Literature DB >> 31414025

Variation and Change Over Time in PROMIS-29 Survey Results Among Primary Care Patients With Type 2 Diabetes.

Juell Homco1, Kristin Rodriguez1, David R Bardach2, Elizabeth A Hahn3, Suzanne Morton2, Daren Anderson4, David Kendrick1, Sarah Hudson Scholle2.   

Abstract

PURPOSE: We sought to describe results of patient-reported outcome measures implemented among primary care patients with diabetes and explore factors associated with changes in scores over time.
METHODS: Two organizations serving diverse patient populations collected the PROMIS-29 survey at baseline and 3-month follow-up for patients with type 2 diabetes. Bayesian regression analysis was used to examine the relationship between patient characteristics and changes in PROMIS-29 scores. Exploratory analyses assessed relationships between goal-setting and changes in scores.
RESULTS: The study population reported substantially more problems with physical functioning (mean: 42.5 at Site 1 and 38.9 at Site 2) and pain interference (mean: 58.0 at Site 1 and 61.1 at Site 2) compared to the general population (mean: 50; standard deviation: 10). At least 33% of patients had a clinically meaningful change (ie, at least half the standard deviation, or 5 points) in each PROMIS domain. For pain interference, 55% had no change, 22% improved by 5 or more points, and 23% worsened by 5 or more points. Bayesian regression analyses suggest that chronic conditions, insurance status, and Hispanic ethnicity are likely associated with decreased functioning over time. Exploratory analyses found that setting a mental health goal did not appear to be associated with improvement for anxiety or depression.
CONCLUSIONS: Use of patient-reported outcome measures in routine clinical care identified areas of functional limitations among people with diabetes. However, changes in participants' PROMIS-29 scores over time were minimal. Research is needed to understand patterns of change in global and domain-specific functioning, particularly among racial/ethnic minorities.

Entities:  

Keywords:  health care planning; health-related quality of life; outcome measurement; patient-reported outcomes

Year:  2019        PMID: 31414025      PMCID: PMC6676762          DOI: 10.17294/2330-0698.1694

Source DB:  PubMed          Journal:  J Patient Cent Res Rev        ISSN: 2330-068X


  25 in total

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Authors:  D J Spiegelhalter; J P Myles; D R Jones; K R Abrams
Journal:  BMJ       Date:  1999-08-21

Review 2.  Interpretation of changes in health-related quality of life: the remarkable universality of half a standard deviation.

Authors:  Geoffrey R Norman; Jeff A Sloan; Kathleen W Wyrwich
Journal:  Med Care       Date:  2003-05       Impact factor: 2.983

3.  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

4.  Representativeness of the Patient-Reported Outcomes Measurement Information System Internet panel.

Authors:  Honghu Liu; David Cella; Richard Gershon; Jie Shen; Leo S Morales; William Riley; Ron D Hays
Journal:  J Clin Epidemiol       Date:  2010-08-05       Impact factor: 6.437

5.  The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005-2008.

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Journal:  J Clin Epidemiol       Date:  2010-08-04       Impact factor: 6.437

Review 6.  Implementing patient-reported outcomes assessment in clinical practice: a review of the options and considerations.

Authors:  Claire F Snyder; Neil K Aaronson; Ali K Choucair; Thomas E Elliott; Joanne Greenhalgh; Michele Y Halyard; Rachel Hess; Deborah M Miller; Bryce B Reeve; Maria Santana
Journal:  Qual Life Res       Date:  2011-11-03       Impact factor: 4.147

Review 7.  Communication interventions make a difference in conversations between physicians and patients: a systematic review of the evidence.

Authors:  Jaya K Rao; Lynda A Anderson; Thomas S Inui; Richard M Frankel
Journal:  Med Care       Date:  2007-04       Impact factor: 2.983

8.  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

9.  Responsiveness and minimal important differences for patient reported outcomes.

Authors:  Dennis A Revicki; David Cella; Ron D Hays; Jeff A Sloan; William R Lenderking; Neil K Aaronson
Journal:  Health Qual Life Outcomes       Date:  2006-09-27       Impact factor: 3.186

10.  Can teaching agenda-setting skills to physicians improve clinical interaction quality? A controlled intervention.

Authors:  Hector P Rodriguez; Michael P Anastario; Richard M Frankel; Esosa G Odigie; William H Rogers; Ted von Glahn; Dana G Safran
Journal:  BMC Med Educ       Date:  2008-01-14       Impact factor: 2.463

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Journal:  Thyroid       Date:  2020-04-16       Impact factor: 6.568

2.  Symptoms in the general Norwegian adult population - prevalence and associated factors.

Authors:  Hilde Krogstad; Jon Håvard Loge; Kjersti S Grotmol; Stein Kaasa; Cecilie E Kiserud; Øyvind Salvesen; Marianne Jensen Hjermstad
Journal:  BMC Public Health       Date:  2020-06-23       Impact factor: 3.295

3.  The Prevalence of Depression Symptoms and Their Socioeconomic and Health Predictors in a Local Community with a High Deprivation: A Cross-Sectional Studies.

Authors:  Maciej Polak; Grzegorz Józef Nowicki; Katarzyna Naylor; Robert Piekarski; Barbara Ślusarska
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