Literature DB >> 23181579

Distress associated with patients' symptoms and depression in a sample of Mexican caregivers of individuals with MS.

Tara Lehan1, Juan Carlos Arango-Lasprilla, Miguel Ángel Macias, Adriana Aguayo, Teresita Villaseñor.   

Abstract

PURPOSE/
OBJECTIVE: The objectives of this quantitative correlational study were to: (a) determine the frequency and level of distress associated with patients' symptoms as reported by caregivers of individuals with multiple sclerosis (MS), (b) determine the prevalence of depression in these caregivers, and (c) examine the relationship between these caregivers' total symptom distress and depression after controlling for patient, caregiver, and illness characteristics. METHOD/
DESIGN: In this quantitative correlational study, data from 79 caregivers of individuals with MS in Mexico were analyzed.
RESULTS: The patient symptoms with the highest average level of distress for caregivers were depression, difficulty talking, difficulty hearing, becoming upset easily, and upsetting other people. Patient symptoms with the lowest average level of distress for caregivers included difficulty learning, seizures, trouble reading, difficulty eating, and difficulty writing. Forty percent of the caregivers met the criteria for probable major depressive disorder. Results of a multivariate regression analysis showed that caregiver total symptom distress was significantly related to caregiver depression, after controlling for patient marital status, caregiver gender, caregiver relationship to patient, caregiver current employment, and months spent caregiving.
CONCLUSIONS: These findings have implications for MS patients and caregivers as well as larger society, as depression in caregivers often results in the institutionalization of individuals with chronic illnesses and disabilities, which is costly for both individuals and society. In addition, there might be increased expenditures associated with the caregivers' own declining health. For these reasons, it is important to develop a better understanding of its risk factors to identify caregivers who might benefit from intervention. PsycINFO Database Record (c) 2012 APA, all rights reserved.

Entities:  

Mesh:

Year:  2012        PMID: 23181579     DOI: 10.1037/a0030764

Source DB:  PubMed          Journal:  Rehabil Psychol        ISSN: 0090-5550


  8 in total

1.  Effects of change in arthritis severity on spouse well-being: The moderating role of relationship closeness.

Authors:  Courtney A Polenick; Lynn M Martire; Rachel C Hemphill; Mary Ann Parris Stephens
Journal:  J Fam Psychol       Date:  2015-06

2.  Care Partners and Multiple Sclerosis: Differential Effect on Men and Women.

Authors:  Tamara McKenzie; Mary Elizabeth Quig; Tuula Tyry; Ruth Ann Marrie; Gary Cutter; Edward Shearin; Kamau Johnson; James Simsarian
Journal:  Int J MS Care       Date:  2015 Nov-Dec

Review 3.  The incidence and prevalence of psychiatric disorders in multiple sclerosis: a systematic review.

Authors:  Ruth Ann Marrie; Stephen Reingold; Jeffrey Cohen; Olaf Stuve; Maria Trojano; Per Soelberg Sorensen; Gary Cutter; Nadia Reider
Journal:  Mult Scler       Date:  2015-01-12       Impact factor: 6.312

Review 4.  A systematic review of the incidence and prevalence of comorbidity in multiple sclerosis: overview.

Authors:  Ruth Ann Marrie; Jeffrey Cohen; Olaf Stuve; Maria Trojano; Per Soelberg Sørensen; Stephen Reingold; Gary Cutter; Nadia Reider
Journal:  Mult Scler       Date:  2015-01-26       Impact factor: 6.312

5.  Providing care to relatives with mental illness: reactions and distress among primary informal caregivers.

Authors:  Sherilyn Chang; Yunjue Zhang; Anitha Jeyagurunathan; Ying Wen Lau; Vathsala Sagayadevan; Siow Ann Chong; Mythily Subramaniam
Journal:  BMC Psychiatry       Date:  2016-03-25       Impact factor: 3.630

6.  Mediational Model of Multiple Sclerosis Impairments, Family Needs, and Caregiver Mental Health in Guadalajara, Mexico.

Authors:  Melody N Mickens; Paul B Perrin; Adriana Aguayo; Brenda Rabago; Miguel A Macías-Islas; Juan Carlos Arango-Lasprilla
Journal:  Behav Neurol       Date:  2018-01-17       Impact factor: 3.342

7.  A home-based comprehensive care model in patients with Multiple Sclerosis: A study pre-protocol.

Authors:  Lufei Young; Kathleen Healey; Mary Charlton; Kendra Schmid; Rana Zabad; Rebecca Wester
Journal:  F1000Res       Date:  2015-09-18

8.  A Disproportionate Burden of Care: Gender Differences in Mental Health, Health-Related Quality of Life, and Social Support in Mexican Multiple Sclerosis Caregivers.

Authors:  Paul B Perrin; Ivan Panyavin; Alejandra Morlett Paredes; Adriana Aguayo; Miguel Angel Macias; Brenda Rabago; Sandra J Fulton Picot; Juan Carlos Arango-Lasprilla
Journal:  Behav Neurol       Date:  2015-10-11       Impact factor: 3.342

  8 in total

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