Literature DB >> 33170400

Patient-reported experience with patient-reported outcome measures in adult patients seen in rheumatology clinics.

Brittany R Lapin1,2, Ryan Honomichl3,4, Nicolas Thompson3,4, Susannah Rose5, Abby Abelson6, Chad Deal6, Irene L Katzan4.   

Abstract

OBJECTIVES: Patient-reported outcome measures (PROMs) are increasingly utilized in the evaluation of patients with rheumatic diseases. The aim of our study was to assess the patient experience with completing PROMs within rheumatology clinics, and identify patient characteristics associated with a more positive experience.
METHODS: We conducted a retrospective cross-sectional study of adult patients seen in rheumatology clinics between 1/1/2017 and 6/30/2017. Patients were included in the study if they completed at least one patient-reported experience question following completion of PROMs. Patient characteristics associated with more positive experiences were identified through multivariable proportional odds models.
RESULTS: 12,597 adult patients (mean age 59 ± 15; 76% female; 84% white) completed PROMs, as well as questions on their experience completing PROMs. Patients agreed/strongly agreed that PROM questions were easy to understand (97%), useful (84%), helped their physician understand their health (78%), improved communication with their provider (78%) and improved control over their own care (70%). Predictors of better experience with PROMs included being younger, non-white, having lower income, and being a new patient. Worse self-reported health also predicted better experience with PROMs.
CONCLUSION: Our study found a positive patient experience with PROMs, which is a crucial component of their successful implementation and utilization. Findings from this study suggest PROMs may be particularly beneficial in new patients, minorities, those with lower income, and worse self-reported quality of life. Collecting PROMs could provide opportunities to improve patient-provider communication and enhance control over care for rheumatology patients who could most benefit.

Entities:  

Keywords:  Depression; Outcome measures; Primary care rheumatology; Quality of health care; Quality of life

Mesh:

Year:  2020        PMID: 33170400     DOI: 10.1007/s11136-020-02692-2

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


  36 in total

1.  Perceptions of Patients, Caregivers, and Healthcare Providers of Idiopathic Inflammatory Myopathies: An International OMERACT Study.

Authors:  Christopher A Mecoli; Jin Kyun Park; Helene Alexanderson; Malin Regardt; Merrilee Needham; Ingrid de Groot; Catherine Sarver; Ingrid E Lundberg; Beverley Shea; Marianne de Visser; Yeong Wook Song; Clifton O Bingham; Lisa Christopher-Stine
Journal:  J Rheumatol       Date:  2018-09-15       Impact factor: 4.666

2.  Patient-Reported Symptom Monitoring During Chemotherapy-Reply.

Authors:  Ethan Basch; Allison M Deal; Amylou C Dueck
Journal:  JAMA       Date:  2017-11-21       Impact factor: 56.272

3.  Impact of patient-reported outcomes in oncology: a longitudinal analysis of patient-physician communication.

Authors:  Elena E Takeuchi; Ada Keding; Noha Awad; Ursula Hofmann; Lyndsay J Campbell; Peter J Selby; Julia M Brown; Galina Velikova
Journal:  J Clin Oncol       Date:  2011-06-20       Impact factor: 44.544

Review 4.  Patient-Reported Outcomes Measurement Information System Versus Legacy Instruments: Are They Ready for Prime Time?

Authors:  Vivian P Bykerk
Journal:  Rheum Dis Clin North Am       Date:  2019-05       Impact factor: 2.670

Review 5.  The Promise of Patient-Reported Outcomes Measurement Information System-Turning Theory into Reality: A Uniform Approach to Patient-Reported Outcomes Across Rheumatic Diseases.

Authors:  James P Witter
Journal:  Rheum Dis Clin North Am       Date:  2016-05       Impact factor: 2.670

6.  Establishing clinical severity for PROMIS® measures in adult patients with rheumatic diseases.

Authors:  Vivek Nagaraja; Constance Mara; Puja P Khanna; Rajaie Namas; Amber Young; David A Fox; Timothy Laing; William J McCune; Carol Dodge; Debra Rizzo; Maha Almackenzie; Dinesh Khanna
Journal:  Qual Life Res       Date:  2017-10-05       Impact factor: 4.147

7.  Reliability and Validity of Selected PROMIS Measures in People with Rheumatoid Arthritis.

Authors:  Susan J Bartlett; Ana-Maria Orbai; Trisha Duncan; Elaine DeLeon; Victoria Ruffing; Katherine Clegg-Smith; Clifton O Bingham
Journal:  PLoS One       Date:  2015-09-17       Impact factor: 3.240

8.  PRO-based follow-up as a means of self-management support - an interpretive description of the patient perspective.

Authors:  Caroline Trillingsgaard Mejdahl; Liv Marit Valen Schougaard; Niels Henrik Hjollund; Erik Riiskjær; Sally Thorne; Kirsten Lomborg
Journal:  J Patient Rep Outcomes       Date:  2018-09-05

Review 9.  A systematic review of the impact of routine collection of patient reported outcome measures on patients, providers and health organisations in an oncologic setting.

Authors:  Jack Chen; Lixin Ou; Stephanie J Hollis
Journal:  BMC Health Serv Res       Date:  2013-06-11       Impact factor: 2.655

Review 10.  How do patient reported outcome measures (PROMs) support clinician-patient communication and patient care? A realist synthesis.

Authors:  Joanne Greenhalgh; Kate Gooding; Elizabeth Gibbons; Sonia Dalkin; Judy Wright; Jose Valderas; Nick Black
Journal:  J Patient Rep Outcomes       Date:  2018-09-15
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  4 in total

1.  Impetus of US hospital leaders to invest in patient-reported outcome measures (PROMs): a qualitative study.

Authors:  Danny Mou; Christer Mjaset; Claire M Sokas; Azan Virji; Barbara Bokhour; Marilyn Heng; Rachel C Sisodia; Andrea L Pusic; Meredith B Rosenthal
Journal:  BMJ Open       Date:  2022-07-06       Impact factor: 3.006

2.  From individualised treatment goals to personalised rehabilitation in osteoarthritis: a longitudinal prospective mapping study using the WHO international classification for functioning, disability and health.

Authors:  Sinisa Stefanac; Claudia Oppenauer; Michael Zauner; Martina Durechova; Daffodil Dioso; Daniel Aletaha; Gerhard Hobusch; Reinhard Windhager; Tanja Stamm
Journal:  Ann Med       Date:  2022-12       Impact factor: 5.348

3.  Validation and Adjustment of the Patient Experience Questionnaire (PEQ): A Regional Hospital Study in Norway.

Authors:  Seth Ayisi Addo; Reidar Johan Mykletun; Espen Olsen
Journal:  Int J Environ Res Public Health       Date:  2021-07-03       Impact factor: 3.390

4.  Patients' and parents' perspective on the implementation of Patient Reported Outcome Measures in pediatric clinical practice using the KLIK PROM portal.

Authors:  Maud M van Muilekom; Lorynn Teela; Hedy A van Oers; Johannes B van Goudoever; Martha A Grootenhuis; Lotte Haverman
Journal:  Qual Life Res       Date:  2021-07-29       Impact factor: 4.147

  4 in total

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