Literature DB >> 20856267

Life issues in multiple sclerosis.

Rex D Simmons1.   

Abstract

A diagnosis of multiple sclerosis (MS), an incurable condition, introduces great uncertainty into virtually all aspects of a person's life. From early in the disease course, people with MS are vulnerable to disempowerment, poor psychological health, and social exclusion including high unemployment. Current health-care research for people with MS is reviewed here within the context of three philosophies of disability and health-care service provision: the biomedical, biopsychosocial and sociopolitical models. Some of the uncertainties concerning the patient's life that result from MS have been reduced by improved diagnostic tools, advances in immunotherapy, multidisciplinary rehabilitation, community programs, and provision of information specifically designed to facilitate shared decision-making and empowerment. Such progress is modest, however, and substantial improvements to the psychological health, empowerment, and quality of life of people with MS requires more sociopolitically oriented research.

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Year:  2010        PMID: 20856267     DOI: 10.1038/nrneurol.2010.143

Source DB:  PubMed          Journal:  Nat Rev Neurol        ISSN: 1759-4758            Impact factor:   42.937


  116 in total

1.  Natural history of multiple sclerosis.

Authors:  G C Ebers
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-12       Impact factor: 10.154

Review 2.  Psychosomatic medicine: the scientific foundation of the biopsychosocial model.

Authors:  Dennis H Novack; Oliver Cameron; Elissa Epel; Robert Ader; Shari R Waldstein; Susan Levenstein; Michael H Antoni; Alicia Rojas Wainer
Journal:  Acad Psychiatry       Date:  2007 Sep-Oct

Review 3.  Stress and multiple sclerosis.

Authors:  David C Mohr
Journal:  J Neurol       Date:  2007-05       Impact factor: 4.849

Review 4.  Taking part in life: enhancing participation in multiple sclerosis.

Authors:  Kathryn M Yorkston; Kurt L Johnson; Estelle R Klasner
Journal:  Phys Med Rehabil Clin N Am       Date:  2005-05       Impact factor: 1.784

5.  Doctor-patient dilemmas in multiple sclerosis.

Authors:  A Burnfield
Journal:  J Med Ethics       Date:  1984-03       Impact factor: 2.903

6.  The value of diagnostic information to patients with suspected multiple sclerosis. Rochester-Toronto MRI Study Group.

Authors:  A I Mushlin; C Mooney; V Grow; C E Phelps
Journal:  Arch Neurol       Date:  1994-01

7.  Physical activity and quality of life in multiple sclerosis: intermediary roles of disability, fatigue, mood, pain, self-efficacy and social support.

Authors:  Robert W Motl; Edward McAuley; Erin M Snook; Rachael C Gliottoni
Journal:  Psychol Health Med       Date:  2009-01       Impact factor: 2.423

8.  Multiple sclerosis.

Authors:  Alastair Compston; Alasdair Coles
Journal:  Lancet       Date:  2008-10-25       Impact factor: 79.321

Review 9.  The needs and experiences of caregivers of individuals with multiple sclerosis: a systematic review.

Authors:  L P McKeown; A P Porter-Armstrong; G D Baxter
Journal:  Clin Rehabil       Date:  2003-05       Impact factor: 3.477

Review 10.  Multidisciplinary rehabilitation for adults with multiple sclerosis.

Authors:  F Khan; L Turner-Stokes; L Ng; T Kilpatrick
Journal:  Cochrane Database Syst Rev       Date:  2007-04-18
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  12 in total

1.  Longitudinal changes in quality of life and related psychosocial variables in australians with multiple sclerosis.

Authors:  Judy Ann Wollin; Nancy Spencer; Elizabeth McDonald; Gary Fulcher; Maureen Bourne; Rex D Simmons
Journal:  Int J MS Care       Date:  2013

2.  Intolerance of Uncertainty: Shaping an Agenda for Research on Coping with Multiple Sclerosis.

Authors:  Kevin N Alschuler; Meghan L Beier
Journal:  Int J MS Care       Date:  2015 Jul-Aug

3.  Health-related quality of life outcomes at 1 and 5 years after a residential retreat promoting lifestyle modification for people with multiple sclerosis.

Authors:  Emily J Hadgkiss; George A Jelinek; Tracey J Weiland; Greg Rumbold; Claire A Mackinlay; Siegfried Gutbrod; Ian Gawler
Journal:  Neurol Sci       Date:  2012-02-25       Impact factor: 3.307

4.  Keeping cool: use of air conditioning by australians with multiple sclerosis.

Authors:  Michael P Summers; Rex D Simmons; George Verikios
Journal:  Mult Scler Int       Date:  2012-03-28

5.  Fatigue in Multiple Sclerosis Compared to Stroke.

Authors:  Claudia Lukoschek; Annette Sterr; Dolores Claros-Salinas; Rolf Gütler; Christian Dettmers
Journal:  Front Neurol       Date:  2015-05-26       Impact factor: 4.003

6.  Anxiety, emotional processing and depression in people with multiple sclerosis.

Authors:  Marie-Claire Gay; Catherine Bungener; Sarah Thomas; Pierre Vrignaud; Peter W Thomas; Roger Baker; Sébastien Montel; Olivier Heinzlef; Caroline Papeix; Rana Assouad; Michèle Montreuil
Journal:  BMC Neurol       Date:  2017-02-23       Impact factor: 2.474

7.  Psychological consequences of COVID-19 pandemic in Italian MS patients: signs of resilience?

Authors:  Rocco Capuano; Manuela Altieri; Alvino Bisecco; Alessandro d'Ambrosio; Renato Docimo; Daniela Buonanno; Federica Matrone; Federica Giuliano; Gioacchino Tedeschi; Gabriella Santangelo; Antonio Gallo
Journal:  J Neurol       Date:  2020-07-28       Impact factor: 4.849

8.  Economic burden of multiple sclerosis on Kuwait health care system.

Authors:  Maryam S Alowayesh; Samar F Ahmed; Jasem Al-Hashel; Raed Alroughani
Journal:  PLoS One       Date:  2019-05-14       Impact factor: 3.240

9.  Is it worth it?: The experiences of persons with multiple sclerosis as they access health care to manage their condition.

Authors:  Julie Pétrin; Catherine Donnelly; Mary-Ann McColl; Marcia Finlayson
Journal:  Health Expect       Date:  2020-07-22       Impact factor: 3.377

10.  The impact of social media use on depression in multiple sclerosis patients.

Authors:  Hamid Reza Farpour; Amir Human Hoveidaei; Leila Habibi; Mahsa Moosavi; Sima Farpour
Journal:  Acta Neurol Belg       Date:  2020-06-21       Impact factor: 2.471

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