SyphilisBMJ 2019; 365 doi: https://doi.org/10.1136/bmj.l4159 (Published 28 June 2019) Cite this as: BMJ 2019;365:l4159
- Patrick O'Byrne, associate professor, nurse practitioner1 2,
- Paul MacPherson, infectious disease specialist3
- 1School of Nursing, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada
- 2Sexual Health Clinic, Ottawa Public Health, Ottawa, Ontario K1N 5P9
- 3Division of Infectious Diseases, Ottawa Hospital General Campus, Ottawa, Ontario
- Correspondence to: P O'Byrne
What you need to know
Incidence rates of syphilis have increased substantially around the world, mostly affecting men who have sex with men and people infected with HIV
Have a high index of suspicion for syphilis in any sexually active patient with genital lesions or rashes
Primary syphilis classically presents as a single, painless, indurated genital ulcer (chancre), but this presentation is only 31% sensitive; lesions can be painful, multiple, and extra-genital
Diagnosis is usually based on serology, using a combination of treponemal and non-treponemal tests. Syphilis remains sensitive to benzathine penicillin G
Staging syphilis is important because it is the basis of management (treatment, expected treatment response, follow-up periods, and partner follow-up)
Patients with syphilis should be screened for HIV, gonorrhoea, and chlamydia
Caused by the bacteria Treponema pallidum,12 syphilis is transmitted through direct (usually sexual) contact with infected mucosal lesions. Other bodily fluids are also infectious when patients are bacteraemic. With infectivity up to 10-30% per sexual contact or 60% per relationship,3 syphilis rates have risen 300% since 2000 in many Western countries.4567 While most infections involve men who have sex with men, infections among people with opposite sex partners also occur.4567 In addition to increasing rates, syphilis can cause early complications such as irreversible loss of vision, so awareness of the infection is important for primary care clinicians.8910
What symptoms should alert me to this diagnosis?
Symptoms of syphilis by stage of infection (see fig 1)
Symptoms appear 10-90 days (mean 21 days) after exposure
Main symptom is a <2 cm chancre:
Progresses from a macule to papule to ulcer over 7 days
Painless, solitary, indurated, clean base (98% specific, 31% sensitive)
On glans, corona, labia, fourchette, or perineum
A third are extragenital in men who have sex with men and in women
Localised painless adenopathy
Symptoms appear 2 weeks to 6 months (mean 2-12 weeks) after exposure. Can be concurrent with, or up to 8 weeks after, chancre
Rash—Diffuse, symmetric, on trunk (often subtle or atypical)
Mucus lesions, condylomata lata
Patchy alopecia (4-11%)
Fever, headaches, generalised painless adenopathy
Neurologic symptoms—Cranial nerve palsies (II,VIII), eye redness or pain, meningitis, changes to mental status or memory
In early latent stage (<12 months* or <24 months† after exposure) 25% of subjects relapse to secondary syphilis (90% of these in first year, 94% within 2 years)
In late latent stage (>12* or 24† months after exposure), no relapse and not infectious
1-46 years after exposure
Neurologic—paresis, tabes dorsalis
Gummatous—necrotic granulomatous lesions
Primary syphilis—Patients with primary syphilis (fig 1) have a chancre at the site of inoculation—classically a solitary, painless, indurated, non-exudative ulcer (fig 2).1719 While often on the glans, corona, labia, fourchette, or perineum, it may occur in the mouth (fig 3), rectum, or vagina.17 Chancres can be inconspicuous (fig 4) and resolve in 3-10 weeks, possibly explaining why 60% of patients do not recall this lesion. Chancres may be multiple, painful, or atypical due to coinfection with other bacteria or herpesvirus.20 Depending on inoculum size, chancres appear 10-90 days after exposure (mean 21 days).17 Localised painless adenopathy may occur.17
Secondary syphilis—Secondary syphilis is a manifestation of bacterial dissemination and classically presents as a diffuse, symmetric, copper, maculopapular, possibly pruritic rash of any morphology except vesicular (fig 5).172021 A rash on the palms or soles is common (11-70%, fig 6). Mucus lesions (fig 7), patchy alopecia, fever, headaches, and generalised painless adenopathy may also occur.1718192021 Early neurosyphilis develops in 25-60% of people (box 1).9171819202122 Secondary symptoms appear 2-24 weeks after infection, concurrently with or up to eight weeks after chancres, and disappear spontaneously after several weeks with or without marking.1719
Latent syphilis—Syphilis then becomes latent, although symptoms of secondary syphilis recur in 25% of people, mostly (90%) within one year of acquiring the infection.17 Latent syphilis has early and late stages.17 Early latent disease includes the period of potential symptom relapse, classified by the WHO14 and European15 guidelines as <2 years since inoculation and as <1 year by US,11 UK,12 and Canadian13 guidelines. As symptom relapse indicates bacterial replication, early latent disease can be infectious. Late latent syphilis occurs >1-2 years after acquisition and is non-infectious (see fig 1).
