Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-30T22:01:46.408Z Has data issue: false hasContentIssue false

The resurgence of syphilis in high-income countries in the 2000s: a focus on Europe

Published online by Cambridge University Press:  13 March 2019

G. Spiteri*
Affiliation:
European Centre for Disease Prevention and Control, Stockholm, Sweden
M. Unemo
Affiliation:
Department of Laboratory Medicine, Microbiology, Faculty of Medicine and Health, WHO Collaborating Centre for Gonorrhoea and other STIs, Örebro University, Örebro, Sweden
O. Mårdh
Affiliation:
European Centre for Disease Prevention and Control, Stockholm, Sweden
A. J. Amato-Gauci
Affiliation:
European Centre for Disease Prevention and Control, Stockholm, Sweden
*
Author for correspondence: G. Spiteri, E-mail: gianfranco.spiteri@ecdc.europa.eu
Rights & Permissions [Opens in a new window]

Abstract

Syphilis can cause severe complications and sequelae. Following a decrease in reported cases in European Union/European Economic Area (EU/EEA) and other high-income countries in the 1980s and 1990s as a result of the HIV epidemic and ensuing changes in sexual behaviour, trends started to increase in the 2000s in a number of EU/EEA Member States with higher rates among men and a large proportion of cases reported among men who have sex with men (MSM), particularly HIV-positive MSM. Trends in EU/EEA Member States vary however with some countries continuing to report decreases in the number of reported cases (mostly in the Eastern part of EU/EEA) whereas many Western European countries report increasing numbers of cases. Increasing rates among women, although still relatively low, have been observed in a number of countries leading to concerns around mother-to-child transmission of syphilis and congenital syphilis. Similar overall trends are observed in other high-income countries with the exception of Japan where rates among heterosexual men and women have been rising at alarming levels. Control of syphilis requires use of comprehensive, evidence-based strategies which take into account lessons learned from previous control efforts as well as consideration of biomedical interventions.

Type
Review
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s) 2019

Introduction

Syphilis is caused by the spirochaete Treponema pallidum subspecies pallidum. The infection is mainly sexually transmitted, except for transfusion of blood or blood products and congenital syphilis (mother-to-child transmission (MTCT) of syphilis), which is transmitted vertically during pregnancy. Following infection, syphilis may present as a chancre (primary syphilis) 10–90 days (average 3 weeks) after exposure [Reference Holmes1]. If untreated, the chancre will heal, but within a few weeks or months symptoms of secondary syphilis may appear. Symptoms may vary and include rashes, alopecia, condylomata lata as well as unspecific symptoms including malaise, sore throat, weight loss and low-grade fever. Symptoms of secondary syphilis disappear within some weeks, even without treatment. Latent syphilis then follows where patients do not show any symptoms but may remain infectious for up to a year following infection [Reference Singh and Romanowski2]. Latent infection may last for decades; if untreated, tertiary syphilis may develop with symptoms depending on the organ involved. Tertiary complications are rare at the present time, likely due to the impact of intermittent antibiotic use. Neurosyphilis, however, can still be observed and may present at any stage of syphilis. There are many diverse clinical manifestations of neurosyphilis [Reference Holmes1]. Benzathine penicillin G is the recommended treatment for syphilis and no bacterial resistance has been confirmed yet [Reference Janier3Reference Kingston6].

Historically, prior to the advent of penicillin, syphilis caused a significant public health burden with rates of infection in the general population of some countries of 5–10% [Reference Szreter7]. Syphilis was an important cause of neurological and cardiovascular complications and congenital syphilis was a significant cause of perinatal mortality. The rates of syphilis rapidly decreased following the widespread use of penicillin in the 1940s [Reference Mohammed8, 9]. Since then, syphilis has followed social trends with, for example, increases related to the sexual liberation of the 1960s, the crack-cocaine epidemics in the USA in the late 1980s and 1990s as well as decreases following the HIV epidemic in the 1980s and the subsequent changes in sexual behaviour [Reference Rolfs, Goldberg and Sharrar10, Reference Aral, Fenton and Holmes11]. However, since the 2000s, syphilis rates have again been increasing in developed countries, with rates rising most rapidly among men who have sex with men (MSM), but also increasing in other population groups [12]. The interaction with HIV co-infection, changes in sexual behaviour following wider availability of effective antiretroviral HIV treatment, the changing means and ease of finding sexual partners as a consequence of Internet and mobile dating applications have increased the complexity of the syphilis epidemiology, and particularly its control.

The aim of this review was to describe the recent epidemiology of syphilis in high-income countries, focusing on the European Union and the European Economic Area (EU/EEA) and to highlight emerging issues in syphilis epidemiology and control. This was done by reviewing syphilis surveillance data published by the European Centre for Disease Prevention and Control (ECDC), including surveillance reports and online databases. Additional key publications supporting the surveillance results were identified by reviewing the peer-reviewed published literature. A similar approach was used for other high-income countries and for MTCT of syphilis. Emerging issues were identified following discussion between coauthors and through reviewing peer-reviewed publications, where available from countries in the EU/EEA, but otherwise from other high-income countries.

