Skip to main content
Top
Published in: Health and Quality of Life Outcomes 1/2013

Open Access 01-12-2013 | Commentary

The case for an international patient-reported outcomes measurement information system (PROMIS®) initiative

Authors: Jordi Alonso, Susan J Bartlett, Matthias Rose, Neil K Aaronson, John E Chaplin, Fabio Efficace, Alain Leplège, Aiping LU, David S Tulsky, Hein Raat, Ulrike Ravens-Sieberer, Dennis Revicki, Caroline B Terwee, Jose M Valderas, David Cella, Christopher B Forrest, for the PROMIS International group

Published in: Health and Quality of Life Outcomes | Issue 1/2013

Login to get access

Abstract

Patient-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.
Appendix
Available only for authorised users
Literature
1.
go back to reference McHorney CA: Health status assessment methods for adults: past accomplishments and future challenges. Annu Rev Public Health 1999, 20: 309–335. 10.1146/annurev.publhealth.20.1.309PubMedCrossRef McHorney CA: Health status assessment methods for adults: past accomplishments and future challenges. Annu Rev Public Health 1999, 20: 309–335. 10.1146/annurev.publhealth.20.1.309PubMedCrossRef
2.
go back to reference Calvert M, Blazeby J, Altman DG, Revicki DA, Moher D, Brundage MD: Reporting of patient-reported outcomes in randomized trials: the CONSORT PRO extension. JAMA 2013, 309: 814–822. 10.1001/jama.2013.879PubMedCrossRef Calvert M, Blazeby J, Altman DG, Revicki DA, Moher D, Brundage MD: Reporting of patient-reported outcomes in randomized trials: the CONSORT PRO extension. JAMA 2013, 309: 814–822. 10.1001/jama.2013.879PubMedCrossRef
3.
go back to reference Valderas JM, Kotzeva A, Espallargues M, Guyatt G, Ferrans CE, Halyard MY, Revicki DA, Symonds T, Parada A, Alonso J: The impact of measuring patient-reported outcomes in clinical practice: a systematic review of the literature. Qual Life Res 2008, 17: 179–193. 10.1007/s11136-007-9295-0PubMedCrossRef Valderas JM, Kotzeva A, Espallargues M, Guyatt G, Ferrans CE, Halyard MY, Revicki DA, Symonds T, Parada A, Alonso J: The impact of measuring patient-reported outcomes in clinical practice: a systematic review of the literature. Qual Life Res 2008, 17: 179–193. 10.1007/s11136-007-9295-0PubMedCrossRef
4.
go back to reference Black N: Patient reported outcome measures could help transform healthcare. BMJ 2013, 346: f167. 10.1136/bmj.f167PubMedCrossRef Black N: Patient reported outcome measures could help transform healthcare. BMJ 2013, 346: f167. 10.1136/bmj.f167PubMedCrossRef
5.
go back to reference Cella D, Riley W, Stone A, Rothrock N, Reeve B, Yount S, Amtmann D, Bode R, Buysse D, Choi S, et al.: The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008. J Clin Epidemiol 2010, 63: 1179–1194. 10.1016/j.jclinepi.2010.04.011PubMedCentralPubMedCrossRef Cella D, Riley W, Stone A, Rothrock N, Reeve B, Yount S, Amtmann D, Bode R, Buysse D, Choi S, et al.: The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008. J Clin Epidemiol 2010, 63: 1179–1194. 10.1016/j.jclinepi.2010.04.011PubMedCentralPubMedCrossRef
6.
go back to reference Forrest CB, Bevans KB, Tucker C, Riley AW, Ravens-Sieberer U, Gardner W, Pajer K: Commentary: the patient-reported outcome measurement information system (PROMIS(R)) for children and youth: application to pediatric psychology. J Pediatr Psychol 2012, 37: 614–621. 10.1093/jpepsy/jss038PubMedCentralPubMedCrossRef Forrest CB, Bevans KB, Tucker C, Riley AW, Ravens-Sieberer U, Gardner W, Pajer K: Commentary: the patient-reported outcome measurement information system (PROMIS(R)) for children and youth: application to pediatric psychology. J Pediatr Psychol 2012, 37: 614–621. 10.1093/jpepsy/jss038PubMedCentralPubMedCrossRef
