Evidence map›Paper›PMID 38240873›Full record

ArticleMikrochimica acta2024

Micromotor-based dual aptassay for early cost-effective diagnosis of neonatal sepsis.

José M Gordón Pidal, Luis Arruza, María Moreno-Guzmán, Miguel Ángel López, Alberto Escarpa

Abstract read
In one paragraph

Article in Mikrochimica acta, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Magnetoelectrochemical Rotation of Light Emitting Graphene Monolayers.Small (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  3. Review
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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

5 authors.

José M Gordón PidalDepartment of Analytical Chemistry, Physical Chemistry and Chemical Engineering, Faculty of Sciences, University of Alcalá, Ctra. Madrid-Barcelona, Km. 33.600, Alcalá de Henares, 28802, Madrid, Spain.
Luis ArruzaDepartment of Neonatology, Instituto del Niño y del Adolescente, Hospital Clínico San Carlos-IdISSC, 28040, Madrid, Spain.
María Moreno-GuzmánDepartment of Chemistry in Pharmaceutical Sciences, Analytical Chemistry, Faculty of Pharmacy, Complutense University of Madrid, Plaza Ramón y Cajal, S/N, 28040, Madrid, Spain.
Miguel Ángel LópezDepartment of Analytical Chemistry, Physical Chemistry and Chemical Engineering, Faculty of Sciences, University of Alcalá, Ctra. Madrid-Barcelona, Km. 33.600, Alcalá de Henares, 28802, Madrid, Spain. miguelan.lopez@uah.es.
Alberto EscarpaDepartment of Analytical Chemistry, Physical Chemistry and Chemical Engineering, Faculty of Sciences, University of Alcalá, Ctra. Madrid-Barcelona, Km. 33.600, Alcalá de Henares, 28802, Madrid, Spain. alberto.escarpa@uah.es.ORCID http://orcid.org/0000-0002-7302-0948

Funding

Comunidad de Madrid DISCOVER-UAH-CM Project (Ref. REACT UE-CM2021-01)Comunidad de Madrid TRANSNANOAVANSES program (S2018/NMT-4349 )Ministerio de Ciencia e Innovación Grant PID2020-118154 GB-I00 funded by MCIN/AEI/ 10.13039/501100011033
6 · The paper itself

Abstract

Given the long-life expectancy of the newborn, research aimed at improving sepsis diagnosis and management in this population has been recognized as cost-effective, which at early stages continues to be a tremendous challenge. Despite there is not an ideal-specific biomarker, the simultaneous detection of biomarkers with different behavior during an infection such as procalcitonin (PCT) as high specificity biomarker with one of the earliest biomarkers in sepsis as interleukin-6 (IL-6) increases diagnostic performance. This is not only due to their high positive predictive value but also, since it can also help the clinician to rule out infection and thus avoid the use of antibiotics, due to their high negative predictive value. To this end, we explore a cutting-edge micromotor (MM)-based OFF-ON dual aptassay for simultaneous determination of both biomarkers in 15 min using just 2 μL of sample from low-birth-weight neonates with gestational age less than 32 weeks and birthweight below 1000 g with clinical suspicion of late-onset sepsis. The approach reached the high sensitivities demanded in the clinical scenario (LOD

Indexed as

Neonatal SepsisSepsisAnti-Bacterial AgentsBiomarkersCalcitoninCost-Benefit AnalysisC-Reactive ProteinHumansInfantInfant, NewbornInterleukin-6ProcalcitoninReproducibility of ResultsAnti-Bacterial AgentsBiomarkersCalcitoninC-Reactive ProteinInterleukin-6ProcalcitoninAptamersBedside/point-of-care technologiesFluorescence microscopyInterleukin-6ProcalcitoninSepsis biomarkers

Identifiers

PMID38240873
PMCPMC10798920

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Registered trials

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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.