Risk Factors for Maternal Chagas Disease and Vertical Transmission in a Bolivian Hospital

Author:

Klein Melissa D1ORCID,Tinajeros Freddy2,del Carmen Menduiña María3,Málaga Edith4,Condori Beth J4,Verástegui Manuela4,Urquizu Federico3,Gilman Robert H5,Bowman Natalie M1

Affiliation:

1. Department of Medicine, Division of Infectious Diseases, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA

2. Asociación Benéfica PRISMA, Lima, Peru

3. Hospital Percy Boland Rodríguez, Ministerio de Salud Bolivia, Santa Cruz, Bolivia

4. Infectious Diseases Research Laboratory, Department of Cellular and Molecular Sciences, Universidad Peruana Cayetano Heredia, Lima, Peru

5. Department of International Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA

Abstract

Abstract Background Vertical transmission of Trypanosoma cruzi infection accounts for a growing proportion of new cases of Chagas disease. Better risk stratification is needed to predict which women are more likely to transmit the infection. Methods This study enrolled women and their infants at the Percy Boland Women’s Hospital in Santa Cruz, Bolivia. Pregnant women were screened for Chagas disease by rapid test and received confirmatory serology. Infants of seropositive mothers underwent diagnostic testing with quantitative polymerase chain reaction (qPCR). Results Among 5828 enrolled women, 1271 (21.8%) screened positive for Chagas disease. Older maternal age, family history of Chagas disease, home conditions, lower educational level, and history of living in a rural area were significantly associated with higher adjusted odds of maternal infection. Of the 1325 infants of seropositive mothers, 65 infants (4.9%) were diagnosed with congenital Chagas disease. Protective factors against transmission included cesarean delivery (adjusted odds ratio [aOR]: .60; 95% confidence interval [CI]: .36–.99) and family history of Chagas disease (aOR: .58; 95% CI: .34–.99). Twins were significantly more likely to be congenitally infected than singleton births (OR: 3.32; 95% CI: 1.60–6.90). Among congenitally infected infants, 32.3% had low birth weight, and 30.8% required hospitalization after birth. Conclusions Although improved access to screening and qPCR increased the number of infants diagnosed with congenital Chagas disease, many infants remain undiagnosed. A better understanding of risk factors and improved access to highly sensitive and specific diagnostic techniques for congenital Chagas disease may help improve regional initiatives to reduce disease burden.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference36 articles.

1. World health Organization. Chagas disease in Latin America: an epidemiological update based on 2010 estimates;Wkly Epidemiol Rec,2015

2. Chagas’ disease;Bern;N Engl J Med,2015

3. Chagas’ disease: pregnancy and congenital transmission;Cevallos;Biomed Res Int,2014

4. Frequency of the congenital transmission of Trypanosoma cruzi: a systematic review and meta-analysis;Howard;BJOG,2014

5. Modelling congenital transmission of Chagas’ disease;Raimundo;Biosystems,2010

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