Literature DB >> 19738215

Patient perspective on outcomes in rheumatology -- a position paper for OMERACT 9.

John R Kirwan1, Stanton Newman, Peter S Tugwell, George A Wells.   

Abstract

The inclusion of patient participants at OMERACT has resulted in direct incorporation of the patient perspective in the development of outcome assessments in rheumatology. Fatigue has been adopted as a recommended measure in all studies, and further work is now under way on the assessment of sleep, effective healthcare consumers, and the effects of psychological or educational interventions. This position paper draws this work together in preparation for the Patient Perspective Workshop at OMERACT 9, and introduces the concept that other core outcomes relevant to patients might be required in assessing interventions designed to help patients live with their disease.

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Year:  2009        PMID: 19738215     DOI: 10.3899/jrheum.090359

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  13 in total

Review 1.  Patient empowerment as a component of health system reforms: rights, benefits and vested interests.

Authors:  Cinzia Colombo; Lorenzo Moja; Marien Gonzalez-Lorenzo; Alessandro Liberati; Paola Mosconi
Journal:  Intern Emerg Med       Date:  2012-01-26       Impact factor: 3.397

2.  Development of Clinical Trial Assessments for the Study of Interstitial Lung Disease in Patients who have Connective Tissue Diseases-Methodological Considerations.

Authors:  Dörte Huscher; Lesley Ann Saketkoo; David Pittrow; Dinesh Khanna
Journal:  Curr Rheumatol Rev       Date:  2010-05-01

3.  Selection of items for a computer-adaptive test to measure fatigue in patients with rheumatoid arthritis: a Delphi approach.

Authors:  Stephanie Nikolaus; Christina Bode; Erik Taal; Mart A F J vd Laar
Journal:  Qual Life Res       Date:  2011-07-31       Impact factor: 4.147

4.  Pain and difficulties performing valued life activities in women and men with rheumatoid arthritis.

Authors:  Inger Ahlstrand; Mathilda Björk; Ingrid Thyberg; Torbjörn Falkmer
Journal:  Clin Rheumatol       Date:  2015-01-25       Impact factor: 2.980

5.  "If i wasn't this robust": patients' expectations and experiences at the Outcome Measures in Rheumatology Conference 2010.

Authors:  Maarten P T de Wit; Marije S Koelewijn-van Loon; Sarah Collins; Tineke A Abma; John Kirwan
Journal:  Patient       Date:  2013       Impact factor: 3.883

Review 6.  Using the Delphi technique to determine which outcomes to measure in clinical trials: recommendations for the future based on a systematic review of existing studies.

Authors:  Ian P Sinha; Rosalind L Smyth; Paula R Williamson
Journal:  PLoS Med       Date:  2011-01-25       Impact factor: 11.069

7.  Patient-initiated research in rheumatic diseases in Sweden--dignity, identity and quality of life in focus when patients set the research agenda.

Authors:  U Bergsten; A-M Andrey; L Bottner; M Nylander; G Persson; E Petersson; S Bergman
Journal:  Musculoskeletal Care       Date:  2014-04-30

8.  Construct Validation of a Multidimensional Computerized Adaptive Test for Fatigue in Rheumatoid Arthritis.

Authors:  Stephanie Nikolaus; Christina Bode; Erik Taal; Harald E Vonkeman; Cees A W Glas; Mart A F J van de Laar
Journal:  PLoS One       Date:  2015-12-28       Impact factor: 3.240

9.  Doctors' insights into the patient perspective: a qualitative study in the field of chronic pain.

Authors:  Claudia Zanini; Piercarlo Sarzi-Puttini; Fabiola Atzeni; Manuela Di Franco; Sara Rubinelli
Journal:  Biomed Res Int       Date:  2014-05-18       Impact factor: 3.411

10.  Rheumatoid arthritis patients' experience of climate care.

Authors:  Katrin Vaks; Rita Sjöström
Journal:  J Exerc Rehabil       Date:  2015-12-31
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