Literature DB >> 21958918

The PROMIS initiative: involvement of rehabilitation stakeholders in development and examples of applications in rehabilitation research.

Dagmar Amtmann1, Karon F Cook, Kurt L Johnson, David Cella.   

Abstract

To fully capture the impact of a disease or condition on the lives of individuals, patient-reported outcomes are considered a necessary component of health measurement in rehabilitation. This article provides an overview of the involvement of rehabilitation stakeholders in the development of sound measurement tools for the Patient-Reported Outcomes Measurement Information System (PROMIS), a National Institutes of Health-funded initiative. PROMIS is a multisite study that included many different populations. We focus on the involvement of people with several chronic conditions, including multiple sclerosis, spinal cord injury, and arthritis, in the development of PROMIS measures. We describe both qualitative and quantitative methods used, including expert panels, focus groups, cognitive interviews, and item response theory modeling, which resulted in enhanced utility of PROMIS measures in rehabilitation. Measures include a set of global health items and 12 item banks representing 6 domains. Scores are reported in the T score metric (mean ± SD, 50 ± 10) and centered on mean values from the U.S. general population. The PROMIS item banks measure quality of life and symptoms of people with chronic conditions and have the potential to enhance research and clinical practice by facilitating comparisons of scores across domains and populations.
Copyright © 2011 American Congress of Rehabilitation Medicine. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21958918      PMCID: PMC3668854          DOI: 10.1016/j.apmr.2011.04.025

Source DB:  PubMed          Journal:  Arch Phys Med Rehabil        ISSN: 0003-9993            Impact factor:   3.966


  43 in total

1.  Psychometric evaluation and calibration of health-related quality of life item banks: plans for the Patient-Reported Outcomes Measurement Information System (PROMIS).

Authors:  Bryce B Reeve; Ron D Hays; Jakob B Bjorner; Karon F Cook; Paul K Crane; Jeanne A Teresi; David Thissen; Dennis A Revicki; David J Weiss; Ronald K Hambleton; Honghu Liu; Richard Gershon; Steven P Reise; Jin-shei Lai; David Cella
Journal:  Med Care       Date:  2007-05       Impact factor: 2.983

2.  The future of outcomes measurement: item banking, tailored short-forms, and computerized adaptive assessment.

Authors:  David Cella; Richard Gershon; Jin-Shei Lai; Seung Choi
Journal:  Qual Life Res       Date:  2007-03-31       Impact factor: 4.147

3.  Development of a PROMIS item bank to measure pain interference.

Authors:  Dagmar Amtmann; Karon F Cook; Mark P Jensen; Wen-Hung Chen; Seung Choi; Dennis Revicki; David Cella; Nan Rothrock; Francis Keefe; Leigh Callahan; Jin-Shei Lai
Journal:  Pain       Date:  2010-07       Impact factor: 6.961

4.  Health status identifies heart failure outpatients at risk for hospitalization or death.

Authors:  Paul A Heidenreich; John A Spertus; Philip G Jones; William S Weintraub; John S Rumsfeld; Saif S Rathore; Eric D Peterson; Frederick A Masoudi; Harlan M Krumholz; Edward P Havranek; Mark W Conard; Randall E Williams
Journal:  J Am Coll Cardiol       Date:  2006-01-26       Impact factor: 24.094

Review 5.  Patient-reported outcomes in cystic fibrosis.

Authors:  Christopher H Goss; Alexandra L Quittner
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

6.  Development and validation of the Congestion Quantifier seven-item test (CQ7): a screening tool for nasal congestion.

Authors:  Donald E Stull; John Krouse; Eli O Meltzer; Laurie Roberts; Susan Kim; Lori Frank; Robert Naclerio; Valerie Lund; Aidan Long
Journal:  Value Health       Date:  2007 Nov-Dec       Impact factor: 5.725

7.  Evaluation of item candidates: the PROMIS qualitative item review.

Authors:  Darren A DeWalt; Nan Rothrock; Susan Yount; Arthur A Stone
Journal:  Med Care       Date:  2007-05       Impact factor: 2.983

8.  The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years.

Authors:  David Cella; Susan Yount; Nan Rothrock; Richard Gershon; Karon Cook; Bryce Reeve; Deborah Ader; James F Fries; Bonnie Bruce; Mattias Rose
Journal:  Med Care       Date:  2007-05       Impact factor: 2.983

9.  Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance.

