Literature DB >> 16609318

Multiple sclerosis: disability profile and quality of life in an Australian community cohort.

Fary Khan1, Tracey McPhail, Caroline Brand, Lynne Turner-Stokes, Trevor Kilpatrick.   

Abstract

The objective of this study was to determine the experience of disability and reported symptoms in multiple sclerosis in an Australian community sample, comparing the perceptions of patients, carers and treating doctors, and to examine effects on quality of life, carer stress and utilization of health services. The study design used a prospective cross sectional community survey. The participants were persons with a confirmed diagnosis of multiple sclerosis, with quantified neurological, mobility and cognitive deficits, from a tertiary hospital database (n=101), who lived at home, and their carers and doctors. The study method used demographic, diagnostic and disease severity data extracted from the database. Structured interviews conducted at home included: (1) open questionnaires for participant, carer and general practitioner, prioritizing symptoms/problems affecting daily living; and (2) standardized assessments for patient quality of life, caregiver strain and perceived burden of care. The mean age was 49 years (range 28-64). Those more severely affected had a significantly reduced quality of life and increased carer burden than those with milder disability, but discordance between patients, carers and doctors was noted in their perception of problems and symptom experience. Rates of depression (67%) and work-related problems were high, but vocational support was rarely provided. Forty persons used interferon, of whom 20 had secondary progressive multiple sclerosis; 39% reported difficulty in accessing rehabilitation services and only 10% were referred to medical rehabilitation units. In conclusion, the rates of disability and symptom experience were similar to other series; however, access and utilization of appropriate rehabilitation and support services appears to be lacking. There were higher reported rates of depression and poor quality of life. Opportunities may possibly exist to re-deploy resources to develop vocational support, counselling and rehabilitation.

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Year:  2006        PMID: 16609318     DOI: 10.1097/01.mrr.0000194393.56772.62

Source DB:  PubMed          Journal:  Int J Rehabil Res        ISSN: 0342-5282            Impact factor:   1.479


  18 in total

1.  Perceived met and unmet health-care needs in a community population with multiple sclerosis.

Authors:  Scott B Patten; Jeanne V A Williams; Dina H Lavorato; David Terriff; Luanne M Metz; Sandy Berzins; Andrew G M Bulloch
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Review 2.  A review of the psychometric properties of generic utility measures in multiple sclerosis.

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Journal:  Pharmacoeconomics       Date:  2014-08       Impact factor: 4.981

3.  "It's just horrible": a qualitative study of patients' and carers' experiences of bowel dysfunction in multiple sclerosis.

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4.  Validity and Reliability of the Turkish Version of the Monitoring My Multiple Sclerosis Scale.

Authors:  Cansu Polat; Zeliha Tülek; Murat Kürtüncü; Mefkure Eraksoy
Journal:  Noro Psikiyatr Ars       Date:  2017-01-19       Impact factor: 1.339

5.  Neurogenic Bowel Dysfunction Over the Course of Multiple Sclerosis: A Review.

Authors:  Elsie E Gulick
Journal:  Int J MS Care       Date:  2022-06-20

6.  Ten-year follow-up of health-related quality of life among ambulatory persons with multiple sclerosis at baseline.

Authors:  Aki Rintala; Arja Häkkinen; Jaana Paltamaa
Journal:  Qual Life Res       Date:  2016-06-30       Impact factor: 4.147

7.  Symptomatic therapy and rehabilitation in primary progressive multiple sclerosis.

Authors:  Fary Khan; Bhasker Amatya; Lynne Turner-Stokes
Journal:  Neurol Res Int       Date:  2011-10-17

8.  Rasch analysis of the Multiple Sclerosis Impact Scale MSIS-29.

Authors:  Melina Ramp; Fary Khan; Rose Anne Misajon; Julie F Pallant
Journal:  Health Qual Life Outcomes       Date:  2009-06-22       Impact factor: 3.186

9.  The impact of regular physical activity on fatigue, depression and quality of life in persons with multiple sclerosis.

Authors:  Nicole M Stroud; Clare L Minahan
Journal:  Health Qual Life Outcomes       Date:  2009-07-20       Impact factor: 3.186

10.  Anorectal dysfunction in multiple sclerosis: a systematic review.

Authors:  Sanober Nusrat; Elsie Gulick; David Levinthal; Klaus Bielefeldt
Journal:  ISRN Neurol       Date:  2012-07-29
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