Literature DB >> 27288793

Low quality of life and psychological wellbeing contrast with moderate perceived burden in carers of people with severe multiple sclerosis.

Andrea Giordano1, Vincenzo Cimino2, Angela Campanella3, Giovanni Morone4, Augusto Fusco5, Mariangela Farinotti6, Lucia Palmisano7, Paolo Confalonieri8, Alessandra Lugaresi9, Maria Grazia Grasso10, Michela Ponzio11, Simone Veronese12, Francesco Patti13, Alessandra Solari14.   

Abstract

Entities:  

Keywords:  Caregivers; Illness burden; Outcome measure; Palliative care; Primary progressive multiple sclerosis; Quality of life; Secondary progressive multiple sclerosis

Mesh：

Year:  2016        PMID： 27288793     DOI： 10.1016/j.jns.2016.05.016

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN： 0022-510X            Impact factor:   3.181


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  4 in total

1.  Randomized controlled trial of a home-based palliative approach for people with severe multiple sclerosis.

Authors:  Alessandra Solari; Andrea Giordano; Francesco Patti; Maria Grazia Grasso; Paolo Confalonieri; Lucia Palmisano; Michela Ponzio; Claudia Borreani; Rosalba Rosato; Simone Veronese; Paola Zaratin; Mario Alberto Battaglia
Journal:  Mult Scler       Date:  2017-04-06       Impact factor: 6.312

2.  The unmet needs of family members of patients with progressive neurological disease in the Czech Republic.

Authors:  Radka Bužgová; Radka Kozáková; Lubica Juríčková
Journal:  PLoS One       Date:  2019-03-25       Impact factor: 3.240

Review 3.  Caregiver Burden in Multiple Sclerosis: Recent Trends and Future Directions.

Authors:  Rebecca Maguire; Phil Maguire
Journal:  Curr Neurol Neurosci Rep       Date:  2020-05-22       Impact factor: 5.081

4.  Caregiver wellbeing during Covid-19: does being hopeful play a role?

Authors:  Juliana Onwumere; Elizabeth Kuipers; Emilie Wildman; Ava Mason; Daniel Stahl
Journal:  J Affect Disord Rep       Date:  2021-09-17
  4 in total

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