Volume 11 Supplement 3
Lives Saved Tool supplement detection and treatment of syphilis in pregnancy to reduce syphilis related stillbirths and neonatal mortality
© Blencowe et al; licensee BioMed Central Ltd. 2011
Published: 13 April 2011
Globally syphilis is an important yet preventable cause of stillbirth, neonatal mortality and morbidity.
This review sought to estimate the effect of detection and treatment of active syphilis in pregnancy with at least 2.4MU benzathine penicillin (or equivalent) on syphilis-related stillbirths and neonatal mortality.
We conducted a systematic literature review of multiple databases to identify relevant studies. Data were abstracted into standardised tables and the quality of evidence was assessed using adapted GRADE criteria. Where appropriate, meta-analyses were undertaken.
Moderate quality evidence (3 studies) supports a reduction in the incidence of clinical congenital syphilis of 97% (95% c.i 93 – 98%) with detection and treatment of women with active syphilis in pregnancy with at least 2.4MU penicillin. The results of meta-analyses suggest that treatment with penicillin is associated with an 82% reduction in stillbirth (95% c.i. 67 – 90%) (8 studies), a 64% reduction in preterm delivery (95% c.i. 53 – 73%) (7 studies) and an 80% reduction in neonatal deaths (95% c.i. 68 – 87%) (5 studies). Although these effect estimates were large and remarkably consistent across studies, few of the studies adjusted for potential confounding factors and thus the overall quality of the evidence was considered low. However, given these large observed effects and a clear biological mechanism for effectiveness the GRADE recommendation is strong.
Detection and appropriate, timely penicillin treatment is a highly effective intervention to reduce adverse syphilis-related pregnancy outcomes. More research is required to identify the most cost-effective strategies for achieving maximum coverage of screening for all pregnant women, and access to treatment if required.
Transmission of maternal syphilis infection to the foetus during pregnancy has been described in the medical literature as long ago as 1497 and has been much studied over the past 500 years . However, despite the availability of diagnostic tests for a century and of cheap, effective therapy for over 50 years, WHO currently estimates between 730,000 and 1,500,000 adverse pregnancy outcomes are caused by untreated maternal syphilis each year, of which about 650,000 are foetal and newborn deaths [2, 3]. In many regions congenital syphilis remains an important public health problem, e.g Latin America and Africa , and the incidence is increasing in some countries, for example China [4, 5]. In 2007 WHO launched a programme for the global elimination of congenital syphilis through strengthening existing maternal and newborn health (MNCH) systems in highly affected nations .
In 2001, twelve million people globally were estimated to be infected with the causative agent of syphilis, the spirochete Treponema pallidum (T.pallidum) . Syphilis classically presents in its primary stage with a painless, spontaneously resolving ulcer (chancre), lasting 3 – 6 weeks, that typically occurs around 21 days, but which may occur up to 3 months post infection. This is followed, 6 – 8 weeks later, by the secondary stage, which consists of a more diffuse inflammatory response characterised by an exanthema which manifests variably and for which healthcare is often not sought even if available. This stage also resolves spontaneously and is followed by an asymptomatic ‘latent period’. Untreated, 15 – 40% of infected individuals develop late ‘tertiary’ complications that may occur years after the initial infection: e.g. granulomas, neuropathic joint disease, cardiovascular and neurological complications.
Syphilis can be difficult to diagnose, since T pallidum cannot be cultured in vitro, and PCR-based tests are unavailable outside research settings. While direct diagnosis of characteristic treponemes with darkfield microscopy is highly sensitive and specific, this requires exudate obtained from a lesion during the brief primary stage. Thus most infections are identified using serologic tests that support, rather than establish, a syphilis diagnosis. Serologic tests fall into 2 broad categories: non-treponemal tests (e.g., RPR, VDRL) measure antibody to a component of mammalian cell membranes modified by T pallidum. Positive RPR tests are reported as the highest titre for which tests are still positive after dilution, with titre correlating with recentness of infection and stage of disease and falling over time or with treatment. In general, titres >1:4 have been considered to represent “active” infections, more likely to be more recently acquired and infectious. With treatment, titres typically return to negative. Treponemal tests (e.g., TPHA, MHA-TP) detect T pallidum antibody, and are reported as either positive or negative. Because these tests typically remain positive even after treatment, a positive treponemal test could indicate either recent active or old (or previously treated) infection. Currently available, rapid point-of-care tests (e.g., ICS strip) are treponemal tests.
Effects of syphilis on pregnancy outcome
The risk of syphilis to the foetus is dependent upon the stage of maternal infection and on the stage of pregnancy at which the foetus is exposed. Primary, secondary, early latent, and in some cases late latent, stage maternal syphilis infection can lead to haematogenous spread to the foetus, resulting in a systemic inflammatory response . Although spirochetes can cross the placenta to the foetus from early pregnancy , foetal immune systems are not mature enough to mount a consistent immune response until about 18 to 22 weeks gestation. After this time the characteristic features of congenital syphilis may be seen. In addition, placental infiltration with reduced blood flow to the foetus can lead to growth restriction which, if severe, may result in foetal death . Foetal involvement occurs most consistently in pregnant women with ‘active’ infections (i.e. RPR titre >1:4), that is inadequately or not treated infections acquired in the five years preceding the pregnancy. This review therefore focuses on this group of pregnant women with active infection. Based on the available data, an expert panel has estimated , that in the absence of effective treatment, 25% of pregnancies to such women will result in a 2nd trimester miscarriage or stillbirth, 11% of pregnancies in a neonatal death at term, 13% in a preterm or low birth weight infant and an additional 20% with clinical signs of congenital syphilis that are attributable to syphilis. Hence, of the 75% of the pregnancies resulting in a liveborn infant, 15% would be expected to result in a neonatal death at term and 17% in a preterm or low birth weight infant, with a further 27% of babies who survive to 28 days developing clinical signs of congenital syphilis . Congenital syphilis in the first 2 years of life may present with hepato-splenomegaly, anaemia, jaundice, rash, snuffles and pseudo-paralysis . Later manifestations of congenital syphilis, after the first 2 years of life may be an important treatable cause of neurological, developmental, and musculoskeletal problems and death in infants and children in low-income settings . In view of the ongoing morbidity and mortality associated with congenital syphilis, and because of the challenges of making a specific diagnosis, both CDC and WHO now recommend a 10 day course of intravenous or intramuscular penicillin treatment for all infants born to mothers with untreated or inadequately treated syphilis in pregnancy , regardless of symptoms or clinical findings [12, 13].
