Literature DB >> 29350345

Measurement invariance and general population reference values of the PROMIS Profile 29 in the UK, France, and Germany.

Felix Fischer1, Chris Gibbons2,3, Joël Coste4,5, Jose M Valderas6, Matthias Rose7,8, Alain Leplège4,9.   

Abstract

PURPOSE: Comparability of patient-reported outcome measures over different languages is essential to allow cross-national research. We investigate the comparability of the PROMIS Profile 29, a generic health-related quality of life measure, in general population samples in the UK, France, and Germany and present general population reference values.
METHODS: A web-based survey was simultaneously conducted in the UK (n = 1509), France (1501), and Germany (1502). Along with the PROMIS Profile 29, we collected sociodemographic information as well as the EQ-5D. We tested measurement invariance by means of multigroup confirmatory factor analysis (CFA). Differences in the health-related quality of life between countries were modeled by linear regression analysis. We present general population reference data for the included PROMIS domains utilizing plausible value imputation and quantile regression.
RESULTS: Multigroup CFA of the PROMIS Profile 29 showed that factor means are insensitive to potential measurement bias except in one item. We observed significant differences in patient-reported health between countries, which could be partially explained by the differences in overall ratings of health. The physical function and pain interference scales showed considerable floor effects in the normal population in all countries.
CONCLUSIONS: Scores derived from the PROMIS Profile 29 are largely comparable across the UK, France, and Germany. Due to the use of plausible value imputation, the presented general population reference values can be compared to data collected with other PROMIS short forms or computer-adaptive tests.

Entities:  

Keywords:  Cross-cultural equivalence; General population reference; Item response theory; Patient-reported outcomes; Plausible value imputation; Self-reported health

Mesh:

Year:  2018        PMID: 29350345     DOI: 10.1007/s11136-018-1785-8

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  57 in total

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Authors:  Adam W Meade; Emily C Johnson; Phillip W Braddy
Journal:  J Appl Psychol       Date:  2008-05

2.  The factor structure of the SF-36 Health Survey in 10 countries: results from the IQOLA Project. International Quality of Life Assessment.

Authors:  J E Ware; M Kosinski; B Gandek; N K Aaronson; G Apolone; P Bech; J Brazier; M Bullinger; S Kaasa; A Leplège; L Prieto; M Sullivan
Journal:  J Clin Epidemiol       Date:  1998-11       Impact factor: 6.437

3.  Comparison of health-related quality of life in patients with neuroendocrine tumors with quality of life in the general US population.

Authors:  Jennifer L Beaumont; David Cella; Alexandria T Phan; Seung Choi; Zhimei Liu; James C Yao
Journal:  Pancreas       Date:  2012-04       Impact factor: 3.327

4.  Using Patient Health Questionnaire-9 item parameters of a common metric resulted in similar depression scores compared to independent item response theory model reestimation.

Authors:  Gregor Liegl; Inka Wahl; Anne Berghöfer; Sandra Nolte; Christoph Pieh; Matthias Rose; Felix Fischer
Journal:  J Clin Epidemiol       Date:  2015-10-22       Impact factor: 6.437

5.  Development and validation of patient-reported outcome measures for sleep disturbance and sleep-related impairments.

Authors:  Daniel J Buysse; Lan Yu; Douglas E Moul; Anne Germain; Angela Stover; Nathan E Dodds; Kelly L Johnston; Melissa A Shablesky-Cade; Paul A Pilkonis
Journal:  Sleep       Date:  2010-06       Impact factor: 5.849

6.  Performance of the Patient-Reported Outcomes Measurement Information System 29-Item Profile in Rheumatoid Arthritis, Osteoarthritis, Fibromyalgia, and Systemic Lupus Erythematosus.

Authors:  Patricia Katz; Sofia Pedro; Kaleb Michaud
Journal:  Arthritis Care Res (Hoboken)       Date:  2017-08-08       Impact factor: 4.794

7.  Montreal Accord on Patient-Reported Outcomes (PROs) use series - Paper 6: creating national initiatives to support development and use-the PROMIS example.

