health education
/ Health Knowledge, Attitudes, Practice
/ Health literacy
/ Hepatitis
/ Humans
/ Information dissemination
/ Internet
/ Literacy
/ Medical diagnosis
/ Medicine
/ Medicine and Health Sciences
/ Middle Aged
/ Oncology
/ Organizations
/ Patients
/ People and places
/ Primary care
/ Qualitative research
/ Safety
/ Safety and security measures
/ Social Sciences
/ Studies
/ Survival
/ Survival Rate
/ Survivor
/ Survivors - psychology
/ Symptom management
/ United States
2016
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Survivorship Care Plan Information Needs: Perspectives of Safety-Net Breast Cancer Patients
Journal Article
Survivorship Care Plan Information Needs: Perspectives of Safety-Net Breast Cancer Patients
2016
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Overview
Despite the Institute of Medicine's (IOM) 2005 recommendation, few care organizations have instituted standard survivorship care plans (SCPs). Low health literacy and low English proficiency are important factors to consider in SCP development. Our study aimed to identify information needs and survivorship care plan preferences of low literacy, multi-lingual patients to support the transition from oncology to primary care and ongoing learning in survivorship.
We conducted focus groups in five languages with African American, Latina, Russian, Filipina, White, and Chinese medically underserved breast cancer patients. Topics explored included the transition to primary care, access to information, knowledge of treatment history, and perspectives on SCPs.
Analysis of focus group data identified three themes: 1) the need for information and education on the transition between \"active treatment\" and \"survivorship\"; 2) information needed (and often not obtained) from providers; and 3) perspectives on SCP content and delivery.
Our data point to the need to develop a process as well as written information for medically underserved breast cancer patients. An SCP document will not replace direct communication with providers about treatment, symptom management and transition, a communication that is missing in participating safety-net patients' experiences of cancer care. Women turned to peer support and community-based organizations in the absence of information from providers.
\"Clear and effective\" communication of survivorship care for safety-net patients requires dedicated staff trained to address wide-ranging information needs and uncertainties.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
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