Evidence map›Paper›PMID 34488677›Full record

ArticleBMC infectious diseases2021

The potential value of plasma receptor interacting protein 3 in neonates with culture-positive late-onset sepsis.

Chuchu Gao, Zongtai Feng, Lixia Wang, Xingxing Zhao, Kai Fu, Shurong Ma, Zuming Yang, Sannan Wang, Shenglin Yu

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Chuchu Gao *Department of Neonatology, Children's Hospital of Soochow University, Suzhou, 215025, China.
Zongtai Feng *Department of Neonatology, The Affiliated Suzhou Hospital of Nanjing Medical University (Suzhou Municipal Hospital), Suzhou, 215002, China.
Lixia Wang *Department of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Xingxing ZhaoDepartment of Neonatology, The Affiliated Suzhou Hospital of Nanjing Medical University (Suzhou Municipal Hospital), Suzhou, 215002, China.
Kai FuDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Shurong MaDepartment of Neonatology, Children's Hospital of Soochow University, Suzhou, 215025, China.
Zuming YangDepartment of Neonatology, The Affiliated Suzhou Hospital of Nanjing Medical University (Suzhou Municipal Hospital), Suzhou, 215002, China.
Sannan WangDepartment of Neonatology, The Affiliated Suzhou Hospital of Nanjing Medical University (Suzhou Municipal Hospital), Suzhou, 215002, China. wangsn2002@sina.com.
Shenglin YuDepartment of Neonatology, Children's Hospital of Soochow University, Suzhou, 215025, China. wm1971@sina.com.
Nanjing Medical University · CNSoochow University · CNSuzhou Municipal Hospital · CNSecond Affiliated Hospital of Soochow University · CN

Funding

Jiangsu Province Women and Children Health Research Project No. F202021Science and Technology Development Fund Project of Nanjing Medical University No. NMUB2019330Science and Technology Project of Suzhou No. SYS2019095Science and Technology Project of Suzhou SYS2018070the Advanced Research Fund for the Second Affiliated Hospital of Soochow University No. SDFEYQN1805
6 · The paper itself

Abstract

backgroundLate-onset sepsis (LOS) is a systemic inflammatory response syndrome in neonates, and the molecular mechanism of LOS is incompletely characterized. The purpose of this study was to explore the potential value of receptor interacting protein 3 (RIP3) in LOS.

methods63 neonates with LOS supported by positive culture and 79 neonates without sepsis were enrolled in this study from September 2019 to March 2021. Plasma RIP3 was detected by enzyme-linked immunosorbent assay (ELISA) and assessed along with the whole blood hypersensitive C-reactive protein (hs-CRP) level and platelet count (PLT). Differences in RIP3, hs-CRP and PLT between the two groups were compared. Changes in the three indicators in sepsis were also observed after treatment. The diagnostic value of indicators for LOS was evaluated by receiver operating characteristic (ROC) curve analysis.

resultsIn the sepsis group, RIP3 and hs-CRP levels were significantly higher than those in the control group (RIP3, p < 0.0001; hs-CRP, p < 0.0001), and PLT was significantly lower than that in the control group (p < 0.0001). After treatment, RIP3 and hs-CRP levels among septic survivors were significantly decreased (p < 0.0001) and PLT significantly improved (p = 0.0216). With RIP3 > 15,845.19 pg/mL, hs-CRP > 5.00 mg/L, and PLT < 204.00 × 10

conclusionsRIP3 may contribute to the early diagnosis of LOS and monitoring of treatment effect. The combined detection of RIP3, hs-CRP and PLT may be more effective than individual detection in the diagnosis of LOS.

Indexed as

SepsisBiomarkersC-Reactive ProteinEarly DiagnosisHumansInfant, NewbornPlatelet CountROC CurveBiomarkersC-Reactive ProteinLate-onset sepsisNeonateReceptor interacting protein 3

Identifiers

PMID34488677
PMCPMC8422743
OpenAlexW3197745467

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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.