Social, psychological and existential well-being in patients with glioma and their caregivers: a qualitative study

被引:101
作者
Cavers, Debbie [1 ]
Hacking, Belinda [2 ]
Erridge, Sara E. [2 ]
Kendall, Marilyn [1 ]
Morris, Paul G. [1 ]
Murray, Scott A. [1 ]
机构
[1] Univ Edinburgh, Primary Palliat Care Res Grp, Ctr Populat Hlth Sci, Gen Practice Sect,Med Sch, Edinburgh, Midlothian, Scotland
[2] Western Gen Hosp, Edinburgh Canc Ctr, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
SUPPORTIVE-CARE NEEDS; BRAIN-TUMOR PATIENTS; CANCER-PATIENTS; UNDERSTAND PATIENTS; CEREBRAL GLIOMA; HEART-FAILURE; LUNG-CANCER; OF-LIFE; DEATH; END;
D O I
10.1503/cmaj.111622
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Cerebral glioma has a devastating impact on cognitive, physical, social, psychological and spiritual well-being. We sought to understand the multidimensional experience of patients with this form of cancer as they progressed from receiving a diagnosis to the terminal phase of the disease. Methods: We recruited patients with a suspected brain tumour from a tertiary referral centre in the United Kingdom. We interviewed patients and their caregivers at key stages of the illness: before receiving a formal diagnosis, at the start of initial treatment, after initial treatment was completed and at six months' follow-up; caregivers were also interviewed postbereavement. We interviewed the patients' general practitioners once, after treatment had been completed. We transcribed the interviews and analyzed them thematically using the constant comparative method of a grounded theory approach. Results: We conducted in-depth interviews with 26 patients, 23 of their relatives and 19 general practitioners. We saw evidence of physical, social, psychological and existential distress even before a diagnosis was confirmed. Social decline followed a similar trajectory to that of physical decline, whereas psychological and existential distress were typically acute around diagnosis and again after initial treatment. Each patient's individual course varied according to other factors including the availability of support and individual and family resources (e.g., personal resilience and emotional support). Interpretation: There are practical ways that clinicians can care for patients with glioma and their caregivers, starting from before a diagnosis is confirmed. Understanding the trajectories of physical, social, psychological and existential well-being for these patients allows health care professionals to predict their patients' likely needs so they can provide appropriate support and sensitive and effective communication.
引用
收藏
页码:E373 / E382
页数:10
相关论文
共 29 条
[11]   Discussing end-of-life issues with terminally ill cancer patients and their carers: a qualitative study [J].
Clayton, JM ;
Butow, PN ;
Arnold, RM ;
Tattersall, MHN .
SUPPORTIVE CARE IN CANCER, 2005, 13 (08) :589-599
[12]   Longitudinal study on quality of life and social support in cancer patients [J].
Courtens, AM ;
Stevens, FCJ ;
Crebolder, HFJM ;
Philipsen, H .
CANCER NURSING, 1996, 19 (03) :162-169
[13]   Opportunities for improving the quality of care in malignant cerebral glioma [J].
Davies, E ;
Bannon, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1999, 66 (05) :693-693
[14]  
DAVIES E, 1997, IMPROVING CARE PATIE
[15]   Supportive care needs of people with brain tumours and their carers [J].
Janda, Monika ;
Eakin, Elizabeth G. ;
Bailey, Lucy ;
Walker, David ;
Troy, Kate .
SUPPORTIVE CARE IN CANCER, 2006, 14 (11) :1094-1103
[16]   Effect of different forms of information produced for cancer patients on their use of the information, social support, and anxiety: randomised trial [J].
Jones, RB ;
Pearson, J ;
Cawsey, AJ ;
Bental, D ;
Barrett, A ;
White, J ;
White, CA ;
Gilmour, WH .
BRITISH MEDICAL JOURNAL, 2006, 332 (7547) :942-946A
[17]   Use of multiperspective qualitative interviews to understand patients' and carers' beliefs, experiences, and needs [J].
Kendall, Marilyn ;
Murray, Scott A. ;
Carduff, Emma ;
Worth, Allison ;
Harris, Fiona ;
Lloyd, Anna ;
Cavers, Debbie ;
Grant, Liz ;
Boyd, Kirsty ;
Sheikh, Aziz .
BMJ-BRITISH MEDICAL JOURNAL, 2009, 339 :b4122
[18]  
Khalili Yasmin, 2007, Axone, V28, P5
[19]   Liminality: A major category of the experience of cancer illness [J].
Little, M ;
Jordens, CFC ;
Paul, K ;
Montgomery, K ;
Philipson, B .
SOCIAL SCIENCE & MEDICINE, 1998, 47 (10) :1485-1494
[20]   Exploring the spiritual needs of people dying of lung cancer or heart failure: a prospective qualitative interview study of patients and their carers [J].
Murray, SA ;
Kendall, M ;
Boyd, K ;
Worth, A ;
Benton, TF .
PALLIATIVE MEDICINE, 2004, 18 (01) :39-45