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Bridging the Gap in Palliative Care Access for Head and Neck Cancer Patients : = A Bioethical Evaluation.
紀錄類型:
書目-語言資料,手稿 : Monograph/item
正題名/作者:
Bridging the Gap in Palliative Care Access for Head and Neck Cancer Patients :/
其他題名:
A Bioethical Evaluation.
作者:
Jegede, Victor.
面頁冊數:
1 online resource (36 pages)
附註:
Source: Masters Abstracts International, Volume: 85-11.
Contained By:
Masters Abstracts International85-11.
標題:
Oncology. -
電子資源:
click for full text (PQDT)
ISBN:
9798382755045
Bridging the Gap in Palliative Care Access for Head and Neck Cancer Patients : = A Bioethical Evaluation.
Jegede, Victor.
Bridging the Gap in Palliative Care Access for Head and Neck Cancer Patients :
A Bioethical Evaluation. - 1 online resource (36 pages)
Source: Masters Abstracts International, Volume: 85-11.
Thesis (M.A.)--Temple University, 2024.
Includes bibliographical references
Palliative care is a specialty focused on improving the quality of life for patients with serious illnesses through symptom management and emotional/spiritual support. Despite its documented benefits, it remains largely underutilized among head and neck cancer patients, especially those in urban environments. This thesis reviews obstacles to accessing care in these environments and proposes practical solutions to enhance palliative care accessibility and effectiveness. Disparities in the access and utilization of palliative care are largely influenced by socio-economic status, cultural discrepancies, and healthcare infrastructure, with limited patient awareness further impacting its use. Addressing these challenges requires a comprehensive strategy that includes policy reform, educational outreach, and localized community interventions. Such approaches should be culturally sensitive and tailored to local needs to bridge the gap between medical services and community expectations. By working with patients to recognize palliative care as an integral part of comprehensive cancer care, rather than merely an end-of-life option, we can improve the quality of life for patients with head and neck cancer.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2024
Mode of access: World Wide Web
ISBN: 9798382755045Subjects--Topical Terms:
593951
Oncology.
Subjects--Index Terms:
Urban bioethicsIndex Terms--Genre/Form:
554714
Electronic books.
Bridging the Gap in Palliative Care Access for Head and Neck Cancer Patients : = A Bioethical Evaluation.
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Palliative care is a specialty focused on improving the quality of life for patients with serious illnesses through symptom management and emotional/spiritual support. Despite its documented benefits, it remains largely underutilized among head and neck cancer patients, especially those in urban environments. This thesis reviews obstacles to accessing care in these environments and proposes practical solutions to enhance palliative care accessibility and effectiveness. Disparities in the access and utilization of palliative care are largely influenced by socio-economic status, cultural discrepancies, and healthcare infrastructure, with limited patient awareness further impacting its use. Addressing these challenges requires a comprehensive strategy that includes policy reform, educational outreach, and localized community interventions. Such approaches should be culturally sensitive and tailored to local needs to bridge the gap between medical services and community expectations. By working with patients to recognize palliative care as an integral part of comprehensive cancer care, rather than merely an end-of-life option, we can improve the quality of life for patients with head and neck cancer.
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