Evidence map›Paper›PMID 36191370›Full record

ArticleMultiple sclerosis and related disorders2022

Exploring the impact of the COVID-19 pandemic on social isolation and mental health in people with MS.

Shu Ling, Brandon Moss, Zhini Wang, Amy B Sullivan

Abstract read
In one paragraph

Article in Multiple sclerosis and related disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Shu LingMellen Center for Multiple Sclerosis Treatment and Research, Cleveland Clinic, 9500, Euclid Ave., U-10, Cleveland, OH 44195, USA.
Brandon MossMellen Center for Multiple Sclerosis Treatment and Research, Cleveland Clinic, 9500, Euclid Ave., U-10, Cleveland, OH 44195, USA.
Zhini WangDepartment of Quantitative Health Science, Lerner Research Institute, Cleveland Clinic, 9500 Euclid Ave., Cleveland, OH 44195, USA.
Amy B SullivanMellen Center for Multiple Sclerosis Treatment and Research, Cleveland Clinic, 9500, Euclid Ave., U-10, Cleveland, OH 44195, USA. Electronic address: sulliva5@ccf.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeople with multiple sclerosis (MS) may be disproportionally impacted by the coronavirus disease of 2019 (COVID-19) as various factors important to their functioning and quality of life are at-risk and/or compromised during the pandemic. In particular, the social distancing and quarantine practice during the pandemic maybe detrimental to MS patients' social and emotional health. Compared with the general population, MS patients may be under increased social strain and suffer worse health consequences from social isolation. To date, there has been no research examining the social consequences of the pandemic on MS patients' emotional and social health.

methodsThis is a retrospective longitudinal study of 266 adults with MS who were followed at a large academic medical center in the Midwest. Each participant completed monthly surveys including depression, anxiety, and social health variables.

resultsT-Tests shows worse anxiety (95% CI [-5.03, -3.05]; p-value < 0.001), worse depression (95% CI [-2.67, -1.03]; p-value < 0.001), and worse satisfaction with social roles (95% CI [2.37, 3.95]; p-value < 0.001) since the COVID-19 outbreak (March 2020). Social isolation is associated with worse anxiety (95% CI [-8.98, -4.58]; p-value < 0.001) and depression (95% CI [-6.88, -3.24]; p-value < 0.001). However, individuals who had in-person visits before and after the outbreak did not experience any changes in anxiety, depression, or social health.

conclusionMS patients' anxiety, depression, and social participation worsened during the COVID-19 pandemic. Social isolation is found to be associated with worse anxiety and depression. However, those who attended in-person visits for their MS treatment did not experience negative changes in their emotional or social health. This study highlights the importance of healthcare provider's alertness to MS patients' social health and the interplay between social and emotional health during the COVID-19 pandemic.

Indexed as

COVID-19Multiple SclerosisAdultAnxietyDepressionHumansLongitudinal StudiesMental HealthPandemicsQuality of LifeRetrospective StudiesSARS-CoV-2Social IsolationCOVIDIsolationMental healthMoodMultiple sclerosis

Identifiers

PMID36191370
PMCPMC9489964

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.