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How do patient reported outcome measures (PROMs) support clinician-patient communication and patient care? A realist synthesis

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TLDR
The findings show thatPROMs completion is not a neutral act of information retrieval but can change how patients think about their condition and reveal that the ways in which clinicians use PROMs is shaped by their relationships with patients and professional roles and boundaries.
Abstract
In this paper, we report the findings of a realist synthesis that aimed to understand how and in what circumstances patient reported outcome measures (PROMs) support patient-clinician communication and subsequent care processes and outcomes in clinical care We tested two overarching programme theories: (1) PROMs completion prompts a process of self-reflection and supports patients to raise issues with clinicians and (2) PROMs scores raise clinicians’ awareness of patients’ problems and prompts discussion and action We examined how the structure of the PROM and care context shaped the ways in which PROMs support clinician-patient communication and subsequent care processes PROMs completion prompts patients to reflect on their health and gives them permission to raise issues with clinicians However, clinicians found standardised PROMs completion during patient assessments sometimes constrained rather than supported communication In response, clinicians adapted their use of PROMs to render them compatible with the ongoing management of patient relationships Individualised PROMs supported dialogue by enabling the patient to tell their story In oncology, PROMs completion outside of the consultation enabled clinicians to identify problematic symptoms when the PROM acted as a substitute rather than addition to the clinical encounter and when the PROM focused on symptoms and side effects, rather than health related quality of life (HRQoL) Patients did not always feel it was appropriate to discuss emotional, functional or HRQoL issues with doctors and doctors did not perceive this was within their remit This paper makes two important contributions to the literature First, our findings show that PROMs completion is not a neutral act of information retrieval but can change how patients think about their condition Second, our findings reveal that the ways in which clinicians use PROMs is shaped by their relationships with patients and professional roles and boundaries Future research should examine how PROMs completion and feedback shapes and is influenced by the process of building relationships with patients, rather than just their impact on information exchange and decision making

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Patient-Reported Outcome Measures and Their Clinical Applications in Dermatology

TL;DR: In this article , the authors combine available literature with expert views to discuss overcoming barriers and helping dermatologists incorporate patient-reported outcome measures (PROMs) into routine patient-centered care.
Journal ArticleDOI

Role of parents in fatigue of children with a chronic disease: a cross-sectional study

TL;DR: In this paper, the authors explored the association between parental factors and fatigue in children with a chronic disease and found that more parental empowerment was associated with less paediatric fatigue on both subscales of the PedsQL multidimensional fatigue scale.
Journal ArticleDOI

Partnered decision support: Parental perspectives of completing a pre-visit pediatric asthma questionnaire via the patient portal.

TL;DR: In this paper, the authors conducted semi-structured interviews with caregivers of children 5-11 years old with asthma in the University of California, Los Angeles (UCLA) Health System and identified eight themes related to caregiver-physician communication, perception of portal questionnaires, facilitators and barriers to portal questionnaire use.
Journal ArticleDOI

Development and Content Validity of the Bilateral Vestibulopathy Questionnaire

TL;DR: The BVQ, which was developed to assess the spectrum of BVP symptoms and its impact on daily life, proved to have good face and content validity and can be used to characterize current self-reported symptoms and disability and to evaluate symptom burden before and after therapeutic interventions in future research and clinical practice.
Posted ContentDOI

Patient-Reported Outcome and Experience Measures in Perinatal Care to Guide Clinical Practice: Prospective Observational Study (Preprint)

TL;DR: The International Consortium for Health Outcomes Measurement has published a set of patient-centered outcome measures for pregnancy and childbirth (PCB set), including patientreported outcome measures (PROMs) and patient-reported experience measures (PREMs) as discussed by the authors .
References
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Journal ArticleDOI

Crossing the Quality Chasm: A New Health System for the 21st Century

Alastair Baker
- 17 Nov 2001 - 
TL;DR: Analyzing health care organizations as complex systems, Crossing the Quality Chasm also documents the causes of the quality gap, identifies current practices that impede quality care, and explores how systems approaches can be used to implement change.
Journal ArticleDOI

Checklists for improving rigour in qualitative research: a case of the tail wagging the dog?

TL;DR: It is argued that there is no substitute for systematic and thorough application of the principles of qualitative research and technical fixes will achieve little unless they are embedded in a broader understanding of the rationale and assumptions behind qualitative research.
Journal ArticleDOI

Truth and method

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How does communication heal? Pathways linking clinician-patient communication to health outcomes.

TL;DR: Clinicians and patients should maximize the therapeutic effects of communication by explicitly orienting communication to achieve intermediate outcomes associated with improved health.
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