7.
go back to reference Reeve BB, Hays RD, Bjorner JB, Cook KF, Crane PK, Teresi JA, Thissen D, Revicki DA, Weiss DJ, Hambleton RK, et al.: Psychometric evaluation and calibration of health-related quality of life item banks: plans for the Patient-Reported Outcomes Measurement Information System (PROMIS). Med Care 2007, 45: S22-S31. 10.1097/01.mlr.0000250483.85507.04PubMedCrossRef Reeve BB, Hays RD, Bjorner JB, Cook KF, Crane PK, Teresi JA, Thissen D, Revicki DA, Weiss DJ, Hambleton RK, et al.: Psychometric evaluation and calibration of health-related quality of life item banks: plans for the Patient-Reported Outcomes Measurement Information System (PROMIS). Med Care 2007, 45: S22-S31. 10.1097/01.mlr.0000250483.85507.04PubMedCrossRef
8.
go back to reference Dewalt DA, Rothrock N, Yount S, Stone AA: Evaluation of item candidates: the PROMIS qualitative item review. Med Care 2007, 45: S12-S21. 10.1097/01.mlr.0000254567.79743.e2PubMedCentralPubMedCrossRef Dewalt DA, Rothrock N, Yount S, Stone AA: Evaluation of item candidates: the PROMIS qualitative item review. Med Care 2007, 45: S12-S21. 10.1097/01.mlr.0000254567.79743.e2PubMedCentralPubMedCrossRef
9.
go back to reference Gershon RC, Rothrock N, Hanrahan R, Bass M, Cella D: The use of PROMIS and assessment center to deliver patient-reported outcome measures in clinical research. J Appl Meas 2010, 11: 304–314.PubMedCentralPubMed Gershon RC, Rothrock N, Hanrahan R, Bass M, Cella D: The use of PROMIS and assessment center to deliver patient-reported outcome measures in clinical research. J Appl Meas 2010, 11: 304–314.PubMedCentralPubMed
10.
go back to reference Bullinger M, Alonso J, Apolone G, Leplege A, Sullivan M, Wood-Dauphinee S, Gandek B, Wagner A, Aaranson NK, Bech P, et al.: Translating health status questionnaires and evaluating their quality: the IQOLA Project approach. International Quality of Life Assessment. J Clin Epidemiol 1998, 51: 913–923. 10.1016/S0895-4356(98)00082-1PubMedCrossRef Bullinger M, Alonso J, Apolone G, Leplege A, Sullivan M, Wood-Dauphinee S, Gandek B, Wagner A, Aaranson NK, Bech P, et al.: Translating health status questionnaires and evaluating their quality: the IQOLA Project approach. International Quality of Life Assessment. J Clin Epidemiol 1998, 51: 913–923. 10.1016/S0895-4356(98)00082-1PubMedCrossRef
11.
go back to reference Eremenco SL, Cella D, Arnold BJ: A comprehensive method for the translation and cross-cultural validation of health status questionnaires. Eval Health Prof 2005, 28: 212–232. 10.1177/0163278705275342PubMedCrossRef Eremenco SL, Cella D, Arnold BJ: A comprehensive method for the translation and cross-cultural validation of health status questionnaires. Eval Health Prof 2005, 28: 212–232. 10.1177/0163278705275342PubMedCrossRef
Metadata
Title
The case for an international patient-reported outcomes measurement information system (PROMIS®) initiative
Authors
Jordi Alonso
Susan J Bartlett
Matthias Rose
Neil K Aaronson
John E Chaplin
Fabio Efficace
Alain Leplège
Aiping LU
David S Tulsky
Hein Raat
Ulrike Ravens-Sieberer
Dennis Revicki
Caroline B Terwee
Jose M Valderas
David Cella
Christopher B Forrest
for the PROMIS International group
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Health and Quality of Life Outcomes / Issue 1/2013
Electronic ISSN: 1477-7525
DOI
https://doi.org/10.1186/1477-7525-11-210

Other articles of this Issue 1/2013

Health and Quality of Life Outcomes 1/2013 Go to the issue