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Record W2078443837 · doi:10.1186/ar4652

Serological features of systemic lupus erythematosus diagnosed after referral through a rheumatology triage system because of positive antinuclear antibodies

2014· article· en· W2078443837 on OpenAlexafffund
Marvin J. Fritzler, Whitney Steber, Terri Lupton, Christie Fitch-Rogalsky, Liam Martin, Susan G. Barr, Ann E. Clarke

Bibliographic record

VenueArthritis Research & Therapy · 2014
Typearticle
Languageen
FieldMedicine
TopicSystemic Lupus Erythematosus Research
Canadian institutionsUniversity of Calgary
FundersNational Institute of Allergy and Infectious DiseasesCanadian Institutes of Health ResearchCanadian Arthritis NetworkNational Institute of Arthritis and Musculoskeletal and Skin DiseasesArthritis SocietyLupus Research AllianceNational Institutes of HealthLupus Foundation of AmericaCentral New York Community Foundation
KeywordsRheumatologyMedicineAnti-nuclear antibodyTriageInternal medicineSerologyReferralSystemic lupus erythematosusSystemic lupusAutoantibodyAntibodyPhysical therapyDermatologyImmunologyFamily medicineEmergency medicineDisease

Abstract

fetched live from OpenAlex

The initial diagnosis of systemic lupus erythematosus (SLE) is made in a number of clinical settings, which include referrals to a specialist because of a constellation of symptoms and/or abnormal laboratory findings. Although a positive antinuclear antibody (ANA) test has been regarded a serological hallmark of SLE, it is also associated with a number of other systemic autoimmune rheumatic diseases (SARD). We studied the serological features of patients who were referred through a central triage (CT) system because of positive ANA and were then diagnosed as having SLE by the consulting rheumatologist. Patients who met four criteria were included in the SLE cohort: referred to CT over 3 years; reason for referral was positive ANA; evaluated by a certified rheumatologist; and diagnosed as SLE. Clinical information from the first rheumatologic visit was extracted from the consultant's report. An anonymous CT database was developed to contain clinical information and an anonymous serological database was used for autoantibody test results. A total of 15,357 patients were referred through the CT; 643 (4.1%) because of positive ANA and, of these 263 (40.9%) were evaluated by a rheumatologist. In 24/263 (9.1%) ANA-positive patients, the rheumatologist provided a diagnosis of SLE, while 39 (14.8%) had a diagnosis of another autoantibody-related rheumatic disease (AARD), 69 (26.2%) had no evidence of any disease, 29 (11%) had conditions that did not meet classification criteria for an AARD and the remainder (102, 38.8%) had a variety of rheumatologic diagnoses. The age range of the SLE patients was 25 to 73 years (mean 44.4 years), 95.8% were female, 87.5% were referred by a family physician and the average waiting time was 137.3 days. The serological profile of the 24 SLE patients included 29.1% anti-Sm, 25% anti-U1RNP, 25% anti-ribosomal P, 25% anti-SS-A/Ro60, 25% anti-Ro52/TRIM21, 8.3% anti-dsDNA but none were anti-DFS70-positive. This is the first study to evaluate the serological features of patients who were diagnosed on their first visit as having SLE after they were referred through a CT system because of positive ANA. Approximately 10% of the ANA referral patients were diagnosed as SLE and anti-Sm was the most common (~29%) autoantibody detected. This study provides an assessment of patients referred for positive ANA and implies that serological parameters might be helpful in determining the level of urgency of the referral.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.004
metaresearch head score (Gemma)0.002
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.577
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0040.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0020.000
Bibliometrics0.0010.001
Science and technology studies0.0000.001
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0000.000

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 head0.043
GPT teacher head0.343
Teacher spread0.300 · 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 teacher head, not a consensus.

Study designObservational
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
Published2014
Admission routes2
Has abstractyes

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