Improving psychotropic medication use among persons with dementia

2016 ◽  
Vol 28 (10) ◽  
pp. 1587-1588 ◽  
Author(s):  
Donovan T. Maust

The use of psychotropic medication among persons with dementia (PWD) both in nursing home (Wetzels et al., 2011) and community settings (Maust et al., 2016) far exceeds what might be expected based on their limited evidence for benefit (Kales et al., 2015). This relatively high use persists despite years of evidence about the potential harms associated with their use in older adults generally and PWD in particular (e.g. Wang et al., 2001; Schneider et al., 2005). However, the solution to relatively high psychotropic use is not to end all psychotropic use, as there are individual patients for whom use of such medication is appropriate. For example, a policy that defines all antipsychotic use as inappropriate may simply lead to increased use of alternatives with even less evidence of benefit, as suggested by the response to antipsychotics’ black box warning in the United States (Kales et al., 2011).

2014 ◽  
Vol 65 (10) ◽  
pp. 1218-1225 ◽  
Author(s):  
Marisa Elena Domino ◽  
William H. Dow ◽  
Fernando Coto-Yglesias

Author(s):  
Jennifer Ailshire ◽  
Margarita Osuna ◽  
Jenny Wilkens ◽  
Jinkook Lee

Abstract Objectives Family is largely overlooked in research on factors associated with place of death among older adults. We determine if family caregiving at the end of life is associated with place of death in the United States and Europe. Methods We use the Harmonized End of Life data sets developed by the Gateway to Global Aging Data for the Survey of Health, Ageing and Retirement in Europe (SHARE) and the Health and Retirement Study (HRS). We conducted multinomial logistic regression on 7,113 decedents from 18 European countries and 3,031 decedents from the United States to determine if family caregiving, defined based on assistance with activities of daily living, was associated with death at home versus at a hospital or nursing home. Results Family caregiving was associated with reduced odds of dying in a hospital and nursing home, relative to dying at home in both the United States and Europe. Care from a spouse/partner or child/grandchild was both more common and more strongly associated with place of death than care from other relatives. Associations between family caregiving and place of death were generally consistent across European welfare regimes. Discussion This cross-national examination of family caregiving indicates that family-based support is universally important in determining where older adults die. In both the United States and in Europe, most care provided during a long-term illness or disability is provided by family caregivers, and it is clear families exert tremendous influence on place of death.


2018 ◽  
Vol 69 (5) ◽  
pp. 605-608 ◽  
Author(s):  
T. Scott Stroup ◽  
Tobias Gerhard ◽  
Stephen Crystal ◽  
Cecilia Huang ◽  
Zhiqiang Tan ◽  
...  

2010 ◽  
Vol 19 (8) ◽  
pp. 834-842 ◽  
Author(s):  
Dima M. Qato ◽  
Stacy Tessler Lindau ◽  
Rena M. Conti ◽  
L. Philip Schumm ◽  
G. Caleb Alexander

2015 ◽  
Vol 8 (6) ◽  
pp. 273-285 ◽  
Author(s):  
Lenny Chiang-Hanisko ◽  
Christine L. Williams ◽  
David Newman ◽  
Ruth M. Tappen

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