Parenteral penicillin was identified as effective in the treatment of syphilis shortly after its introduction in 1943, and is still the recommended drug for treatment of syphilis, whether acquired sexually or through transmission from mother to child during pregnancy . Studies have established that penicillin is treponemocidal at fairly low serum concentrations (>0.1 mug/ml), and that longer duration regimens are more effective than shorter duration regimens, even those achieving higher concentrations . These provide the therapeutic rationale for use of relatively low doses of longer acting penicillin G formulations (e.g. 2.4 million units benzathine penicillin). Current CDC and WHO guidelines recommend a single dose of long acting penicillin to treat early syphilis, and three injections of benzathine penicillin at weekly intervals for infections of > 1 year (or unknown) duration for infected adults, including pregnant women . For women with infection of > 1 year duration (i.e. latent infection), clinical studies suggest that a single penicillin dose effectively treats the foetus in at least 95% of cases [16, 17]; while subsequent doses treat the mother. Other antibiotics, such as oral tetracyclines and macrolides (e.g., erythromycin, azithromycin) have been used to treat syphilis in adults, but are not recommended either due to their toxicity in the foetus (tetracyclines) or because they do not cross the placental barrier (macrolides) and thus do not treat foetal infection at all. Macrolide antibiotics have also been associated with development of resistance [15, 18]. Parenteral ceftriaxone has been used to treat syphilis in penicillin-allergic patients, but as no controlled studies among pregnant women have assessed its efficacy in treating the foetus, this is not recommended in pregnancy [13, 14].
Many factors limit the quality of evidence available concerning the magnitude of the effects of penicillin treatment on foetal and neonatal mortality. Syphilis in pregnancy is a dynamic disease; the timing of infection, re-infection and treatment can all vary, and there are a variety of possible non-specific outcomes (including stillbirth, preterm birth and neonatal and infant death) that are associated with many different, and potentially confounding factors (e.g. other infections, maternal well-being and adherence to recommendations). Given the longstanding recommendations regarding identification and treatment of maternal syphilis randomised controlled trials of the effect of penicillin compared to no treatment would not be ethical. Many observational studies control for potential confounders inadequately or not at all. In summary, despite evidence and widespread policy acceptance of the importance of identifying and treating syphilis during pregnancy, there are limited data regarding the magnitude of the effect such detection and treatment has on foetal and neonatal mortality.
The objective of this paper is to provide quantitative estimates of the effect of antenatal syphilis detection based on serological screening in pregnancy combined with treatment with at least 2.4 million units penicillin (at least a single dose of benzathine penicillin or the equivalent multiple dose schedule of shorter acting penicillin) on syphilis related stillbirths, neonatal mortality and morbidity related to maternal syphilis infection. These effect estimates are inputs to the Lives Saved Tool (LiST)  and are derived according to set rules .
We systematically reviewed the published literature to identify studies of detection and treatment of syphilis in pregnancy for the prevention of congenital syphilis mortality (latest searches performed December 2009). There are two broad causal pathways by which active syphilis in pregnancy may lead to mortality in the foetus/ neonate – through direct infection of the foetus and leading to an overwhelming inflammatory response (leading to sepsis, stillbirth or preterm birth) or indirectly through reduced placental blood flow (leading to stillbirth or low birth weight), though this is less frequent. We searched PubMed, EMBASE, Cochrane Libraries, and all World Health Organisation Regional Databases and included publications in any language . Snowball searching was used whereby literature referenced in key papers was included. Combinations of the following search terms were used: “congenital syphilis/ syphilis” “pregnancy” “neonate/ newborn” “mortality” “screening” “syphilis/ drug therapy” “antibiotics” “preterm” “stillbirth/ foetal death” “perinatal mortality”.
Inclusion/ exclusion criteria
Abstraction, analyses and summary measures
All studies meeting the criteria above were abstracted onto a standardised abstraction form for each outcome of interest . Each study was assessed for limitations and graded according to the CHERG adaptation of the GRADE technique . The evidence was summarised by outcome including a qualitative assessment of study quality and sources of bias adapted from the Cochrane review handbook. CHERG Rules for Evidence Review were applied to the collective evidence to provide an estimate for reduction in stillbirth and congenital syphilis related neonatal mortality.
Separate meta-analyses were planned for the effect of penicillin on incidence of stillbirth, preterm delivery, congenital syphilis, and neonatal mortality. Meta-analyses were conducted with STATA version 10.0 statistical software . Heterogeneity was assessed using I2 and the chi-squared test. When evidence of heterogeneity was present (p<0.10), a random effects model was used, otherwise a fixed effect was assumed. Summary risk ratios and corresponding 95% confidence intervals (CI) are reported.
The search strategy from all listed databases and reference lists identified 3126 records (Figure 2). After initial screening of the title or abstract we reviewed 58 papers. Twenty five papers, all observational studies were abstracted and included in the final database. (Additional file 1) Some studies took into account important potential confounders such as co-infection with malaria or anaemia, while others did not. Additionally, some studies assessed pregnancy outcomes in women who were uninfected with syphilis, while others did not. One Cochrane Review (“Antibiotics for syphilis diagnosed during pregnancy”) was retrieved, but included no studies .
1. Evidence for the effectiveness of detection and treatment of active syphilis in pregnancy in reducing stillbirths and perinatal mortality
Eight observational studies reported the incidence of stillbirths in treated, infected women compared with untreated infected women. None of the studies made any attempt to control this comparison for systematic differences between treated and untreated women (confounding). Women not attending antenatal clinics or not adhering to complex penicillin treatment regimes may differ in their risk profiles for stillbirth, preterm delivery and neonatal death from fully compliant infected women.
Two early, observational studies from the United States report very large reductions in stillbirths to pregnant women identified as ‘syphilitic’ by physical examination and serological testing and treated with at least 2.4 million units of penicillin G compared to untreated syphilis positive women diagnosed at delivery (RRs of 0.15 (95%c.i. 0.10 – 0.25) and 0.06 (95%c.i. 0.01 – 0.27)) [24, 25]. Four further studies reported RRs of 0.65 (95% c.i 0.29 – 1.45), 0.17 (0.02 – 1.25)  , 0.19 (95% c.i. 0.10 – 0.38) and 0.53 (95%c.i. 0.03 – 9.68) for stillbirth. One study reported no stillbirths in a group of 111 adequately treated RPR-positive women compared to 5 stillbirths in 45 untreated pregnancies RR=0.04 (95%c.i. 0.00 – 0.66) . Two Tanzanian cohorts paired in setting and time [17, 31] found three stillbirths amongst 133 women with high titre syphilis who received treatment , compared to 18 stillbirths amongst 73 women with high titre syphilis who were untreated RR 0.09 (95% c.i. 0.03 – 0.30).
Five studies compared stillbirth rates in uninfected women compared to infected women who were treated during pregnancy. In three of the studies the observed stillbirth rate were slightly higher among infected women receiving treatment than among uninfected women (RR 1.3; 95% c.i. 0.81 – 2,13: RR 1.4; 95% c.i. 0.34 – 5.75: RR 1.4; 95% c.i. 1.05 – 1.86 ) while two studies found no elevated stillbirth risk (RR 0.94: 95% c.i. 0.90 – 0.98 : RR 0.68; 95% c.i. 0.2 – 2.4 ).
Four studies investigated the effect of syphilis detection and penicillin treatment on perinatal mortality (i.e. stillbirths and live born infants who died in the first week of life) without distinguishing stillbirths from early neonatal deaths. Two of these studies attempted to control confounding. In one cohort of 158 women with syphilis diagnosed at first ANC visit in rural South Africa, 5/26 untreated pregnancies with known outcomes resulted in perinatal death, compared to 10/116 with at least 2.4 MU penicillin (adjusted RR=0.45: 95%c.i. 0.17 – 1.12) . Another South African study reported a reduction in perinatal mortality of 35% with each dose of penicillin received (adjusted RR = 0.65: 95% c.i. 0.5 – 0.85) . These results are broadly consistent with the two further observational studies that did not control for confounding. A study from South Africa reported a RR of 0.34 (0.11 – 1.03)  while a study from Swaziland observed 7/24 perinatal deaths in untreated pregnant women, 0/8 in treated women and 4/145 in those negative for syphilis .
