Evidence map›Paper›PMID 35238334›Full record

ArticleRheumatology (Oxford, England)2022

Patient preferences for the treatment of systemic sclerosis-associated interstitial lung disease: a discrete choice experiment.

Cosimo Bruni, Sebastian Heidenreich, Ashley Duenas, Anna-Maria Hoffmann-Vold, Armando Gabrielli, Yannick Allanore, Emmanuel Chatelus, Jörg H W Distler, Eric Hachulla, Vivien M Hsu and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 15 institutions in 6 countries.

Cosimo BruniDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.ORCID 0000-0003-2813-2083
Sebastian HeidenreichPatient-Centered Research, Evidera, London, UK.
Ashley DuenasPatient-Centered Research, Evidera, London, UK.
Anna-Maria Hoffmann-VoldDepartment of Rheumatology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0001-6467-7422
Armando GabrielliDepartment of Clinical and Molecular Sciences, Università Politecnica delle Marche, Ancona, Italy.
Yannick AllanoreDepartment of Rheumatology A, Cochin Hospital, Paris Descartes University, Paris.
Emmanuel ChatelusDepartment of Rheumatology, University Hospital of Strasbourg, Hôpital de Hautepierre, Strasbourg, France.
Jörg H W DistlerDepartment of Internal Medicine 3, University of Erlangen-Nuremberg, Erlangen, Germany.
Eric HachullaDepartment of Internal Medicine and Clinical Immunology, Referral Centre for Centre for rare systemic autoimmune diseases North and North-West of France (CeRAINO), CHU Lille, University of Lille, Inserm, U1286 - INFINITE-Institute for Translational Research in Inflammation, Lille, France.
Vivien M HsuDepartment of Medicine, Division of Rheumatology, Rutgers-Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Nicolas HunzelmannDepartment of Dermatology, University of Cologne, Cologne, Germany.
Dinesh KhannaScleroderma Program.
Marie-Elise TruchetetDepartment of Rheumatology, CHU Bordeaux, Bordeaux, France.
Ulrich A WalkerDepartment of Rheumatology, University Hospital Basel, Basel, Switzerland.
Margarida AlvesTA Inflammation, Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany.
Nils SchoofTA Inflammation, Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany.
Lesley Ann SaketkooNew Orleans Scleroderma and Sarcoidosis Patient Care and Research Center.
Oliver DistlerDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Boehringer Ingelheim (Germany) · DECentre Hospitalier Universitaire de Bordeaux · FRDélégation Paris 5 · FRFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHôpital d'Hautepierre · FRInserm · FRMarche Polytechnic University · ITOslo University Hospital · NORutgers, The State University of New Jersey · USTulane University · USUniversity Hospital of Basel · CHUniversity of Cologne · DEUniversity of Florence · ITUniversity of Michigan · USUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTreatments for SSc-associated interstitial lung disease (SSc-ILD) differ in attributes, i.e. mode of administration, adverse events (AEs) and efficacy. As physicians and patients may perceive treatments differently, shared decision-making can be essential for optimal treatment provision. We therefore aimed to quantify patient preferences for different treatment attributes.

methodsSeven SSc-ILD attributes were identified from mixed-methods research and clinician input: mode of administration, shortness of breath, skin tightness, cough, tiredness, risk of gastrointestinal AEs (GI-AEs) and risk of serious and non-serious infections. Patients with SSc-ILD completed an online discrete choice experiment (DCE) in which they were asked to repeatedly choose between two alternatives characterized by varying severity levels of the included attributes. The data were analysed using a multinomial logit model; relative attribute importance and maximum acceptable risk measures were calculated.

resultsOverall, 231 patients with SSc-ILD completed the DCE. Patients preferred twice-daily oral treatments and 6-12 monthly infusions. Patients' choices were mostly influenced by the risk of GI-AEs or infections. Improvement was more important in respiratory symptoms than in skin tightness. Concerning trade-offs, patients accepted different levels of increase in GI-AE risk: +21% if it reduced the infusions' frequency; +15% if changing to an oral treatment; up to +37% if it improved breathlessness; and up to +36% if it reduced the risk of infections.

conclusionsThis is the first study to quantitatively elicit patients' preferences for treatment attributes in SSc-ILD. Patients showed willingness to make trade-offs, providing a firm basis for shared decision-making in clinical practice.

Indexed as

Lung Diseases, InterstitialScleroderma, SystemicChoice BehaviorHumansPatient PreferenceSurveys and Questionnairesdiscrete choice experimentinterstitial lung diseasepatient preferenceSSc

Identifiers

PMID35238334
PMCPMC9536797
OpenAlexW4214610485

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.