Self-perceived burden to others: Patient and, family caregiver correlates

被引:68
作者
Mcpherson, Christine J. [1 ]
Wilson, Keith G. [2 ]
Lobchuk, Michelle M. [3 ]
Brajtman, Susan [1 ]
机构
[1] Univ Ottawa, Sch Nursing, Ottawa, ON, Canada
[2] Ottawa Hosp, Rehabil Ctr, Ottawa, ON, Canada
[3] Univ Manitoba, Fac Nursing, Winnipeg, MB, Canada
关键词
D O I
10.1177/082585970702300303
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
Aims: To provide further evidence about-the prevalence and correlates of the sense of "self-perceived burden" (SPB) to others, and to examine its association with caregiver reports of burden. Methods: The participants were 65 patients with advanced cancer and their family caregivers. Patients completed measures of SPB and family members completed a caregiver burden scale. Results: SPB was experienced at minimal to mild levels by 35% of patients, and at moderate to extreme levels by another 28%. It was correlated with some physical symptoms, but more frequently with psychological symptoms. The family members of patients who reported that SPB was a significant problem had higher scores on the caregiver burden scale than family members of other patients (p=0.048), although the overall correlation was modest. Conclusions: SPB is a common and distressing concern for many patients receiving palliative care and is associated with a number of other distressing concerns.
引用
收藏
页码:135 / 142
页数:8
相关论文
共 48 条
[1]
Suicidality in terminally ill Japanese patients with cancer - Prevalence, patient perceptions, contributing factors, and longitudinal [J].
Akechi, T ;
Okuyama, T ;
Sugawara, Y ;
Nakano, T ;
Shima, Y ;
Uchitomi, Y .
CANCER, 2004, 100 (01) :183-191
[2]
Palliative performance scale (PPS): A new tool [J].
Anderson, F ;
Downing, GM ;
Hill, J ;
Casorso, L ;
Lerch, N .
JOURNAL OF PALLIATIVE CARE, 1996, 12 (01) :5-11
[3]
Physician-assisted suicide and euthanasia in Washington State - Patient requests and physician responses [J].
Back, AL ;
Wallace, JI ;
Starks, HE ;
Pearlman, RA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (12) :919-925
[4]
Breitbart W, 1996, AM J PSYCHIAT, V153, P238
[5]
Chang VT, 2000, CANCER, V89, P1162, DOI 10.1002/1097-0142(20000901)89:5<1162::AID-CNCR26>3.0.CO
[6]
2-Y
[7]
Caregiver burden and patients' perception of being a burden in ALS [J].
Chiò, A ;
Gauthier, A ;
Calvo, A ;
Ghiglione, P ;
Mutani, R .
NEUROLOGY, 2005, 64 (10) :1780-1782
[8]
Dignity in the terminally ill: a developing empirical model [J].
Chochinov, HM ;
Hack, T ;
McClement, S ;
Kristjanson, L ;
Harlos, M .
SOCIAL SCIENCE & MEDICINE, 2002, 54 (03) :433-443
[9]
What determines the quality of life of terminally ill cancer patients from their own perspective? [J].
Cohen, SR ;
Leis, A .
JOURNAL OF PALLIATIVE CARE, 2002, 18 (01) :48-58
[10]
FACTORS INFLUENCING HOSPITAL PATIENTS PREFERENCES IN THE UTILIZATION OF LIFE-SUSTAINING TREATMENTS [J].
COHENMANSFIELD, J ;
DROGE, JA ;
BILLIG, N .
GERONTOLOGIST, 1992, 32 (01) :89-95