Evidence map›Paper›PMID 40756153›Full record

ArticleJournal of the Pediatric Orthopaedic Society of North America2025

Risk Factors for Corticosteroid-associated Osteonecrosis in Children: A National Database Study.

Gabriella B Smith, Nicole S Pham, Amin Alayleh, Stephanie Smith, Karen Chao, Stuart B Goodman, Kevin G Shea

Abstract read
In one paragraph

Article in Journal of the Pediatric Orthopaedic Society of North America, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Gabriella B SmithStanford University School of Medicine, Department of Orthopaedic Surgery, Division of Pediatric Orthopaedics, Stanford, CA, USA.
Nicole S PhamStanford University School of Medicine, Department of Orthopaedic Surgery, Division of Pediatric Orthopaedics, Stanford, CA, USA.
Amin AlaylehStanford University School of Medicine, Department of Orthopaedic Surgery, Division of Pediatric Orthopaedics, Stanford, CA, USA.
Stephanie SmithStanford University School of Medicine, Department of Pediatrics, Division of Pediatric Hematology, Oncology, Stanford, CA, USA.
Karen ChaoStanford University School of Medicine, Department of Pediatrics, Division of Pediatric Hematology, Oncology, Stanford, CA, USA.
Stuart B GoodmanStanford University School of Medicine, Department of Orthopaedic Surgery, Division of Pediatric Orthopaedics, Stanford, CA, USA.
Kevin G SheaStanford University School of Medicine, Department of Orthopaedic Surgery, Division of Pediatric Orthopaedics, Stanford, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Corticosteroid-associated osteonecrosis presents a risk for severe pain and joint collapse. While the relationship between corticosteroid treatment and osteonecrosis in pediatric patients is well-documented, less is known about which patients are at greatest risk across medical conditions. The purpose of this study was to identify high-risk pediatric populations for developing osteonecrosis following corticosteroid treatment across autoimmune, inflammatory, and oncologic conditions. Methods: The Merative MarketScan Research Databases (2007-2022) were queried to identify pediatric patients with an outpatient oral or intravenous corticosteroid prescription. Demographic, clinical, and prescription differences between osteonecrosis and non-osteonecrosis patients were analyzed using t-tests, Fisher's exact, and chi-square tests. Factors associated with time to osteonecrosis were assessed using a multivariable Cox proportional-hazards regression model. Results: We identified 5,606,781 pediatric patients who received corticosteroids, and 131 developed osteonecrosis. The mean time to osteonecrosis following corticosteroid administration was 7.1 months (SD = 5.2). Osteonecrosis patients were significantly older at the age of corticosteroid administration (12.1 [SD = 4.9] vs. 8.2 [5.6], Conclusions: Our national database study highlights the need for targeted screening of pediatric patients treated with high-dose corticosteroids. This investigation may inform multidisciplinary studies and interventions in children treated with corticosteroids. Key Concepts: (1)Corticosteroid-associated osteonecrosis presents a risk for severe pain and joint collapse, yet little is known regarding which pediatric patients are at greatest risk across medical conditions.(2)Adjusting for other covariates, pediatric patients with acute lymphoblastic leukemia, systemic lupus erythematous, Crohn's disease, juvenile idiopathic arthritis, solid organ transplants, patients prescribed dexamethasone, patients prescribed corticosteroids for greater total days, and older patients were at increased risk for osteonecrosis in our national database study.(3)Our findings highlight the need for targeted screening of pediatric patients treated with high-dose corticosteroids.(4)Future prospective multidisciplinary screening and intervention protocols should be studied in children treated with corticosteroids. Level of Evidence: Level III: Case-control study or retrospective cohort study.

Indexed as

Acute lymphoblastic leukemiaAvascular necrosisCorticosteroidsOsteonecrosisSystemic lupus erythematous

Identifiers

PMID40756153
PMCPMC12317409

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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.