Evidence map›Paper›PMID 29564549›Full record

ReviewRheumatology international2018

Call for action: how to improve use of patient-reported outcomes to guide clinical decision making in rheumatoid arthritis.

Bruno Fautrel, Rieke Alten, Bruce Kirkham, Inmaculada de la Torre, Frederick Durand, Jane Barry, Thorsten Holzkaemper, Walid Fakhouri, Peter C Taylor

Open access · hybridAbstract readReview
In one paragraph

Review in Rheumatology international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 3 pooled it
14.4field-weighted citation impact, top 1% of its field
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

61 citing papers in PubMed, 3 syntheses or guidelines pooled it, 123 citations in OpenAlex.

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1 more citing papers are in PubMed but not listed here.

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

9 authors at 7 institutions in 4 countries.

Bruno FautrelInstitut Pierre Louis d'Epidémiologie et de Santé Publique, Sorbonne Universités, UPMC Universitaire Paris 06, Paris, France.
Rieke AltenSchlosspark-Klinik University Medicine, 14059, Berlin, Germany.
Bruce KirkhamDepartment of Rheumatology, Guys and St Thomas' NHS Trust, Great Maze Pond, London, SE1 9RT, UK.
Inmaculada de la TorreEli Lilly and Company, Indianapolis, IN, USA.
Frederick DurandLilly France, Neuilly-sur-Seine, France.
Jane BarryEli Lilly and Company, Basingstoke, Hampshire, UK.
Thorsten HolzkaemperLilly Deutschland GmbH, Bad Homburg, Germany.
Walid FakhouriEli Lilly and Company, Indianapolis, IN, USA.
Peter C TaylorBotnar Research Centre, NDORMS, University of Oxford, Oxford, UK. peter.taylor@kennedy.ox.ac.uk.
Eli Lilly (United States) · USEli Lilly (Germany) · DEEli Lilly (United Kingdom) · GBHôpital américain de paris · FRInstitut Pierre Louis d‘Épidémiologie et de Santé Publique · FRSchlosspark-Klinik · DEUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current guidelines for the management of rheumatoid arthritis (RA) recommend early treatment and a treat-to-target goal of remission or low disease activity. Over the past decade, this approach has been extremely successful in reducing disease activity and joint damage in patients with RA. At the same time, however, overall patient perception of well-being appears to have decreased with respect to outcome measures considered important by patients themselves, such as pain, fatigue, physical function and quality of life. The timely and effective use of patient-reported outcomes (PROs) could encourage physicians to focus more on the impact of RA on patients and how patients are feeling. This in turn would facilitate shared decision making between patients and physicians, ultimately leading to a more patient-centered approach and improved patient care. Indeed, PROs provide information about individual patients that complements information provided by physical assessment and composite scores, and can also be used to guide patient care, such as determining whether a clinic visit is needed or whether treatment modifications are necessary. This is particularly important for patients who do not achieve the aspirational target of remission or low disease activity with pharmacological treatment. A number of validated PRO questionnaires are available, but how and which PROs should be incorporated into rheumatology clinical practice as part of the decision-making process is still controversial. Combining PROs with technology, such as computer adaptive tests, electronic PRO systems, web-based platforms and patient dashboards, could further aid PRO integration into daily rheumatology clinical practice.

Indexed as

Clinical Decision-MakingPatient Reported Outcome MeasuresQuality of LifeAntirheumatic AgentsArthritis, RheumatoidBiological ProductsDisease ProgressionHumansPatientsPerceptionTreatment OutcomeAntirheumatic AgentsBiological ProductsFatiguePainPatient-reported outcomesQuality of lifeRheumatoid arthritis

Identifiers

PMID29564549
PMCPMC5953992
OpenAlexW2792722775

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.