Evidence map›Paper›PMID 38191998›Full record

ArticleRheumatology (Oxford, England)2025

How do patient-reported outcome measures affect treatment intensification and patient satisfaction in the management of psoriatic arthritis? A cross sectional study of 503 patients.

Conor Coyle, Lily Watson, Caroline Whately-Smith, Mel Brooke, Uta Kiltz, Ennio Lubrano, Ruben Queiro, David Trigos, Jan Brandt-Juergens, Ernest Choy and 21 more

Open access · hybridAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

31 authors at 20 institutions in 8 countries.

Conor CoyleOxford University, John Radcliffe Hospital, Oxford University Hospitals, Oxford, UK.ORCID 0000-0003-1795-0099
Lily WatsonDepartment of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.ORCID 0000-0003-2005-2708
Caroline Whately-SmithConsultant Biostatistician, Whately-Smith Ltd, Herts, UK.
Mel BrookeRoyal National Hospital for Rheumatic Diseases, Royal United Hospitals, Bath, UK.
Uta KiltzRuhr-Universität Bochum, and Rheumazentrum Ruhrgebiet, Bochum, Germany.ORCID 0000-0001-5668-4497
Ennio LubranoAcademic Rheumatology Unit, Department of Medicine and Health Sciences "Vincenzo Tiberio", University of Molise, Campobasso, Italy.ORCID 0000-0001-6189-5328
Ruben QueiroRheumatology & ISPA Translational Immunology Division, Faculty of Medicine, Rheumatology Service & the Principality of Asturias Institute for Health Research (ISPA), Universidad de Oviedo, Oviedo, Spain.ORCID 0000-0002-8418-7145
David TrigosAcción Psoriasis, Barcelona, Spain.
Jan Brandt-JuergensRheumatologische Schwerpunktpraxis, Berlin, Germany.
Ernest ChoyCREATE Centre, Division of Infection and Immunity, Cardiff University, Cardiff, UK.ORCID 0000-0003-4459-8609
Salvatore D'AngeloRheumatology Department of Lucania, San Carlo Hospital, Potenza, Italy.
Andrea Delle SedieRheumatology Unit, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
Emmanuelle DernisRheumatology Department, Centre Hospitalier du Mans, Le Mans, France.
Théo WirthRheumatology Department, INSERM UMRs1097 Autoimmune Arthritis, Aix Marseille University, Marseille, France.
Sandrine GuisRheumatology Department, Aix Marseille University, Arthrites Autoimmunes, Marseille, France.
Philip HelliwellLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK.ORCID 0000-0002-4155-9105
Pauline HoThe Kellgren Centre for Rheumatology, Manchester University NHS Foundation Trust, Manchester, UK.
Axel HueberDivision of Rheumatology, Klinikum Nürnberg, Paracelsus Medical University, Nürnberg, Germany.
Beatriz JovenRheumatology Department, Hospital Universitario 12 Octubre, Madrid, Spain.
Michaela KoehmRheumatology, Universitiy Hospital Frankfurt, Fraunhofer-Institute for Translational Medicine and Cluster of Excellence Immune-Mediated Diseases CIMD, Frankfurt am Main, Germany.
Carlos Montilla MoralesRheumatology Department, Hospital Universitario Salamanca, Salamanca, Spain.
Jon PackhamAcademic Unit of Population and Lifespan Sciences, University of Nottingham, Nottingham, UK.
Jose Antonio Pinto TasendeRheumatology Department, INIBIC. CHU A Coruña, A Coruña, Spain.
Julio RamírezArthritis Unit, Rheumatology Department, Hospital Clinic, Barcelona, Spain.
Adeline Ruyssen-WitrandRheumatology Center, Toulouse University Hospital, CIC 1436 Inserm, Rheumatology, Tolouse, France.
Rossana ScrivoRheumatology Unit, Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy.ORCID 0000-0002-2889-8962
Sarah TwiggRheumatology, Bradford Teaching Hospitals NHS Foundation Trust, Bradford, UK.
Martin WelckerMVZ für Rheumatologie Dr M. Welcker GmbH, Planegg, Germany.
Martin SoubrierRheumatology Department, Gabriel-Montpied Teaching Hospital of Clermont-Ferrand, Clermont-Ferrand, France.ORCID 0000-0001-9349-0720
Laure GossecRheumatology Department, Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, FR. & AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Laura C CoatesNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.ORCID 0000-0002-4756-663X
Inserm · FRAix-Marseille Université · FRAzienda Ospedaliera Universitaria Pisana · ITBiostatistical Consulting (United States) · USBradford Teaching Hospitals NHS Foundation Trust · GBCentre Hospitalier du Mans · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRComplejo Hospitalario de Salamanca · ESComplexo Hospitalario Universitario A Coruña · ESFraunhofer Institute for Translational Medicine and Pharmacology · DEHospital Clínic de Barcelona · ESInstitute of Infection and Immunity · CAJohn Radcliffe Hospital · GBManchester University NHS Foundation Trust · GBMedizinisches Versorgungszentrum Prof. Mathey, Prof. Schofer · DENuffield Orthopaedic Centre · GBOspedale San Carlo · ITParacelsus Medical University · ATPraxis für Hämatologie und Onkologie · DEPsoriasis Association · GB