Present situation: EU/EEA

Syphilis surveillance data reported at the EU/EEA level showed an overall decreasing trend from 8.4 cases per 1 00 000 population in 2000 to 4.4 in 2010, followed by an increase up to 6.1 cases per 1 00 000 in 2016 when 29 365 cases of syphilis were reported in 28 EU/EEA countries (Fig. 1) [12, 13]. This overall trend, however, masks the heterogeneity in trends observed across different countries. Syphilis rates in the Eastern part of the EU/EEA peaked around the late 1990s and early 2000s at very high rates (e.g. Latvia (in 1996): 126 per 1 00 000 and Romania (in 2002): 55 per 1 00 000 persons) and decreased thereafter. Rates in most Western and Central EU/EEA countries started from very low levels in the early 2000s and have been increasing steadily since then at different rates, although they still have not reached levels seen in Eastern Europe in the early 2000s (Fig. 2). At the EU/EEA level, there are gender differences, with rates among women decreasing overall since the peak in 1997. In contrast, rates among men decreased from 2005 to 2010 but have since increased to the highest rates reported since surveillance started at EU/EEA level (1990) (Figs 1 and 2 and [14]). These gender-specific patterns also vary by region within the EU/EEA, with large increases in rates reported among women in the Eastern part in the early 2000s, whereas Western and Central EU/EEA countries reported lowest rates among women in the early 2000s. Since then, cases among women in Western and Central EU/EEA countries such as the Czech Republic, Denmark, France, Germany and the UK have increased although rates are still lower than in Eastern EU/EEA countries (Fig. 2). Trends among men in Eastern EU/EEA countries followed similar patterns as for women, peaking in the mid-1990s and early 2000s, then decreasing and stabilising since 2010 [1214].

Source: Country reports from Bulgaria, Cyprus, the Czech Republic, Denmark, Estonia, Finland, Germany, Ireland, Italy, Latvia, Luxembourg, Malta, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Sweden and the UK.

Fig. 1. Rate of confirmed syphilis cases per 1 00 000 population by gender and year, EU/EEA countries reporting consistently, 2007–2016 (from [13]).

Fig. 2. Changes in number of reported syphilis cases overall and among men and women, between 2010 and 2016 (adapted from [14]).

The increases in syphilis cases among men in the EU/EEA have been driven by transmission among MSM (Fig. 3) [12Reference Abara17]. This is clearly the case for Western EU/EEA countries; however, although data are limited, similar observations have been reported from certain cities in Eastern and Central EU/EEA, for example, Gdansk and Warsaw in Poland [Reference Orzechowska18]. In addition, syphilis seropositivity among MSM in Bucharest was over 16% in a respondent-driven sampling study in 2012–2013, indicating a significant burden of syphilis among among MSM there [Reference Massimo Mirandola, Nigel, Igor, Ulrich, Susanne, Barbara, Cinta and Magdalena19]. The number of cases reported among MSM in the EU/EEA has more than doubled (164% increase) from 2010 to 2016 (Fig. 3). Increases in number of infections among MSM have been reported among HIV-negative and HIV-positive MSM, with some studies reporting greater increases among HIV-positive MSM [Reference Abara17]. Trends among heterosexual men at the EU/EEA level have, on the other hand, remained stable overall, although slight increases have been reported in 2015 and 2016 [13].

Source: Country reports from the Czech Republic, Denmark, Finland, France, Germany, Hungary, Iceland, Ireland, Latvia, Lithuania, Malta, the Netherlands, Norway, Portugal, Romania, Slovakia, Slovenia, Sweden and the UK.

Fig. 3. Number of confirmed syphilis cases by gender, transmission mode (sexual orientation) and year, EU/EEA countries reporting consistently, 2010–2016 (from [13]).

Other high-income countries

Similar trends as in Western EU/EEA countries have been described in high-income countries outside of Europe. In the USA, primary and secondary syphilis cases increased by 74% from 2003 to 2017, from 5.5 cases per 1 00 000 persons to 9.5, continuing an increasing trend since a nadir in 2001. Men accounted for 88% of syphilis cases in the USA in 2017 and 58% of all cases were among MSM [20]. In Canada, infectious syphilis rates increased from 5.0 to 9.3 per 1 00 000 persons from 2010 to 2015, an increase of 86%. The increase in Canada was more pronounced among males (90% compared with 28% among females) and males accounted for 94% of cases of infectious syphilis in 2015 [Reference Choudhri21]. In Australia, the overall syphilis notification rate increased by 107% from 6.9 cases per 1 00 000 persons in 2012 to 14.3 in 2016. Notification rates in Australia have increased among both males and females during this time with increases being proportionately more marked among females. However, males accounted for 87% of infectious syphilis cases in 2016. Notification rates were 5.4 times higher among the Aboriginal and Torres Strait Islander population than in the non-indigenous population. The increase from 2012 to 2016 was also higher among the Aboriginal and Torres Strait Islander population compared with the non-indigenous population (193% vs. 100% increase, respectively) [22]. In Japan, syphilis cases had increased in 2016 to levels not seen since the 1970s [Reference Takahashi23]. Although initially the increase was seen mostly among MSM [Reference Sugishita24], since 2013 the number of reported syphilis cases in Japan among heterosexual men and women have increased dramatically and each group accounted for more diagnoses in 2016 than MSM [Reference Takahashi23] leading to concerns about the re-emergence of congenital syphilis.

