Biomarkers for Pediatric Bacterial Musculoskeletal Infections in Lyme Disease-Endemic Regions.


Journal

Pediatrics
ISSN: 1098-4275
Titre abrégé: Pediatrics
Pays: United States
ID NLM: 0376422

Informations de publication

Date de publication:
01 Aug 2023
Historique:
accepted: 27 04 2023
pubmed: 6 7 2023
medline: 6 7 2023
entrez: 6 7 2023
Statut: ppublish

Résumé

Bacterial musculoskeletal infections (MSKIs) are challenging to diagnose because of the clinical overlap with other conditions, including Lyme arthritis. We evaluated the performance of blood biomarkers for the diagnosis of MSKIs in Lyme disease-endemic regions. We conducted a secondary analysis of a prospective cohort study of children 1 to 21 years old with monoarthritis presenting to 1 of 8 Pedi Lyme Net emergency departments for evaluation of potential Lyme disease. Our primary outcome was an MSKI, which was defined as septic arthritis, osteomyelitis or pyomyositis. We compared the diagnostic accuracy of routinely available biomarkers (absolute neutrophil count, C-reactive protein, erythrocyte sedimentation rate, and procalcitonin) to white blood cells for the identification of an MSKI using the area under the receiver operating characteristic curve (AUC). We identified 1423 children with monoarthritis, of which 82 (5.8%) had an MSKI, 405 (28.5%) Lyme arthritis, and 936 (65.8%) other inflammatory arthritis. When compared with white blood cell count (AUC, 0.63; 95% confidence interval [CI], 0.55-0.71), C-reactive protein (0.84; 95% CI, 0.80-0.89; P < .05), procalcitonin (0.82; 95% CI, 0.77-0.88; P < .05), and erythrocyte sedimentation rate (0.77; 95% CI, 0.71-0.82; P < .05) had higher AUCs, whereas absolute neutrophil count (0.67; 95% CI, 0.61-0.74; P < .11) had a similar AUC. Commonly available biomarkers can assist in the initial approach to a potential MSKI in a child. However, no single biomarker has high enough accuracy to be used in isolation, especially in Lyme disease-endemic areas.

Identifiants

pubmed: 37409396
pii: 192509
doi: 10.1542/peds.2023-061329
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 by the American Academy of Pediatrics.

Auteurs

Caroline G Kahane (CG)

Division of Emergency Medicine, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.

Lise E Nigrovic (LE)

Division of Emergency Medicine, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.

Anupam B Kharbanda (AB)

Department of Emergency Medicine, Children's Minnesota, Minneapolis, Minnesota.

Desiree Neville (D)

Division of Emergency Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.

Amy D Thompson (AD)

Division of Emergency Medicine, Nemours Children's Hospital and Sidney Kimmel Medical College of Thomas Jefferson University, Wilmington, Delaware.

Fran Balamuth (F)

Department of Pediatrics, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, Pennsylvania.

Laura Chapman (L)

Division of Pediatric Emergency Medicine, Rhode Island Hospital and Warren Alpert Medical School of Brown University, Providence, Rhode Island.

Michael N Levas (MN)

Department of Pediatric Emergency Medicine, Children's Hospital of Wisconsin and Medical College of Wisconsin, Milwaukee, Wisconsin.

John A Branda (JA)

Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.

Mark D Kellogg (MD)

Department of Laboratory Medicine, Boston Children's Hospital and Department of Pathology, Harvard Medical School, Boston, Massachusetts.

Michael C Monuteaux (MC)

Division of Emergency Medicine, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.

Todd W Lyons (TW)

Division of Emergency Medicine, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.

Classifications MeSH