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Evaluating congenital syphilis in a reverse sequence testing environment
May W Chen1, Ibukunoluwa C Akinboyo2,3, Paul K Sue2,4
1Division of Neonatology, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Insights
Maternal reverse-sequence (RS) syphilis screening did not improve infant management for congenital syphilis (CS). In a high-risk group, RS testing did not identify additional CS cases, with discordant results often relying on clinical judgment.
Area of Science:
- Infectious Diseases
- Maternal-Fetal Medicine
- Clinical Diagnostics
Background:
- Congenital syphilis (CS) poses significant risks to newborns.
- Accurate maternal syphilis screening is crucial for preventing CS.
- Reverse-sequence (RS) testing is a diagnostic approach for syphilis.
Purpose of the Study:
- To evaluate the impact of maternal RS syphilis screening on the management of infants at risk for CS.
- To assess if RS testing aids in identifying additional CS cases in a high-risk population.
Main Methods:
- Retrospective study (2011-2014) at an academic medical center.
- Utilized RS testing including chemiluminescent immunoassay (CIA), rapid plasma reagin (RPR), and fluorescent treponemal antibody-absorption (FTA-ABS).
- Compared clinical management and outcomes of infants born to mothers with discordant serology (CIA+/RPR-/FTA+) against guidelines.
Main Results:
- Sixty-three infants were analyzed: 21 discordant, 16 presumed false positive, and 26 true positive.
- Only 24% of infants in the discordant group received the recommended full evaluation.
- No infants in the evaluated discordant group (n=8) were diagnosed with CS.
Conclusions:
- Management of infants with discordant maternal RS serology often depends on clinical judgment.
- RS testing in this high-risk population did not lead to the identification of additional CS cases.
- Standardized approaches to CS prevention and infant management require further investigation.
Objectives:
To examine the effect of maternal reverse-sequence (RS) syphilis screening on management of infants at risk for congenital syphilis (CS) using a standardized approach.
Study Design:
A retrospective study from 2011 to 2014 at an academic medical center using RS testing, involving chemiluminescent immunoassay (CIA), rapid plasma reagin (RPR), and fluorescent treponemal antibody-absorption (FTA-ABS) assays for syphilis. Clinical management and outcomes of infants born to mothers with discordant (CIA+/RPR-/FTA+) serology were compared with national or internal guidelines.
Results:
Sixty-three infants were classified as discordant (n = 21), presumed false positive (CIA+/RPR-/FTA-; n = 16), or true positive (CIA+/RPR+; n = 26) based on maternal serology. Only 24% of cases in the discordant group underwent recommended full evaluation. None of the evaluated infants in the discordant group (n = 8) were diagnosed with CS.
Conclusions:
Management of infants with discordant maternal RS serology remained reliant on clinical judgment. In our high-risk population, RS testing did not identify additional cases of CS.
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