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dc.contributor.authorAlonso, J
dc.contributor.authorBartlett, SJ
dc.contributor.authorRose, M
dc.contributor.authorAaronson, NK
dc.contributor.authorChaplin, JE
dc.contributor.authorEfficace, F
dc.contributor.authorLeplege, A
dc.contributor.authorLu, A
dc.contributor.authorTulsky, DS
dc.contributor.authorRaat, H
dc.contributor.authorRavens-Sieberer, U
dc.contributor.authorRevicki, D
dc.contributor.authorTerwee, CB
dc.contributor.authorValderas, JM
dc.contributor.authorCella, D
dc.contributor.authorForrest, CB
dc.contributor.authorPROMIS International Group
dc.date.accessioned2015-04-10T08:04:07Z
dc.date.issued2013-12-20
dc.description.abstractPatient-reported outcomes (PROs) play an increasingly important role in clinical practice and research. Modern psychometric methods such as item response theory (IRT) enable the creation of item banks that support fixed-length forms as well as computerized adaptive testing (CAT), often resulting in improved measurement precision and responsiveness. Here we describe and discuss the case for developing an international core set of PROs building from the US PROMIS® network. PROMIS is a U.S.-based cooperative group of research sites and centers of excellence convened to develop and standardize PRO measures across studies and settings. If extended to a global collaboration, PROMIS has the potential to transform PRO measurement by creating a shared, unifying terminology and metric for reporting of common symptoms and functional life domains. Extending a common set of standardized PRO measures to the international community offers great potential for improving patient-centered research, clinical trials reporting, population monitoring, and health care worldwide. Benefits of such standardization include the possibility of: international syntheses (such as meta-analyses) of research findings; international population monitoring and policy development; health services administrators and planners access to relevant information on the populations they serve; better assessment and monitoring of patients by providers; and improved shared decision making. The goal of the current PROMIS International initiative is to ensure that item banks are translated and culturally adapted for use in adults and children in as many countries as possible. The process includes 3 key steps: translation/cultural adaptation, calibration, and validation. A universal translation, an approach focusing on commonalities, rather than differences across versions developed in regions or countries speaking the same language, is proposed to ensure conceptual equivalence for all items. International item calibration using nationally representative samples of adults and children within countries is essential to demonstrate that all items possess expected strong measurement properties. Finally, it is important to demonstrate that the PROMIS measures are valid, reliable and responsive to change when used in an international context. IRT item banking will allow for tailoring within countries and facilitate growth and evolution of PROs through contributions from the international measurement community. A number of opportunities and challenges of international development of PROs item banks are discussed.en_GB
dc.identifier.citationHealth and Quality of Life Outcomes, 2013, Vol. 11:210en_GB
dc.identifier.doi10.1186/1477-7525-11-210
dc.identifier.urihttp://hdl.handle.net/10871/16707
dc.language.isoenen_GB
dc.publisherBioMed Centralen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/24359143en_GB
dc.rights© 2013 Alonso et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectPatient-reported outcomesen_GB
dc.subjectHealth-related quality of life researchen_GB
dc.subjectPatients' experiencesen_GB
dc.subjectQuestionnairesen_GB
dc.subjectCross-cultural equivalenceen_GB
dc.subjectHealth information systemsen_GB
dc.subjectClinical decision makingen_GB
dc.subjectComparative effectiveness researchen_GB
dc.subjectPatient empowermenten_GB
dc.subjectCross-national comparisonsen_GB
dc.titleThe case for an international patient-reported outcomes measurement information system (PROMIS (R)) initiativeen_GB
dc.typeArticleen_GB
dc.date.available2015-04-10T08:04:07Z
dc.identifier.issn1477-7525
exeter.article-numberARTN 210
dc.descriptionThis is a freely-available open access publication. Please cite the published version which is available via the DOI link in this record.en_GB
dc.identifier.journalHealth and Quality of Life Outcomesen_GB


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