Tertiary syphilis—Without treatment, 14-40% of people with syphilis progress to tertiary disease—irreversible damage to any organ—within 1-46 years. The damage is primarily neurologic, cardiovascular, or gummatous (necrotic granulomatous lesions pathognomonic of tertiary syphilis).217
Which diagnostic test should be done (table 1)?
Treponema pallidum may be visualised from lesions using dark field microscopy, direct fluorescent antibody testing, or polymerase chain reaction.1112131415 Because these tests are not widely available, diagnosis predominantly relies on serology.172627 While serologic tests and laboratory algorithms vary, testing usually begins with a screening treponemal test, such as an enzyme or chemiluminescence immunoassay (EIA or CLIA) to detect treponemal antibodies. A positive screening test should be followed by a confirmatory treponemal test, typically the T pallidum particle agglutination (TPPA). If both tests are positive, infection with syphilis is confirmed. Thereafter, the rapid plasma reagin (RPR) test (a quantitative non-treponemal test) should be used to measure disease activity and to track response to treatment (although 15-41% of patients remain reactive even after successful treatment).28
Screening treponemal tests (EIA or CLIA) usually become reactive first, often within two weeks of the chancre. However, patients with negative results who have syphilis-like symptoms or who report a high risk contact should be re-tested after a further two to four weeks.13
The RPR test may remain non-reactive for up to four weeks after the chancre, so it is often negative in primary syphilis, but it is 98-100% sensitive in secondary syphilis. However, because the RPR is a test of non-specific tissue damage, it may be positive for reasons other than syphilis.15
In the absence of treatment, a negative non-treponemal test three months after potential exposure effectively rules out a new syphilis infection.
Note that treponemal tests cannot distinguish active from treated infections and generally remain positive for life (see table 2).
Staging of syphilis
Staging of syphilis cannot be done based on laboratory results alone, and requires history and examination. Primary and secondary syphilis are symptomatic; early and late latent syphilis are generally asymptomatic. Careful examination to identify any symptoms not noticed by the patient is important and should include thorough anogenital and dermatologic inspection.21
The staging criteria for early latent syphilis are given in box 2. Asymptomatic patients with positive serology who do not fulfil the criteria of early latent syphilis could be staged as latent syphilis or as having syphilis of unknown duration.
Patients with early latent syphilis are asymptomatic, with one of the following:
New positive serology with a documented negative test within previous 12* or 24† months
≥4-fold increase in the RPR titre relative to a previous test done within 12* or 24† months
Unequivocal symptoms of primary or secondary syphilis within the previous 12* or 24† months
Only one possible exposure, which occurred within previous 12* or 24† months
What should I do with inconclusive results?
Generally, inconclusive results arise in early infection or from waning antibody levels in late infection. The most common combinations are:
A positive RPR with negative treponemal screening (EIA/CLIA) and confirmatory tests (TPPA) suggests the RPR result is a false positive
A positive screen (EIA/CLIA) with negative confirmatory test (TPPA) and negative RPR is likely a false positive but could indicate early infection
A positive screen (EIA/CLIA) with indeterminant confirmatory test (TPPA) and negative RPR could represent waning antibody levels after a previous, treated infection or a new infection.
When results are inconclusive, clinicians should inquire about previous syphilis infection and treatment, and, if early syphilis is possible, retest in two to four weeks.13 If results are unchanged, interpretation is based on history—consider the possibility of late untreated infection, treated infection, or non-venereal treponemal disease in adults from endemic countries in South and Central America, South-East Asia, and Africa.
