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BMJ. 2019 Jan 24;364:k5267. doi: 10.1136/bmj.k5267.

Maximising the impact of patient reported outcome assessment for patients and society.

Author information

1
Centre for Patient Reported Outcomes Research (CPROR), Institute of Applied Health Research, and NIHR, Birmingham Biomedical Research Centre, University of Birmingham B15 2TT UK m.calvert@bham.ac.uk.
2
Centre for Patient Reported Outcomes Research (CPROR), Institute of Applied Health Research, and NIHR, Birmingham Biomedical Research Centre, University of Birmingham B15 2TT UK.
3
NIHR PenCLAHRC and Institute for Health Services Research, University of Exeter Medical School, St Luke's Campus, St Leonards, Exeter EX1 2LU, UK.
4
AmbuFlex/WestChronic, Regional Hospital West Jutland, Herning, Denmark, and Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.
PMID:
30679170
DOI:
10.1136/bmj.k5267

Conflict of interest statement

Competing interests: We have read and understood BMJ policy on conflicts of interest and declare the following: MC has received personal fees from Astellas, Takeda, and Glaukos outside the submitted work and grants from the NIHR and is a coinvestigator at Health Data Research UK Midlands. DK is supported by the NIHR postdoctoral fellowship scheme (PDF-2016-09-009). JMV has received grants and fellowships from NIHR and Instituto de Salud Carlos III (Spain), grants from MRC, CRUK, Royal Devon and Exeter Trust, Fondo de Investigaciones Sanitarias (Spain), consultancy fees from the World Health Organization, and Technische Krankenkasse (Germany) and currently is chairman (unpaid) of the International Consortium for Health Outcomes Measurement panel for the development of core sets of outcomes for Health Overall Adult Health. GP and NHH declare no competing interests.

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