2. Evidence for the effectiveness of detection and treatment of active syphilis in pregnancy in reducing neonatal mortality
3. Evidence for the effectiveness of detection and treatment of active syphilis in pregnancy in reducing preterm births
Since none of these studies controlled for confounding in this analysis, other factors may have contributed to the association between penicillin treatment and reduced risk of preterm delivery. However the consistency and strength of association and further analyses of the Tanzania cohorts paired in setting and time, which adjusted for potential confounders such as reproductive tract infections, HIV, malaria and anaemia, provide some evidence that the effect seen is not entirely explained by uncontrolled confounding factors. The Tanzania study reported the risk of preterm birth to be 6.1 (95% c.i. 2.5 – 15.3) times higher in women with high titre RPR positivity (i.e., active syphilis) compared to uninfected women, while women with high titre RPR positivity who were treated with penicillin had no increased risk of preterm birth (RR =0.58; 95% c.i. 0.3 – 1.1) .
4. Evidence for the effectiveness of detection and treatment of active syphilis in pregnancy in reducing the incidence of congenital syphilis in live born infants
Three studies were identified addressing the effect of penicillin for pregnant women with active syphilis on the incidence of congenital syphilis. Two early cohort studies in the United States report risk ratios of 0.05 (95% c.i. 0.01 – 0.16) and 0.05 (95% c.i. 0.03 – 0.09) for congenital syphilis [24, 25].
A large, population-based study in 6 districts in China screened 477,656 pregnant women using Toluidine Red Unheated Serum Test, a non-treponemal serological test similar to RPR, for detecting current infection [40, 41]. Among 2208 (0.5%) test-positive women, the risk of congenital syphilis was 0.004 (7/1855) in those treated with at least 2.4MU IM benzathine benzylpenicillin, and 0.23 (81/353) in those not receiving treatment (RR = 0.02 (95% c.i. 0.01 – 0.04)) .
These results are consistent with a small prospective uncontrolled series examining 11 VDRL positive women identified between fourteen and nineteen weeks gestation. Amniocentesis confirmed foetal infection in four out of 11 cases. All four mothers were treated with 2 doses of 2.4 million units Penicillin G 1 week apart. No infant had serological evidence of congenital infection . Another larger case series of penicillin-treated antenatal attendees with active syphilis reported that 98.2% (95% c.i 96.2 – 99.3%) of pregnancies resulted in an uninfected infant . Timing of treatment is very important in subsequent risk of congenital syphilis. In a large prospective cohort study in China, women commencing treatment before 20 weeks gestation had a lower rate of congenital syphilis RR=0.50 (95%c.i. 0.38 – 0.64)  than women treated after 20 weeks.
Quality of the evidence for estimation of the effect of at least 2.4MU penicillin treatment in pregnant women with active syphilis
Quality assessment of evidence for treatment with at least 2.4MU penicillin for women with active syphilis in pregnancy to prevent adverse pregnancy and neonatal outcomes:
Summary of Findings
Treated women with active syphilis
Untreated women with active syphilis
No of studies (ref)
Generalizability to population of interest
Generalizability to intervention of interest
GRADE of evidence
Number of births
Number of births
Effect size (95% CI)
At least 2.4MU penicillin
no or insufficient controlling for important potential confounding variables
(0.10 - 0.33)
PerinatalMortality (stillbirth and early neonatal mortality):
At least 2.4MU penicillin
Both from South Africa
Both from South Africa
RR= 0.49 - 0.65
Neonatal Mortality (All Cause):
At least 2.4MU penicillin
no or insufficient controlling for important potential confounding variables
(0.13 - 0.32)
At least 2.4MU penicillin
no or insufficient controlling for important potential confounding variables
(0.27 - 0.47)
At least 2.4MU penicillin
no or insufficient controlling for important potential confounding variables but as very specific outcome unlikely to be confounded
(0.02 - 0.07)
1. Evidence of effect on perinatal deaths and stillbirths
Combining data from eight cohort studies that did not control for potential confounding results in an estimate for the reduction in stillbirth amongst women with active syphilis in pregnancy of 82% (95% c.i. 67 – 90%) with penicillin treatment (figure 3). There is a very large, biologically plausible and consistent effect size. Since none of these studies adequately controlled for potential confounding factors, other factors may have contributed to this apparent relationship, although the strength and the consistency of the association makes it rather unlikely that that the association can be entirely explained by confounding factors. Also, several studies included a comparison group of uninfected women and noted similar stillbirth rates in this group to the rates in syphilis-infected women who were treated, providing further evidence that the observed reductions in stillbirths were due to treatment of syphilis. However, without adjustment for confounding factors the quality of evidence is considered low.
Four studies which examined perinatal mortality were all consistent with a substantial reduction with penicillin treatment.
2. Cause-specific evidence of effect on congenital syphilis on deaths in the neonatal period
There is no high or moderate quality direct evidence for the effect of treating women with syphilis in pregnancy on reduction of congenital syphilis specific-neonatal deaths. In five observational studies, treatment was consistently associated with a reduction all-cause neonatal mortality of 80% (95% c.i. 68 – 87%) (figure 4). Some studies included a comparison group of uninfected women and noted that neonatal mortality in syphilis-infected women who were treated was similar. This provides some circumstantial evidence that the observed reductions in neonatal mortality may have been due to treatment of syphilis. None of the studies controlled for possible confounding factors and hence the quality of the evidence is low.
3. Cause-specific evidence of effect on preterm birth
Seven observational cohort studies which did not control for potential confounders in this analysis consistently reported reductions in preterm births with penicillin of 64% (95% c.i. 53 – 73%) (figure 5). The overall quality of evidence is low and distal to the mortality effect. Some studies included a comparison group of uninfected women with birth outcomes similar to infected women treated with penicillin. This provides some supportive evidence that the observed reductions in preterm birth may have been due to treatment of syphilis. The quality of the evidence is low.
4. Evidence of effect on incidence of congenital syphilis
Combining data from 3 observational studies results in an estimated reduction in the incidence of clinical congenital syphilis of 97% (95% c.i. 93 – 98%) with penicillin (figure 6). There is a very large, biologically plausible and broadly consistent effect size which, given the very specific outcome, is unlikely to be confounded by other factors, so GRADE rules result in upgrading the quality of evidence from low to moderate.
Estimation of effect on neonatal mortality
A recent expert consensus panel reviewing published data has estimated that approximately 15% of livebirths in women with active syphilis in pregnancy result in a neonatal death from congenital syphilis and that a further 27% have clinical evidence of syphilis in the first year of life . Current practice, based on both the WHO and CDC guidelines for the management of presumptive congenital syphilis, includes parenteral penicillin treatment for all infants born to untreated or inadequately treated mothers[12, 13]. Whilst this will markedly reduce the incidence and later morbidity and mortality of congenital syphilis it is likely to have less impact on neonatal mortality as most of the neonatal deaths from congenital syphilis occur on the first day of life [44, 45].
