Evidence map›Paper›PMID 30719594›Full record

ArticleClinical rheumatology2019

Unmet needs in psoriatic arthritis patients receiving immunomodulatory therapy: results from a large multinational real-world study.

Rieke Alten, P G Conaghan, V Strand, E Sullivan, S Blackburn, H Tian, K Gandhi, S M Jugl, A Deodhar

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Clinical rheumatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 23 citations in OpenAlex.

  1. State of the Art Review on the Treatment of Psoriatic Disease.Mediterranean journal of rheumatology · 2024
    Review
  2. Observational
  3. Article
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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

9 authors at 7 institutions in 4 countries.

Rieke AltenInternal Medicine II, Rheumatology bei Schlosspark-Klinik, University Medicine, Berlin, Germany. Rieke.Alten@schlosspark-klinik.de.
P G ConaghanLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds & NIHR Leeds Biomedical Research Centre, Leeds, UK.
V StrandStanford University, Palo Alto, CA, USA.
E SullivanAdelphi Real World, Manchester, UK.
S BlackburnAdelphi Real World, Manchester, UK.
H TianNovartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
K GandhiNovartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
S M JuglNovartis Pharma AG, Basel, Switzerland.
A DeodharOregon Health & Science University, Portland, OR, USA.
Adelphi Group (United Kingdom) · GBNovartis (United States) · USNovartis (Switzerland) · CHOregon Health & Science University · USSchlosspark-Klinik · DEStanford University · USUniversity of Leeds · GB

Funding

Novartis Pharmaceuticals Corporation na
6 · The paper itself

Abstract

objectiveThere are limited data on therapy selection and switching in psoriatic arthritis (PsA). This 18 country, real-world study assessed use and switching of immunomodulatory therapy (biologic/apremilast), the extent of treatment failure and its association with reduced physical functioning, health-related quality of life (HRQoL), and work productivity and activity impairment (WPAI).

methodsPsA patients under routine care and their treating physicians provided demographics, current therapy, reasons for switching, duration of first therapy, HRQoL, HAQ-DI, and WPAI. Current immunomodulatory therapy was determined as "failing" if, after ≥ 3 months, physician-rated disease severity had worsened, remained severe, was "unstable/deteriorating," or they were dissatisfied with disease control and/or did not consider treatment a "success."

resultsIncluded were 3714 PsA patients; 1455 (40.6%) had never received immunomodulatory therapy; 1796 (50.1%) had ever received 1 immunomodulatory therapy and 331 (9.2%) ≥ 1. Lack of efficacy with first immunomodulatory therapy was the most common reason for switching; patients whose physicians indicated "primary lack of efficacy" as the reason, switched after a mean of 9.4 months. Patients currently failing immunomodulator therapies (n = 246) had poorer HRQoL compared with treatment success (n = 1472) measured by EQ-5D-3L (0.60 vs 0.77%; P < 0.0001); SF-36 PCS (40.8% vs 46.1%; P < 0.0001) MCS (41.1% vs 45.3%; P < 0.0001). Physical functioning, activity, and work productivity were also more impaired (HAQ-DI: 0.88 vs 0.56; activity impairment: 46.7% vs 29.7%; overall work impairment: 35.4% vs 26.1%; all P < 0.0001).

conclusionsPoor treatment response in PsA is associated with substantial negative patient impact. In cases of primary treatment failure, timely switching is needed.

Indexed as

Drug SubstitutionImmunomodulationPatient Reported Outcome MeasuresAdultArthritis, PsoriaticBiological ProductsDisease ManagementFemaleHumansImmunologic FactorsInternationalityLinear ModelsMaleMiddle AgedQuality of LifeRetrospective StudiesBiological ProductsImmunologic FactorsHealth-related quality of lifePsoriatic arthritisTNFiTreatmentWork

Identifiers

PMID30719594
OpenAlexW2914424636

What OpenQuestion holds

Textmetadata
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.