Patient and Provider Insights into the Impact of Multiple Sclerosis on Mental Health: A Narrative Review

20Citations
Citations of this article
216Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Multiple sclerosis (MS) is a chronic disease in which the immune system attacks the central nervous system, causing inflammation and neurodegeneration. People living with MS may experience a variety of symptoms as a consequence of this process, including many “invisible” symptoms that are internally manifested and not seen by others. Of the invisible symptoms of MS, which we have reviewed in a companion article, mood and mental health disorders are of particular concern due to their high prevalence and significant impact on patient quality of life. In this review, we showcase the experiences of patient authors alongside perspectives from healthcare provider authors as we promote awareness of the common mental health conditions faced by those living with MS, such as depression, anxiety, adjustment disorder, bipolar disorder, psychosis, and suicidal ideation. Many of these conditions stem in part from the increased stress levels and the many uncertainties that come with managing life with MS, which have been exacerbated by the environment created by the coronavirus disease 2019 (COVID-19) pandemic. A patient-centered interdisciplinary approach, routine screening for mental health changes, and referral to specialists when needed can normalize discussions of mental health and increase the likelihood that people living with MS will receive the support and care they need. Management techniques such as robust social support, cognitive behavioral therapy, mindfulness-based interventions, and/or pharmacotherapy may be implemented to build resilience and promote healthy coping strategies. Increasingly, patients have access to telehealth options as well as digital apps for mental health management. Taken together, these approaches form an integrative care model in which people living with MS benefit from the care of medical professionals, a variety of support networks/resources, and self-management techniques for optimal mental health care. Graphical Plain Language Summary: [Figure not available: see fulltext.]

References Powered by Scopus

A global measure of perceived stress.

22398Citations
N/AReaders
Get full text

Validation and utility of a self-report version of PRIME-MD: The PHQ Primary Care Study

8056Citations
N/AReaders
Get full text

You want to measure coping but your protocol' too long: Consider the brief cope

5299Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Comprehensive Approach to Management of Multiple Sclerosis: Addressing Invisible Symptoms—A Narrative Review

63Citations
N/AReaders
Get full text

High-Efficacy Therapies for Treatment-Naïve Individuals with Relapsing–Remitting Multiple Sclerosis

50Citations
N/AReaders
Get full text

Long-term consequences of COVID-19 on mental health and the impact of a physically active lifestyle: a narrative review

9Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Davis, B. E., Lakin, L., Binns, C. C., Currie, K. M., & Rensel, M. R. (2021, June 1). Patient and Provider Insights into the Impact of Multiple Sclerosis on Mental Health: A Narrative Review. Neurology and Therapy. Adis. https://doi.org/10.1007/s40120-021-00240-9

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 47

64%

Researcher 14

19%

Professor / Associate Prof. 7

9%

Lecturer / Post doc 6

8%

Readers' Discipline

Tooltip

Psychology 33

45%

Medicine and Dentistry 21

28%

Nursing and Health Professions 14

19%

Biochemistry, Genetics and Molecular Bi... 6

8%

Article Metrics

Tooltip
Social Media
Shares, Likes & Comments: 43

Save time finding and organizing research with Mendeley

Sign up for free