Search tips
Search criteria 


Logo of straninfSexually Transmitted InfectionsVisit this articleSubmit a manuscriptReceive email alertsContact usBMJ
Sex Transm Infect. 2007 August; 83(5): 345–346.
PMCID: PMC2659019

Antenatal screening for syphilis

Short abstract

Congenital syphilis is preventable if the mother's infection is diagnosed early in pregnancy and treated promptly

The morbidity and mortality associated with congenital syphilis are preventable; screening in pregnancy enables treatment of the mother, fetus and sexual partners. Maternal syphilis leads to stillbirth, prematurity, clinical congenital syphilis and infant death, with the highest transmission rates and most deaths occurring in early syphilis. A recent study in Russia showed that 26% of infants with congenital syphilis had fatal outcomes,1 while 51% of all stillbirths in Tanzania were attributed to syphilis.2 While maternal screening and treatment of syphilis are extremely cost‐effective health interventions even when the prevalence of infection is very low,3,4 many countries do not have universal antenatal screening. In a survey of 22 countries in sub‐Saharan Africa, 17 had antenatal screening, but although 73% of pregnant women had antenatal care, only 38% were screened for syphilis.5

Globally, the World Health Organization (WHO) estimates that around 360 000 fetal and perinatal deaths occur annually due to syphilis and a further 270 000 babies suffer serious and permanent effects.6 A study conducted in four countries (Argentina, Cuba, Saudi Arabia and Thailand) participating in the WHO antenatal care trial estimated an overall prevalence of 0.9% with a range of 0.1% to 2.2% across the four countries.7 Much higher prevalence has been reported in other developing countries, for example, a prevalence of 7.7% has been described in Tanzania.3 Cheng et al8 report in this issue on the screening of half a million pregnant women in China. Syphilis was detected in 2208 (0.46%) women and the authors showed that screening was effective in preventing congenital syphilis. Although prevalence is low nationally, the sheer size of the population in China means that there are likely to be very many cases of congenital syphilis.

Far less congenital syphilis is seen in the developed world. In the UK, only 14 cases of congenital syphilis in infants under 2 years old were reported from genito‐urinary medicine (GUM) clinics in 2005.9 These low figures are partially due to a well established antenatal screening programme and low rates of syphilis in heterosexual women, although rates are increasing. The constantly changing epidemiology of syphilis in the adult population highlights the need for continued compliance with the universal screening policy.

In light of this substantial burden of disease, the WHO recommends that all pregnant women should be screened at their first antenatal visit and that the test should be repeated early in the third trimester.7,10 Treponemal tests such as EIA or TPPA/TPHA or cardiolipin tests such as RPR/VDRL are used for screening. The latter test diagnoses early syphilis but misses many cases of late syphilis and there may be problems with biological false positives if no confirmatory test is performed as well as false negative in early syphilis from the prozone phenomenon.

Decentralisation of antenatal care may assist in the uptake of screening. Some of the problems are late presentation to antenatal clinic and failure to reattend for results and treatment. However, the advent of point of care (POC) treponemal tests enables immediate diagnosis and treatment at the initial visit. The POC test has to be affordable, sensitive, specific, user‐friendly, rapid/robust, equipment‐free and deliverable (ASSURED),11 and has to be accompanied by immediate treatment provision. A South African study showed that “complicated” RPR POC tests, although they reduced treatment delay, did not lead to a better treatment rate or a reduction in perinatal mortality. This may be due to the poor treatment rate of 64% resulting from women not staying because of the delay between testing and treatment.12 Significantly more cases are detected and treated when POC tests with immediate results are used.7 Treponemal and POC tests cannot differentiate between new and previously treated syphilis and RPR/VDRL titres are required to assess reinfection or recrudescence.

Minimum treatment is a single injection of IM benzathine penicillin 2.4 MU for early syphilis and possibly a further injection before delivery.3,10 However, there is a need for single dose oral treatment. While azithromycin 2 g orally is effective for adults,13 it is not recommended for pregnant women because poor placental penetration means that the fetus is not adequately treated. There is also concern regarding macrolide resistant strains14 and if a macrolide is used the baby should also be treated at birth. It is essential that partners are treated to prevent reinfection as otherwise the prevention efforts will be undone.