In a high prevalence setting in Malawi in 1990, with a “very high” neonatal mortality NMR typology of 47/1000, about 30% (14 per 1000) of all neonatal deaths would be expected to be due to sepsis . With a prevalence of active syphilis of 3.6%, without treatment in pregnancy, for every 1000 pregnant women 36 women would be infected with active syphilis of whom 9 (25%) would be expected to have a stillbirth and 27 a livebirth. Overall 4 women (11% of pregnancies, 15% of livebirths) would expect to result in a term neonatal death attributable to syphilis i.e. a “sepsis” death. Assuming 97% efficacy about 8% (3.88/47) of overall neonatal deaths and 28% (3.88/14) of neonatal sepsis deaths in women with syphilis could be averted.
This is likely to be a conservative estimate. Additional neonatal deaths attributable to maternal syphilis are expected due to the effect of syphilis in pregnancy on preterm delivery and low birth weight, with their associated increased neonatal mortality. Four recent studies report 17% (90/536) of live births in women with syphilis in pregnancy were preterm [27, 31, 47, 48]. Preterm delivery was reported six times more frequently in RPR positive women compared with RPR negative women .
Cause specific mortality effect and quality grade of the estimate for the effect of at least 2.4MU penicillin treatment for active syphilis in pregnancy
Cause specific mortality to act on:
The proportion of stillbirth mortality that is related to syphilis.
The proportion of preterm mortality that is related to syphilis.
The proportion of neonatal sepsis mortality that is due to congenital syphilis.
Cause specific estimate of effect in affected pregnancies and range:
Reduction in stillbirth of 82% (95% c.i. 67 – 90%)
Reduction in the incidence of preterm delivery of 64% (95% c.i. 53 – 73%)
Reduction in the incidence of clinical congenital syphilis of 97% (95% c.i. 93 – 98%)
Assuming 15% of livebirths from syphilis affected pregnancies result in a neonatal death attributable to congenital syphilis (expert consensus) and that treatment does not affect case fatality, 97% (95%c.i. 93 – 98%) of these deaths could be averted.
Quality of input evidence:
For stillbirth – There is a large and consistent effect size from 8 observational studies. The GRADE quality of evidence is low.
For preterm - There is a large and consistent effect size from 7 observational studies. The GRADE quality of evidence is low.
There is a large and consistent effect size on incidence of clinical congenital syphilis and confounding is unlikely, so GRADE rules result in upgrading the low to moderate quality evidence.
The GRADE recommendation is STRONG, based on large and consistent effect sizes across studies, and biological plausibility.
Proximity of the data to cause specific mortality effect:
For the effect on preterm and neonatal sepsis due to congenital syphilis, the evidence is on incidence and distal to mortality estimate.
Possible adverse effects:
Penicillin allergic symptoms may occur in 2% of individuals ; however, severe allergic reactions (e.g. anaphylaxis) are rare events, estimated to occur in 10 to 50 of every 100,000 exposed individuals [90, 91]. Up to 40% of patients with primary or secondary syphilis may experience Jarisch-Herxheimer reactions with antibiotic treatment. These reactions involving malaise, anxiety, fever, headache, sweating, or rigors are believed caused by microbial lysis. If the reaction occurs late pregnancy it could lead to fetal distress, uterine contractions and preterm delivery [92, 93]. There is some evidence of possible increased maternal infection after antepartum treatment 
The information used on the extent to which maternal syphilis infection affects pregnancy outcome is based on a variety of sources. Randomised controlled trials of the effect of penicillin compared to no treatment would not be ethical. Studies reporting on the effect of syphilis in pregnancy on pregnancy outcome e.g. stillbirth, neonatal death, infected infant most commonly compare the outcome of untreated pregnancies with treated pregnancies or outcome of infected pregnancies versus non-affected pregnancies. In both cases the two groups may differ with respect to other risk factors for neonatal outcome, potential confounders (e.g. maternal age), co-infections (e.g. malaria and HIV) and maternal anaemia. Two recent studies which sought to control for potential confounding variables, have reported on the association of untreated active syphilis in pregnancy (RPR/VDRL titre >= 1:4 and reactive MHA-TP assay) with peri- and neonatal outcomes in low income settings. A study from Malawi, in a population with a prevalence of active syphilis of 3.6%, reported an adjusted odds ratio (OR) of 10.89 (95% c.i 6.61 – 17.93) for stillbirth and 4.86 (95% c.i. 2.73 – 10.36) for neonatal death . An estimated 11% (95% c.i. 6 – 17%) of neonatal deaths and 26% (95% c.i.18 – 35%) of stillbirths in this population were attributable to syphilis. A cohort study in Tanzania in which 7.7% of women tested seropositive for syphilis, reported adjusted risk ratios (RR) of 18.1 (95% c.i.5.5 – 59.6) for stillbirth, of 3.3 (95% c.i. 2.0 – 5.4) for low birth weight (LBW), of 6.1 (95% c.i. 2.5 – 15.3) for preterm birth, and of 2.1 (95% c.i. 1.0 – 4.2) for intra-uterine growth retardation (IUGR) .
A limitation of the GRADE approach, well illustrated in the present context, is its potential to produce results which could be misinterpreted by the reader who glances at the results but does not have time to read them and the conclusions carefully. There can be no doubt, based on our understanding of biological mechanisms, and the consistent and large effects seen across multiple studies, that timely diagnosis and treatment with benzathine penicillin of active syphilis infection in pregnant women substantially reduces the risk of stillbirth, and neonatal morbidity and mortality. However, all of the available quantitative evidence regarding the precise magnitude of these reductions comes from observational studies. Such evidence is automatically classified as "low quality" by the GRADE process unless one can essentially rule out any confounding (or other threats to validity). One is very rarely in a position to do this. The GRADE approach is, however, a two stage process, first grading the quality of evidence and secondarily the strength of recommendation. This is an intervention which should clearly be strongly recommended (GRADE recommendation STRONG) in areas where syphilis is prevalent even though it comes with a tag of "low quality evidence" attached. We should also emphasise the distinction between the quality of the evidence assigned by the GRADE process and the quality of individual studies contributing to that evidence. In many cases, well designed and executed observational studies will produce only “low quality evidence” in GRADE terms.
We assessed interventions that involved any treatment with at least 2.4 million units of penicillin, and did not attempt to compare longer versus shorter penicillin regimens. Foetal syphilis infection is, by definition, of less than one year duration, and thus falls under WHO and CDC treatment recommendations for early infection of a single intramuscular dose of 2.4 million units of benzathine penicillin (although effective treatment of a mother with latent infection would require additional doses per those recommendations). Watson-Jones found such a single dose treatment to be effective in preventing syphilis-associated adverse pregnancy outcomes among Tanzanian women attending ANC and, importantly, that 229 women ≤ 28 weeks gestation who received a single dose of penicillin had no increased risk for adverse pregnancy outcome compared with seronegative women. Gestational age at treatment is likely quite important, as foetal inflammatory response to treponemal infection occurs in the latter part of the 2nd trimester of pregnancy. Detection and treatment of syphilis infection later than 24 to 28 weeks gestation may be too late to prevent occurrence of some foetal losses, stillbirths or preterm births. Completing 3 penicillin doses has been observed to be highly correlated with gestational age at diagnosis, with women attending ANC later in pregnancy less likely to receive all 3 doses . While some studies have reported multiple penicillin doses to be more effective than single dose regimens in reducing adverse pregnancy outcomes associated with maternal syphilis infection, these did not report results by gestational age at first treatment [26, 34]. It is possible that longer regimens may confer some additional benefit in reducing adverse pregnancy outcomes, particularly among women co-infected with HIV  or in women with secondary infection ; however we were not able to assess this using existing data.