MTCT of syphilis

Apart from the increases in MSM, the USA, Canada, Australia and some Western EU/EEA countries have observed an increase in infections among heterosexual women. Although absolute rates among women continue to be low, these increases are worrying due to the risk of MTCT of syphilis. Indeed, there have been recent increases in cases of congenital syphilis in the USA and Japan [Reference Takahashi23, Reference Bowen25]. In Europe, congenital syphilis rates have decreased in recent years although cases are likely under-reported [26]. The countries reporting the largest numbers of cases have seen the largest decreases, for example, Bulgaria and Romania [14]. Despite this, cases are still reported in many EU/EEA countries (10 of the 23 reporting countries in 2016) and there have been recent reports of cases from the UK among mothers who screened negative in the first trimester of pregnancy [Reference Kingston27]. An ecological analysis found that these cases occurred in areas with increases in syphilis among women and MSM and relatively high proportion of behaviourally bisexual MSM which might have led to bridging of the syphilis epidemic from MSM to heterosexuals [Reference Furegato28]. These cases emphasise the need for strengthened antenatal syphilis screening, subsequent appropriate treatment and follow-up of screening-positive cases during the phase of elimination of MTCT of syphilis and HIV infections as declared by the World Health Organization [29].

Ocular syphilis

Recent reports of clusters of ocular syphilis in the USA [Reference Woolston30] created concerns of possible oculotropic strains. However, preliminary molecular epidemiological typing investigations have so far not confirmed the presence of a single oculotropic strain [Reference Oliver31]. It is still unclear whether the increase in ocular syphilis is a result of increased recognition and subsequent testing of ocular manifestations, a real increase in the proportion of cases with ocular manifestations, and/or a consequence of the increase in syphilis cases being observed among MSM. A report describing observations from eight jurisdictions in the USA showed that reported ocular syphilis cases from 2014 to 2015 had an epidemiology that appeared to reflect that of syphilis in the USA in terms of predominance among men, proportion among MSM and percentage HIV-positive [Reference Oliver32]. Authors from UK also report that trends of ocular syphilis in Manchester have increased in line with the epidemic of early syphilis. Of the 34 cases in their 2002–2016 case series, almost all were male (94%), 75% were MSM and 29% (all men) were HIV-positive. They estimate a risk of 1% for ocular involvement among those with early syphilis infection [Reference Wells33].

Reinfection

One aspect of the recent increases in syphilis among MSM observed in some countries has been the large proportion of repeat infections. In Antwerp, Belgium, for example, the majority of syphilis episodes from 1992 to 2012 were reported among MSM reporting more than one syphilis episode [Reference Kenyon34]. Observations from San Diego county in the USA also showed a substantial proportion of repeat syphilis [Reference Katz35]. HIV-positive MSM, those with 10 or more partners in the interval when syphilis was most likely acquired, as well as MSM who fail to attend for follow-up of the initial episode have been associated with a higher risk of repeat infection [Reference Kenyon34, Reference Dolan36].

Outbreaks

Despite the increase in reported syphilis across Europe, defined syphilis outbreaks are not often described in the EU/EEA. Key features associated with reported outbreaks include transmission among MSM, involvement of MSM often showing high prevalence of co-infections including HIV and hepatitis C, large number of recent sexual partners, including new and unknown partners, per time unit, as well as the use of geospatial networking apps to source partners [Reference Seppings and Hamill37Reference Cox40]. The increasing use of social media applications for finding sexual partners, particularly among MSM, has been frequently associated with increases in sexually transmitted infection (STI) despite limited evidence. Geospatial apps and websites, however, also provide an opportunity to reach key groups with public health messaging, although such campaigns need to be effectively designed to allow for an impact on outbreak control [Reference Thomas39, Reference Ross41, 42].

Newer epidemiological methods such as space-time clustering have been used to investigate syphilis epidemiology in the UK and the Netherlands. These identified previously undetected outbreaks among HIV-positive and HIV-negative MSM [Reference van Aar15, Reference Petersen43]. Such analyses could support syphilis control, management and guide public health interventions.

