Literature DB >> 16240492

Uncommon dementia and the carer's perspective.

D LoGiudice1, A Hassett.   

Abstract

There is much caregiving literature describing factors that affect carer burden, and interventions that may be useful for carers of those with common dementias such as Alzheimer's disease (AD). By contrast, relatively little information and few data are available on potentially diverse issues facing carers of those with uncommon dementias, such as frontotemporal dementia (FTD), Huntington's disease (HD) and human immunodeficiency virus (HIV) dementia. This paper highlights particular characteristics of caregiving for those with uncommon dementias, and the unique needs that may arise for this group of carers who often "fall between the net" of services and supports available. Further research into this area is required.

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Year:  2005        PMID: 16240492     DOI: 10.1017/s1041610205002048

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  8 in total

1.  A new scale to measure family members' perception of community health care services for persons with Huntington disease.

Authors:  Valmi D Sousa; Janet K Williams; Jack J Barnette; David A Reed
Journal:  J Eval Clin Pract       Date:  2010-03-11       Impact factor: 2.431

2.  Observational themes of social behavioral disturbances in frontotemporal dementia.

Authors:  Joseph P Barsuglia; Frances R Nedjat-Haiem; Jill S Shapira; Christina Velasco; Elvira E Jimenez; Michelle J Mather; Mario F Mendez
Journal:  Int Psychogeriatr       Date:  2014-05-20       Impact factor: 3.878

3.  Family carer personal concerns in Huntington disease.

Authors:  Janet K Williams; Heather Skirton; James Jackson Barnette; Jane S Paulsen
Journal:  J Adv Nurs       Date:  2011-06-12       Impact factor: 3.187

4.  In their own words: reports of stigma and genetic discrimination by people at risk for Huntington disease in the International RESPOND-HD study.

Authors:  Janet K Williams; Cheryl Erwin; Andrew R Juhl; Michelle Mengeling; Yvonne Bombard; Michael R Hayden; Kimberly Quaid; Ira Shoulson; Sandra Taylor; Jane S Paulsen
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2010-09       Impact factor: 3.568

5.  Development of the Huntington disease family concerns and strategies survey from focus group data.

Authors:  Janet K Williams; J Jackson Barnette; David Reed; Valmi D Sousa; Debra L Schutte; Meghan McGonigal-Kenney; Lori Jarmon; Emily Phillips; Toni Tripp-Reimer; Jane S Paulsen
Journal:  J Nurs Meas       Date:  2010

6.  The emotional experiences of family carers in Huntington disease.

Authors:  Janet K Williams; Heather Skirton; Jane S Paulsen; Toni Tripp-Reimer; Lori Jarmon; Meghan McGonigal Kenney; Emily Birrer; Bonnie L Hennig; Joann Honeyford
Journal:  J Adv Nurs       Date:  2009-02-09       Impact factor: 3.187

7.  Living with idiopathic basal ganglia calcification 3: a qualitative study describing the lives and illness of people diagnosed with a rare neurological disease.

Authors:  Tomiko Takeuchi; Koko Muraoka; Megumi Yamada; Yuri Nishio; Isao Hozumi
Journal:  Springerplus       Date:  2016-10-04

Review 8.  A meta-review of stress, coping and interventions in dementia and dementia caregiving.

Authors:  K J Gilhooly; M L M Gilhooly; M P Sullivan; A McIntyre; L Wilson; E Harding; R Woodbridge; S Crutch
Journal:  BMC Geriatr       Date:  2016-05-18       Impact factor: 3.921

  8 in total

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