What are the recommended treatment options? (box 3)
Recommended treatments for syphilis
Primary, secondary, and early latent disease
First line treatment
Benzathine penicillin G 2.4×106 units, single intramuscular dose*†
Doxycycline 100 mg, taken orally twice daily for 14 days*†
Ceftriaxone 1 g, intravenous or intramuscular once daily for 10 days*
Procaine penicillin G 1.2×106 units, intramuscular once daily for 10 days†
Azithromycin 2 g, single oral dose†
Late latent disease
First line treatment
Benzathine penicillin G 2.4×106 units, intramuscular dose once weekly for 3 weeks*†
Doxycycline 100 mg, taken orally twice daily for 28 days*†
Ceftriaxone 1 g, intravenous or intramuscular once daily for 10 days*
Procaine penicillin G 1.2×106 units, intramuscular once daily for 14-21 days†
For primary, secondary, and early latent syphilis, in the absence of neurologic findings, first-line treatment is benzathine penicillin G (BPG) 2.4×106 units as a single intramuscular injection. Late latent syphilis is treated with the same dose of BPG weekly for three weeks with no more than 14 days between doses (no more than 7 days for pregnant women).1112131415 Additional BPG doses do not improve treatment outcomes for patients with early syphilis,282930 although some guidelines suggest pregnant women with early syphilis can receive up to two doses.13 BPG has not been evaluated in controlled trials, but remains the first-line treatment because it is long acting (so covering the long dividing time of T pallidum) and because penicillin-resistant syphilis has not been documented in 60 years of the drug’s use.283031
Non-pregnant patients who are allergic to penicillin can be given doxycycline 100 mg by mouth twice daily for two weeks for primary, secondary, and early latent syphilis, or for four weeks for late latent syphilis,1112131415 although doxycycline, compared with BPG, may yield more treatment failures (defined according to the CDC as a fourfold or higher increase in RPR titre).283031 There is no alternative treatment to BPG for pregnant women.
Counsel patients about the possibility of Jarish-Herxheimer reactions, which start two to four hours after treatment and usually resolve within 24 hours. Symptoms include fever and systemic symptoms (such as chills, rigors, myalgias, arthralgias) with worsening rash or chancre.17 While UK guidelines12 state prednisolone can be used for symptom management, other guidelines11131415 recommend only over-the-counter antipyretics.
What about follow-up?
Because syphilis has no test-of-cure, conversion to a non-reactive RPR is the best evidence of successful treatment.28 Patients should be tested at the start of treatment and monitored at six and 12 months. No clinical data guide interpretation of RPR titres after treatment, and guidelines are based on expert opinion. See table 3 for recommendations from European, UK, US, Canadian, and WHO guidelines.1112131415
When should I consider evaluation of cerebrospinal fluid?
Indications for lumbar puncture and evaluation of cerebrospinal fluid (CSF) include neurologic symptoms or tertiary disease (table 3).1112131415 CSF evaluation can also be considered for the 10-20% of patients with earlier disease who do not achieve a fourfold decline in RPR titres by 6-12 months after treatment.1112131415
Because BPG poorly penetrates CSF,11 neurosyphilis should be treated with aqueous penicillin G, 4×106 units intravenously every 4 hours for 10-14 days. If neurosyphilis is ruled out, optimal management is unclear.11 Clinicians may monitor the RPR titre until it is low or non-reactive, or repeat the treatment for early or late latent syphilis.11 Factors limiting post-treatment RPR declines in the absence of neurosyphilis include prior infection, longer duration of infection, older age, HIV co-infection, and low pre-treatment titres.11121415
Referral to secondary care may be necessary for patients requiring CSF evaluation and should be considered for those with uncertain diagnoses or poor response to treatment.
Are there specific considerations for patients with HIV?
Syphilis and HIV infection often co-exist.3233 Patients with syphilis should be screened for HIV and, if negative, offered pre-exposure prophylaxis.323334 They should also be screened for gonorrhoea and chlamydia. HIV-positive patients have additional indications for CSF evaluation (see table 3). Otherwise, diagnosis and treatment are unchanged.31353637
How should I manage contact tracing?
Contacts (people who have had sex with a person diagnosed with infectious (early) syphilis) within 90 days should receive treatment with one dose of BPG even if their serology results are is negative; asymptomatic contacts who had sex with an infected person more than 90 days ago could defer treatment until their serology results are available, but only if follow-up is assured. Discussions about contact tracing should be non-stigmatising and sensitive to patients’ concerns about confidentiality. Explain that contact tracing has important benefits for the individual concerned and their contacts. It helps to limit ongoing transmission of a serious infection and prevent re-infection. Patients need help and support to notify contacts confidentially.
How this article was created
This article was created based on a review of international guidelines, expert opinion (local public health unit, STI clinic, and infectious disease department), and through a review of Medline and CINAHL, using the search term “syphilis.” We also undertook a manual review of the reference lists of identified articles.
Education into practice
Do you consider syphilis as a differential diagnosis of genital lesions and rashes among sexually active patients?
How would you approach a conversation about contact tracing with a young man, recently diagnosed?
How patients were involved in this article
We reviewed the contents of this material with Max Ottawa, a local “community-based organisation that focuses on maximising the health and wellness of gay, bisexual, Two-spirit, queer, and other guys who are into guys, both cis and trans.”
PO’B holds a research chair in public health and HIV prevention from the Ontario HIV Treatment Network.
Competing interests: We have read and understood the BMJ policy on declaration of interests and have no relevant interests to declare.
Provenance and peer review: Commissioned; externally peer reviewed.
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