Syphilis treatment

Syphilis treatment continues to be based on benzathine penicillin G, and decades of clinical experience, clinical case studies, laboratory considerations and biological plausibility support its effectiveness [Reference Workowski4, Reference Kingston6, Reference Janier44]. Use of the appropriate preparation is essential as some forms of penicillin do not reach sequestered sites in the body and there have been reports of inadvertent use of inappropriate penicillin formulations [45]. Data on the effectiveness of alternative regimens are limited. The European syphilis management guideline recommends intramuscular procaine penicillin for 10–14 days as second-line therapy option if benzathine penicillin G is not available with additional options, such as doxycycline, ceftriaxone or azithromycin, in case of bleeding disorders, penicillin allergy or refusal of parenteral treatment [Reference Janier44]. All three alternatives are effective; however, a recent meta-analysis found that doxycycline/tetracycline recipients had a higher treatment failure rate than those treated with benzathine penicillin G [Reference Dai46Reference Riedner50]. In addition, azithromycin resistance and treatment failures have been described in the USA, Europe, Australia, China and elsewhere and azithromycin should therefore only be used as a last resort and when treatment can be followed up closely [Reference Kingston6, Reference Janier44, Reference Stamm51].

Discussion

The main epidemiological trends of syphilis in the EU/EEA in recent years are driven by increased cases among MSM. This observed increase among MSM is likely multifactorial and linked to increased numbers of partners, particularly casual partners, sero-adaptive behaviours and reduced condom use particularly among HIV-positive MSM [Reference Jansen16, Reference van den Boom52Reference Aghaizu54]. In more recent years, it is likely that the impact of effective HIV treatment as prevention and, even more recently, the introduction of HIV pre-exposure prophylaxis (PrEP) have led to increased risk behaviours and consequently syphilis transmission [Reference Montaño55Reference Molina57]. Control of syphilis, as well as other STIs, among MSM is challenging in the era of PrEP and highly active antiretroviral treatment [Reference Unemo58].

Apart from the challenges in controlling syphilis among MSM, the rapid change in the epidemiology of syphilis in Japan [Reference Takahashi23], with increased infections among heterosexual men and women together with the increase in MTCT of syphilis, highlights another significant public health issue that might also affect many additional high income countries. Indeed, the USA and a number of EU/EEA countries have already started observing increases in syphilis rates among women and in certain cases increases in MTCT of syphilis. Effective antenatal screening programmes, including appropriate screening and subsequent treatment and follow-up of screening-positive cases, are implemented in most parts of the EU/EEA and some countries already implement repeat screening in the third trimester of pregnancy [59]. In areas with ongoing outbreaks where repeat screening is not implemented, women at risk should be considered for such a second screening opportunity during the third trimester or even at delivery. In such situations, rapid serological point-of-care tests could also be considered for use when a pregnant woman who has not been screened earlier, with unknown screening results or who has been exposed since her screening test attends for delivery [60]. Unfortunately, women at risk can be difficult to identify [Reference Furegato28]. The EU/EEA rate of MTCT of syphilis is already below the World Health Organization elimination target (50 per 1 00 000 live births). With the re-emergence of syphilis, however, attention should be given to monitoring the performance of antenatal screening programmes and to increasing awareness among healthcare professionals. In addition, public health agencies should consider evaluating confirmed MTCT of syphilis in detail to identify ways of optimising antenatal programmes to prevent future infections. Standardised case definitions need to be used to ensure that all episodes of MTCT of syphilis are captured.

Syphilis control requires a multi-targeted approach using all available tools, and also new opportunities. Existing tools, such as primary and secondary prevention interventions, including enhanced awareness in the general population, persons at risk and among health care professionals, facilitation and expansion of testing and subsequent treatment and follow-up of patients, and partner notification need to be implemented as widely as possible [61]. Many of these interventions could be further enhanced through the use of geospatial apps and websites as mentioned earlier. Focusing particularly on regular STI testing of MSM, particularly when on PrEP, as recommended in guidelines, is essential [Reference Workowski4, Reference Kingston6, 61, Reference Templeton62]. Expansion of syphilis testing can be supplemented through community-based initiatives, successful examples of which have been implemented in the EU/EEA [Reference Coll63, Reference Manavi, Williams and Newton64]. Although many community-based settings focus mostly on HIV testing, syphilis testing should be routinely included in the context of high prevalence rates. Such expansion of testing could be established through rapid point-of-care testing technologies including combined HIV and syphilis testing methodologies once these have been thoroughly validated [Reference Zorzi65Reference Holden67].

Recently, post-exposure prophylaxis with doxycycline for syphilis has been investigated and found to be effective in reducing syphilis [Reference Molina68, Reference Bolan69]. Further research is needed to investigate the use of such an intervention in the context of core transmitter groups with high incidence of infection and re-infection. Although there are concerns around the development of antimicrobial resistance in T. pallidum and particularly in other bacterial species, the use of post-exposure prophylaxis for a limited period of time in groups with a high intensity of syphilis transmission as part of a comprehensive prevention intervention as suggested by Molina et al. warrants further investigation [Reference Molina68]. In addition, an effective oral therapy for syphilis would be valuable and a randomised controlled clinical trial evaluating cefixime for treatment is currently being planned [70]. Availability of alternative treatment options are particularly important due to shortages of benzathine penicillin G reported in many countries in recent years. These shortages have been in part linked to producers of the active product ingredient exiting the market as a consequence of the low market price and high production costs [Reference Nurse-Findlay71]. Despite the potential of alternative treatments, securing the availability of benzathine penicillin G is essential for global syphilis control.

