# Treatment of Syphilis in Pregnancy and Congenital Syphilis: Current Evidence, Challenges, and Future Directions

**Authors:** Serena Salomè, Chryssoula Tzialla

PMC · DOI: 10.3390/antibiotics15030305 · Antibiotics · 2026-03-18

## TL;DR

This paper reviews the treatment of syphilis during pregnancy and congenital syphilis, emphasizing the challenges with penicillin and the need for alternative solutions.

## Contribution

The paper highlights the current treatment challenges and proposes future directions for addressing gaps in syphilis management during pregnancy.

## Key findings

- Penicillin remains the only proven treatment for preventing congenital syphilis.
- Global shortages and mislabeling of penicillin allergy hinder effective treatment.
- Alternative antimicrobial agents show promise but lack evidence for use in pregnancy.

## Abstract

Syphilis remains a global public health concern, with maternal infection posing a substantial risk for congenital syphilis, a preventable condition associated with severe morbidity and mortality. Penicillin, particularly benzathine penicillin G, remains the cornerstone of treatment and the only therapy with proven efficacy in preventing vertical transmission during pregnancy. However, recurrent global shortages, limited manufacturing capacity, mislabeling of penicillin allergy, and the absence of validated alternative regimens for pregnant women and neonates threaten progress toward elimination goals. This review summarizes current evidence on the treatment of syphilis in pregnancy and congenital syphilis, highlighting the established maternal and neonatal regimens, diagnostic and therapeutic challenges, and clinical consequences of delayed or inadequate treatment. We examine the scope and drivers of benzathine penicillin G shortages, the overestimation of penicillin allergy and its impact on care, and the role of neonatal management when maternal therapy is suboptimal. Emerging data on alternative antimicrobial agents, including cephalosporins, tetracyclines, lipoglycopeptides, and novel compounds are discussed considering recent advances in Treponema pallidum culture and susceptibility testing. While several non-penicillin agents show promise for non-pregnant populations, robust evidence supporting their use during pregnancy and for the prevention of congenital syphilis is lacking. Addressing these gaps through coordinated supply chain strategies, guideline harmonization, and targeted clinical research is essential to ensure resilient and equitable syphilis control and advance global efforts toward the elimination of congenital syphilis.

## Linked entities

- **Chemicals:** penicillin (PubChem CID 2349), benzathine penicillin G (PubChem CID 15232), cephalosporins (PubChem CID 25058126)
- **Diseases:** syphilis (MONDO:0005976), congenital syphilis (MONDO:0005714)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** intellectual disability (MESH:D008607), penicillin allergies (MESH:D008586), rash (MESH:D005076), anemia (MESH:D000740), miscarriage (MESH:D000022), headache (MESH:D006261), neurologic impairment (MESH:D009422), tachycardia (MESH:D013610), hepatosplenomegaly (MESH:C535727), skeletal abnormalities (MESH:D009139), sensorineural hearing loss (MESH:D006319), cutaneous lesions (MESH:D009059), HIV infection (MESH:D015658), injury to (MESH:D014947), Neurosyphilis (MESH:D009494), latent syphilis (MESH:D013592), congenital infection (MESH:D007239), Clostridioides difficile colonization and (MESH:D003015), perinatal death (MESH:D066087), deaths (MESH:D003643), bone and dental deformities (MESH:D001847), hyperbilirubinemia (MESH:D006932), maternal (MESH:D000079262), infectious disease (MESH:D003141), fetal growth restriction (MESH:D005317), /Congenital Syphilis (MESH:D013590), Treponema pallidum (MESH:C531782), hearing impairment (MESH:D034381), stillbirth (MESH:D050497), Jarisch-Herxheimer reaction (MESH:D006967), thrombocytopenia (MESH:D013921), Allergy (MESH:D004342), anaphylaxis (MESH:D000707), Stevens-Johnson syndrome (MESH:D013262), fetal distress (MESH:D005316), tachypnea (MESH:D059246), Syphilis (MESH:D013587), prematurity (MESH:C536271), phlebitis (MESH:D010689), myalgia (MESH:D063806), rhinitis (MESH:D012220), sepsis (MESH:D018805), chills (MESH:D023341), fetal disease (MESH:D005315), visual deficits (MESH:D014786)
- **Chemicals:** Ampicillin (MESH:D000667), lipoglycopeptides (MESH:D000077427), Ceftriaxone (MESH:D002443), potassium (MESH:D011188), probenecid (MESH:D011339), beta-lactam (MESH:D047090), calcium (MESH:D002118), API (-), Dalbavancin (MESH:C469289), tetracyclines (MESH:D013754), benzathine (MESH:C010044), amoxicillin (MESH:D000658), penicillin G (MESH:D010400), Azithromycin (MESH:D017963), cefazolin (MESH:D002437), tetracycline (MESH:D013752), Linezolid (MESH:D000069349), BPG (MESH:D010401), cephalosporin (MESH:D002511), Doxycycline (MESH:D004318), macrolide (MESH:D018942), Cefixime (MESH:D020682), Erythromycin (MESH:D004917), Penicillin (MESH:D010406), Zoliflodacin (MESH:C000599190), Minocycline (MESH:D008911), procaine penicillin (MESH:D010402)
- **Species:** Homo sapiens (human, species) [taxon 9606], Treponema pallidum (species) [taxon 160], Neisseria gonorrhoeae (species) [taxon 485], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13024649/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC13024649/full.md

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Source: https://tomesphere.com/paper/PMC13024649