Detecting and measuring accurately the incidence of congenital syphilis is problematic even in countries with comprehensive surveillance systems . False positives may occur with RPR/ VDRL for example with yaws, viral infections, autoimmune conditions and pregnancy. These tests are user-dependent and onsite testing reduces sensitivity [47, 53–55] whilst laboratory-based screening involves women returning for the result. This delay in initiating treatment may result in fewer women receiving treatment or in insufficient time for treatment to be adequately effective prior to delivery. The most practical approach in low income settings is to ensure early screening and prompt, ideally same visit, treatment of positives, with follow-up treatment of mothers with additional penicillin doses if required e.g. late latent or tertiary syphilis. In settings lacking laboratory capacity for RPR testing this may be best achieved through use of point-of-care treponemal tests . This approach is currently being implemented in several countries. A recent cluster randomised trial found using point-of-care treponemal tests and first dose of penicillin in a one-stop clinic reduced congenital syphilis by 93.5% (95% c.i 66.0%–98.6%) compared with off-site RPR testing and penicillin treatment at next ANC visit . However, current point-of-care tests do not distinguish between past and present infection  and thus may result in some over-treatment of positive mothers who have been previously treated. Studies suggest that risks to the mother and costs of unnecessary treatment are small [14, 59]; however, introduction of a dual treponemal/non-treponemal point of care test, anticipated in the near future, should help address this problem.
Whilst policies for syphilis control are present in over three-quarters of 22 countries surveyed in Sub-Saharan Africa, in practice many women remain unscreened and untreated. Even amongst those receiving treatment, it is often only received after the critical first 24 weeks of pregnancy . In a study in Tanzania, only 43% of women attending ANC were screened and only 61% of those positive and 37% of their partners were treated . Other studies report similar figures [47, 62–68]. To prevent syphilis related adverse pregnancy outcomes women must access ANC sufficiently early, be tested, receive results promptly, be treated adequately, and remain uninfected for the rest of pregnancy . Implementing programmes can be difficult and even in high income countries cases of syphilis-related stillbirth and congenital syphilis still occur . Contributing factors include failure to attend ANC or attending only in the third trimester, lack of testing supplies/ transport for specimens and treatment available at the antenatal site, not returning for results/ treatment, infection or re-infection during pregnancy, and (rarely) failure of treatment [70–72]. Resolving some of these operational issues may be easier with decentralised approaches but concerns exist regarding sustainability [73–75].
How to screen most efficiently for syphilis is currently the major issue for low income countries . The economic cost of screening and treating cases of syphilis in pregnancy in Tanzania has been estimated to be $1.44 per women screened, $20 per woman treated and $186 per case of stillbirth or low birth weight averted . Modelling has suggested on-site testing with ICS to be the most effective and least costly strategy  and translation of these results into effective routine programmes has been demonstrated [59, 75]. Discussion surrounds whether screening should be carried out once or twice during pregnancy, though ensuring screening once for every woman would represent a major step forward. 0.4 – 2.8% of pregnant women in high prevalence areas were found to have become seropositive for syphilis between testing in the 1st and the 3rd trimester [17, 78–80]. Contact tracing of partners to reduce the risk of re-infection is resource intensive and rarely carried out . It is unclear what proportion of cases of congenital syphilis attributed to ‘penicillin treatment failure’ are actually due to re-infection [65, 80–84].
Co-infection with HIV infection compromises the serological response to and probably effectiveness of syphilis treatment of syphilis in adults [51, 85]. The effect of HIV on treatment of syphilis in pregnancy is not known. However syphilis may increase the transmission of congenital HIV infection [86, 87]. Introducing a functioning programme of syphilis screening and treatment into already established prenatal HIV testing services may be a cost-effective strategy and an opportunity for cohesion to maximise prevention of mother to child transmission of both HIV and syphilis [59, 88].
Evidence supports that at least 2.4MU penicillin given at least 28 days prior to delivery is effective in the treatment of syphilis in pregnant women to prevent congenital syphilis, with greatest effect when given early in pregnancy (before 24 -28 weeks). Our estimates suggest such treatment results in at least a 97% reduction in the incidence of congenital syphilis. Assuming that penicillin treatment does not alter case fatality from congenital syphilis, 97% of neonatal deaths from congenital syphilis may be averted by appropriate timely penicillin treatment for the affected mother during pregnancy. In addition, low grade evidence consistently supports large reductions amongst infected women in risks of stillbirth (82%), preterm birth (64%) and neonatal mortality (80%) with appropriate and timely treatment but uncontrolled confounding factors may account for part of these apparent effects.
Detection and appropriate timely penicillin treatment is an effective intervention to reduce adverse syphilis-related pregnancy outcomes. The strength of GRADE recommendation is strong based on biological plausibility and consistent and large effects seen across all studies reviewed. More research is required to identify the most cost effective strategy for achieving maximum coverage of screening for all pregnant women and access to treatment if required.
This work was supported in part by a grant to the US Fund for UNICEF from the Bill &Melinda Gates Foundation (grant 43386) to “Promote evidence-based decision making in designing maternal, neonatal and child health interventions in low- and middle-income countries”, and by a grant to Save The Children USA from the Bill & Melinda Gates Foundation (Grant 50124) for "Saving Newborn Lives".
We are grateful to Fujie Xu for insightful comments on an earlier draft of this paper.
This article has been published as part of BMC Public Health Volume 11 Supplement 3, 2011: Technical inputs, enhancements and applications of the Lives Saved Tool (LiST). The full contents of the supplement are available online at http://www.biomedcentral.com/1471-2458/11?issue=S3.
