Literature DB >> 26153787

Psychosocial Challenges Experienced by Partners of People With Parkinson Disease.

Summer Carnett Martin1.   

Abstract

Although researchers have examined issues related to partners providing care for a person with Parkinson disease (PWP), few have explored partners' broader psychosocial experiences. To investigate this underexplored area, individual, in-depth interviews with 23 partners of PWPs were conducted. Participants reported significant psychosocial challenges, including having the PWP withdraw from communication, being unable to "rescue" the PWP, being the recipient of the PWP's frustration, expressing impatience with the PWP, shouldering increased responsibility, being confronted with possibly losing the PWP, losing valued activities, feeling housebound, being unable to predict the PWP's daily well-being, and experiencing uncertainty about future caregiving and disease progression. These results indicate that being the partner of a PWP involves serious, complex psychosocial challenges related to both caregiving and noncaregiving issues. This research highlights the need for a family-centered approach to Parkinson care and provides valuable insight that can inform interventions and nursing practice for this population.

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Mesh:

Year:  2015        PMID: 26153787     DOI: 10.1097/JNN.0000000000000141

Source DB:  PubMed          Journal:  J Neurosci Nurs        ISSN: 0888-0395            Impact factor:   1.230


  5 in total

1.  The role of dispositional mindfulness in a stress-health pathway among Parkinson's disease patients and caregiving partners.

Authors:  Allison Hicks; Kala Phillips; Chelsea Siwik; Paul Salmon; Irene Litvan; Megan E Jablonski; J Vincent Filoteo; Karen Kayser; Sandra E Sephton
Journal:  Qual Life Res       Date:  2019-06-14       Impact factor: 4.147

2.  The self-management balancing act of spousal care partners in the case of Parkinson's disease.

Authors:  Sue Berger; Tiffany Chen; Jenna Eldridge; Cathi A Thomas; Barbara Habermann; Linda Tickle-Degnen
Journal:  Disabil Rehabil       Date:  2017-12-12       Impact factor: 3.033

Review 3.  The subjective experience of family caregivers of people living with Parkinson's disease: a meta-ethnography of qualitative literature.

Authors:  Yiping Chen; Wentao Zhou; Liyuan Hou; Xianhui Zhang; Qiaohong Wang; Jing Gu; Ru Zhang; Hui Yang
Journal:  Aging Clin Exp Res       Date:  2021-10-14       Impact factor: 4.481

4.  Risk factors for neuropsychiatric symptoms in patients with Parkinson's disease during COVID-19 pandemic in Japan.

Authors:  Fukiko Kitani-Morii; Takashi Kasai; Go Horiguchi; Satoshi Teramukai; Takuma Ohmichi; Makiko Shinomoto; Yuzo Fujino; Toshiki Mizuno
Journal:  PLoS One       Date:  2021-01-22       Impact factor: 3.240

5.  Psychological Impact of Parkinson Disease Delusions on Spouse Caregivers: A Qualitative Study.

Authors:  Caroline J Deutsch; Noelle Robertson; Janis M Miyasaki
Journal:  Brain Sci       Date:  2021-06-29
  5 in total

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