Literature DB >> 30498892

In proportion: approaches for displaying patient-reported outcome research study results as percentages responding to treatment.

Elliott Tolbert1,2, Michael Brundage3, Elissa Bantug4, Amanda L Blackford4,5, Katherine Smith6,4,7, Claire Snyder8,6,4,9.   

Abstract

PURPOSE: Patient-reported outcome (PRO) data from clinical trials can promote valuable patient-clinician communication and aid the decision-making process regarding treatment options. Despite these benefits, both patients and doctors face challenges in interpreting PRO scores. The purpose of this study was to identify best practices for presenting PRO results expressed as proportions of patients with changes from baseline (improved/stable/worsened) for use in patient educational materials and decision aids.
METHODS: We electronically surveyed adult cancer patients/survivors, oncology clinicians, and PRO researchers, and conducted one-on-one cognitive interviews with patients/survivors and clinicians. Participants saw clinical trial data comparing two treatments as proportions changed using three different formats: pie charts, bar graphs, icon arrays. Interpretation accuracy, clarity, and format preference were analyzed quantitatively and online survey comments and interviews, qualitatively.
RESULTS: The internet sample included 629 patients, 139 clinicians, and 249 researchers; 10 patients and 5 clinicians completed interviews. Bar graphs were less accurately interpreted than pie charts (OR 0.39; p < .0001) and icon arrays (OR 0.47; p < .0001). Bar graphs and icon arrays were less likely to be rated clear than pie charts (OR 0.37 and OR 0.18; both p < .0001). Qualitative data informed interpretation of these findings.
CONCLUSIONS: For communicating PROs as proportions changed in patient educational materials and decision aids, these results support the use of pie charts.

Entities:  

Keywords:  Cancer; Communication; Decision aids; Decision-making; Educational materials; Patient-reported outcomes (PROs)

Mesh:

Year:  2018        PMID: 30498892      PMCID: PMC6387635          DOI: 10.1007/s11136-018-2065-3

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


  19 in total

1.  Oncologists' use of quality of life information: results of a survey of Eastern Cooperative Oncology Group physicians.

Authors:  A Bezjak; P Ng; R Skeel; A D Depetrillo; R Comis; K M Taylor
Journal:  Qual Life Res       Date:  2001       Impact factor: 4.147

2.  Use of patient-reported outcomes in clinical practice.

Authors:  Claire F Snyder; Neil K Aaronson
Journal:  Lancet       Date:  2009-08-01       Impact factor: 79.321

3.  A knowledge translation challenge: clinical use of quality of life data from cancer clinical trials.

Authors:  Michael Brundage; Brenda Bass; Ringash Jolie; Kimberley Foley
Journal:  Qual Life Res       Date:  2011-01-29       Impact factor: 4.147

Review 4.  Added value of health-related quality of life measurement in cancer clinical trials: the experience of the NCIC CTG.

Authors:  Heather-Jane Au; Jolie Ringash; Michael Brundage; Michael Palmer; Harriet Richardson; Ralph M Meyer
Journal:  Expert Rev Pharmacoecon Outcomes Res       Date:  2010-04       Impact factor: 2.217

5.  Assessing the conceptual clarity and evidence base of quality criteria/standards developed for evaluating decision aids.

Authors:  Heather McDonald; Cathy Charles; Amiram Gafni
Journal:  Health Expect       Date:  2011-11-03       Impact factor: 3.377

6.  Further insight into the perception of quantitative information: judgments of gist in treatment decisions.

Authors:  Deb Feldman-Stewart; Michael D Brundage; Vladimir Zotov
Journal:  Med Decis Making       Date:  2007 Jan-Feb       Impact factor: 2.583

Review 7.  Issues and challenges with integrating patient-reported outcomes in clinical trials supported by the National Cancer Institute-sponsored clinical trials networks.

Authors:  Deborah Watkins Bruner; Charlene J Bryan; Neil Aaronson; C Craig Blackmore; Michael Brundage; David Cella; Patricia A Ganz; Carolyn Gotay; Pamela S Hinds; Alice B Kornblith; Benjamin Movsas; Jeff Sloan; Lari Wenzel; Giles Whalen
Journal:  J Clin Oncol       Date:  2007-11-10       Impact factor: 44.544

8.  The applications of PROs in clinical practice: what are they, do they work, and why?

Authors:  Joanne Greenhalgh
Journal:  Qual Life Res       Date:  2008-12-23       Impact factor: 4.147

9.  Incorporating the patient's perspective into drug development and communication: an ad hoc task force report of the Patient-Reported Outcomes (PRO) Harmonization Group meeting at the Food and Drug Administration, February 16, 2001.

Authors:  Catherine Acquadro; Rick Berzon; Dominique Dubois; Nancy Kline Leidy; Patrick Marquis; Dennis Revicki; Margaret Rothman
Journal:  Value Health       Date:  2003 Sep-Oct       Impact factor: 5.725

10.  Toward Minimum Standards for Certifying Patient Decision Aids: A Modified Delphi Consensus Process.

Authors:  Natalie Joseph-Williams; Robert Newcombe; Mary Politi; Marie-Anne Durand; Stephanie Sivell; Dawn Stacey; Annette O'Connor; Robert J Volk; Adrian Edwards; Carol Bennett; Michael Pignone; Richard Thomson; Glyn Elwyn
Journal:  Med Decis Making       Date:  2013-08-20       Impact factor: 2.583

View more
  2 in total

1.  The PROTEUS-Trials Consortium: Optimizing the use of patient-reported outcomes in clinical trials.

Authors:  Claire Snyder; Norah Crossnohere; Madeleine King; Bryce B Reeve; Andrew Bottomley; Melanie Calvert; Elissa Thorner; Albert W Wu; Michael Brundage
Journal:  Clin Trials       Date:  2022-01-31       Impact factor: 2.599

2.  Communicating treatment risks and benefits to cancer patients: a systematic review of communication methods.

Authors:  L F van de Water; J J van Kleef; W P M Dijksterhuis; I Henselmans; H G van den Boorn; N M Vaarzon Morel; K F Schut; J G Daams; E M A Smets; H W M van Laarhoven
Journal:  Qual Life Res       Date:  2020-04-24       Impact factor: 4.147

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.