Quality of Life and Symptom Burden in Cancer Patients Admitted to an Acute Palliative Care Unit

被引:35
作者
Jones, Jennifer M. [1 ]
Cohen, S. Robin [2 ,3 ,4 ]
Zimmermann, Camilla [5 ]
Rodin, Gary [6 ]
机构
[1] Univ Toronto, Princess Margaret Hosp, Univ Hlth Network, Dept Psychosocial Oncol & Palliat Care,Dept Psych, Toronto, ON M5G 2C4, Canada
[2] McGill Univ, Dept Oncol, Montreal, PQ, Canada
[3] McGill Univ, Dept Med, Montreal, PQ, Canada
[4] McGill Univ, Jewish Gen Hosp, Lady Davis Inst Res, Montreal, PQ H3T 1E2, Canada
[5] Univ Toronto, Dept Med, Toronto, ON M5G 2C4, Canada
[6] Univ Toronto, Dept Psychiat, Toronto, ON M5G 2C4, Canada
关键词
MEMORY-CONCENTRATION TEST; PERFORMANCE SCALE; MEDICATION PROFILES; RESPONSE SHIFT; QUESTIONNAIRE; VALIDATION; DISTRESS; IMPACT; DEPRESSION; VALIDITY;
D O I
10.1177/082585971002600205
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
This paper describes the quality of life and symptom burden of 211 cancer patients admitted to an acute palliative care unit (PCU) in a comprehensive cancer centre. Participants completed the McGill Quality of Life Questionnaire (MQOL), Edmonton Symptom Assessment Scale (ESAS), Short Orientation-Memory-Concentration Test, and Palliative Performance Scale within 24 hours of admission to the PCU. The mean MQOL total was 6.1 +/- 1.4, and the mean single-item scale score was 4.9 +/- 2.4. The mean total ESAS score was 36.3 +/- 15.8, with a median of six reported symptoms. Women and younger patients reported a lower quality of life (QoL) and a higher symptom burden. Regression and correlational analyses highlighted the importance of the existential and psychological domains to overall QoL. These findings emphasize the need for interdisciplinary, collaborative approaches to managing the complex physical, psychosocial, and existential needs of cancer patients admitted to acute PCUs.
引用
收藏
页码:94 / 102
页数:9
相关论文
共 90 条
  • [1] Measuring quality of life - Who should measure quality of life?
    Addington-Hall, J
    Kalra, L
    [J]. BRITISH MEDICAL JOURNAL, 2001, 322 (7299): : 1417 - 1420
  • [2] Palliative performance scale (PPS): A new tool
    Anderson, F
    Downing, GM
    Hill, J
    Casorso, L
    Lerch, N
    [J]. JOURNAL OF PALLIATIVE CARE, 1996, 12 (01) : 5 - 11
  • [3] [Anonymous], 1996, GLOBAL BURDEN DIS IN
  • [4] [Anonymous], 2009, WHO Definition of palliative care
  • [5] Validation of the McGill Quality of Life Questionnaire in home hospice settings in Israel
    Bentur, N
    Resnizky, S
    [J]. PALLIATIVE MEDICINE, 2005, 19 (07) : 538 - 544
  • [6] Billings J A, 2001, J Palliat Med, V4, P309, DOI 10.1089/109662101753123913
  • [7] Symptom distress in patients attending an outpatient palliative radiotherapy clinic
    Bradley, N
    Davis, L
    Chow, E
    [J]. JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2005, 30 (02) : 123 - 131
  • [8] The aggressiveness of cancer care in the last three months of life: A retrospective single centre analysis
    Braga, Sofia
    Miranda, Ana
    Fonseca, Rute
    Passos-Coelho, J. L.
    Fernandes, Aires
    Costa, J. D.
    Moreira, Antonio
    [J]. PSYCHO-ONCOLOGY, 2007, 16 (09) : 863 - 868
  • [9] VALIDATING THE SF-36 HEALTH SURVEY QUESTIONNAIRE - NEW OUTCOME MEASURE FOR PRIMARY CARE
    BRAZIER, JE
    HARPER, R
    JONES, NMB
    OCATHAIN, A
    THOMAS, KJ
    USHERWOOD, T
    WESTLAKE, L
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 1992, 305 (6846): : 160 - 164
  • [10] Monitoring symptoms in patients with advanced illness in long-term care: A pilot study
    Brechtl, John R.
    Murshed, Shaiqua
    Homel, Peter
    Bookbinder, Marilyn
    [J]. JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2006, 32 (02) : 168 - 174