Authors: 
Journal:  Health Qual Life Outcomes       Date:  2006-10-11       Impact factor: 3.186

10.  Validation of two generic patient-reported outcome measures in patients with type 2 diabetes.

Authors:  Louis S Matza; Kristina S Boye; Nicole Yurgin
Journal:  Health Qual Life Outcomes       Date:  2007-07-31       Impact factor: 3.186

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  44 in total

1.  The relationship of age, function, and psychological distress in multiple sclerosis.

Authors:  Salene M W Jones; Dagmar Amtmann
Journal:  Psychol Health Med       Date:  2014-11-04       Impact factor: 2.423

2.  Querying stakeholders to inform comparative effectiveness research.

Authors:  Yoon Duk Hong; Daisuke Goto; C Daniel Mullins
Journal:  J Comp Eff Res       Date:  2017-05-09       Impact factor: 1.744

3.  Conducting Accessible Research: Including People With Disabilities in Public Health, Epidemiological, and Outcomes Studies.

Authors:  Dianne Rios; Susan Magasi; Catherine Novak; Mark Harniss
Journal:  Am J Public Health       Date:  2016-10-13       Impact factor: 9.308

4.  Development of items that assess physical function in children who use wheelchairs.

Authors:  Cheryl I Kerfeld; Brian J Dudgeon; Joyce M Engel; Deborah Kartin
Journal:  Pediatr Phys Ther       Date:  2013       Impact factor: 3.049

5.  Do measures of depressive symptoms function differently in people with spinal cord injury versus primary care patients: the CES-D, PHQ-9, and PROMIS®-D.

Authors:  Karon F Cook; Michael A Kallen; Charles Bombardier; Alyssa M Bamer; Seung W Choi; Jiseon Kim; Rana Salem; Dagmar Amtmann
Journal:  Qual Life Res       Date:  2016-07-14       Impact factor: 4.147

6.  Symptoms and quality of life indicators among children with chronic medical conditions.

Authors:  Jiseon Kim; Hyewon Chung; Dagmar Amtmann; Rana Salem; Ryoungsun Park; Robert L Askew
Journal:  Disabil Health J       Date:  2013-10-12       Impact factor: 2.554

7.  Use of cognitive interviews in the development of the PLUS-M item bank.

Authors:  Sara J Morgan; Dagmar Amtmann; Daniel C Abrahamson; Andre J Kajlich; Brian J Hafner
Journal:  Qual Life Res       Date:  2014-01-20       Impact factor: 4.147

8.  Development of a novel positive psychology-based intervention for couples post-stroke.

Authors:  Alexandra L Terrill; Maija Reblin; Justin J MacKenzie; Beth Cardell; Jackie Einerson; Cynthia A Berg; Jennifer J Majersik; Lorie Richards
Journal:  Rehabil Psychol       Date:  2018-02

9.  Measuring pain phenomena after spinal cord injury: Development and psychometric properties of the SCI-QOL Pain Interference and Pain Behavior assessment tools.

Authors:  Matthew L Cohen; Pamela A Kisala; Trevor A Dyson-Hudson; David S Tulsky
Journal:  J Spinal Cord Med       Date:  2017-02-10       Impact factor: 1.985

10.  The International Spinal Cord Injury Pain Extended Data Set (Version 1.0).

Authors:  E Widerström-Noga; F Biering-Sørensen; T N Bryce; D D Cardenas; N B Finnerup; M P Jensen; J S Richards; E J Richardson; P J Siddall
Journal:  Spinal Cord       Date:  2016-04-12       Impact factor: 2.772

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