Literature DB >> 15571900

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

Joanne Greenhalgh1, Andrew F Long, Rob Flynn.   

Abstract

This paper applies a theory-driven approach to explore why the use of patient-reported outcome (PRO) measures in clinical practice, in particular, health-related quality of life (HRQoL) instruments, has little or no apparent influence on clinical decision making. A theory-driven approach involves combining knowledge of whether and how an intervention works. It is argued that such an approach is currently lacking within the literature evaluating the effectiveness of feeding back HRQoL information to clinicians. The paper identifies a number of mechanisms that might give rise to the expected outcomes that are currently implicit within the design of the intervention and hypotheses specified within the trials evaluating the use of HRQoL measures in clinical practice. It then examines how far current clinical practice matches these mechanisms and in doing so, a number of possible explanations for the lack of impact of HRQoL on clinical decision making are reviewed. The influence of HRQoL information on clinical decision making depends on a large number of factors related to the design of the intervention, patients' and clinicians' desire to discuss HRQoL issues within the consultation and the legitimacy that clinicians give to HRQoL instruments. To date, knowledge of how the feedback of HRQoL information to clinicians might improve doctor-patient communication or clinical decision making has yet to sufficiently inform an assessment of whether these aspects of patient care are improved. The paper concludes by specifying how the feedback of HRQoL information to clinicians might be modified to maximise its impact on clinical decision making.

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Mesh:

Year:  2005        PMID: 15571900     DOI: 10.1016/j.socscimed.2004.06.022

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  146 in total

1.  How to interpret multidimensional quality of life questionnaires for patients with schizophrenia?

Authors:  Pierre Michel; Pascal Auquier; Karine Baumstarck; Anderson Loundou; Badih Ghattas; Christophe Lançon; Laurent Boyer
Journal:  Qual Life Res       Date:  2015-04-09       Impact factor: 4.147

2.  Data collection challenges in community settings: insights from two field studies of patients with chronic disease.

Authors:  Richard J Holden; Amanda M McDougald Scott; Peter L T Hoonakker; Ann S Hundt; Pascale Carayon
Journal:  Qual Life Res       Date:  2014-08-26       Impact factor: 4.147

Review 3.  [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

4.  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

5.  Linking data to decision-making: applying qualitative data analysis methods and software to identify mechanisms for using outcomes data.

Authors:  Vaishali N Patel; Anne W Riley
Journal:  J Behav Health Serv Res       Date:  2007-07-24       Impact factor: 1.505

6.  [Health-related quality of life].

Authors:  Luis Lizán Tudela
Journal:  Aten Primaria       Date:  2009-05-15       Impact factor: 1.137

7.  One-Year Linear Trajectories of Symptoms, Physical Functioning, Cognitive Functioning, Emotional Well-being, and Spiritual Well-being Among Patients Receiving Dialysis.

Authors:  Mi-Kyung Song; Sudeshna Paul; Sandra E Ward; Constance A Gilet; Gerald A Hladik
Journal:  Am J Kidney Dis       Date:  2018-02-01       Impact factor: 8.860

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.  Health perceptions and symptom burden in primary care: measuring health using audio computer-assisted self-interviews.

Authors:  Keiki Hinami; Jennifer Smith; Catherine D Deamant; Romina Kee; Diana Garcia; William E Trick
Journal:  Qual Life Res       Date:  2014-12-07       Impact factor: 4.147

Review 10.  Quality of life in cirrhosis.

Authors:  Anthony Loria; Carey Escheik; N Lynn Gerber; Zobair M Younossi
Journal:  Curr Gastroenterol Rep       Date:  2013-01
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