Quality and acceptability of patient-reported outcome measures used in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME): a systematic review

Author:

Haywood Kirstie L.,Staniszewska Sophie,Chapman Sarah

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health

Reference127 articles.

1. Department of Health. (2002). Report of the CFS/ME working group. Para.1.4.2, p6. Accessed 2 March 2009 http://www.dh.gov.uk/en/Publicationsandstatistics/Publications/PublicationsPolicyAndGuidance/DH_4064840 .

2. Bibby, J., & Kershaw, A. (2006). How much is M.E. costing the country? Report prepared by the survey & Statistical Research Centre. Sheffield, England: Sheffield Hallam University.

3. Reynolds, K. J., Vernon, S. D., Bouchery, E., & Reeves, W. C. (2004). The economic impact of chronic fatigue syndrome. Cost Effectiveness and Resource Allocation, 2(1), 4.

4. Liberating the NHS: legislative framework and next steps. (2010). UK Department of Health. Accessed 4 April 2011. http://www.dh.gov.uk/prod_consum_dh/groups/dh_digitalassets/@dh/@en/@ps/documents/digitalasset/dh_122707.pdf .

5. Staley, K. (2009). Exploring impact: Public involvement in NHS, public health and social care research. Eastleigh: INVOLVE. Accessed 4 April 2011. http://www.invo.org.uk/pdfs/Involve_Exploring_Impactfinal28.10.09.pdf .

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