Literature DB >> 17101077

Patient-reported Outcome Measures in Multiple Sclerosis.

A Riazi1.   

Abstract

Patient-reported outcome (PRO) measures are being used more frequently in epidemiological studies, health service research and in clinical trials to evaluate therapeutic interventions from the patient's perspective. In MS, where evaluations of treatments are becoming increasingly important, outcome measures that are rigorous and appropriate to patients are needed. This article examines the value of PRO measures in MS and the criteria of evaluating such measures, and provides a brief description of MS-specific PRO measures that are currently available.

Entities:  

Mesh:

Year:  2006        PMID: 17101077

Source DB:  PubMed          Journal:  Int MS J        ISSN: 1352-8963


  9 in total

1.  Neuro-QOL: brief measures of health-related quality of life for clinical research in neurology.

Authors:  D Cella; J-S Lai; C J Nowinski; D Victorson; A Peterman; D Miller; F Bethoux; A Heinemann; S Rubin; J E Cavazos; A T Reder; R Sufit; T Simuni; G L Holmes; A Siderowf; V Wojna; R Bode; N McKinney; T Podrabsky; K Wortman; S Choi; R Gershon; N Rothrock; C Moy
Journal:  Neurology       Date:  2012-05-09       Impact factor: 9.910

2.  Multiple Sclerosis Patients Valuing Their Own Health Status: Valuation and Psychometric Properties of the 15D.

Authors:  Ioannis E Dagklis; Vasilis H Aletras; Efthymia Tsantaki; Anastasios Orologas; Dimitrios Niakas
Journal:  Neurol Int       Date:  2016-09-30

3.  Exploring cued and non-cued motor imagery interventions in people with multiple sclerosis: a randomised feasibility trial and reliability study.

Authors:  Barbara Seebacher; Raija Kuisma; Angela Glynn; Thomas Berger
Journal:  Arch Physiother       Date:  2018-03-02

4.  Outcomes of natalizumab treatment within 3 years of relapsing-remitting multiple sclerosis diagnosis: a prespecified 2-year interim analysis of STRIVE.

Authors:  Jai Perumal; Robert J Fox; Roumen Balabanov; Laura J Balcer; Steven Galetta; Shavy Makh; Sourav Santra; Christophe Hotermans; Lily Lee
Journal:  BMC Neurol       Date:  2019-06-08       Impact factor: 2.474

5.  Mobile-phone-based e-diary derived patient reported outcomes: Association with clinical disease activity, psychological status and quality of life of patients with multiple sclerosis.

Authors:  Daniel Golan; Smadar Sagiv; Lea Glass-Marmor; Ariel Miller
Journal:  PLoS One       Date:  2021-05-05       Impact factor: 3.240

6.  Comparison of employment among people with Multiple Sclerosis across Europe.

Authors:  David Ellenberger; Tina Parciak; Waldemar Brola; Jan Hillert; Rod Middleton; Alexander Stahmann; Christoph Thalheim; Peter Flachenecker
Journal:  Mult Scler J Exp Transl Clin       Date:  2022-04-27

Review 7.  Health-related quality of life in mucopolysaccharidosis: looking beyond biomedical issues.

Authors:  Christian J Hendriksz; Kenneth I Berger; Christina Lampe; Susanne G Kircher; Paul J Orchard; Rebecca Southall; Sarah Long; Stephen Sande; Jeffrey I Gold
Journal:  Orphanet J Rare Dis       Date:  2016-08-26       Impact factor: 4.123

8.  Levels of Patient Satisfaction on Integrative Medicine Before and After Implementation of Diagnosis-related Groups.

Authors:  Tobias Romeyke; Elisabeth Noehammer; Hans Christoph Scheuer; Harald Stummer
Journal:  Glob Adv Health Med       Date:  2018-02-27

Review 9.  Measuring the cost-effectiveness of treatments for people with multiple sclerosis: Beyond quality-adjusted life-years.

Authors:  Annie Hawton; Elizabeth Goodwin; Kate Boddy; Jennifer Freeman; Sarah Thomas; Jeremy Chataway; Colin Green
Journal:  Mult Scler       Date:  2020-09-03       Impact factor: 6.312

  9 in total

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