Evidence map›Paper›PMID 31168410›Full record

ArticleRMD open2019

Validating 10-joint juvenile arthritis disease activity score cut-offs for disease activity levels in non-systemic juvenile idiopathic arthritis.

Maria Backström, Pirjo Tynjälä, Kristiina Aalto, Minna-Maija Grönlund, Heikki Ylijoki, Anne Putto-Laurila, Johanna Kärki, Paula Keskitalo, Sirja Sard, Heini Pohjankoski and 5 more

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

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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

15 authors at 10 institutions in 1 country.

Maria BackströmPediatric Department, Vaasan keskussairaala, Vaasa, Finland.ORCID 0000-0002-8632-8634
Pirjo TynjäläDepartment of Pediatrics, South Karelia Central Hospital, Lappeenranta, Finland.
Kristiina AaltoHospital for Children and Adolescents, University of Helsinki Hospital for Children and Adolescents, Helsinki, Finland.
Minna-Maija GrönlundDepartment of Pediatrics, Turku University Hospital, Turku, Finland.
Heikki YlijokiDepartment of Pediatrics, Satakunta Central Hospital, Pori, Finland.
Anne Putto-LaurilaDepartment of Pediatrics, Turku University Hospital, Turku, Finland.
Johanna KärkiDepartment of Pediatrics, Kanta-Häme Central Hospital, Hämeenlinna, Finland.
Paula KeskitaloDepartment of Paediatrics, Oulu University Hospital, Oulu, Finland.
Sirja SardDepartment of Paediatrics, Oulu University Hospital, Oulu, Finland.
Heini PohjankoskiDepartment of Pediatrics, Päijät-Häme Central Hospital, Lahti, Finland.
Maiju HietanenDepartment of Pediatrics, Päijät-Häme Central Hospital, Lahti, Finland.
Silke WitterDepartment of Pediatrics, Central Finland Hospital District, Jyvaskyla, Finland.
Helena LehtoDepartment of Pediatrics, South Karelia Central Hospital, Lappeenranta, Finland.
Eliisa LöyttyniemiDepartment of Biostatistics, University of Turku, Turku, Finland.
Paula VähäsaloDepartment of Paediatrics, Oulu University Hospital, Oulu, Finland.ORCID 0000-0002-2712-3903
Oulu University Hospital · FIPäijät-Hämeen Keskussairaala · FITurku University Hospital · FIUniversity of Helsinki · FICentral Finland Health Care District · FIKanta-Hämeen Keskussairaala · FISatakunta Central Hospital · FISouth Karelia Central Hospital · FIUniversity of Turku · FIVaasa Central Hospital · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To validate cut-offs of the Juvenile Arthritis Disease Activity Score 10 (JADAS10) and clinical JADAS10 (cJADAS10) and to compare them with other patient cohorts. Methods: In a national multicentre study, cross-sectional data on recent visits of 337 non-systemic patients with juvenile idiopathic arthritis (JIA) were collected from nine paediatric outpatient units. The cut-offs were tested with receiver operating characteristic curve-based methods, and too high, too low and correct classification rates (CCRs) were calculated. Results: Our earlier presented JADAS10 cut-offs seemed feasible based on the CCRs, but the cut-off values between low disease activity (LDA) and moderate disease activity (MDA) were adjusted. When JADAS10 cut-offs for clinically inactive disease (CID) were increased to 1.5 for patients with oligoarticular disease and 2.7 for patients with polyarticular disease, as recently suggested in a large multinational register study, altogether 11 patients classified as CID by the cut-off had one active joint. We suggest JADAS10 cut-off values for oligoarticular/polyarticular disease to be in CID: 0.0-0.5/0.0-0.7, LDA: 0.6-3.8/0.8-5.1 and MDA: >3.8/5.1. Suitable cJADAS10 cut-offs are the same as JADAS10 cut-offs in oligoarticular disease. In polyarticular disease, cJADAS10 cut-offs are 0-0.7 for CID, 0.8-5.0 for LDA and >5.0 for MDA. Conclusion: International consensus on JADAS cut-off values is needed, and such a cut-off for CID should preferably exclude patients with active joints in the CID group.

Indexed as

AdolescentArthritis, JuvenileBiomarkersChildChild, PreschoolDiagnosis, DifferentialFemaleHumansInfantMaleReference ValuesROC CurveSeverity of Illness IndexBiomarkersdisease activityjuvenile idiopathic arthritisoutcomes research

Identifiers

PMID31168410
PMCPMC6525603
OpenAlexW2941534281

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Registered trials

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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.