Funding

Biomedical Research CentreClinical Research NetworkDepartment of HealthNational Health ServiceNational Institute for Health ResearchNational Institute for Health Research Clinician ScientistNIHR
6 · The paper itself

Abstract

objectivesThe AsseSSing Impact in pSoriatic Treatment (ASSIST) study investigated prescribing in routine PsA care and whether the patient-reported outcome-PsA Impact of Disease questionnaire (PsAID-12)-impacted treatment. This study also assessed a range of patient and clinician factors and their relationship to PsAID-12 scoring and treatment modification.

methodsPatients with PsA were selected across the UK and Europe between July 2021 and March 2022. Patients completed the PsAID questionnaire and the results were shared with their physician. Patient characteristics, disease activity, current treatment methods, treatment strategies, medication changes and patient satisfaction scores were recorded.

resultsA total of 503 patients were recruited. Some 36.2% had changes made to treatment, and 88.8% of these had treatment escalation. Overall, the mean PsAID-12 score was higher for patients with treatment escalation; increase in PSAID-12 score is associated with increased odds of treatment escalation (odds ratio 1.58; P < 0.0001). However, most clinicians reported that PsAID-12 did not impact their decision to escalate treatment, instead supporting treatment reduction decisions. Physician's assessment of disease activity had the most statistically significant effect on likelihood of treatment escalation (odds ratio 2.68, per 1-point score increase). Escalation was more likely in patients not treated with biologic therapies. Additional factors associated with treatment escalation included: patient characteristics, physician characteristics, disease activity and disease impact.

conclusionThis study highlights multiple factors impacting treatment decision-making for individuals with PsA. PsAID-12 scoring correlates with multiple measures of disease severity and odds of treatment escalation. However, most clinicians reported that the PsAID-12 did not influence treatment escalation decisions. Psoriatic Arthritis Impact of Disease (PsAID) scoring could be used to increase confidence in treatment de-escalation.

Indexed as

Arthritis, PsoriaticPatient Reported Outcome MeasuresPatient SatisfactionAdultAgedAntirheumatic AgentsCross-Sectional StudiesFemaleHumansMaleMiddle AgedSeverity of Illness IndexSurveys and QuestionnairesUnited KingdomAntirheumatic AgentsASSISTEQ-5D-5LHAQpatient-reported outcomesPsAPsAIDPsAID-12psoriatic arthritisquality of life

Identifiers

PMID38191998
PMCPMC11701309
OpenAlexW4390737644

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.