- A History of Syphilis. Edited by: Dennie, C.C., I. Springfield, Charles C. Thomas. 1962
- Schmid GP, et al: The need and plan for global elimination of congenital syphilis. Sexually Transmitted Diseases. 2007, 34 (7 Suppl): S5-10. 10.1097/01.olq.0000261456.09797.1b.View ArticlePubMedGoogle Scholar
- World Health Organization and Department of Reproductive Health and Research: Investment Case for Eliminating Congenital Syphilis: Promoting Better Maternal and Child Health Outcomes and Stronger Health Systems. 2010, WHO Geneva SwitzerlandGoogle Scholar
- Cheng JQ, et al: Syphilis screening and intervention in 500,000 pregnant women in Shenzhen, the People's Republic of China. Sexually Transmitted Infections. 2007, 83 (5): 347-50. 10.1136/sti.2006.023655.PubMed CentralView ArticlePubMedGoogle Scholar
- Tucker JD, Chen XS, Peeling RW: Syphilis and social upheaval in China. N Engl J Med. 2010, 362 (18): 1658-61. 10.1056/NEJMp0911149.View ArticlePubMedGoogle Scholar
- Meredith S: The Global Elimination of Congenital syphilis: rationale and strategy for action. 2007, Geneva: WHOGoogle Scholar
- Global prevalence and incidence of selected curable sexually transmitted infections overview and estimates. [http://www.who.int/hiv/pub/sti/who_hiv_aids_2001.02.pdf]
- Hollier LM, et al: Fetal syphilis: clinical and laboratory characteristics. Obstetrics & Gynecology. 2001, 97 (6): 947-53. 10.1016/S0029-7844(01)01367-9.View ArticleGoogle Scholar
- Nathan L, et al: In utero infection with Treponema pallidum in early pregnancy. Prenat Diagn. 1997, 17 (2): 119-23. 10.1002/(SICI)1097-0223(199702)17:2<119::AID-PD39>3.0.CO;2-T.View ArticlePubMedGoogle Scholar
- Sexually Transmitted Diseases. Edited by: Holmes, K.T. 2008, McGraw-Hill: New York, 4
- Stokes JHB: Modern Clinical Syphilology: Diagnosis, Treatment, Case Study. 1944, WB Saunders, 1: 3Google Scholar
- Workowski B: CDC Sexually Transmitted Diseases Treatment guidelines 2006. 2006, MMWR - Morbidity & Mortality Weekly Report, 55 (RR-11): 1-94.Google Scholar
- WHO: Prevention of Mother-to-Child Transmission of syphilis. [http://www.who.int/reproductive-health/publications/standards/prevention_mtct_syphilis.pdf]
- Centers for Disease, C: STD Treatment Guidelines 2006. [http://www.cdc.gov/std/treatment/2006/congenital-syphilis.htm]
- Rein MF: Biopharmacology of syphilotherapy. J Am Vener Dis Assoc. 1976, 3 (2 Pt 2): 109-27.PubMedGoogle Scholar
- Alexander JM, et al: Efficacy of treatment for syphilis in pregnancy. Obstetrics & Gynecology. 1999, 93 (1): 5-8. 10.1016/S0029-7844(98)00338-X.View ArticleGoogle Scholar
- Watson-Jones D, et al: Syphilis in pregnancy in Tanzania. II. The effectiveness of antenatal syphilis screening and single-dose benzathine penicillin treatment for the prevention of adverse pregnancy outcomes. J Infect Dis. 2002, 186 (7): 948-57. 10.1086/342951.View ArticlePubMedGoogle Scholar
- Stoner BP: Current controversies in the management of adult syphilis. Clinical Infectious Diseases. 2007, 44 (Suppl 3): S130-46. 10.1086/511426.View ArticlePubMedGoogle Scholar
- Boschi-Pinto C, Young M, Black RE: The Child Health Epidemiology Reference Group reviews of the effectiveness of interventions to reduce maternal, neonatal and child mortality. International Journal of Epidemiology. 2010, 39 (Suppl 1): i3-6. 10.1093/ije/dyq018.PubMed CentralView ArticlePubMedGoogle Scholar
- Walker N, F.-W. C, Bryce J, Bahl R, Cousens S: Standards for CHERG Reviews of Intervention Effects on Child Survival. International Journal of Epidemiology. 2010, 39 (suppl 1): i21-31. 10.1093/ije/dyq036.PubMed CentralView ArticlePubMedGoogle Scholar
- Atkins D, et al: Grading quality of evidence and strength of recommendations. BMJ. 2004, 328 (7454): 1490-10.1136/bmj.328.7454.1490.View ArticlePubMedGoogle Scholar
- STATA/IC 10.1, in Statistical Program. 2008, TX:STATA Corporation: College Station
- Walker GJ: Antibiotics for syphilis diagnosed during pregnancy. Cochrane Database Syst Rev. 2001, CD001143-3
- Wammock V: Penicillin therapy of the syphilitic pregnant woman: its practical application to a large urban obstetrical service. American Journal of Obstetrics & Gynecology. 1950, 59 (4): 806-17.View ArticleGoogle Scholar
- Ingraham NR: The value of penicillin alone in the prevention and treatment of congenital syphilis. Acta Derm Venereol Suppl (Stockh). 1950, 31 (Suppl 24): 60-87.Google Scholar
- Myer L, et al: Treatment of maternal syphilis in rural South Africa: effect of multiple doses of benzathine penicillin on pregnancy loss. Trop Med Int Health. 2004, 9 (11): 1216-21. 10.1111/j.1365-3156.2004.01330.x.View ArticlePubMedGoogle Scholar
- Gichangi P, et al: Congenital syphilis in a Nairobi maternity hospital. East Afr Med J. 2004, 81 (11): 589-93.PubMedGoogle Scholar
- Tikhonova L, et al: Congenital syphilis in the Russian Federation: magnitude, determinants, and consequences. Sexually Transmitted Infections. 2003, 79 (2): 106-10. 10.1136/sti.79.2.106.PubMed CentralView ArticlePubMedGoogle Scholar
- Lu J, Huang C, Zeng Y: Syphilis in pregnancy women. Zhonghua Fu Chan Ke Za Zhi. 2001, 36 (8): 456-9.PubMedGoogle Scholar
- Rutgers S: Syphilis in pregnancy: a medical audit in a rural district. Central African Journal of Medicine. 1993, 39 (12): 248-53.PubMedGoogle Scholar
- Watson-Jones D, et al: Syphilis in pregnancy in Tanzania. I. Impact of maternal syphilis on outcome of pregnancy. J Infect Dis. 2002, 186 (7): 940-7. 10.1086/342952.View ArticlePubMedGoogle Scholar
- Southwick KL, et al: Barriers to prenatal care and poor pregnancy outcomes among women with syphilis in the Russian Federation. Int J STD AIDS. 2007, 18 (6): 392-395. 10.1258/095646207781024748.View ArticlePubMedGoogle Scholar
- Rotchford K, et al: Impact on perinatal mortality of missed opportunities to treat maternal syphilis in rural South Africa: baseline results from a clinic randomized controlled trial. Trop Med Int Health. 2000, 5 (11): 800-804. 10.1046/j.1365-3156.2000.00636.x.View ArticlePubMedGoogle Scholar
- Donders GG, et al: Apparent failure of one injection of benzathine penicillin G for syphilis during pregnancy in human immunodeficiency virus-seronegative African women. Sexually Transmitted Diseases. 1997, 24 (2): 94-101. 10.1097/00007435-199702000-00007.View ArticlePubMedGoogle Scholar
