Patient-reported outcome measures: Clinical applications in the field of chronic pain self-management
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Elander & Spitz 2017 PROMs and ...
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Abstract
Chronic pain is a major influence on patient-reported quality of life. This chapter examines ways that information from patient-reported outcome measures (PROMs) can be translated into clinical practice to improve the management and self-management of chronic pain among people with rheumatic disorders and haemophilia. This includes: 1) evidence about how PROMs can be used to improve routine clinical practice and self-management programmes in rheumatic disorders and haemophilia; 2) evidence about a DVD intervention with patient perspectives about living and coping with chronic joint pain, which improved patient-reported readiness to self-manage pain; 3) evidence about pain acceptance and pain coping as influences on patient-reported quality of life among people with haemophilia; and 4) recommendations for clinical and treatment interventions to improve patient-reported outcomes for people with haemophilia-related joint pain.Citation
Elander, J. and Spitz, E. (2017). 'Patient-reported outcome measures: clinical applications in the field of chronic pain self-management.'. In Guillemin, F., Leplege, A., Briancon, S., Spitz, E., and Coste, J. (Eds.). 'Perceived Health and Adaptation in Chronic Disease'. London: Routledge, pp. 276-293.Publisher
Routledge, Taylor and Francis GroupAdditional Links
https://www.routledge.com/Perceived-Health-and-Adaptation-in-Chronic-Disease/Guillemin-Leplege-Briancon-Spitz-Coste/p/book/9781315155074Type
Book chapterLanguage
enISBN
9781315155074Collections
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