Assessing advanced cancer pain in older adults with dementia at the end-of-life

被引:52
|
作者
Monroe, Todd [1 ,2 ]
Carter, Michael [3 ]
Feldt, Karen [4 ]
Tolley, Betsey [3 ]
Cowan, Ronald L. [5 ,6 ]
机构
[1] Vanderbilt Univ, Sch Nursing, Nashville, TN 37240 USA
[2] Vanderbilt Univ, Inst Imaging Sci, Nashville, TN USA
[3] Univ Tennessee, Coll Nursing, Hlth Sci Ctr, Memphis, TN USA
[4] Seattle Univ, Coll Nursing, Washington, DC USA
[5] Vanderbilt Univ Sch Med, Nashville, TN USA
[6] Vanderbilt Univ, Psychiat Neuroimaging Program, Nashville, TN USA
关键词
Alzheimer's disease; cancer pain; Cognitive Performance Scale (CPS); Discomfort Behavioural Scale (DBS); pain; pain behaviours; MINIMUM DATA SET; COGNITIVE IMPAIRMENT; PEOPLE; PREVALENCE; BEHAVIORS; SCALE;
D O I
10.1111/j.1365-2648.2011.05929.x
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Monroe T., Carter M., Feldt K., Tolley B. & Cowan R.L. (2012) Assessing advanced cancer pain in older adults with dementia at the end-of-life. Journal of Advanced Nursing68(9), 20702078. Abstract Aim. To assess advanced cancer pain in older adults with dementia at the end-of-life. Background. Self-report is the gold standard for pain assessment; however, people with Alzheimers disease may lose the ability to report pain. Biochemical and neuropathological changes occur in Alzheimers disease that impairs the affective, sensory, and motor pain processing regions of the brain. Because people with severe Alzheimers disease may lose the ability to report their sensory and emotional response to pain verbally, external motor displays of pain, such as grimacing, have been suggested for use in people with Alzheimers Disease. Design. Between groups cross sectional study. Method. Retrospective chart audits of people with Alzheimers disease in nine nursing homes in the US in 2009. Participants were nursing home residents (n = 48) with mild to very severe dementia, pain and cognitive measures were collected during the final 3 months of life. The primary outcome variable was the Discomfort Behaviour Scale score (a measure of observed pain behaviour) and the main predictor variable was the Cognitive Performance Scale score (a measure of Alzheimers disease severity). Medication administration (opioid, non-narcotic, and psychotropic medications) recorded over the final 2 weeks of life was collected as a covariate of interest. Results. Alzheimers disease severity was negatively associated with pain behaviours. Post hoc procedures showed that this difference was due to the difference in pain behaviours between individuals with moderate and very severe Alzheimers disease. Total amount of opioid analgesic, total number of doses of non-narcotic medications, and psychotropic medications administered over the last 2 weeks of life were not statistically significantly correlated with pain behaviour. An inverse correlation was found between cognitive ability (Cognitive Performance Scale score) and total amount of opioid medication indicating that individuals with severe Alzheimers disease received less opioid. Conclusion. Because people with worsening Alzheimers disease have fewer pain behaviours, assessing pain using behavioural indicators can be a challenge. Improving methods to assess for pain in people with Alzheimers disease is of critical public health importance. Moreover, future studies are urgently needed to further examine the sensory, emotional, and behavioural responses to pain in people with Alzheimers disease.
引用
收藏
页码:2070 / 2078
页数:9
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