Evidence map›Paper›PMID 38321298›Full record

ReviewNature reviews. Rheumatology2024

Treatment of non-systemic juvenile idiopathic arthritis.

Susan Shenoi, Gerd Horneff, Amita Aggarwal, Angelo Ravelli

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Rheumatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Observational
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. [Rheumatic shoulder joints in childhood].Zeitschrift fur Rheumatologie · 2025
    Article
  8. Review
  9. Article
  10. Angular assessment of joints in juvenile idiopathic arthritis.Rheumatology and immunology research · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Juvenile idiopathic arthritis and associated uveitis: A review of pathogenesis, diagnosis, and management.Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society
    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

4 authors at 4 institutions in 4 countries.

Susan ShenoiSeattle Children's Hospital and Research Centre, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-2495-594X
Gerd HorneffDepartment of General Paediatrics, Asklepios Clinic Sankt Augustin, Sankt Augustin, Germany.
Amita AggarwalDepartment of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Angelo RavelliDirezione Scientifica, IRCCS Istituto Giannina Gaslini, Genoa, Italy. angeloravelli@gaslini.org.ORCID http://orcid.org/0000-0001-9658-0385
Asklepios Klinik Sankt Augustin · DEIstituto Giannina Gaslini · ITSanjay Gandhi Post Graduate Institute of Medical Sciences · INSeattle Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the past two decades, the treatment of juvenile idiopathic arthritis (JIA) has evolved markedly, owing to the availability of a growing number of novel, potent and relatively safe therapeutic agents and the shift of management strategies towards early achievement of disease remission. However, JIA encompasses a heterogeneous group of diseases that require distinct treatment approaches. Furthermore, some old drugs, such as methotrexate, sulfasalazine and intraarticular glucocorticoids, still maintain an important therapeutic role. In the past 5 years, information on the efficacy and safety of drug therapies for JIA has been further enriched through the accomplishment of several randomized controlled trials of newer biologic and synthetic targeted DMARDs. In addition, a more rational therapeutic approach has been fostered by the promulgation of therapeutic recommendations and guidelines. A multinational collaborative effort has led to the development of the recommendations for the treat-to-target strategy in JIA. There is currently increasing interest in establishing the optimal time and modality for discontinuation of treatment in children with JIA who achieve sustained clinical remission. The aim of this Review is to summarize the current evidence and discuss the therapeutic approaches to the management of non-systemic phenotypes of JIA, including oligoarthritis, polyarthritis, enthesitis-related arthritis and psoriatic arthritis.

Indexed as

Antirheumatic AgentsArthritis, JuvenileArthritis, PsoriaticChildHumansMethotrexateSulfasalazineTreatment OutcomeAntirheumatic AgentsMethotrexateSulfasalazine

Identifiers

PMID38321298
OpenAlexW4391579112

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.