Evidence map›Paper›PMID 25991448›Full record

ArticleBMJ open2015

Perspectives from health, social care and policy stakeholders on the value of a single self-report outcome measure across long-term conditions: a qualitative study.

Cheryl Hunter, Ray Fitzpatrick, Crispin Jenkinson, Anne-Sophie Emma Darlington, Angela Coulter, Julien E Forder, Michele Peters

Abstract read
In one paragraph

Article in BMJ open, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Living well while providing support: validation of LTCQ-Carer for assessing informal carers' quality of life.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Cheryl HunterAcademic Unit of Primary Care, Leeds Institute of Health Sciences, University of Leeds, Leeds, England.
Ray FitzpatrickHealth Services Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, England.
Crispin JenkinsonHealth Services Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, England.
Anne-Sophie Emma DarlingtonFaculty of Health Sciences, University of Southampton, Southampton, England.
Angela CoulterHealth Services Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, England.
Julien E ForderPSSRU, University of Kent, Canterbury, England PSSRU, London School of Economics and Political Science, London, England.
Michele PetersHealth Services Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, England.

Funding

Department of Health
6 · The paper itself

Abstract

objectivesTo explore the views of a range of stakeholders regarding whether patient-reported outcome measures (PROMs) can be developed to measure key attributes of long-term conditions (LTCs) care in England, and the potential value of a single generic measure.

designQualitative semistructured interview study, analysed using a framework approach. PARTICIPANTS AND

settingInterviews with 31 stakeholders from primary care, secondary care, social care, policy and patient-focused voluntary organisations in England.

resultsThere was broad support for a single PROM that could be used to measure outcomes for patients with any LTCs in any health or social care setting. Interviewees identified three desired uses for a PROM: to improve the quality of individual care; to increase people's engagement in their own care; and to monitor the performance of services. Interviewees felt that a PROM for LTCs should incorporate a mixture of traditional and non-traditional domains, such as functioning, empowerment and social participation, and be codesigned with patients and professional end-users. Stakeholders emphasised the need for a PROM to be feasible for practical implementation at the individual clinical level as a first priority. A number of concerns and potential problems were identified in relation to the application and interpretation of an LTC PROM.

conclusionsThis study has demonstrated support for a single self-report outcome measure that reflects the priorities of people with LTCs, if such a measure can be shown to be meaningful and useful at the individual level. People with LTCs and professional end-users in health and social care should be involved in the development and evaluation of such a measure.

Indexed as

Quality ImprovementChronic DiseaseContinuity of Patient CareEnglandEvidence-Based MedicineFeasibility StudiesHumansPatient Care PlanningPolicy MakingPrimary Health CareProfessional-Patient RelationsQualitative ResearchQuality of Health CareReferral and ConsultationSecondary Health CareSelf ReportPRIMARY CAREQUALITATIVE RESEARCH

Identifiers

PMID25991448
PMCPMC4442190

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.