The potential economic value of a therapeutic Chagas disease vaccine for pregnant women to prevent congenital transmission

Currently, there are no solutions to prevent congenital transmission of Chagas disease during pregnancy, which affects 1–40% of pregnant women in Latin America and is associated with a 5% transmission risk. With therapeutic vaccines under development, now is the right time to determine the economic...

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Published inVaccine Vol. 38; no. 16; pp. 3261 - 3270
Main Authors Bartsch, Sarah M., Stokes-Cawley, Owen J., Buekens, Pierre, Asti, Lindsey, Bottazzi, Maria Elena, Strych, Ulrich, Wedlock, Patrick T., Mitgang, Elizabeth A., Meymandi, Sheba, Falcon-Lezama, Jorge Abelardo, Hotez, Peter J., Lee, Bruce Y.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 03.04.2020
Elsevier Limited
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Summary:Currently, there are no solutions to prevent congenital transmission of Chagas disease during pregnancy, which affects 1–40% of pregnant women in Latin America and is associated with a 5% transmission risk. With therapeutic vaccines under development, now is the right time to determine the economic value of such a vaccine to prevent congenital transmission. We developed a computational decision model that represented the clinical outcomes and diagnostic testing strategies for an infant born to a Chagas-positive woman in Mexico and evaluated the impact of vaccination. Compared to no vaccination, a 25% efficacious vaccine averted 125 [95% uncertainty interval (UI): 122–128] congenital cases, 1.9 (95% UI: 1.6–2.2) infant deaths, and 78 (95% UI: 66–91) DALYs per 10,000 infected pregnant women; a 50% efficacious vaccine averted 251 (95% UI: 248–254) cases, 3.8 (95% UI: 3.6–4.2) deaths, and 160 (95% UI: 148–171) DALYs; and a 75% efficacious vaccine averted 376 (95% UI: 374–378) cases, 5.8 (95% UI: 5.5–6.1) deaths, and 238 (95% UI: 227–249) DALYs. A 25% efficacious vaccine was cost-effective (incremental cost-effectiveness ratio <3× Mexico’s gross domestic product per capita, <$29,698/DALY averted) when the vaccine cost ≤$240 and ≤$310 and cost-saving when ≤$10 and ≤$80 from the third-party payer and societal perspectives, respectively. A 50% efficacious vaccine was cost-effective when costing ≤$490 and ≤$615 and cost-saving when ≤$25 and ≤$160, from the third-party payer and societal perspectives, respectively. A 75% efficacious vaccine was cost-effective when ≤$720 and ≤$930 and cost-saving when ≤$40 and ≤$250 from the third-party payer and societal perspectives, respectively. Additionally, 13–42 fewer infants progressed to chronic disease, saving $0.41-$1.21 million to society. We delineated the thresholds at which therapeutic vaccination of Chagas-positive pregnant women would be cost-effective and cost-saving, providing economic guidance for decision-makers to consider when developing and bringing such a vaccine to market.
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Sarah M. Bartsch contributed to study conception and design, model conceptualization, data collection, data analysis, interpretation of results, and writing of the manuscript.
Patrick T. Wedlock contributed to data analysis and editing of the manuscript.
Credit Author Statement
Elizabeth A. Mitgang contributed to data analysis and editing of the manuscript.
Maria Elena Bottazzi contributed study conception and design, model conceptualization, interpretation of results, and editing of the manuscript.
Bruce Y. Lee contributed to study conception and design, model conceptualization, data analysis, interpretation of results, and writing of the manuscript.
Lindsey Asti contributed to data collection, data analysis, interpretation of results, and writing of the manuscript.
Owen J. Stokes-Cawley contributed to study conception and design, model conceptualization, data collection, data analysis, interpretation of results, and writing of the manuscript.
Pierre Buekens contributed to study conception and design, model conceptualization, interpretation of results, and editing of the manuscript.
Peter J. Hotez contributed to study conception and design, model conceptualization, interpretation of results, and editing of the manuscript.
Ulrich Strych contributed to model conceptualization, interpretation of results, and editing of the manuscript.
Sheba Meymandi contributed to model conceptualization, interpretation of results, and editing of the manuscript.
Jorge Abelardo Falcon-Lezama contributed to data collection, interpretation of results, and editing of the manuscript.
ISSN:0264-410X
1873-2518
DOI:10.1016/j.vaccine.2020.02.078