Volume 164, Issue 3 p. 835-842
REVIEW ARTICLE

Mother-to-child Chagas disease transmission: The challenge of detection and prevention in areas without the risk of vectorial transmission

Santiago Palacios Gil-Antuñano

Corresponding Author

Santiago Palacios Gil-Antuñano

Palacios Institute of Women's Health, Madrid, Spain

Correspondence

Santiago Palacios Gil-Antuñano, Instituto Palacios, Calle Antonio Acuña, 9 – 28009, Madrid, Spain.

Email: [email protected]

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Silvia Gold

Silvia Gold

Mundo Sano Foundation, Buenos Aires, Argentina

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Marcelo Abril

Marcelo Abril

Mundo Sano Foundation, Buenos Aires, Argentina

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Manuel Segovia Hernández

Manuel Segovia Hernández

Microbiology and Parasitology Service, Universitary Hospital Virgen de la Arrixaca, Murcia University, Murcia, Spain

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Maria Jesus Cancelo-Hidalgo

Maria Jesus Cancelo-Hidalgo

Obstetrics and Gynaecology Service, Universitary Hospital of Guadalajara, Gynaecology and Obstetrics Alcala de Henares Universitiy, Madrid, Spain

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Maria Flores-Chávez

Maria Flores-Chávez

Mundo Sano Foundation – National Centre for Microbiology, Instituto de Salud Carlos III, Madrid, Spain

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Irene Pelayo-Delgado

Irene Pelayo-Delgado

Department of Obstetrics and Gynecology, Alcala de Henares University, Ramon y Cajal Hospital, Madrid, Spain

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First published: 26 July 2023
Citations: 1

Abstract

Chagas disease (CD) is caused by the parasite Trypanosoma cruzi. Although it is endemic in many Latin American (LA) countries, mother-to-child transmission has caused it to expand to other countries and continents. In places where vector transmission is controlled or absent, the epidemiological importance of T. cruzi transmission of the infected mother to her child during pregnancy or childbirth (i.e., perinatal CD) increases. In countries where CD is not endemic, CD screening should be performed in pregnant or fertile women who are native to LA countries or whose mothers are native to LA countries. Diagnosis is established by detecting anti–T. cruzi IgG antibodies in a serum or plasma sample. Antiparasitic treatment cannot be offered during pregnancy, and since the majority of infected newborns are asymptomatic at birth, a diagnosis is made by direct observation or concentration (microhematocrit) or by using molecular testing techniques. Once the infected child receives a diagnosis, it is essential to offer treatment (benznidazole/nifurtimox) as soon as possible, with good tolerance and effectiveness in the first year of life. Even if the diagnosis is negative at birth, the newborn must be followed up for at least the first 9 months of life.

CONFLICT OF INTEREST STATEMENT

All of the authors declare that they have no conflict of interest.

DATA AVAILABILITY STATEMENT

Data sharing is not applicable to this article as no new data were created or analyzed in this study.