Literature DB >> 30448911

Implementing patient-reported outcome measures in clinical practice: a companion guide to the ISOQOL user's guide.

Eric K H Chan1,2, Todd C Edwards3, Kirstie Haywood4, Sean P Mikles5, Louise Newton6.   

Abstract

PURPOSE: The use of patient-reported outcome (PRO) measures in clinical practice is increasing. Following the creation of a 'User's Guide to Implementing PRO Assessment in Clinical Practice' by the International Society for Quality of Life Research (ISOQOL), volunteers from ISOQOL sought to create a Companion Guide to assist health care providers with the scientific and practical considerations involved in implementing and using PRO measures in clinical care by using information from real-world case studies. This paper summarizes the key issues presented in the Companion Guide.
METHODS: Ten respondents, who were members of the ISOQOL's CP-SIG and worked in various clinical areas, participated in a survey or telephone interview. Participants were from Canada (n = 2), Denmark (n = 1), England (n = 2), Holland (n = 1), and the United States (n = 4).
RESULTS: Based on the information provided by respondents, a Companion Guide was produced, organized according to the nine questions presented in the User's Guide. An additional section for key take-home messages was also provided. This guide provides examples of issues and considerations related to the implementation of PRO measures in clinical practice.
CONCLUSIONS: Respondents provided insight into their experiences and emphasized that PRO initiatives were likely to be more successful if there is purposeful, designed integration into clinical practice, meaningful substantive engagement with all stakeholders and access to necessary organizational resources. The ability to leverage existing technology as well as realistic and stakeholder consensus-driven expectations for planning and timing were also key to the successful implementation of PRO measures.

Entities:  

Keywords:  Clinical practice; Guidelines; ISOQOL; Implementation; PRO; Patient-reported outcome

Mesh:

Year:  2018        PMID: 30448911      PMCID: PMC8084633          DOI: 10.1007/s11136-018-2048-4

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


  8 in total

1.  Continence specialists use of quality of life information in routine practice: a national survey of practitioners.

Authors:  Kirstie L Haywood; Andrew M Garratt; Sandra Carrivick; Joanne Mangnall; Suzanne M Skevington
Journal:  Qual Life Res       Date:  2009-03-07       Impact factor: 4.147

2.  The triple aim: care, health, and cost.

Authors:  Donald M Berwick; Thomas W Nolan; John Whittington
Journal:  Health Aff (Millwood)       Date:  2008 May-Jun       Impact factor: 6.301

3.  Linking clinical variables with health-related quality of life. A conceptual model of patient outcomes.

Authors:  I B Wilson; P D Cleary
Journal:  JAMA       Date:  1995-01-04       Impact factor: 56.272

Review 4.  The impact of measuring patient-reported outcomes in clinical practice: a systematic review of the literature.

Authors:  J M Valderas; A Kotzeva; M Espallargues; G Guyatt; C E Ferrans; M Y Halyard; D A Revicki; T Symonds; A Parada; J Alonso
Journal:  Qual Life Res       Date:  2008-01-04       Impact factor: 4.147

5.  Using patient-reported outcomes in clinical practice: challenges and opportunities.

Authors:  Kathleen N Lohr; Bradley J Zebrack
Journal:  Qual Life Res       Date:  2008-11-25       Impact factor: 4.147

6.  Measuring quality of life in routine oncology practice improves communication and patient well-being: a randomized controlled trial.

Authors:  Galina Velikova; Laura Booth; Adam B Smith; Paul M Brown; Pamela Lynch; Julia M Brown; Peter J Selby
Journal:  J Clin Oncol       Date:  2004-02-15       Impact factor: 44.544

7.  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

Review 8.  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

  8 in total
  22 in total

1.  Feasibility of health-related quality of life (HRQoL) assessment for cancer patients using electronic patient-reported outcome (ePRO) in daily clinical practice.

