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Evaluation and Management of Congenital Chagas Disease in the United States.
- Source :
-
Journal of the Pediatric Infectious Diseases Society [J Pediatric Infect Dis Soc] 2019 Nov 06; Vol. 8 (5), pp. 461-469. - Publication Year :
- 2019
-
Abstract
- Chagas disease is underappreciated as a health concern in the United States. Approximately 40 000 women of childbearing age living in the United States have chronic Chagas disease. Most of them are unaware that they have an infection that is transmissible to their offspring. The estimated US maternal-to-infant transmission rate of Trypanosoma cruzi is 1% to 5%. Ten percent to 40% of neonates with congenital T cruzi infection have clinical signs consistent with a congenital infection but no findings are unique to Chagas disease. If left untreated, 20% to 40% of infants with Chagas disease will later develop potentially fatal cardiac manifestations. Molecular testing can confirm the diagnosis in neonates. Treatment is well tolerated in infancy and usually results in cure. Screening of at-risk women during pregnancy can identify maternal infection and allow early assessment and treatment for congenital T cruzi infection.<br /> (© The Author(s) 2019. Published by Oxford University Press on behalf of The Journal of the Pediatric Infectious Diseases Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
- Subjects :
- Chagas Disease therapy
Chagas Disease transmission
Female
Humans
Infant
Infant, Newborn
Molecular Diagnostic Techniques
Polymerase Chain Reaction
Pregnancy
Pregnancy Complications, Parasitic therapy
Risk Factors
Trypanosoma cruzi
United States
Chagas Disease diagnosis
Infectious Disease Transmission, Vertical
Pregnancy Complications, Parasitic diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 2048-7207
- Volume :
- 8
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Journal of the Pediatric Infectious Diseases Society
- Publication Type :
- Academic Journal
- Accession number :
- 31016324
- Full Text :
- https://doi.org/10.1093/jpids/piz018