MétaCan
Menu
Back to cohort
Record W2006894316 · doi:10.1186/1546-0096-10-s1-a64

Diagnostic evaluation and medication usage in a cohort of subjects with juvenile dermatomyositis from the CARRAnet registry

2012· article· en· W2006894316 on OpenAlexaff
Angela Byun Robinson, Mark F. Hoeltzel, Ann M. Reed, Adam M. Huber, Brian M. Feldman

Bibliographic record

VenuePediatric Rheumatology · 2012
Typearticle
Languageen
FieldMedicine
TopicInflammatory Myopathies and Dermatomyositis
Canadian institutionsHospital for Sick ChildrenIzaak Walton Killam Health Centre
Fundersnot available
KeywordsMedicineJuvenile dermatomyositisRheumatologyIncidence (geometry)CohortInternal medicineDermatomyositisObservational studyPediatricsEpidemiologyCohort studyDisease registryDiseasePhysical therapyDatabaseFamily medicine

Abstract

fetched live from OpenAlex

Children under 21 yrs with onset of JDM prior to 16 yrs were included, and subjects or their guardians were consented for the study. IRB approval was obtained at each enrolling site. JDM was diagnosed by modified Bohan and Peter criteria. Clinical data were collected from the subjects, guardians, and providers using both general and JDM-specific case report forms at the time of enrollment. Data regarding demographics, diagnostic assessment, and medication exposure were collected. Data were pooled and stored in a secure centralized database and de-identified prior to analysis. Between May 28, 2010 and December 28, 2010, 102 subjects meeting modified criteria for JDM were enrolled from 23 sites in the U.S. Diagnostic studies commonly used include electromyography (EMG), muscle biopsy, and magnetic resonance imaging (MRI). Overall, MRI was more likely than EMG or muscle biopsy to show abnormalities. (Table 1 ) 48 of subjects had 2 or more studies performed and 54.2% of these subjects reported at least 1 negative study. In terms of medications, 100% of subjects have been exposed to corticosteroids during their course of treatment, and 97% of subjects have been exposed to methotrexate, suggesting that these medications are almost universally prescribed for JDM. Medication history in order of frequency of usage is shown in Table 2 . MRI was the most common diagnostic modality used and was the most likely to show abnormalities consistent with JDM. The false negative rates for MRI, EMG, and muscle biopsy alone were higher than expected if ascertainment is correct. Corticosteroids and methotrexate appear to be standard first line medications used by US pediatric rheumatologists for JDM. Pulse corticosteroids, intravenous gammaglobulin, and hydroxychloroquine have been used by about half of subjects and further investigation as to which subgroups receive these medications is warranted.

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)0.001
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.012
Threshold uncertainty score0.417

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
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 head0.008
GPT teacher head0.246
Teacher spread0.238 · 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.

The models applied no category: nothing in the taxonomy fit this work.
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

Citations1
Published2012
Admission routes1
Has abstractyes

Explore more

Same venuePediatric RheumatologySame topicInflammatory Myopathies and DermatomyositisFrench-language works237,207