The limited data and lack of reported syphilis outbreaks in many parts of Europe in a context of increasing trends highlight the challenges in prioritising STI surveillance and public health response in many countries. There is scope for a wider response to the resurgence of syphilis in Europe. In the USA, plans for syphilis control were launched in 1999 and 2006 with the 2006 plan proposing a reduction in primary and secondary syphilis, a reduction in congenital syphilis and reduced racial disparities by 2010. Three goals were proposed: investment in and enhancement of public health services; prioritisation of evidence-based, culturally competent interventions; and creating accountable services and interventions [72]. The targets were not reached and further increases in syphilis and MTCT of syphilis have since been reported. The experience from the USA provides a number of lessons which are useful for most countries trying to deal with this epidemic, including improving access to care, expanding partnerships (e.g. with other disease programmes), tailoring control activities to the epidemic and ensuring programme evaluation [Reference Valentine and Bolan73].

The syphilis epidemic should however not be taken as an isolated issue. Other STIs are on the increase both among MSM and heterosexuals [Reference Unemo58]. Increasing trends and/or outbreaks of gonorrhoea, lymphogranuloma venereum, and sexually transmitted shigellosis and hepatitis A have been reported in high-income countries around the globe over the last few years [Reference Rivas7477], indicating a need to focus more widely on improving sexual health rather than targeting specific infections. An integrated cross-disease approach would also result in synergies with other public health programmes which are often better resourced, such as HIV control.

One of the key challenges in syphilis control in EU/EA is the diversity in populations, resources, healthcare systems and public health services including surveillance. A one-size-fits-all approach is therefore unlikely to be effective. The lessons from the experience of the syphilis control plans in the USA certainly need to be borne in mind. The paucity of data on the syphilis epidemic from some parts of Europe is an additional point that needs to be kept in mind for an effective syphilis response in Europe. Ensuring that surveillance and other data are available at sufficient quality across EU/EEA is essential in order to guide an effective response. A better understanding of the key groups affected by syphilis across Europe, including (but not only) through better collection of data on sexual orientation, would allow for better understanding of the drivers of the epidemic, particularly in terms of socio-economic factors which clearly have an impact on syphilis epidemiology.

Conclusion

The resurgence of syphilis over the last decade in high-income countries of EU/EEA has clearly been driven by epidemics among MSM. Although this is a burden which needs to be addressed through specific interventions, the increase in cases among women, combined with increases in some settings of MTCT of syphilis, are worrying due to high risk of still birth and many additional severe complications and sequelae in affected newborn infants. Control of the current syphilis epidemic will not be achieved through any single intervention. Approaching syphilis control through a comprehensive strategy which applies all available evidence-based prevention interventions, including increased condom use, regular testing, behavioural interventions, together with effective treatment as well as further investigation of emerging biomedical tools and development of novel prevention approaches adapted to current social, behavioural and epidemiological contexts provides the best chance for success.

