Evidence map›Paper›PMID 34175928›Full record

Observational studyRheumatology (Oxford, England)2022

Prevalence of avascular necrosis in idiopathic inflammatory myopathies: a single-centre experience.

Khalil I Bourji, Christopher A Mecoli, Julie J Paik, Jemima Albayda, Eleni Tiniakou, William Kelly, Thomas E Lloyd, Andrew Mammen, Shivani Ahlawat, Lisa Christopher-Stine

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Rheumatology (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 45% of its field
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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
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 at 4 institutions in 1 country.

Khalil I BourjiDivision of Rheumatology, Wayne State University/Henry Ford Health System, Detroit, MI.ORCID 0000-0001-9878-4074
Christopher A MecoliDivision of Rheumatology.ORCID 0000-0002-1429-8392
Julie J PaikDivision of Rheumatology.ORCID 0000-0001-8436-1601
Jemima AlbaydaDivision of Rheumatology.
Eleni TiniakouDivision of Rheumatology.
William KellyDivision of Rheumatology.
Thomas E LloydDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore.
Andrew MammenDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore.
Shivani AhlawatDepartment of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Lisa Christopher-StineDivision of Rheumatology.
Center for Rheumatology · USJohns Hopkins University · USHenry Ford Health System · USNational Institutes of Health · US

Funding

Muscle Disease UnitZIAAR041203 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI MAMMEN, ANDREW · 2015 to 2025
$19.7M
RNA: Polymerase III specific CD8+ T cells: a mechanistic insight into cancer-induced autoimmunity in sclerodermaK08AR077732 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TINIAKOU, ELENI · 2021 to 2025
$794k
Optimizing the Approach to Identify Cancer-Associated MyositisK23AR075898 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI MECOLI, CHRISTOPHER · 2019 to 2023
$773k
NIAMS NIH HHS K08 AR077732NIAMS NIH HHS K23 AR075898
6 · The paper itself

Abstract

objectivesTo assess the prevalence of avascular necrosis (AVN) in a large cohort of patients with idiopathic inflammatory myopathies (IIM) and define the major associated risk factors.

methodsWe retrospectively reviewed the electronic medical records of all patients with a definitive diagnosis of IIM enrolled in our registry between 2003 and 2017, and followed until 2020. Pertinent demographic, clinical, serologic and imaging data were collected. A matched group of patients without AVN was then selected for comparison.

resultsA total of 1680 patients were diagnosed with IIM. Fifty-one patients developed AVN, with an overall prevalence of 3%. Musculoskeletal MRI was available for 1085 patients and AVN was present in 46 patients (43 lower extremities and 3 upper extremities MRI studies), with a relative prevalence of 4.2%. Most patients with AVN were Caucasian females (57%) with a mean (s.d.) age at diagnosis of 44.5 (12.4) years. Sixty-one percent had DM and 29% had PM. The median time from onset of IIM to diagnosis of AVN was 46 months. The hip joint was most commonly involved in 76% of cases, followed by the knee joint in 15% and shoulder joint in 9%. Some 81% of patients were asymptomatic. Established risk factors for AVN were not found to be associated with the development of AVN in IIM patients.

conclusionAlthough mostly asymptomatic and incidental, the overall prevalence of AVN in IIM was 3% and the prevalence by MRI was 4.2%. None of the established risk factors was found to be associated with AVN development.

Indexed as

AdultFemaleHumansMagnetic Resonance ImagingMaleMyositisOsteonecrosisPrevalenceRegistriesRetrospective Studiesavascular necrosisAVNmyositisosteonecrosis

Identifiers

PMID34175928
PMCPMC9123897
OpenAlexW3176958188

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.