Assessing disease experience across the life span for individuals with osteogenesis imperfecta: challenges and opportunities for patient-reported outcomes (PROs) measurement: a pilot study

Assessing disease experience across the life span for individuals with osteogenesis imperfecta: challenges and opportunities for patient-reported outcomes (PROs) measurement: a pilot study

Abstract Background Patient reported outcome (PRO) information is crucial for establishing better patient-provider communication, improving shared decision-making between clinicians and patients, assessing patient responses to therapeutic interventions, and increasing satisfaction with care. We used...

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Détails bibliographiques
Auteurs principaux: Laura L. Tosi, Marianne K. Floor, Christina M. Dollar, Austin P. Gillies, Members of the Brittle Bone Disease Consortium, Tracy S. Hart, David D. Cuthbertson, V. Reid Sutton, Jeffrey P. Krischer
Format: Article
Langue:English
Publié: BMC 2019-01-01
Collection:Orphanet Journal of Rare Diseases
Sujets:
Patient reported outcomes
Patient-reported outcome measurement information system® (PROMIS®)
Health-related quality of life (HRQoL)
Osteogenesis imperfecta
Rare disease
Registry
Accès en ligne:http://link.springer.com/article/10.1186/s13023-019-1004-x

Internet

http://link.springer.com/article/10.1186/s13023-019-1004-x

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