Author ORCIDs

Gianfranco Spiteri, 0000-0002-8877-059X

References

1.Holmes, KK. (2008) Sexually Transmitted Diseases. 4th Edn. New York: McGraw-Hill Medical, pp. xxv, 2166 p.Google Scholar
2.Singh, AE and Romanowski, B (1999) Syphilis: review with emphasis on clinical, epidemiologic, and some biologic features. Clinical Microbiology Reviews 12, 187209.Google Scholar
3.Janier, M et al. (2016) 2014 European guideline on the management of syphilis: giving evidence priority. Journal of the European Academy of Dermatology and Venereology 30, e78e79.Google Scholar
4.Workowski, KA et al. (2015) Sexually transmitted diseases treatment guidelines, 2015. MMWR Recommendations and Reports 64, 1137.Google Scholar
5.World Health Organization (2016) WHO Guidelines for the Treatment of Treponema pallidum (Syphilis). Geneva: World Health Organization.Google Scholar
6.Kingston, M et al. (2016) UK national guidelines on the management of syphilis 2015. International Journal of STD and AIDS 27, 421446.Google Scholar
7.Szreter, S (2014) The prevalence of syphilis in England and Wales on the eve of the Great War: re-visiting the estimates of the Royal Commission on Venereal Diseases 1913–1916. Social History of Medicine 27, 508529.Google Scholar
8.Mohammed, H et al. (2018) 100 years of STIs in the UK: a review of national surveillance data. Sexually Transmitted Infections 94, 553558.Google Scholar
9.Centers for Disease Control and Prevention (2017) Sexually Transmitted Disease Surveillance 2016. Atlanta: U.S. Department of Health and Human Services.Google Scholar
10.Rolfs, RT, Goldberg, M and Sharrar, RG (1990) Risk factors for syphilis: cocaine use and prostitution. American Journal of Public Health 80, 853857.Google Scholar
11.Aral, SO, Fenton, KA and Holmes, KK (2007) Sexually transmitted diseases in the USA: temporal trends. Sexually Transmitted Infections 83, 257266.Google Scholar
12.European Centre for Disease Prevention and Control (2012) Sexually Transmitted Infections in Europe 1990–2010. Stockholm: European Centre for Disease Prevention and Control.Google Scholar
13.European Centre for Disease Prevention and Control (2018) Syphilis. In: ECDC. Annual epidemiological report for 2016. Stockholm: European Centre for Disease Prevention and Control.Google Scholar
14.Surveillance Atlas of Infectious Diseases. Available at https://atlas.ecdc.europa.eu/public/index.aspx (Accessed 28 September 2018).Google Scholar
15.van Aar, F et al. (2017) Outbreaks of syphilis among men who have sex with men attending STI clinics between 2007 and 2015 in the Netherlands: a space-time clustering study. Sexually Transmitted Infections 93, 390395.Google Scholar
16.Jansen, K et al. (2016) Increased incidence of syphilis in men who have sex with men and risk management strategies, Germany, 2015. Euro Surveillance 21(43). pii=30382. https://doi.org/10.2807/1560-7917.ES.2016.21.43.30382.Google Scholar
17.Abara, WE et al. (2016) Syphilis trends among men who have sex with men in the United States and Western Europe: a systematic review of trend studies published between 2004 and 2015. PLoS ONE 11, e0159309.Google Scholar
18.Orzechowska, M et al. (2018) Epidemiological characteristics of patients with syphilis in Gdansk and Warsaw in 2016. Przeglad Epidemiologiczny 72, 223234.Google Scholar
19.Massimo Mirandola, LG, Nigel, S, Igor, T, Ulrich, M, Susanne, S, Barbara, S, Cinta, F, Magdalena, R (eds) (2016) The Sialon II project. Report on a bio-behavioural survey among MSM in 13 European cities: Cierre Grafica. ISBN 978-88-98768-55-4.Google Scholar
20.Centers for Disease Control and Prevention (2018) Sexually Transmitted Disease Surveillance 2017. Atlanta: Department of Health and Human Services.Google Scholar
21.Choudhri, Y et al. (2018) Infectious and congenital syphilis in Canada, 2010–2015. Canada Communicable Disease Report 44, 4348.Google Scholar
22.Kirby Institute (2017) HIV, viral hepatitis and sexually transmissible infections in Australia: annual surveillance report 2017. Sydney: Kirby Institute, UNSW.Google Scholar
23.Takahashi, T et al. (2018) Rapid increase in reports of syphilis associated with men who have sex with women and women who have sex with men, Japan, 2012 to 2016. Sexually Transmitted Diseases 45, 139143.Google Scholar
24.Sugishita, Y et al. (2016) Increase in primary and secondary syphilis notifications in men in Tokyo, 2007–2013. Japanese Journal of Infectious Diseases 69, 154157.Google Scholar
25.Bowen, V et al. (2015) Increase in incidence of congenital syphilis – United States, 2012–2014. MMWR Morbidity and Mortality Weekly Report 64, 12411245.Google Scholar
26.European Centre for Disease Prevention and Control (2018) Congenital syphilis. In: ECDC. Annual epidemiological report for 2016. Stockholm: European Centre for Disease Prevention and Control.Google Scholar
27.Kingston, M et al. (2017) Congenital syphilis in England and amendments to the BASHH guideline for management of affected infants. International Journal of STD and AIDS 28, 13611362.Google Scholar
28.Furegato, M et al. (2017) Factors associated with four atypical cases of congenital syphilis in England, 2016 to 2017: an ecological analysis. Euro Surveillance 22(49). pii=17-00750. https://doi.org/10.2807/1560-7917.ES.2017.22.49.17-00750.Google Scholar
