Evidence map›Paper›PMID 34363343›Full record

ArticleArthritis care & research2023

Development and Validation of a Juvenile Spondyloarthritis Disease Flare Measure: Ascertaining Flare in Patients With Inactive Disease.

Pamela F Weiss, Timothy G Brandon, Meghan E Ryan, Erin B Treemarcki, Stephanie Armendariz, Tracey B Wright, Chetna Godiwala, Matthew L Stoll, Rui Xiao, Daniel Lovell

Abstract read
In one paragraph

Article in Arthritis care & research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

10 authors.

Pamela F WeissUniversity of Pennsylvania and Children's Hospital of Philadelphia, Philadelphia.ORCID 0000-0002-9724-0443
Timothy G BrandonChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-1305-4871
Meghan E RyanUniversity of Minnesota Masonic Children's Hospital, Minneapolis.
Erin B TreemarckiUniversity of Utah and Primary Children's Hospital, Salt Lake City.ORCID 0000-0003-3858-7065
Stephanie ArmendarizScottish Rite Hospital for Children, Dallas, Texas.
Tracey B WrightUniversity of Texas Southwestern Medical Center and Scottish Rite Hospital for Children, Dallas.
Chetna GodiwalaScottish Rite Hospital for Children, Dallas, Texas.
Matthew L StollUniversity of Alabama at Birmingham.ORCID 0000-0002-6225-3690
Rui XiaoUniversity of Pennsylvania, Philadelphia.
Daniel LovellCincinnati Children's Hospital Medical Center, Cincinnati, Ohio.ORCID 0000-0003-1604-0130

Funding

Refining entry criteria and outcome measures for children with axial disease and spondyloarthritis: preparation for clinical trialsR01AR074098 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI WEISS, PAMELA FITCH · 2019 to 2021
$678k
NIAMS NIH HHS R01 AR074098
6 · The paper itself

Abstract

objectiveOur objective was to develop and validate a composite disease flare definition for juvenile spondyloarthritis (SpA) that would closely approximate the clinical decision made to reinitiate or not reinitiate systemic therapy after therapy de-escalation.

methodsRetrospective chart reviews of children with SpA who underwent systemic therapy de-escalation of biologic or conventional disease-modifying antirheumatic drugs were used to develop and validate the flare outcome. Data on independent cohorts for development (1 center) and validation (4 centers) were collected from large tertiary health care systems. Core measure thresholds and candidate disease flare outcomes were assessed using sensitivity, specificity, positive predictive values (PPVs) and negative predictive values (NPVs), and the receiver operating characteristic (ROC) area under the curve (AUC), with physician assessment of active disease plus re-initiation of standard dose of systemic therapy as the reference standard.

resultsOf the candidate definitions, clinically meaningful worsening in ≥3 of the following 5 core measures performed best: caregiver/patient assessment of well-being; physician assessment of disease activity; caregiver/patient assessment of pain, physical function, and active joint count. The ROC AUC was 0.91, PPV 87.5%, NPV 98.1%, sensitivity 82.4%, and specificity 98.7%. Cronbach's α was 0.81, signifying internal consistency, and factor analysis demonstrated that the outcome measured 1 construct. The Juvenile SpA Flare measure had face validity according to 21 surveyed pediatric rheumatologists. Juvenile SpA Flare had an ROC AUC of 0.85, a PPV of 92.3%, and an NPV of 96.8% in the validation cohort.

conclusionThere is initial support for the validity of the Juvenile SpA Flare measure as a tool to identify disease flare in juvenile SpA patients de-escalating therapy, and the measure is potentially applicable in clinical practice, observational studies, and therapeutic trials.

Indexed as

Antirheumatic AgentsArthritis, JuvenileSpondylarthritisSpondylitis, AnkylosingChildHumansRetrospective StudiesSymptom Flare UpAntirheumatic Agents

Identifiers

PMID34363343
PMCPMC8818809

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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.