Evidence map›Paper›PMID 41624828›Full record

ArticleFrontiers in pediatrics2025

High CRP and white blood cell counts are not reliable indicators of early-onset neonatal infection in full-term infants.

Liang Liu, Xueou Liu, Lulu Zhang, Junling Ma, Fangrui Ding

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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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

5 authors.

Liang Liu *Department of Neonatology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin, China.
Xueou Liu *Tianjin Institute of Gynecology Obstetrics, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin, China.
Lulu ZhangDepartment of Neonatology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin, China.
Junling MaDepartment of Neonatology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin, China.
Fangrui DingDepartment of Neonatology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Diagnosing neonatal early-onset sepsis (EOS) is challenging, making it difficult to determine infection indicator characteristics and cutoff values in full-term infants. This study retrospectively analyzed full-term infants with high-risk factors for neonatal EOS but tested negative for EOS, aiming to identify infection indicator characteristics and their association with perinatal factors without antibiotic intervention. Methods: Full-term infants at high risk for EOS who were admitted to rooming-in from 1 July 2023 to 29 February 2024 were included in the study. Blood routine examinations and C-reactive protein (CRP) levels were dynamically monitored after birth. All demographic data and medical records were collected from the electronic medical records system. Results: Among 103 neonates, only 2 had normal infection indicators. Within 24-48 h after birth, an additional 28 displayed normal infection indicators. Although most of the infants exhibited normal WBC within 24-48 h, 33 patients still had higher neutrophil percentages, and 62 had higher CRP levels. Moreover, several high-risk perinatal factors for abnormal infection indicators have been identified. Conclusions: This study demonstrates that infection indicators frequently showed abnormalities in full-term infants at high risk for EOS who tested negative. Few infants had normal infection indicators within 24 h, and although WBC levels normalized by 24-48 h, CRP levels remained elevated. Specific perinatal factors were also associated with abnormal infection markers. These findings reinforce the need for cautious interpretation of isolated biomarker elevations and support antimicrobial stewardship by highlighting the high frequency of abnormal indicators in uninfected infants, thereby reducing unnecessary antibiotic exposure.

Indexed as

antibiotic stewardshipbiomarkersinfectious diseaseneonatesepsis

Identifiers

PMID41624828
PMCPMC12852385

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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.