Literature DB >> 24314680

Caregiving in multiple sclerosis.

Lynda Hillman1.   

Abstract

Thirty percent of persons with multiple sclerosis (pwMS) require caregiving owing to their disability, and 80% of care to pwMS is provided by informal unpaid caregivers. The average caregiver is male, in a spousal/partner relationship with the pwMS, and provides more than 4 hours per day of care for many years. The physical, emotional, and time-intensive nature of caregiving for pwMS frequently impairs the caregiver's own physical and emotional health. Rehabilitation medicine professionals should be aware of the high risk of caregiver burden. Assessment of caregiver needs and appropriate intervention will help minimize the burden on caregivers.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Caregiver burden; Caregiving; Disability; Informal care; Multiple sclerosis

Mesh:

Year:  2013        PMID: 24314680     DOI: 10.1016/j.pmr.2013.06.007

Source DB:  PubMed          Journal:  Phys Med Rehabil Clin N Am        ISSN: 1047-9651            Impact factor:   1.784


  7 in total

1.  Validity and Reliability of the Scale to Report Emotional Stress Signs-Multiple Sclerosis (STRESS-MS) in Assessing Abuse and Neglect of Adults With Multiple Sclerosis.

Authors:  Elizabeth H Morrison; Dara Sorkin; Laura Mosqueda; Napatkamon Ayutyanont
Journal:  Int J MS Care       Date:  2021-06-30

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

3.  Burden for Parents of Patients With Schizophrenia-A Nationwide Comparative Study of Parents of Offspring With Rheumatoid Arthritis, Multiple Sclerosis, Epilepsy, and Healthy Controls.

Authors:  Ellenor Mittendorfer-Rutz; Syed Rahman; Antti Tanskanen; Maila Majak; Juha Mehtälä; Fabian Hoti; Erik Jedenius; Dana Enkusson; Amy Leval; Jan Sermon; Heidi Taipale; Jari Tiihonen
Journal:  Schizophr Bull       Date:  2019-06-18       Impact factor: 9.306

4.  The burden of family caregiving in the United States: work productivity, health care resource utilization, and mental health among employed adults.

Authors:  Markay Hopps; Laura Iadeluca; Margaret McDonald; Geoffrey T Makinson
Journal:  J Multidiscip Healthc       Date:  2017-12-06

5.  Psychological Shift in Partners of People with Multiple Sclerosis Who Undertake Lifestyle Modification: An Interpretive Phenomenological Study.

Authors:  Sandra L Neate; Keryn L Taylor; George A Jelinek; Alysha M De Livera; Chelsea R Brown; Tracey J Weiland
Journal:  Front Psychol       Date:  2018-01-31

6.  Fatigue and Mood States in Nursing Home and Nonambulatory Home-Based Patients with Multiple Sclerosis.

Authors:  Zilfah Younus; Caila B Vaughn; Shaik Ahmed Sanai; Katelyn S Kavak; Sahil Gupta; Muhammad Nadeem; Barbara E Teter; Katia Noyes; Robert Zivadinov; Keith Edwards; Patricia K Coyle; Andrew Goodman; Bianca Weinstock-Guttman
Journal:  Int J MS Care       Date:  2017 Nov-Dec

7.  Measuring burden in caregivers of people with multiple sclerosis: psychometric properties of the CSI questionnaire.

Authors:  Jose M García-Domínguez; María L Martínez-Ginés; Olga Carmona; Ana B Caminero; Daniel Prefasi; Jorge Maurino; Javier Ballesteros
Journal:  Patient Prefer Adherence       Date:  2019-01-09       Impact factor: 2.711

  7 in total

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