Despite the relative ease of screening and treatment, many challenges remain. Problems in developing countries include depleted stocks of drugs and other consumables, lack of appropriate transportation of samples for testing, little training for laboratory staff in performing the tests and a high turn‐over of clinical staff.15 In addition, the biggest challenge is an inadequate healthcare infrastructure. In order for congenital syphilis to be prevented, a woman must access antenatal care early in her pregnancy, undergo a test, get the test results and receive treatment. Women can be lost at all these stages. Women in developing countries may live far from a healthcare facility or be unable to afford transport costs and therefore be unable to attend, while in the developed world high rates of immigration may result in groups of women being unaware of the healthcare options available to them.

All cases of congenital syphilis are preventable if the mother's infection is diagnosed and treated promptly. However, in order for this to occur good pathways of care must be in place and sufficient resources must be available. This requires commitment from governments and strong programme leadership, as shown by Cheng et al.8 The expansion and improvement of free antenatal care should be a priority followed by a specific commitment to prevent congenital syphilis. As high priority is already given to the prevention of vertical transmission of HIV, there is great potential for the integration, expansion and improvement of syphilis programmes. The WHO Millennium Development Goals of reducing the mortality of children under 5 years of age by 66% and improving maternal health by 2015 present a significant challenge and opportunity: the prevention of congenital syphilis is an integral aspect of these aims and requires leadership action.


Competing interests: None declared.

See linked article p 347


1. Tikhonova L, Salakhov E, Southwick K. et al Congenital syphilis in the Russian Federation: magnitude, determinants and consequences. Sex Transm Infect 2003. 79106–110.110 [PMC free article] [PubMed]
2. Watson‐Jones D, Changalucha J, Gumodoka B. et al Syphilis and pregnancy outcomes in Tanzania. I. Impact of maternal syphilis on outcome of pregnancy in Mwanza Region, Tanzania. J Infect Dis 2002. 186940–947.947 [PubMed]
3. Watson‐Jones D, Gumodoka B, Weiss H. et al Syphilis in pregnancy in Tanzania. II. The effectiveness of antenatal screening and single dose benzathine penicillin treatment for the prevention of adverse pregnancy outcomes. J Infect Dis 2002. 186948–957.957 [PubMed]
4. Schmid G. Economic and programmatic aspects of congenital syphilis prevention. Bull World Health Organ 2004. 82(6)402–409.409 [PubMed]
5. Gloyd S, Chai S, Mercer M A. Antenatal screening in sub‐Saharan Africa: missed opportunities for mortality reduction. Health Policy Plan 2001. 1629–34.34 [PubMed]
6. Finelli L, Berman S M, Koumans E H. et al Congenital syphilis. Bull World Health Organ 1998. 76(Suppl 2)126–128.128 [PubMed]
7. Lumbiganon P, Piaggio G, Viller J. et al The epidemiology of syphilis in pregnancy. Int J STD AIDS 2002. 13486–494.494 [PubMed]
8. Cheng J Q, Zhou H, Hong F C. et al Syphilis screening and intervention of 500,000 pregnant women in Shenzhen, the People's Republic of China. Sex Transm Infect 2007. 83347–350.350 [PMC free article] [PubMed]
9. Health Protection Agency KC60 data tables. All new diagnoses made at genitourinary medicine (GUM) clinics: 1996–2005, United Kingdom and country specific tables. (accessed 2 July 2007)
10. World Health Organization Sexually transmitted and other reproductive tract infections ‐ a guide to essential practice.‐health/publications/rtis_gep/index.htm (accessed 2 July 2007)
11. Peeling R W, Holmes K K, Mabey D. et al Rapid tests for sexually transmitted infections (STIs): the way forward. Sex Transm Infect 2006. 82(Suppl V)v1–v6.v6 [PMC free article] [PubMed]
12. Myer L, Wilkinson D, Lombard C. et al Impact of on‐site testing for maternal syphilis on treatment delays, treatment rates, and perinatal mortality in rural South Africa: a randomised controlled trial. Sex Transm Infect 2003. 79208–213.213 [PMC free article] [PubMed]
13. Hook E W, Nartin D H, Stephens J. et al A randomized, comparative pilot study of azithromycin versus benzathine penicillin G for treatment of early syphilis. Sex Transm Dis 2002. 29486–490.490 [PubMed]
14. Lukehart S H, Godornes C, Molini B J. et al Macrolide resistance in Treponema pallidum in the United States and Ireland. N Engl J Med 2004. 351154–158.158 [PubMed]
15. Deperthes B D, Meheus A, O'Reillty K. et al Maternal and congenital syphilis programmes: case studies in Bolivia, Kenya and South Africa. Bull World Health Organ 2004. 82410–416.416 [PubMed]

Articles from Sexually Transmitted Infections are provided here courtesy of BMJ Publishing Group