Literature DB >> 27942273

A clinical perspective on electronically collecting patient-reported outcomes at the point-of-care for overactive bladder.

Darren Desantis1, Richard J Baverstock2, Andrea Civitarese1, R Trafford Crump3, Kevin V Carlson2.   

Abstract

INTRODUCTION: Collecting patient-reported outcomes (PROs) can inform the treatment and management of overactive bladder (OAB). However, collecting these data at the point-of-care can be time-consuming and have a negative impact on a clinic's workflow. The purpose of this study was to pilot a digital system for collecting PROs at the point-of-care and qualitatively assess clinicians' perspectives in terms of the system's impact on the delivery of care for OAB.
METHODS: Patients visiting a urology clinic for OAB completed several PRO instruments using a tablet while awaiting assessment. Clinicians reviewed their responses using a digital dashboard during clinical encounters. Qualitative interviews were conducted with the clinicians, to assess the collection system's impact in terms of: 1) logistics, 2) workflow; 3) patient communication; 4) influence on clinical decisions; 5) user experiences; and 6) the care model.
RESULTS: Six interviews were conducted and thematic saturation was met, with several themes emerging. All participants were generally positive regarding the use of the digital collecting system. Participants felt that the dashboard improved workflow and enhanced communication with patients, but it was not thought to be any more influential on clinical decision-making than conventional collection methods. Several aspects of the digital PRO collection system were identified as needing improvement.
CONCLUSIONS: The digital PRO collection system used at the point-of-care had a positive impact on the delivery of care for OAB. The results from this study could provide insight to other urologists who are interested in collecting PROs in their clinic.

Entities:  

Year:  2016        PMID: 27942273      PMCID: PMC5140027          DOI: 10.5489/cuaj.3757

Source DB:  PubMed          Journal:  Can Urol Assoc J        ISSN: 1911-6470            Impact factor:   1.862


  16 in total

Review 1.  Redefining response in overactive bladder syndrome.

Authors:  Christopher K Payne; Con Kelleher
Journal:  BJU Int       Date:  2007-01       Impact factor: 5.588

2.  Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups.

Authors:  Allison Tong; Peter Sainsbury; Jonathan Craig
Journal:  Int J Qual Health Care       Date:  2007-09-14       Impact factor: 2.038

3.  Issues in the design of Internet-based systems for collecting patient-reported outcomes.

Authors:  James B Jones; Claire F Snyder; Albert W Wu
Journal:  Qual Life Res       Date:  2007-08-01       Impact factor: 4.147

4.  The American Urological Association symptom index for benign prostatic hyperplasia. The Measurement Committee of the American Urological Association.

Authors:  M J Barry; F J Fowler; M P O'Leary; R C Bruskewitz; H L Holtgrewe; W K Mebust; A T Cockett
Journal:  J Urol       Date:  1992-11       Impact factor: 7.450

5.  Validation of an overactive bladder awareness tool for use in primary care settings.

Authors:  Karin S Coyne; Teresa Zyczynski; Mary Kay Margolis; Victor Elinoff; Richard G Roberts
Journal:  Adv Ther       Date:  2005 Jul-Aug       Impact factor: 3.845

6.  Equivalence of electronic and paper-and-pencil administration of patient-reported outcome measures: a meta-analytic review.

Authors:  Chad J Gwaltney; Alan L Shields; Saul Shiffman
Journal:  Value Health       Date:  2008 Mar-Apr       Impact factor: 5.725

7.  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

Review 8.  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

9.  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

Review 10.  Patient reported outcomes as endpoints in medical research.

Authors:  Diane L Fairclough
Journal:  Stat Methods Med Res       Date:  2004-04       Impact factor: 3.021

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  1 in total

Review 1.  Examining perspectives on the adoption and use of computer-based patient-reported outcomes among clinicians and health professionals: a Q methodology study.

Authors:  Shirley V Burton; Annette L Valenta; Justin Starren; Joanna Abraham; Therese Nelson; Karl Kochendorfer; Ashley Hughes; Bhrandon Harris; Andrew Boyd
Journal:  J Am Med Inform Assoc       Date:  2022-01-29       Impact factor: 4.497

  1 in total

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