Evidence map›Paper›PMID 38685851›Full record

ArticlePharmacoepidemiology and drug safety2024

Validation of new medication use algorithms as proxies for worsening disease activity in patients with juvenile idiopathic arthritis.

Kyoko Saito, Avinash Gabbeta, Evan Mulvihill, Lina Al-Jaberi, Timothy Beukelman, James D Lewis, Carlos D Rose, Brian L Strom, Daniel B Horton

Abstract readValidation StudyMulticenter Study
In one paragraph

Article in Pharmacoepidemiology and drug safety, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

9 authors.

Kyoko SaitoBrown University, Providence, Rhode Island, USA.
Avinash GabbetaSt. Christopher's Hospital for Children, Philadelphia, Pennsylvania, USA.
Evan MulvihillNemours Children's Hospital, Wilmington, Delaware, USA.
Lina Al-JaberiArkansas Children's Hospital, Little Rock, Arkansas, USA.
Timothy BeukelmanChildhood Arthritis & Rheumatology Research Alliance, Washington, DC, USA.
James D LewisDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Carlos D RoseNemours Children's Hospital, Wilmington, Delaware, USA.
Brian L StromRutgers Biomedical and Health Sciences, Newark, New Jersey, USA.
Daniel B HortonRutgers Center for Pharmacoepidemiology and Treatment Science, Institute for Health, Health Care Policy and Aging Research, New Brunswick, New Jersey, USA.ORCID 0000-0002-1831-1339

Funding

New Jersey Alliance for Clinical Translational Science: NJ ACTSUL1TR003017 · NCATS · RUTGERS BIOMEDICAL/HEALTH SCIENCES-RBHS · PI PANETTIERI, REYNOLD ALEXANDER · 2019 to 2023
$28.9M
Antibiotics, Juvenile Idiopathic Arthritis, and Antirheumatic Treatment ResponseR01AR074436 · NIAMS · RUTGERS, THE STATE UNIV OF N.J. · PI HORTON, DANIEL BENJAMIN · 2019 to 2022
$2.1M
Drugs, Germs, and Joints: Antibiotics, Gut Microbiota, and Juvenile Idiopathic ArthritisK23AR070286 · NIAMS · RBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL · PI HORTON, DANIEL BENJAMIN · 2016 to 2020
$909k
NCATS NIH HHS UL1 TR003017NCATS NIH HHS UL1TR003017NIAMS NIH HHS K23 AR070286NIAMS NIH HHS K23AR070286NIAMS NIH HHS R01 AR074436NIAMS NIH HHS R01AR074436
6 · The paper itself

Abstract

purposeTo facilitate claims-based research on populations with juvenile idiopathic arthritis (JIA), we sought to validate an algorithm of new medication use as a proxy for worsening JIA disease activity.

methodsUsing electronic health record data from three pediatric centers, we defined new JIA medication use as (re)initiation of disease-modifying antirheumatic drugs or glucocorticoids (oral or intra-articular). Data were collected from 201 randomly selected subjects with (101) or without (100) new medication use. We assessed the positive predictive value (PPV) and negative predictive value (NPV) based on a reference standard of documented worsening of JIA disease activity. The algorithm was refined to optimize test characteristics.

resultsOverall, the medication-based algorithm had suboptimal performance in representing worsening JIA disease activity (PPV 69.3%, NPV 77.1%). However, algorithm performance improved for definitions specifying longer times after JIA diagnosis (≥1-year post-diagnosis: PPV 82.9%, NPV 80.0%) or after initiation of prior JIA treatment (≥1-year post-treatment: PPV 89.7%, NPV 80.0%).

conclusionAn algorithm for new JIA medication use appears to be a reasonable proxy for worsening JIA disease activity, particularly when specifying new use ≥1 year since initiating a prior JIA medication. This algorithm will be valuable for conducting research on JIA populations within administrative claims databases.

Indexed as

AlgorithmsAntirheumatic AgentsArthritis, JuvenileElectronic Health RecordsGlucocorticoidsAdolescentChildChild, PreschoolDisease ProgressionFemaleHumansMalePredictive Value of TestsAntirheumatic AgentsGlucocorticoidsalgorithmsjuvenile arthritispharmacoepidemiologyroutinely collected health datavalidation study

Identifiers

PMID38685851
PMCPMC11541400

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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.