Literature DB >> 19302397

Perceived health status as measured by the SF-36 in patients with multiple sclerosis: a review.

Martina Krokavcova1, Jitse P van Dijk, Iveta Nagyova, Jaroslav Rosenberger, Miriam Gavelova, Zuzana Gdovinova, Johan W Groothoff.   

Abstract

This review of literature gives an overview of recent studies about perceived health status as measured by the Short-Form-36 (SF-36) Health Survey in patients with multiple sclerosis (MS). The SF-36 is one of the tools measuring health status in patients used in international research and clinical practice. It measures two main health concepts - physical and mental. The SF-36 represents a valid instrument able to detect differences in perceived health status in patients. A computer-aided search in Medline and PsycINFO resulted in 504 articles in English published from 1996 to August 2006. After the screening process on the basis of abstracts, eight articles consisting of empirical studies remained in which perceived health status was evaluated using the SF-36 Health Survey. Seven studies focused on disability and perceived health status in the SF-36. Two studies focused on the relationship between depression and perceived health status. These studies showed that MS patients with low disability and minor depression scored significantly better than patients with high disability and major depression in the SF-36 health dimensions. Gender seems to have no influence on perceived health status in MS patients. The longer the disease duration and the more severe the disease, the lower the patients scored in perceived health status. The more disabled, the more depressive and the older the patients, the poorer their perceived health status was. Health providers supporting appropriate treatment might pay more attention to more disabled and more depressive patients, with longer disease duration. Perceived health status can be a predictor of prognosis and intervention outcomes. The study shows the importance of measuring perceived health status in MS patients with implications for their quality of life and provision of care.
© 2009 The Authors. Journal compilation © 2009 Nordic College of Caring Science.

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Year:  2009        PMID: 19302397     DOI: 10.1111/j.1471-6712.2008.00633.x

Source DB:  PubMed          Journal:  Scand J Caring Sci        ISSN: 0283-9318


  8 in total

1.  Disability status and quality of life in multiple sclerosis: non-linearity of the Expanded Disability Status Scale (EDSS).

Authors:  Sabine Twork; Susanne Wiesmeth; Milena Spindler; Markus Wirtz; Sabine Schipper; Dieter Pöhlau; Jörg Klewer; Joachim Kugler
Journal:  Health Qual Life Outcomes       Date:  2010-06-07       Impact factor: 3.186

2.  Aging with multiple sclerosis: A longitudinal study of physical function, mental health, and memory in two cohorts of US women.

Authors:  Marianna Cortese; Kjetil Bjornevik; Tanuja Chitnis; Alberto Ascherio; Kassandra L Munger
Journal:  Mult Scler       Date:  2021-04-16       Impact factor: 6.312

3.  Reliability and validity of the SF-36 Health Survey Questionnaire in patients with brain tumors: a cross-sectional study.

Authors:  Adomas Bunevicius
Journal:  Health Qual Life Outcomes       Date:  2017-05-04       Impact factor: 3.186

4.  Quality of life in multiple sclerosis: The differential impact of motor and cognitive fatigue.

Authors:  Sabina David Ruban; Claudia Christina Hilt; Thor Petersen
Journal:  Mult Scler J Exp Transl Clin       Date:  2021-02-24

Review 5.  Comprehensive Approach to Management of Multiple Sclerosis: Addressing Invisible Symptoms-A Narrative Review.

Authors:  Lynsey Lakin; Bryan E Davis; Cherie C Binns; Keisha M Currie; Mary R Rensel
Journal:  Neurol Ther       Date:  2021-04-20

6.  Burden of disease in myasthenia gravis: taking the patient's perspective.

Authors:  Sophie Lehnerer; Jonas Jacobi; Ralph Schilling; Ulrike Grittner; Derin Marbin; Lea Gerischer; Frauke Stascheit; Maike Krause; Sarah Hoffmann; Andreas Meisel
Journal:  J Neurol       Date:  2021-11-20       Impact factor: 6.682

7.  Quality of Life, Social, and Emotional Aspects of Being Diagnosed With Multiple Sclerosis: What's Grit got to do With it?

Authors:  Susan G Klappa; Kelli Block; Taylor Grant
Journal:  J Patient Exp       Date:  2022-08-15

8.  Quality of Life Assessment in Multiple Sclerosis: Different Perception between Patients and Neurologists.

Authors:  Maria C Ysrraelit; Marcela P Fiol; Maria I Gaitán; Jorge Correale
Journal:  Front Neurol       Date:  2018-01-11       Impact factor: 4.003

  8 in total

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