Literature DB >> 11445630

Does adding MS-specific items to a generic measure (the SF-36) improve measurement?

J A Freeman1, J C Hobart, A J Thompson.   

Abstract

OBJECTIVE: The 36-item Short Form Health Survey Questionnaire (SF-36) is a widely used generic health status measure. Recently it has been adapted to produce a disease-specific measure for MS-the 54-item Multiple Sclerosis Quality of Life Scale (MSQOL-54)-composed of five unchanged SF-36 scales; three altered SF-36 scales (one item added to each scale); and five new scales incorporating 15 additional items. This study evaluates the impact of these additions by comparing the measurement properties of the MSQOL-54 with the SF-36.
METHODS: A total of 150 patients with MS, representing a broad spectrum of disease severity, completed a range of questionnaires, which included the MSQOL-54 (from which the SF-36 score was computed). Of these, 44 people completed the measures before and after inpatient rehabilitation to evaluate responsiveness. Standard psychometric methods were used to evaluate the measurement properties.
RESULTS: The measurement properties of the unchanged scales, inevitably, remain identical. Those of the three altered scales are virtually identical. Of the five new scales, the validity of the two sexual scales is questioned because of the high percentage of missing data, and the validity of the overall quality-of-life scale is limited as demonstrated by the low to moderate correlations with other related and unrelated measures. Responsiveness of the new scales also appears limited.
CONCLUSION: Modifying existing measures by simply adding clinically chosen items may not be as useful as anticipated in improving the measurement properties of an instrument.

Entities:  

Mesh:

Year:  2001        PMID: 11445630     DOI: 10.1212/wnl.57.1.68

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  15 in total

1.  Long-term exercise improves functional impairment but not quality of life in multiple sclerosis.

Authors:  Anders Romberg; Arja Virtanen; Juhani Ruutiainen
Journal:  J Neurol       Date:  2005-03-16       Impact factor: 4.849

2.  Factors that contribute to quality of life outcomes prioritised by people with multiple sclerosis.

Authors:  Maggie Somerset; Tim J Peters; Deborah J Sharp; Rona Campbell
Journal:  Qual Life Res       Date:  2003-02       Impact factor: 4.147

3.  A method to create a standardized generic and condition-specific patient-reported outcome measure for patient care and healthcare improvement.

Authors:  Karen E Schifferdecker; Susan E Yount; Karen Kaiser; Anna Adachi-Mejia; David Cella; Kathleen L Carluzzo; Amy Eisenstein; Michael A Kallen; George J Greene; David T Eton; Elliott S Fisher
Journal:  Qual Life Res       Date:  2017-08-09       Impact factor: 4.147

Review 4.  [Quality of life in multiple sclerosis. Measures, relevance, problems, and perspectives].

Authors:  W Pöllmann; C Busch; R Voltz
Journal:  Nervenarzt       Date:  2005-02       Impact factor: 1.214

Review 5.  Health-related quality of life in multiple sclerosis: current evidence, measurement and effects of disease severity and treatment.

Authors:  Richard A Rudick; Deborah M Miller
Journal:  CNS Drugs       Date:  2008       Impact factor: 5.749

6.  Validation and cross-cultural adaptation of the disease-specific questionnaire MSQOL-54 in Serbian multiple sclerosis patients sample.

Authors:  Tatjana Pekmezovic; Darija Kisic Tepavcevic; Jelena Kostic; Jelena Drulovic
Journal:  Qual Life Res       Date:  2007-07-07       Impact factor: 4.147

7.  Home based management in multiple sclerosis: results of a randomised controlled trial.

Authors:  C Pozzilli; M Brunetti; A M V Amicosante; C Gasperini; G Ristori; L Palmisano; M Battaglia
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-09       Impact factor: 10.154

8.  The MS Symptom and Impact Diary (MSSID): psychometric evaluation of a new instrument to measure the day to day impact of multiple sclerosis.

Authors:  J Greenhalgh; H Ford; A F Long; K Hurst
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-04       Impact factor: 10.154

9.  Measuring the quality of life in patients with multiple sclerosis in clinical practice: a necessary challenge.

Authors:  Karine Baumstarck; Laurent Boyer; Mohamed Boucekine; Pierre Michel; Jean Pelletier; Pascal Auquier
Journal:  Mult Scler Int       Date:  2013-02-28

10.  Responsiveness of the Multiple Sclerosis International Quality of Life questionnaire to disability change: a longitudinal study.

Authors:  Karine Baumstarck; Helmut Butzkueven; Oscar Fernández; Peter Flachenecker; Sergio Stecchi; Egemen Idiman; Jean Pelletier; Mohamed Boucekine; Pascal Auquier
Journal:  Health Qual Life Outcomes       Date:  2013-07-29       Impact factor: 3.186

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