Literature DB >> 20083546

The routine use of patient reported outcome measures in healthcare settings.

Jill Dawson1, Helen Doll, Ray Fitzpatrick, Crispin Jenkinson, Andrew J Carr.   

Abstract

The use of patient reported outcome measures might seem to be quite straightforward; however, a number of pitfalls await clinicians with limited expertise. Jill Dawson and colleagues provide a guide for individuals keen to use patient reported outcome measures at a local level.

Entities:  

Mesh：

Year:  2010        PMID： 20083546     DOI： 10.1136/bmj.c186

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


  156 in total

1.  Measurement of individualised quality of life amongst young people with indicated personality disorder during emerging adulthood using the SEIQoL-DW.

Authors:  Paul Farrand; Joanne Woodford
Journal:  Qual Life Res       Date:  2012-06-04       Impact factor: 4.147

2.  Quality of life in patients with inflammatory bowel disease: translation, validity, reliability and sensitivity to change of the Norwegian version of the short health scale (SHS).

Authors:  Lars-Petter Jelsness-Jørgensen; Tomm Bernklev; Bjørn Moum
Journal:  Qual Life Res       Date:  2011-12-07       Impact factor: 4.147

3.  Measurement issues when assessing quality of life outcomes for different types of hernia mesh repair.

Authors:  Andras Zaborszky; Rita Gyanti; John A Barry; Brian K Saxby; Panchanan Bhattacharya; Fazal A Hasan
Journal:  Ann R Coll Surg Engl       Date:  2011-05       Impact factor: 1.891

4.  Spine Tango registry data collection in a conservative spinal service: a feasibility study.

Authors:  Samuel Morris; James Booth; James Hegarty
Journal:  Eur Spine J       Date:  2016-07-20       Impact factor: 3.134

5.  Translation and Adaptation of the Genetic Counselling Outcome Scale (GCOS-24) for Use in Denmark.

Authors:  Birgitte Rode Diness; Gritt Overbeck; Tina Duelund Hjortshøj; Trine Bjørg Hammer; Susanne Timshel; Else Sørensen; Marion McAllister
Journal:  J Genet Couns       Date:  2017-03-06       Impact factor: 2.537

6.  Overcoming barriers to implementing patient-reported outcomes in an electronic health record: a case report.

Authors:  Christopher A Harle; Alyson Listhaus; Constanza M Covarrubias; Siegfried Of Schmidt; Sean Mackey; Peter J Carek; Roger B Fillingim; Robert W Hurley
Journal:  J Am Med Inform Assoc       Date:  2015-07-09       Impact factor: 4.497

7.  Palliative care-related self-report problems among cancer patients in East Africa: a two-country study.

Authors:  Richard Harding; Richard A Powell; Eve Namisango; Anne Merriman; Nancy Gikaara; Zipporah Ali; Irene J Higginson
Journal:  Support Care Cancer       Date:  2014-06-24       Impact factor: 3.603

8.  Acceptability of Patient-Reported Outcome and Experience Measures for Hepatitis C Treatment Among People Who Use Drugs.

Authors:  Annie Madden; Max Hopwood; Joanne Neale; Carla Treloar
Journal:  Patient       Date:  2019-04       Impact factor: 3.883

9.  Test-Retest Reliability, Agreement and Responsiveness of Productivity Loss (iPCQ-VR) and Healthcare Utilization (TiCP-VR) Questionnaires for Sick Workers with Chronic Musculoskeletal Pain.

Authors:  Timo T Beemster; Judith M van Velzen; Coen A M van Bennekom; Michiel F Reneman; Monique H W Frings-Dresen
Journal:  J Occup Rehabil       Date:  2019-03

10.  Development of a patient-centred, patient-reported outcome measure (PROM) for post-stroke cognitive rehabilitation: qualitative interviews with stroke survivors to inform design and content.

Authors:  Emma L Patchick; Maria Horne; Kate Woodward-Nutt; Andy Vail; Audrey Bowen
Journal:  Health Expect       Date:  2014-12-05       Impact factor: 3.377
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