Evidence map›Paper›PMID 39792926›Full record

ArticlePLoS neglected tropical diseases2025

Congenital Chagas disease: A cohort study to assess molecular diagnostic methods at the Chagas disease national reference center of Argentina.

Constanza Lopez-Albizu, Carolina Inés Cura, Juan Carlos Ramirez, Pamela Peyran, Andrés Benchetrit, Emmaría Danesi, Sergio Sosa-Estani

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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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

7 authors.

Constanza Lopez-AlbizuInstituto Nacional de Parasitología "Dr. Mario Fatala Chaben", Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbran", Buenos, Aires Argentina.ORCID https://orcid.org/0000-0003-0927-8669
Carolina Inés CuraInstituto Nacional de Parasitología "Dr. Mario Fatala Chaben", Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbran", Buenos, Aires Argentina.
Juan Carlos RamirezInstituto Multidisciplinario de Investigaciones en Patologías Pediátricas (IMIPP), CONICET-GCBA, Buenos Aires, Argentina.
Pamela PeyranInstituto Nacional de Parasitología "Dr. Mario Fatala Chaben", Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbran", Buenos, Aires Argentina.
Andrés BenchetritHospital F. J. Muñiz, Buenos Aires, Argentina.
Emmaría DanesiInstituto Nacional de Parasitología "Dr. Mario Fatala Chaben", Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbran", Buenos, Aires Argentina.
Sergio Sosa-EstaniCentro de Investigaciones Epidemiológica y Salud Pública (CIESP-IECS) CONICET.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrypanosoma cruzi is a protozoan parasite which causes Chagas disease. Mother-to-child transmission is the main route of transmission in vector-free areas. Congenital Chagas disease refers specifically to cases arising from this route of transmission. This work evaluates the clinical sensitivity of two qPCR techniques for diagnosis of congenital Chagas disease.

methodsThe study was developed in the National Institute of parasitology (NIP), Argentina, and Pan-American Health Organization/ Word Health Organization Collaborating Center for Chagas Disease. Between July 2014 and May 2018, a prospective cohort study was carried out with 499 children born to seropositive for T. cruzi infection included. The performance of qPCR techniques was compared with the gold standard diagnostic algorithm for Congenital Chagas disease (CCD-GS), which comprises performing more than one parasitological test on children from birth until nine months of age, and serology from ten months of age.

findingsOf the 961 babies born to women seropositive for Chagas disease who were attended at the NIP laboratory, 462 did not meet the study inclusion criteria; 22 cases were diagnosed with congenital Chagas disease. qPCR showed 100% clinical sensitivity and 98 to 100% clinical specificity for the diagnosis of congenital Chagas disease compared with CCD-GS algorithm.

interpretationThe results obtained in this study demonstrate the clinical accuracy and effectiveness of qPCR SatDNA and qPCR kDNA for diagnosis of congenital Chagas disease. It could be a powerful tool for chagas test and treat strategies to reduce late complications of the disease.

fundingThis work was financed by the INP Dr. Mario Fatala Chaben, ANLIS Dr. Carlos G. Malbran.

Indexed as

Chagas DiseaseMolecular Diagnostic TechniquesReal-Time Polymerase Chain ReactionTrypanosoma cruziArgentinaCohort StudiesFemaleHumansInfantInfant, NewbornInfectious Disease Transmission, VerticalMalePregnancyProspective StudiesSensitivity and Specificity

Identifiers

PMID39792926
PMCPMC11825091

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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.