Authors:  Guillaume Mouillet; Antoine Falcoz; Joëlle Fritzsch; Hamadi Almotlak; Pascale Jacoulet; Xavier Pivot; Cristian Villanueva; Laura Mansi; Stefano Kim; Elsa Curtit; Nathalie Meneveau; Olivier Adotevi; Marine Jary; Guillaume Eberst; Angelique Vienot; Fabien Calcagno; Astrid Pozet; Oumelkheir Djoumakh; Christophe Borg; Virginie Westeel; Amélie Anota; Sophie Paget-Bailly
Journal:  Qual Life Res       Date:  2021-01-02       Impact factor: 4.147

2.  Considerations to Support Use of Patient-Reported Outcomes Measurement Information System Pediatric Measures in Ambulatory Clinics.

Authors:  Elizabeth D Cox; Sarah K Dobrozsi; Christopher B Forrest; Wendy E Gerhardt; Harald Kliems; Bryce B Reeve; Nan E Rothrock; Jin-Shei Lai; Jacob M Svenson; Lindsay A Thompson; Thuy Dan N Tran; Carole A Tucker
Journal:  J Pediatr       Date:  2020-11-30       Impact factor: 4.406

3.  Health-related quality of life assessment for patients with advanced or metastatic renal cell carcinoma treated with a tyrosine kinase inhibitor using electronic patient-reported outcomes in daily clinical practice (QUANARIE trial): study protocol.

Authors:  Guillaume Mouillet; Joëlle Fritzsch; Sophie Paget-Bailly; Astrid Pozet; Ikram Es-Saad; Aurelia Meurisse; Dewi Vernerey; Kristina Mouyabi; Diane Berthod; Franck Bonnetain; Amélie Anota; Antoine Thiery-Vuillemin
Journal:  Health Qual Life Outcomes       Date:  2019-02-04       Impact factor: 3.186

4.  Electronic symptom monitoring in patients with metastatic lung cancer: a feasibility study.

Authors:  Rasmus Blechingberg Friis; Niels Henrik Hjollund; Caroline Trillingsgaard Mejdahl; Helle Pappot; Halla Skuladottir
Journal:  BMJ Open       Date:  2020-06-17       Impact factor: 2.692

5.  How do third sector organisations or charities providing health and well-being services in England implement patient-reported outcome measures (PROMs)? A qualitative interview study.

Authors:  Alexis Foster; Alicia O'Cathain; Janet Harris
Journal:  BMJ Open       Date:  2020-10-07       Impact factor: 2.692

6.  Planning for patient-reported outcome implementation: Development of decision tools and practical experience across four clinics.

Authors:  Therese A Nelson; Brigitte Anderson; Jiang Bian; Andrew D Boyd; Shirley V Burton; Kristina Davis; Yi Guo; Bhrandon A Harris; Kelly Hynes; Karl M Kochendorfer; David Liebovitz; Kayla Martin; François Modave; John Moses; Nicholas D Soulakis; Donald Weinbrenner; Sonya H White; Nan E Rothrock; Annette L Valenta; Justin B Starren
Journal:  J Clin Transl Sci       Date:  2020-04-06

7.  Completion of Patient-Reported Outcome Questionnaires Among Older Adults with Advanced Cancer.

Authors:  Marie A Flannery; Supriya Mohile; Eva Culakova; Sally Norton; Charles Kamen; J Nicholas Dionne-Odom; Grace DiGiovanni; Lorraine Griggs; Thomas Bradley; Judith O Hopkins; Jane Jijun Liu; Kah Poh Loh
Journal:  J Pain Symptom Manage       Date:  2021-08-08       Impact factor: 3.612

8.  Acceptability of patient reported outcome measures (PROMs) in a cystic fibrosis data registry.

Authors:  Irushi Ratnayake; Susannah Ahern; Rasa Ruseckaite
Journal:  BMJ Open Respir Res       Date:  2021-07

9.  Clinical Use of PROMIS, Neuro-QoL, TBI-QoL, and Other Patient-Reported Outcome Measures for Individual Adult Clients with Cognitive and Language Disorders.

Authors:  Matthew L Cohen; Alyssa M Lanzi; Aaron J Boulton
Journal:  Semin Speech Lang       Date:  2021-07-14       Impact factor: 1.734

10.  Collection and use of EQ-5D for follow-up, decision-making, and quality improvement in health care - the case of the Swedish National Quality Registries.

Authors:  Olivia Ernstsson; Mathieu F Janssen; Emelie Heintz
Journal:  J Patient Rep Outcomes       Date:  2020-09-16
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