Literature DB >> 21376317

Challenges associated with transition to caregiver role following diagnostic disclosure of Alzheimer disease: a descriptive study.

Francine Ducharme1, Louise Lévesque, Lise Lachance, Marie-Jeanne Kergoat, Renée Coulombe.   

Abstract

BACKGROUND: The prevalence of Alzheimer's disease is rising. The large number of new cases identified each year means that many new families will set upon a long trajectory of caring for a relative with dementia. Diagnostic disclosure of Alzheimer's disease marks the official transition to the caregiver role, yet this early period of the caregiver career have rarely been studied.
OBJECTIVES: Based on Meleis's theoretical framework for role transition, the objectives of this study were to document the characteristics of the caregiving context during the transition to the caregiver role following diagnostic disclosure of Alzheimer's disease and to compare these characteristics by caregiver gender and kinship tie to the relative. DESIGN SETTINGS AND PARTICIPANTS: A descriptive design was used. Data were collected using standardized measures selected in accordance with the role transition theoretical framework. The sample recruited in Quebec (Canada) cognition clinics comprised 122 caregivers of an elderly relative diagnosed with Alzheimer's disease in the past nine months.
RESULTS: Findings reveal the context of care to be marked by several challenges for caregivers. The majority of caregivers receives little informal support, has poor knowledge of available formal services, and has difficulty planning ahead for the relative's future care needs. Caregivers themselves report a lack of preparedness to provide care. Compared with men caregivers, women seem to have more problems controlling disturbing thoughts about their new caregiver role and to experience more family conflicts and psychological distress. Compared with offspring caregivers, spouse caregivers are less able to respond to the relative's disruptive behaviors, make less use of problem-solving strategies, and report fewer family conflicts.
CONCLUSIONS: The challenges faced by caregivers during the transition to the caregiver role are sensitive to nursing interventions. Pro-active interventions from the outset of the caregiving career, such as early assessment of caregiver needs for support and of caregiver preparedness to provide care as well as early psycho-educational interventions, are essential to foster positive caregiver responses to the challenges of their new role.
Copyright © 2011 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21376317     DOI: 10.1016/j.ijnurstu.2011.02.011

Source DB:  PubMed          Journal:  Int J Nurs Stud        ISSN: 0020-7489            Impact factor:   5.837


  16 in total

1.  Transition to the new role of caregiving for families of patients with breast cancer: a qualitative descriptive exploratory study.

Authors:  Masoumeh Hashemi-Ghasemabadi; Fariba Taleghani; Alireza Yousefy; Shahnaz Kohan
Journal:  Support Care Cancer       Date:  2015-08-26       Impact factor: 3.603

2.  Healthcare utilization and costs in primary care patients with dementia: baseline results of the DelpHi-trial.

Authors:  Bernhard Michalowsky; Steffen Flessa; Tilly Eichler; Johannes Hertel; Adina Dreier; Ina Zwingmann; Diana Wucherer; Henriette Rau; Jochen René Thyrian; Wolfgang Hoffmann
Journal:  Eur J Health Econ       Date:  2017-02-03

3.  Living in uncertainty while a spouse is undergoing a cognitive assessment: Voices of women care partners.

Authors:  Ragnhild Hedman; Pernilla Hillerås; Marie Tyrrell
Journal:  Dementia (London)       Date:  2022-09-21

Review 4.  Improving dementia care: the role of screening and detection of cognitive impairment.

Authors:  Soo Borson; Lori Frank; Peter J Bayley; Malaz Boustani; Marge Dean; Pei-Jung Lin; J Riley McCarten; John C Morris; David P Salmon; Frederick A Schmitt; Richard G Stefanacci; Marta S Mendiondo; Susan Peschin; Eric J Hall; Howard Fillit; J Wesson Ashford
Journal:  Alzheimers Dement       Date:  2013-01-30       Impact factor: 21.566

5.  Willingness to pay for informal care in France: the value of funding support interventions for caregivers.

Authors:  Chloé Gervès-Pinquié; Martine M Bellanger; Joel Ankri
Journal:  Health Econ Rev       Date:  2014-12-13

6.  Family carers' experiences of attending a multicomponent psychosocial intervention program for carers and persons with dementia.

Authors:  Aud Johannessen; Frøydis Kristine Bruvik; Solveig Hauge
Journal:  J Multidiscip Healthc       Date:  2015-02-12

7.  Caregiver burden and coping strategies in caregivers of patients with Alzheimer's disease.

Authors:  Alessandro Iavarone; Antonio Rosario Ziello; Francesca Pastore; Angiola Maria Fasanaro; Carla Poderico
Journal:  Neuropsychiatr Dis Treat       Date:  2014-07-29       Impact factor: 2.570

8.  The journey with dementia from the perspective of bereaved family caregivers: a qualitative descriptive study.

Authors:  Shelley C Peacock; Karon Hammond-Collins; Dorothy A Forbes
Journal:  BMC Nurs       Date:  2014-11-27

9.  Evaluation of efficacy and efficiency of a pragmatic intervention by a social worker to support informal caregivers of elderly patients (The ICE Study): study protocol for a randomized controlled trial.

Authors:  Astrid Pozet; Catherine Lejeune; Magalie Bonnet; Sandrine Dabakuyo; Michèle Dion; Philippe Fagnoni; Maryse Gaimard; Geneviève Imbert; Virginie Nerich; Audrey Foubert; Morgane Chotard; Marie Bonin; Amélie Anota; Franck Bonnetain
Journal:  Trials       Date:  2016-11-03       Impact factor: 2.279

10.  Informal caregivers of people with dementia: problems, needs and support in the initial stage and in subsequent stages of dementia: a questionnaire survey.

Authors:  Marieke Zwaanswijk; José M Peeters; Adriana Pa van Beek; Julie Hcm Meerveld; Anneke L Francke
Journal:  Open Nurs J       Date:  2013-01-15
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.