Authors:  Susan J Bartlett; James Witter; David Cella; Sara Ahmed
Journal:  J Clin Epidemiol       Date:  2017-04-20       Impact factor: 6.437

8.  Analysis of longitudinal randomized clinical trials using item response models.

Authors:  Cees A W Glas; Hanneke Geerlings; Mart A F J van de Laar; Erik Taal
Journal:  Contemp Clin Trials       Date:  2008-12-24       Impact factor: 2.226

9.  Standardization of depression measurement: a common metric was developed for 11 self-report depression measures.

Authors:  Inka Wahl; Bernd Löwe; Jakob Bue Bjorner; Felix Fischer; Gernot Langs; Ulrich Voderholzer; Stephen A Aita; Niels Bergemann; Elmar Brähler; Matthias Rose
Journal:  J Clin Epidemiol       Date:  2014-01       Impact factor: 6.437

10.  Why item response theory should be used for longitudinal questionnaire data analysis in medical research.

Authors:  Rosalie Gorter; Jean-Paul Fox; Jos W R Twisk
Journal:  BMC Med Res Methodol       Date:  2015-07-30       Impact factor: 4.615

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  19 in total

1.  PROMIS® Adult Health Profiles: Efficient Short-Form Measures of Seven Health Domains.

Authors:  David Cella; Seung W Choi; David M Condon; Ben Schalet; Ron D Hays; Nan E Rothrock; Susan Yount; Karon F Cook; Richard C Gershon; Dagmar Amtmann; Darren A DeWalt; Paul A Pilkonis; Arthur A Stone; Kevin Weinfurt; Bryce B Reeve
Journal:  Value Health       Date:  2019-05       Impact factor: 5.725

2.  Negligible impact of differential item functioning between Black and White dialysis patients on the Kidney Disease Quality of Life 36-item short form survey (KDQOLTM-36).

Authors:  John D Peipert; Peter Bentler; Kristi Klicko; Ron D Hays
Journal:  Qual Life Res       Date:  2018-05-14       Impact factor: 4.147

3.  PROMIS®-29 v2.0 profile physical and mental health summary scores.

Authors:  Ron D Hays; Karen L Spritzer; Benjamin D Schalet; David Cella
Journal:  Qual Life Res       Date:  2018-03-22       Impact factor: 4.147

4.  Measurement properties of the Dutch PROMIS-29 v2.1 profile in people with and without chronic conditions.

Authors:  Ellen B M Elsman; Leo D Roorda; Nynke Smidt; Henrica C W de Vet; Caroline B Terwee
Journal:  Qual Life Res       Date:  2022-06-25       Impact factor: 3.440

5.  Study Design and Protocol of a Randomized Controlled Trial of the Efficacy of a Smartphone-Based Therapy of Migraine (SMARTGEM).

Authors:  Ana Sofia Oliveira Gonçalves; Inga Laumeier; Maxi Dana Hofacker; Bianca Raffaelli; Philipp Burow; Markus A Dahlem; Simon Heintz; Tim Patrick Jürgens; Steffen Naegel; Florian Rimmele; Simon Scholler; Tobias Kurth; Uwe Reuter; Lars Neeb
Journal:  Front Neurol       Date:  2022-06-16       Impact factor: 4.086

6.  Fatigue in the general population: German normative values of the EORTC QLQ-FA12.

Authors:  Andreas Hinz; Joachim Weis; Elmar Brähler; Anja Mehnert
Journal:  Qual Life Res       Date:  2018-06-16       Impact factor: 4.147

Review 7.  Utility of the Patient-Reported Outcomes Measurement Information System (PROMIS) to measure primary health outcomes in cancer patients: a systematic review.

Authors:  Thi Xuan Mai Tran; Jungeun Park; Joonki Lee; Yuh-Seog Jung; Yoonjung Chang; Hyunsoon Cho
Journal:  Support Care Cancer       Date:  2020-10-15       Impact factor: 3.603

8.  Dutch reference values for the Patient-Reported Outcomes Measurement Information System Scale v1.2 - Global Health (PROMIS-GH).

Authors:  Ellen B M Elsman; Leo D Roorda; Martine H P Crins; Maarten Boers; Caroline B Terwee
Journal:  J Patient Rep Outcomes       Date:  2021-05-12

Review 9.  The National Institutes of Health Patient-Reported Outcomes Measurement Information System (PROMIS): a view from the UK.

Authors:  Jonathan P Evans; Alexander Smith; Chris Gibbons; Jordi Alonso; Jose M Valderas
Journal:  Patient Relat Outcome Meas       Date:  2018-10-24

10.  Factors associated with direct support professionals' behaviour in the physical activity support provided to people with intellectual disabilities.

Authors:  L W M Bossink; A A J van der Putten; M C S Paap; C Vlaskamp
Journal:  J Intellect Disabil Res       Date:  2019-04-03
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