Literature DB >> 20424920

Relevant content for a patient-reported outcomes questionnaire for use in oncology clinical practice: Putting doctors and patients on the same page.

Claire F Snyder1, Roxanne E Jensen, Gail Geller, Michael A Carducci, Albert W Wu.   

Abstract

PURPOSE: To investigate relevant patient-reported outcome (PRO) domains for oncology clinical practice.
METHODS: We conducted cross-sectional semi-structured telephone interviews with patients with breast and prostate cancer and clinicians. Using open-ended questions followed by structured prompts of PRO domains, subjects were asked what they currently discuss during visits and which topics are relevant for a clinical practice PRO. For each domain, we calculated the percentage of patients and clinicians who responded positively. A qualitative thematic content analysis identified barriers and benefits of using PROs in clinical practice.
RESULTS: A total of 41 patients (21 breast cancer and 20 prostate cancer) and 15 clinicians (7 medical oncologists, 5 radiation oncologists, and 3 surgeons) completed the interviews. In general, clinicians and patients reported that the topics explored were relevant. Barriers to using PROs in clinical practice include (1) time constraints, (2) varying relevance of questions, (3) value of the conversational approach, (4) decreased usefulness in established relationships, and (5) respondent burden. Benefits of PROs in clinical practice include (1) identifying problems, (2) serving as a reminder of topics to discuss, and (3) tracking changes over time.
CONCLUSIONS: PROs in clinical practice may help triage issues and focus discussions. Computer-adaptive tests should be explored to tailor questionnaires to patients' specific issues.

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Mesh:

Year:  2010        PMID: 20424920     DOI: 10.1007/s11136-010-9655-z

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


  8 in total

1.  Logistics of collecting patient-reported outcomes (PROs) in clinical practice: an overview and practical examples.

Authors:  Matthias Rose; Andrea Bezjak
Journal:  Qual Life Res       Date:  2009-01-20       Impact factor: 4.147

2.  Taking PROs and patient-centered care seriously: incremental and disruptive ideas for incorporating PROs in oncology practice.

Authors:  Molla Sloane Donaldson
Journal:  Qual Life Res       Date:  2008-11-09       Impact factor: 4.147

3.  Level of agreement between patient self-report and observer ratings of health-related quality of life communication in oncology.

Authors:  Doranne L Hilarius; Paul H A M Kloeg; Symone B Detmar; Martin J Muller; Neil K Aaronson
Journal:  Patient Educ Couns       Date:  2006-07-26

4.  How are you feeling? Who wants to know? Patients' and oncologists' preferences for discussing health-related quality-of-life issues.

Authors:  S B Detmar; N K Aaronson; L D Wever; M Muller; J H Schornagel
Journal:  J Clin Oncol       Date:  2000-09-15       Impact factor: 44.544

5.  Asking the right questions: investigating needs assessments and health-related quality-of-life questionnaires for use in oncology clinical practice.

Authors:  Claire F Snyder; Sydney M Dy; Danetta E Hendricks; Julie R Brahmer; Michael A Carducci; Antonio C Wolff; Albert W Wu
Journal:  Support Care Cancer       Date:  2007-02-21       Impact factor: 3.603

Review 6.  The use of patient reported outcome measures in routine clinical practice: lack of impact or lack of theory?

Authors:  Joanne Greenhalgh; Andrew F Long; Rob Flynn
Journal:  Soc Sci Med       Date:  2005-02       Impact factor: 4.634

7.  Individual-patient monitoring in clinical practice: are available health status surveys adequate?

Authors:  C A McHorney; A R Tarlov
Journal:  Qual Life Res       Date:  1995-08       Impact factor: 4.147

8.  The clinical value of quality of life assessment in oncology practice-a qualitative study of patient and physician views.

Authors:  Galina Velikova; Noha Awad; Rebecca Coles-Gale; E Penny Wright; Julia M Brown; Peter J Selby
Journal:  Psychooncology       Date:  2008-07       Impact factor: 3.894

  8 in total
  24 in total

Review 1.  [The benefits of using patient-reported outcomes in cancer treatment: an overview].

Authors:  Lisa M Wintner; Johannes M Giesinger; Georg Kemmler; Monika Sztankay; Anne Oberguggenberger; Eva-Maria Gamper; Barbara Sperner-Unterweger; Bernhard Holzner
Journal:  Wien Klin Wochenschr       Date:  2012-04-27       Impact factor: 1.704

2.  When using patient-reported outcomes in clinical practice, the measure matters: a randomized controlled trial.

Authors:  Claire F Snyder; Joseph M Herman; Sharon M White; Brandon S Luber; Amanda L Blackford; Michael A Carducci; Albert W Wu
Journal:  J Oncol Pract       Date:  2014-07-01       Impact factor: 3.840

Review 3.  Patient-reported outcome use in oncology: a systematic review of the impact on patient-clinician communication.

Authors:  L Y Yang; D S Manhas; A F Howard; R A Olson
Journal:  Support Care Cancer       Date:  2017-08-28       Impact factor: 3.603

4.  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

Review 5.  Innovations in research and clinical care using patient-generated health data.

Authors:  Heather S L Jim; Aasha I Hoogland; Naomi C Brownstein; Anna Barata; Adam P Dicker; Hans Knoop; Brian D Gonzalez; Randa Perkins; Dana Rollison; Scott M Gilbert; Ronica Nanda; Anders Berglund; Ross Mitchell; Peter A S Johnstone
Journal:  CA Cancer J Clin       Date:  2020-04-20       Impact factor: 508.702

6.  Cancer patients' function, symptoms and supportive care needs: a latent class analysis across cultures.

Authors:  Jennifer Barsky Reese; Amanda Blackford; Jonathan Sussman; Toru Okuyama; Tatsuo Akechi; Daryl Bainbridge; Doris Howell; Claire F Snyder
Journal:  Qual Life Res       Date:  2014-01-31       Impact factor: 4.147

Review 7.  The role of informatics in promoting patient-centered care.

Authors:  Claire F Snyder; Albert W Wu; Robert S Miller; Roxanne E Jensen; Elissa T Bantug; Antonio C Wolff
Journal:  Cancer J       Date:  2011 Jul-Aug       Impact factor: 3.360

8.  Bringing PROMIS to practice: brief and precise symptom screening in ambulatory cancer care.

Authors:  Lynne I Wagner; Julian Schink; Michael Bass; Shalini Patel; Maria Varela Diaz; Nan Rothrock; Timothy Pearman; Richard Gershon; Frank J Penedo; Steven Rosen; David Cella
Journal:  Cancer       Date:  2014-11-06       Impact factor: 6.860

9.  Achieving Coordinated Care for Patients With Complex Cases of Cancer: A Multiteam System Approach.

Authors:  Simon J Craddock Lee; Mark A Clark; John V Cox; Burton M Needles; Carole Seigel; Bijal A Balasubramanian
Journal:  J Oncol Pract       Date:  2016-10-31       Impact factor: 3.840

10.  Setting standards for severity of common symptoms in oncology using the PROMIS item banks and expert judgment.

Authors:  David Cella; Seung Choi; Sofia Garcia; Karon F Cook; Sarah Rosenbloom; Jin-Shei Lai; Donna Surges Tatum; Richard Gershon
Journal:  Qual Life Res       Date:  2014-06-18       Impact factor: 4.147

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