Literature DB >> 31771668

Comparing the physical, psychological, social, and spiritual needs of patients with non-cancer and cancer diagnoses in a tertiary palliative care setting.

Suhair Bandeali1, Amanda Roze des Ordons2,3, Aynharan Sinnarajah2,4,5.   

Abstract

OBJECTIVE: The purpose was to describe the physical, psychological, social, and spiritual needs of patients with non-cancer serious illness diagnoses compared to those of patients with cancer.
METHOD: We conducted a retrospective chart review of all patients with a non-cancer diagnosis admitted to a tertiary palliative care unit between January 2008 and December 2017 and compared their needs to those of a matched cohort of patients with cancer diagnoses. The prevalence of needs within the following four main concerns was recorded and the data analyzed using descriptive statistics and content analysis: •Physical: pain, dyspnea, fatigue, anorexia, edema, and delirium•Psychological: depression, anxiety, prognosis, and dignity•Social: caregiver burden, isolation, and financial•Spiritual: spiritual distress.
RESULTS: The prevalence of the four main concerns was similar among patients with non-cancer and cancer diagnoses. Pain, nausea/vomiting, fatigue, and anorexia were more prevalent among patients with cancer. Dyspnea was more commonly the primary concern in patients with non-cancer diagnoses (39%), who also had a higher prevalence of anxiety and concerns about dignity. Spirituality was addressed more often in patients with cancer. SIGNIFICANCE OF
RESULTS: The majority of patients admitted to tertiary palliative care settings have historically been those with cancer. The tertiary palliative care needs of patients with non-cancer diagnoses have not been well described, despite the increasing prevalence of this population. Our description of the palliative care needs of patients with non-cancer diagnoses will help guide future palliative care for the increasing population of patients with non-cancer serious illness diagnoses.

Entities:  

Keywords:  Cancer; Care needs; Chronic illness; Palliative care; Symptom management

Mesh:

Year:  2020        PMID: 31771668     DOI: 10.1017/S1478951519001020

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  7 in total

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6.  Validation of the Chinese version of the Care Evaluation Scale for measuring the quality of structure and process of end-of-life care from the perspective of bereaved family.

Authors:  Juanjuan Zhao; Liming You; Hongmei Tao; Frances Kam Yuet Wong
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7.  Winners and Losers in Palliative Care Service Delivery: Time for a Public Health Approach to Palliative and End of Life Care.

Authors:  Samar M Aoun; Robyn Richmond; Leanne Jiang; Bruce Rumbold
Journal:  Healthcare (Basel)       Date:  2021-11-23
  7 in total

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