Literature DB >> 20201024

Does age make a difference in caregiver strain? Comparison of young versus older caregivers in early-stage Parkinson's disease.

Julie H Carter1, Karen S Lyons, Barbara J Stewart, Patricia G Archbold, Rebecca Scobee.   

Abstract

Family care research has identified negative outcomes of providing care to a spouse with Parkinson's disease (PD), such as declining physical and mental health. Research has also identified protective variables that decrease negative outcomes such as high mutuality and rewards of meaning. It is important for clinicians to identify "at risk" family caregivers and provide earlier interventions. Despite the importance of age and developmental stage there is a paucity of research comparing young versus older spouse caregivers. This study compared the difference in negative aspects of strain and modulators of strain in young and older PD spouse caregivers. A series of hierarchical multiple regressions were used to examine the contribution of age on both positive and negative aspects of the care situation for 65 (37 young, 28 old) PD spouse caregivers. Negative variables included 3 dimensions of strain; strain from lack of personal resources, strain from worry, and global strain. Positive or protective variables included mutuality, preparedness, and rewards of meaning. Even in early stage disease before significant care is required, young spouses (40-55) were found to be at greater risk for negative consequences of the care situation reporting significantly more strain from lack of personal resources, and lower levels of mutuality and rewards of meaning than older (greater than 70) spouses. As expected, young spouses were more likely to be working, caring for children in the home, and in better physical health than older spouses. Clinicians are well-situated to identify the unique needs of young spouses and intervene early in the caregiving trajectory. These findings provide ideas for targeted interventions. Future larger studies that compare young and older spouses should include later stage disease to more fully understand the developmental differences raised by the present findings. 2010 Movement Disorder Society

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Year:  2010        PMID: 20201024     DOI: 10.1002/mds.22888

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  20 in total

1.  Patterns and predictors of symptom incongruence in older couples coping with prostate cancer.

Authors:  Kerri M Winters-Stone; Karen S Lyons; Jill A Bennett; Tomasz M Beer
Journal:  Support Care Cancer       Date:  2013-12-17       Impact factor: 3.603

2.  The impact of subthalamic deep brain stimulation on caregivers of Parkinson's disease patients: an exploratory study.

Authors:  Catharine J Lewis; Franziska Maier; Nina Horstkötter; Carsten Eggers; Veerle Visser-Vandewalle; Elena Moro; Mateusz Zurowski; Jens Kuhn; Christiane Woopen; Lars Timmermann
Journal:  J Neurol       Date:  2014-11-09       Impact factor: 4.849

3.  Relationship Between Depressive Symptoms and Social Cognitive Processing in Partners of Long-Term Breast Cancer Survivors.

Authors:  Andrea A Cohee; Rebecca N Adams; Betsy L Fife; Diane M Von Ah; Patrick O Monahan; Kathleen A Zoppi; David Cella; Victoria L Champion
Journal:  Oncol Nurs Forum       Date:  2017-01-01       Impact factor: 2.172

4.  Dyadic Perceptions of the Decision Process in Families Living With Lung Cancer.

Authors:  Lyndsey M Miller; Donald R Sullivan; Karen S Lyons
Journal:  Oncol Nurs Forum       Date:  2017-01-01       Impact factor: 2.172

5.  The Roles of Dyadic Appraisal and Coping in Couples With Lung Cancer.

Authors:  Karen S Lyons; Lyndsey M Miller; Michael J McCarthy
Journal:  J Fam Nurs       Date:  2016-10-31       Impact factor: 3.818

6.  Dehumanization and burden of care among caregivers of terminally ill patients.

Authors:  Ines Testoni; Giulia Sicari; Lucia Ronconi; Gianmarco Biancalani; Chiara Franco; Paolo Cottone; Robert Crupi
Journal:  Health Psychol Res       Date:  2021-10-07

7.  What about the caregiver? A journey into Parkinson's disease following the burden tracks.

Authors:  Maria Rita Lo Monaco; Enrico Di Stasio; Maria Caterina Silveri; Anna Rita Bentivoglio; Diego Ricciardi; Marcella Solito; Martina Petracca; Domenico Fusco; Graziano Onder; Giovanni Landi; Giuseppe Zuccalà; Rosa Liperoti; Maria Camilla Cipriani; Caterina Brisi; Roberto Bernabei
Journal:  Aging Clin Exp Res       Date:  2020-06-02       Impact factor: 3.636

8.  Carer quality of life and experiences of health services: a cross-sectional survey across three neurological conditions.

Authors:  Michele Peters; Crispin Jenkinson; Helen Doll; E Diane Playford; Ray Fitzpatrick
Journal:  Health Qual Life Outcomes       Date:  2013-06-25       Impact factor: 3.186

9.  Factors influencing quality of life in caregivers of people with Parkinson's disease and implications for clinical guidelines.

Authors:  D Morley; S Dummett; M Peters; L Kelly; P Hewitson; J Dawson; R Fitzpatrick; C Jenkinson
Journal:  Parkinsons Dis       Date:  2012-12-20

10.  Caregiver strain and symptoms of depression among principal caregivers of patients with schizophrenia and bipolar affective disorder in Sri Lanka.

Authors:  Chaturaka Rodrigo; Tharanga Fernando; Senaka Rajapakse; Varuni De Silva; Raveen Hanwella
Journal:  Int J Ment Health Syst       Date:  2013-01-09
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