- Guinness LF, et al: Influence of antenatal screening on perinatal mortality caused by syphilis in Swaziland. Genitourinary Medicine. 1988, 64 (5): 294-7.PubMed CentralPubMedGoogle Scholar
- Tikhonova L, et al: Congenital syphilis in the Russian Federation: magnitude, determinants, and consequences. Sexually Transmitted Infections. 2003, 79 (2): 106-10. 10.1136/sti.79.2.106.PubMed CentralView ArticlePubMedGoogle Scholar
- Donders GG, et al: The association of gonorrhoea and syphilis with premature birth and low birthweight. Genitourinary Medicine. 1993, 69 (2): 98-101.PubMed CentralPubMedGoogle Scholar
- Salakhov E, et al: Congenital syphilis in Russia: the value of counting epidemiologic cases and clinical cases. Sexually Transmitted Diseases. 2004, 31 (2): 127-32. 10.1097/01.OLQ.0000109516.47951.B8.View ArticlePubMedGoogle Scholar
- Zhang XM, et al: Clinical analysis of 192 pregnant women infected by syphilis. Zhonghua Fu Chan Ke Za Zhi. 2004, 39 (10): 682-6.PubMedGoogle Scholar
- Pettit DE, et al: Toluidine red unheated serum test, a nontreponemal test for syphilis. J Clin Microbiol. 1983, 18 (5): 1141-5.PubMed CentralPubMedGoogle Scholar
- Yin YP, et al: Performance of serological tests for syphilis in sexually transmitted diseases clinics in Guangxi Autonomous Region, China: implications for syphilis surveillance and control. Sex Health. 2009, 6 (1): 5-9. 10.1071/SH08027.View ArticlePubMedGoogle Scholar
- Alexander JM, et al: Efficacy of treatment for syphilis in pregnancy. Obstet Gynecol. 1999, 93 (1): 5-8. 10.1016/S0029-7844(98)00338-X.View ArticlePubMedGoogle Scholar
- Zhu L, et al: Maternal and congenital syphilis in Shanghai, China, 2002 to 2006. Int J Infect Dis. 2010, 14 Suppl 3: e45-e48. 10.1016/j.ijid.2009.09.009.View ArticlePubMedGoogle Scholar
- Tan KL: The re-emergence of early congenital syphilis. Acta Paediatr Scand. 1973, 62 (6): 601-7. 10.1111/j.1651-2227.1973.tb17071.x.View ArticlePubMedGoogle Scholar
- Ricci JM, Fojaco RM, O'Sullivan MJ: Congenital syphilis: the University of Miami/Jackson Memorial Medical Center experience, 1986-1988. Obstet Gynecol. 1989, 74 (5): 687-693.PubMedGoogle Scholar
- Lawn JE, et al: 4 million neonatal deaths: when? Where? Why?. Lancet. 2005, 365 (9462): 891-900. 10.1016/S0140-6736(05)71048-5.View ArticlePubMedGoogle Scholar
- Hira SK, et al: Syphilis intervention in pregnancy: Zambian demonstration project. Genitourinary Medicine. 1990, 66 (3): 159-64.PubMed CentralPubMedGoogle Scholar
- Bhat CJ, et al: Congenital syphilis in Lusaka--II. Incidence at birth and potential risk among hospital deliveries. East Afr Med J. 1982, 59 (5): 306-10.PubMedGoogle Scholar
- McDermott J, et al: Syphilis-associated perinatal and infant mortality in rural Malawi. Bull World Health Organ. 1993, 71 (6): 773-80.PubMed CentralPubMedGoogle Scholar
- Mullick S, Beksinksa M, Msomi S: Treatment for syphilis in antenatal care: compliance with the three dose standard treatment regimen. Sexually Transmitted Infections. 2005, 81 (3): 220-2. 10.1136/sti.2004.011999.PubMed CentralView ArticlePubMedGoogle Scholar
- Musher DM, Hamill RJ, Baughn RE: Effect of human immunodeficiency virus (HIV) infection on the course of syphilis and on the response to treatment. Ann Intern Med. 1990, 113 (11): 872-81.View ArticlePubMedGoogle Scholar
- Simms I, N Broutet: Congenital syphilis re-emerging. Journal der Deutschen Dermatologischen Gesellschaft. 2008, 6 (4): 269-72. 10.1111/j.1610-0387.2008.06490.x.View ArticlePubMedGoogle Scholar
- Peeling RW, Ye H: Diagnostic tools for preventing and managing maternal and congenital syphilis: an overview. Bull World Health Organ. 2004, 82 (6): 439-46.PubMed CentralPubMedGoogle Scholar
- Patel A, Moodley D, Moodley J: An evaluation of on-site testing for syphilis. Trop Doct. 2001, 31 (2): 79-82.PubMedGoogle Scholar
- Delport SD: Serological screening of cord blood for syphilis. S Afr Med J. 1988, 73 (9): 528-9.PubMedGoogle Scholar
- Bronzan RN, et al: On-site rapid antenatal syphilis screening with an immunochromatographic strip improves case detection and treatment in rural South African clinics. Sexually Transmitted Diseases. 2007, 34 (7 Suppl): S55-60. 10.1097/01.olq.0000245987.78067.0c.View ArticlePubMedGoogle Scholar
- Munkhuu B, et al: One-stop service for antenatal syphilis screening and prevention of congenital syphilis in Ulaanbaatar, Mongolia: a cluster randomized trial. Sexually Transmitted Diseases. 2009, 36 (11): 714-20. 10.1097/OLQ.0b013e3181bc0960.View ArticlePubMedGoogle Scholar
- Garcia SG, et al: Demonstrating public health at work: a demonstration project of congenital syphilis prevention efforts in Bolivia. Sexually Transmitted Diseases. 2007, 34 (7 Suppl): S37-41.PubMedGoogle Scholar
- Schackman BR, et al: Cost-effectiveness of rapid syphilis screening in prenatal HIV testing programs in Haiti. PLoS Med. 2007, 4 (5): e183-10.1371/journal.pmed.0040183.PubMed CentralView ArticlePubMedGoogle Scholar
- Gloyd S, Chai S, Mercer MA: Antenatal syphilis in sub-Saharan Africa: missed opportunities for mortality reduction. Health Policy Plan. 2001, 16 (1): 29-34. 10.1093/heapol/16.1.29.View ArticlePubMedGoogle Scholar
- Watson-Jones D, et al: Antenatal syphilis screening in sub-Saharan Africa: lessons learned from Tanzania. Trop Med Int Health. 2005, 10 (9): 934-43. 10.1111/j.1365-3156.2005.01473.x.View ArticlePubMedGoogle Scholar
- Revollo R, et al: Maternal and congenital syphilis in four provinces in Bolivia. Salud Publica Mex. 2007, 49 (6): 422-8. 10.1590/S0036-36342007000600009.View ArticlePubMedGoogle Scholar
- Rodrigues CS, Guimaraes MD, Cesar CC: Missed opportunities for congenital syphilis and HIV perinatal transmission prevention. Revista de Saude Publica. 2008, 42 (5): 851-8. 10.1590/S0034-89102008000500010.View ArticlePubMedGoogle Scholar
- Southwick KL, et al: Maternal and congenital syphilis in Bolivia, 1996: prevalence and risk factors. Bulletin of the World Health Organization. 2001, 79 (1): 33-42.PubMed CentralPubMedGoogle Scholar
- Romoren M, Rahman M: Syphilis screening in the antenatal care: a cross-sectional study from Botswana. BMC Int Health Hum Rights. 2006, 6: 8-10.1186/1472-698X-6-8.PubMed CentralView ArticlePubMedGoogle Scholar
- Bam RH, et al: Syphilis in pregnant patients and their offspring. Int J Gynaecol Obstet. 1994, 44 (2): 113-8. 10.1016/0020-7292(94)90063-9.View ArticlePubMedGoogle Scholar