29.World Health Organization (2007) The Global Elimination of Congenital Syphilis: Rationale and Strategy for Action. Geneva: World Health Organization.Google Scholar
30.Woolston, S et al. (2015) A cluster of ocular syphilis cases – Seattle, Washington, and San Francisco, California, 2014–2015. MMWR Morbidity and Mortality Weekly Report 64, 11501151.Google Scholar
31.Oliver, S et al. (2016) Molecular typing of Treponema pallidum in ocular syphilis. Sexually Transmitted Diseases 43, 524527.Google Scholar
32.Oliver, SE et al. (2016) Ocular syphilis – eight jurisdictions, United States, 2014–2015. MMWR Morbidity and Mortality Weekly Report 65, 11851188.Google Scholar
33.Wells, J et al. (2017) Ocular syphilis: the re-establishment of an old disease. Eye 32, 99.Google Scholar
34.Kenyon, C et al. (2014) Syphilis reinfections pose problems for syphilis diagnosis in Antwerp, Belgium – 1992 to 2012. Euro Surveillance 19, 20958.Google Scholar
35.Katz, KA et al. (2011) Repeat syphilis among men who have sex with men – San Diego County, 2004–2009. Sexually Transmitted Diseases 38, 349352.Google Scholar
36.Dolan, G et al. (2018) Factors associated with repeat diagnosis of syphilis in genitourinary medicine (GUM) clinic attendees in the North East of England, 2002–2014. International Journal of STD and AIDS 29, 790799.Google Scholar
37.Seppings, L and Hamill, M (2016) A review of an early syphilis outbreak in West Berkshire and Reading 2014–2015. Sexually Transmitted Infections 92, 364364.Google Scholar
38.Tsachouridou, O et al. (2016) Syphilis on the rise: a prolonged syphilis outbreak among HIV-infected patients in Northern Greece. Germs 6, 8390.Google Scholar
39.Thomas, DR et al. (2016) Outbreak of syphilis in men who have sex with men living in rural North Wales (UK) associated with the use of social media. Sexually Transmitted Infections 92, 359364.Google Scholar
40.Cox, JH et al. (2015) Audit of the management of the syphilis outbreak in Herefordshire 2011–2013. International Journal of STD and AIDS 26, 357359.Google Scholar
41.Ross, C et al. (2016) Impact of a social media campaign targeting men who have sex with men during an outbreak of syphilis in Winnipeg, Canada. Canada Communicable Disease Report 42, 4549.Google Scholar
42.European Centre for Disease Prevention and Control (2017) Use of Smartphone Application Advertising for HIV Prevention Among Men Who Have Sex With Men in the European Union/European Economic Area – An ECDC Guide to the Effective Use of Digital Platforms for HIV Prevention. Stockholm: European Centre for Disease Prevention and Control.Google Scholar
43.Petersen, J et al. (2016) Identifying and interpreting spatiotemporal variation in diagnoses of infectious syphilis among men, England: 2009 to 2013. Sexually Transmitted Infections 92, 380386.Google Scholar
44.Janier, M et al. (2014) 2014 European guideline on the management of syphilis. Journal of the European Academy of Dermatology and Venereology 28, 15811593.Google Scholar
45.Centers for Disease Control and Prevention (2005) Inadvertent use of Bicillin C-R to treat syphilis infection – Los Angeles, California, 1999–2004. MMWR Morbidity and Mortality Weekly Report 54, 217219.Google Scholar
46.Dai, T et al. (2017) Efficacy of doxycycline in the treatment of syphilis. Antimicrobial Agents and Chemotherapy 61, e0109216.Google Scholar
47.Tsai, JC et al. (2014) Comparison of serological response to doxycycline versus benzathine penicillin G in the treatment of early syphilis in HIV-infected patients: a multi-center observational study. PLoS ONE 9, e109813.Google Scholar
48.Liu, HY et al. (2017) Comparison of efficacy of treatments for early syphilis: a systematic review and network meta-analysis of randomized controlled trials and observational studies. PLoS ONE 12, e0180001.Google Scholar
49.Hook, EW III et al. (2010) A phase III equivalence trial of azithromycin versus benzathine penicillin for treatment of early syphilis. The Journal of Infectious Diseases 201, 17291735.Google Scholar
50.Riedner, G et al. (2005) Single-dose azithromycin versus penicillin G benzathine for the treatment of early syphilis. The New England Journal of Medicine 353, 12361244.Google Scholar
51.Stamm, LV (2015) Syphilis: antibiotic treatment and resistance. Epidemiology and Infection 143, 15671574.Google Scholar
52.van den Boom, W et al. (2012) Serosorting and sexual risk behaviour according to different casual partnership types among MSM: the study of one-night stands and sex buddies. AIDS Care 24, 167173.Google Scholar
53.McDaid, LM and Hart, GJ (2012) Serosorting and strategic positioning during unprotected anal intercourse: are risk reduction strategies being employed by gay and bisexual men in Scotland? Sexually Transmitted Diseases 39, 735738.Google Scholar
54.Aghaizu, A et al. (2016) Sexual behaviours, HIV testing, and the proportion of men at risk of transmitting and acquiring HIV in London, UK, 2000–13: a serial cross-sectional study. The Lancet HIV 3, e431e440.Google Scholar
55.Montaño, MA et al. (2019) Changes in sexual behavior and STI diagnoses among MSM initiating PrEP in a clinic setting. AIDS and Behavior 23, 548.Google Scholar
