Evidence map›Paper›PMID 41163924›Full record

ArticleFrontiers in pediatrics2025

Comparative analysis of CRP and PCT as biomarkers for early diagnosis of pediatric septic arthritis: superior performance of CRP.

Wenchen Xu, Piaoxue Yu, Xiangxuan Wang, Kainan Lin, Hui Chen

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2025. 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

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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. 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

5 authors.

Wenchen XuDepartment of Orthopedics, Fujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center), College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Piaoxue YuDepartment of Ultrasonography, Fuzhou Second Hospital, Fuzhou, China.
Xiangxuan WangDepartment of Orthopedics, Fujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center), College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Kainan LinDepartment of Orthopedics, Fujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center), College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Hui ChenDepartment of Orthopedics, Fujian Children's Hospital (Fujian Branch of Shanghai Children's Medical Center), College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Septic arthritis is a severe pediatric infection that affects joint health and requires early diagnosis to prevent complications. Traditional methods have limitations, and although serum PCT shows promise as a diagnostic marker, its efficacy remains controversial, warranting further studies. Objective: To investigate the value of C-reactive protein (CRP) and procalcitonin (PCT) in the early diagnosis of septic arthritis (SA) in pediatric patients and to compare their diagnostic efficiencies. Methods: This investigation utilized a retrospective cohort methodology to ascertain and compare serum procalcitonin (PCT) and C-reactive protein (CRP) concentrations among a pediatric population comprising 29 individuals diagnosed with septic arthritis and 25 with non-septic arthritis (NSA), all of whom were admitted to our institutional facility over a three-year period from 2019 to 2021. Results: CRP levels (>10 mg/L) were significantly higher in the septic arthritis group than in the non-septic group (26/29 vs. 3/25, Conclusion: Our findings substantiate the substantial superiority of CRP for the early detection and preliminary alert of pediatric septic arthritis. However, due to the small sample size, its significant advantage over procalcitonin (PCT) requires confirmation in larger studies.

Indexed as

biomarkersC-reactive protein (CRP)early diagnosisinfectionpediatricprocalcitonin (PCT)septic arthritis (SA)

Identifiers

PMID41163924
PMCPMC12558828

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