- Lindstrand A, et al: Prevalence of syphilis infection in Mozambican women with second trimester miscarriage and women attending antenatal care in second trimester. Genitourinary Medicine. 1993, 69 (6): 431-3.PubMed CentralPubMedGoogle Scholar
- Wilkinson D, Sach M, Connolly C: Epidemiology of syphilis in pregnancy in rural South Africa: opportunities for control. Trop Med Int Health. 1997, 2 (1): 57-62. 10.1046/j.1365-3156.1997.d01-127.x.View ArticlePubMedGoogle Scholar
- Schmid G: Economic and programmatic aspects of congenital syphilis prevention. Bull World Health Organ. 2004, 82 (6): 402-9.PubMed CentralPubMedGoogle Scholar
- Gust DA, et al: Mortality associated with congenital syphilis in the United States, 1992-1998. Pediatrics. 2002, 109 (5): E79-9. 10.1542/peds.109.5.e79.View ArticlePubMedGoogle Scholar
- Warner L, et al: Missed opportunities for congenital syphilis prevention in an urban southeastern hospital. Sexually Transmitted Diseases. 2001, 28 (2): 92-8.View ArticlePubMedGoogle Scholar
- Deperthes BD, et al: Maternal and congenital syphilis programmes: case studies in Bolivia, Kenya and South Africa. Bulletin of the World Health Organization. 2004, 82 (6): 410-6.PubMed CentralPubMedGoogle Scholar
- Jenniskens F, et al: Syphilis control in pregnancy: decentralization of screening facilities to primary care level, a demonstration project in Nairobi, Kenya. Int J Gynaecol Obstet. 1995, 48 (Suppl): S121-8. 10.1016/0020-7292(95)02326-8.View ArticlePubMedGoogle Scholar
- Fonck K, et al: Syphilis control during pregnancy: effectiveness and sustainability of a decentralized program. American Journal of Public Health. 2001, 91 (5): 705-7. 10.2105/AJPH.91.5.705.PubMed CentralView ArticlePubMedGoogle Scholar
- Gloyd S, et al: Scaling up antenatal syphilis screening in Mozambique: transforming policy to action. Sexually Transmitted Diseases. 2007, 34 (7 Suppl): S31-6. 10.1097/01.olq.0000264586.49616.72.View ArticlePubMedGoogle Scholar
- Terris-Prestholt F, et al: Is antenatal syphilis screening still cost effective in sub-Saharan Africa. Sex Transm Infect. 2003, 79 (5): 375-81. 10.1136/sti.79.5.375.PubMed CentralView ArticlePubMedGoogle Scholar
- Blandford JM, et al: Cost-effectiveness of on-site antenatal screening to prevent congenital syphilis in rural eastern Cape Province, Republic of South Africa. Sexually Transmitted Diseases. 2007, 34 (7 Suppl): S61-6. 10.1097/01.olq.0000258314.20752.5f.View ArticlePubMedGoogle Scholar
- Qolohle DC, et al: Serological screening for sexually transmitted infections in pregnancy: is there any value in re-screening for HIV and syphilis at the time of delivery?. Genitourinary Medicine. 1995, 71 (2): 65-7.PubMed CentralPubMedGoogle Scholar
- Gichangi P, et al: Partner notification of pregnant women infected with syphilis in Nairobi, Kenya. Int J STD AIDS. 2000, 11 (4): 257-261. 10.1258/0956462001915660.View ArticlePubMedGoogle Scholar
- Lumbiganon P, et al: The epidemiology of syphilis in pregnancy. Int J STD AIDS. 2002, 13 (7): 486-494. 10.1258/09564620260079653.View ArticlePubMedGoogle Scholar
- Conover CS, et al: Congenital syphilis after treatment of maternal syphilis with a penicillin regimen exceeding CDC guidelines. Infect Dis Obstet Gynecol. 1998, 6 (3): 134-7. 10.1002/(SICI)1098-0997(1998)6:3<134::AID-IDOG7>3.0.CO;2-X.PubMed CentralView ArticlePubMedGoogle Scholar
- Mascola L, Pelosi R, Alexander CE: Inadequate treatment of syphilis in pregnancy. Am J Obstet Gynecol. 1984, 150 (8): 945-947.View ArticlePubMedGoogle Scholar
- Rawstron SA, Bromberg K: Failure of recommended maternal therapy to prevent congenital syphilis. Sexually Transmitted Diseases. 1991, 18 (2): 102-6. 10.1097/00007435-199118020-00009.View ArticlePubMedGoogle Scholar
- Hardy JB, et al: Failure of penicillin in a newborn with congenital syphilis. JAMA. 1970, 212 (8): 1345-9. 10.1001/jama.212.8.1345.View ArticlePubMedGoogle Scholar
- Ghanem KG, et al: Serological response to syphilis treatment in HIV-positive and HIV-negative patients attending sexually transmitted diseases clinics. Sexually Transmitted Infections. 2007, 83 (2): 97-101. 10.1136/sti.2006.021402.PubMed CentralView ArticlePubMedGoogle Scholar
- Mwapasa V, et al: Maternal syphilis infection is associated with increased risk of mother-to-child transmission of HIV in Malawi. Aids. 2006, 20 (14): 1869-77. 10.1097/01.aids.0000244206.41500.27.View ArticlePubMedGoogle Scholar
- Cowan FM, et al: Maternal Herpes simplex virus type 2 infection, syphilis and risk of intra-partum transmission of HIV-1: results of a case control study. AIDS. 2008, 22 (2): 193-201. 10.1097/QAD.0b013e3282f2a939.View ArticlePubMedGoogle Scholar
- Potter D, et al: Do targeted HIV programs improve overall care for pregnant women?: Antenatal syphilis management in Zambia before and after implementation of prevention of mother-to-child HIV transmission programs. J Acquir Immune Defic Syndr. 2008, 47 (1): 79-85. 10.1097/QAI.0b013e31815d2f71.PubMed CentralView ArticlePubMedGoogle Scholar
- Apter AJ, et al: Represcription of penicillin after allergic-like events. J Allergy Clin Immunol. 2004, 113 (4): 764-70. 10.1016/j.jaci.2003.11.032.View ArticlePubMedGoogle Scholar
- Risk of anaphylaxis in a hospital population in relation to the use of various drugs: an international study. Pharmacoepidemiol Drug Saf. 2003, 12 (3): 195-202. 10.1002/pds.822.
- Greenberger P: Drug allergy, part B: allergic reactions to individual drugs: low molecular weight, in Patterson’s allergic diseases. Edited by: L. Grammer and P. Greenberger. 2002, Lippincott, Williams & Wilkins: Philadelphia, 335-59. 6Google Scholar
- Klein VR, et al: The Jarisch-Herxheimer reaction complicating syphilotherapy in pregnancy. Obstet Gynecol. 1990, 75 (3 Pt 1): 375-380.PubMedGoogle Scholar
- Myles TD, et al: The Jarisch-Herxheimer reaction and fetal monitoring changes in pregnant women treated for syphilis. Obstet Gynecol. 1998, 92 (5): 859-864. 10.1016/S0029-7844(98)00271-3.View ArticlePubMedGoogle Scholar
- Wendel GD, et al: Treatment of syphilis in pregnancy and prevention of congenital syphilis. Clin Infect Dis. 2002, 35 (Suppl 2): S200-9. 10.1086/342108.View ArticlePubMedGoogle Scholar
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