56.Nguyen, VK et al. (2018) Incidence of sexually transmitted infections before and after preexposure prophylaxis for HIV. AIDS 32, 523530.Google Scholar
57.Molina, JM et al. (2017) Efficacy, safety, and effect on sexual behaviour of on-demand pre-exposure prophylaxis for HIV in men who have sex with men: an observational cohort study. The Lancet HIV 4, e402e410.Google Scholar
58.Unemo, M et al. (2017) Sexually transmitted infections: challenges ahead. Lancet Infectious Diseases 17, e235e279.Google Scholar
59.European Centre for Disease Prevention and Control (2016) Antenatal Screening for HIV, Hepatitis B, Syphilis and Rubella Susceptibility in the EU/EEA. Stockholm: European Centre for Disease Prevention and Control.Google Scholar
60.World Health Organization (2017) WHO Guideline on Syphilis Screening and Treatment for Pregnant Women. Geneva: World Health Organization.Google Scholar
61.European Centre for Disease Prevention and Control (2015) HIV and STI Prevention Among Men Who Have Sex With Men. Stockholm: European Centre for Disease Prevention and Control.Google Scholar
62.Templeton, DJ et al. (2014) Australian sexually transmissible infection and HIV testing guidelines for asymptomatic men who have sex with men 2014: a review of the evidence. Sexual Health 11, 217229.Google Scholar
63.Coll, J et al. (2018) Early detection of HIV infection and of asymptomatic sexually transmitted infections among men who have sex with men. Clinical Microbiology and Infection 24, 540545.Google Scholar
64.Manavi, K, Williams, G and Newton, R (2012) The uptake of HIV and syphilis testing in a nurse-delivered service during Gay Pride events. International Journal of STD & AIDS 23, 887889.Google Scholar
65.Zorzi, A et al. (2017) Field evaluation of two point-of-care tests for syphilis among men who have sex with men, Verona, Italy. Sexually Transmitted Infections 93(S4), S51S58.Google Scholar
66.Van Den Heuvel, A et al. (2019) Laboratory evaluation of four HIV/syphilis rapid diagnostic tests. BMC Infectious Diseases 19, 1.Google Scholar
67.Holden, J et al. (2018) An evaluation of the SD Bioline HIV/syphilis duo test. International Journal of STD & AIDS 29, 5762.Google Scholar
68.Molina, JM et al. (2018) Post-exposure prophylaxis with doxycycline to prevent sexually transmitted infections in men who have sex with men: an open-label randomised substudy of the ANRS IPERGAY trial. Lancet Infectious Diseases 18, 308317.Google Scholar
69.Bolan, RK et al. (2015) Doxycycline prophylaxis to reduce incident syphilis among HIV-infected men who have sex with men who continue to engage in high-risk sex: a randomized, controlled pilot study. Sexually Transmitted Diseases 42, 98103.Google Scholar
70.ClinicalTrials.gov. Available at https://clinicaltrials.gov/ct2/show/NCT03660488 (Accessed 1 October 2018).Google Scholar
71.Nurse-Findlay, S et al. (2017) Shortages of benzathine penicillin for prevention of mother-to-child transmission of syphilis: an evaluation from multi-country surveys and stakeholder interviews. PLoS Medicine 14, e1002473.Google Scholar
72.Centers for Disease Control and Prevention (2006) Together We Can. The National Plan to Eliminate Syphilis From the United States. Atlanta, GA: US Department of Health and Human Services.Google Scholar
73.Valentine, JA and Bolan, GA (2018) Syphilis elimination: lessons learned again. Sexually Transmitted Diseases 45(9S Suppl 1), S80S85.Google Scholar
74.Rivas, V et al. (2018) Hepatitis A outbreak since November 2016 affecting men who have sex with men (MSM) in Chile connected to the current outbreak in MSM in Europe, situation up to October 2017. Euro Surveillance 23(9). pii=18-00060. https://doi.org/10.2807/1560-7917.ES.2018.23.9.18-00060.Google Scholar
75.Baker, KS et al. (2015) Intercontinental dissemination of azithromycin-resistant shigellosis through sexual transmission: a cross-sectional study. Lancet Infectious Diseases 15, 913921.Google Scholar
76.European Centre for Disease Prevention and Control (2018) Gonorrhoea. In: ECDC. Annual epidemiological report for 2016. Stockholm: European Centre for Disease Prevention and Control.Google Scholar
77.European Centre for Disease Prevention and Control (2018) Lymphogranuloma venereum. In: ECDC. Annual epidemiological report for 2016, Stockholm: European Centre for Disease Prevention and Control.Google Scholar
Figure 0

Fig. 1. Rate of confirmed syphilis cases per 1 00 000 population by gender and year, EU/EEA countries reporting consistently, 2007–2016 (from [13]).

Source: Country reports from Bulgaria, Cyprus, the Czech Republic, Denmark, Estonia, Finland, Germany, Ireland, Italy, Latvia, Luxembourg, Malta, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Sweden and the UK.
Figure 1

Fig. 2. Changes in number of reported syphilis cases overall and among men and women, between 2010 and 2016 (adapted from [14]).

Figure 2

Fig. 3. Number of confirmed syphilis cases by gender, transmission mode (sexual orientation) and year, EU/EEA countries reporting consistently, 2010–2016 (from [13]).

Source: Country reports from the Czech Republic, Denmark, Finland, France, Germany, Hungary, Iceland, Ireland, Latvia, Lithuania, Malta, the Netherlands, Norway, Portugal, Romania, Slovakia, Slovenia, Sweden and the UK.