MétaCan
Menu
Back to cohort
Record W2764162815 · doi:10.1093/pch/pxx086.081

UNIQUE MONOARTHRITIS PRESENTATIONS IN OLIGOARTICULAR JUVENILE IDIOPATHIC ARTHRITIS: A CASE SERIES

2017· article· en· W2764162815 on OpenAlexaffabout
Natasha Leporé, Megan Cashin, Debra Bartley, Daniela S. Ardelean

Bibliographic record

VenuePaediatrics & Child Health · 2017
Typearticle
Languageen
FieldMedicine
TopicAutoimmune and Inflammatory Disorders Research
Canadian institutionsWestern University
Fundersnot available
KeywordsMonoarthritisMedicineArthritisPediatricsUveitisInternal medicineRetrospective cohort studyCohortRheumatologyOligoarthritisSurgeryPolyarthritisImmunology

Abstract

fetched live from OpenAlex

BACKGROUND: Juvenile idiopathic arthritis (JIA) is a heterogeneous group of seven immune-mediated chronic inflammatory diseases that target the joints in children younger than 16 years of age. In Canada and worldwide, the estimated prevalence of JIA is approximately 1 per 1,000 children. Almost half of JIA patients are diagnosed with oligoarticular juvenile idiopathic arthritis (oligoJIA). OligoJIA, the most common chronic inflammatory arthritis of childhood, usually affects the knees and ankles. OligoJIA monoarthritis presenting with atypical, severe joint involvement is exceedingly rare and may have poor prognosis. OBJECTIVES: To identify the cases of children that presented with atypical monoarthritis and were diagnosed with oligoJIA in our Pediatric Rheumatology Clinic. Our aim is to describe their demographic, clinical, laboratory, and imaging features. In addition, we reviewed ten similar cases published in the literature. DESIGN/METHODS: This is a retrospective case series study. Fifty-three children with JIA from our inception cohort established in September 2015 were screened for the study. Other JIA subtypes and oligoJIA with ≥ 2 joints affected were excluded. RESULTS: Twenty-five out of 53 (47%) children with JIA were diagnosed with oligoJIA. Four of these 25 children (16%) presented with atypical monoarthritis of the hip, wrist or elbow. None had uveitis. All four were girls with a median age of 11.5 ± 3.5 years (range 9-16 years). Median duration of symptoms prior to diagnosis was 9.5 months. Median follow-up was 5.5 ± 3.5 months. All four patients had normal inflammatory markers. Two children were HLA-B27 positive and had hip arthritis. Three out of four (75%) children had second degree relatives with rheumatologic diseases. Three children (75%) diagnosed with hip, wrist and elbow arthritis respectively had cartilage loss and significant bone changes at presentation, including erosions. Only 10 cases of oligoJIA presenting with atypical monoarthritis have been published to date: 7 children with wrist involvement and 3 others with elbow arthritis. Five out of 7 (71%) children presenting with wrist oligoJIA had bone damage, whereas none of those with elbow arthritis had bone changes at presentation. CONCLUSION: Hip, wrist and elbow oligoJIA can have an aggressive course and present with bone damage. Prompt diagnosis is essential in avoiding irreversible bone and joint damage. Early referral to specialized care can improve their diagnosis, treatment and outcome.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Case report · Consensus signal: Case report
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.003
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0020.002
Science and technology studies0.0030.002
Scholarly communication0.0020.002
Open science0.0010.002
Research integrity0.0020.002
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.019
GPT teacher head0.314
Teacher spread0.295 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designCase report
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2017
Admission routes2
Has abstractyes

Explore more

Same venuePaediatrics & Child HealthSame topicAutoimmune and Inflammatory Disorders ResearchFrench-language works237,207