• Finnish Medical Society Duodecim. Syphilis. In: EBM Guidelines. Evidence-Based Medicine [Internet]. Helsinki, Finland: Wiley Interscience. John Wiley & Sons; 2008 Jun 6 [Various].

This is the current release of the guideline.

This guideline updates a previous version: Finnish Medical Society Duodecim. Syphilis. In: EBM Guidelines. Evidence-Based Medicine [Internet]. Helsinki, Finland: Wiley Interscience. John Wiley & Sons; 2006 Jul 25 [Various].

Syphilis, including primary, secondary, and latent syphilis; neurosyphilis and neonatal syphilis

Diagnosis
Management
Prevention
Screening
Treatment

Family Practice
Internal Medicine
Obstetrics and Gynecology
Pediatrics

Health Care Providers
Physicians

Evidence-Based Medicine Guidelines collect, summarize, and update the core clinical knowledge essential in general practice. The guidelines also describe the scientific evidence underlying the given recommendations.

Patients with suspected or confirmed syphilis and patients exposed to syphilis

Diagnosis

1. Assessment of history of exposure and signs and symptoms of syphilis
2. Microscopic assessment of lesion discharge for spirochetes
3. Serologic testing (cardiolipin test, Treponema pallidum haemagglutination test [TPHA], fluorescent treponemal antibody absorption [FTA-abs] test as indicated for special cases)
4. Gene amplification methods for screening

Management/Treatment/Prevention

1. Procaine penicillin
2. Ceftriaxone injections as alternative for patients who are allergic to penicillin
3. Follow-up testing with the cardiolipin and Treponema pallidum haemagglutination tests at specified intervals
4. Identification and screening of partners with cardiolipin test

• Sensitivity and specificity of diagnostic tests
• Effectiveness of antibiotic treatment

Hand-searches of Published Literature (Primary Sources)
Hand-searches of Published Literature (Secondary Sources)
Searches of Electronic Databases

The evidence reviewed was collected from the Cochrane database of systematic reviews and the Database of Abstracts of Reviews of Effectiveness (DARE). In addition, the Cochrane Library and medical journals were searched specifically for original publications.

Not stated

Weighting According to a Rating Scheme (Scheme Given)

Classification of the Quality of Evidence

GRADE (Grading of Recommendations Assessment, Development and Evaluation) Working Group 2007 (modified by the EBM Guidelines Editorial Team).

Systematic Review

Not stated

Not stated

Not applicable

A formal cost analysis was not performed and published cost analyses were not reviewed.

Peer Review

Not stated

Aims

• Suspected syphilis should be verified with the appropriate clinical and serological tests, and the patient should be treated with the most efficient antibiotics.
• Syphilis is a dangerous infectious disease that should be prevented and treated effectively.

Aetiology and Transmission

• The pathogen is the spirochete Treponema pallidum.
• Easily transmitted by sexual intercourse and also from the mother to the foetus.
• Contagiousness is highest (30% to 60%) in the primary and secondary phases. After 2 years, the patient ceases to spread the disease.

Clinical Picture

• Asymptomatic incubation period lasts for 3 to 4 weeks after which two thirds of the patients (not all!) have visible symptoms
  1. Primary symptoms (local infection)
     • An ulcer, the "primary lesion," with a clean, hard base (see picture 1 in the original guideline document) appears in the genital region, sometimes also in anus or the oral region.
     • There is local lymphadenopathy without tenderness.
  2. Secondary stage 6 to 8 weeks after exposure (general infection).
     • General symptoms include indisposition, fever and enlarged lymph nodes.
     • Roseola eczema (see picture 2 in the original guideline document) resembles widely spread viral eczema or drug eruption.
       • Syphilids (i.e., formations of papules) are found in the hands and feet or spread all over the body. May be large, cauliflower-like formations (condylomata latum) around the anus or necrotic in patients with a poor immune response (e.g. human immunodeficiency virus [HIV])
     • Alopecia syphilitica, typical "moth-eaten" spotty baldness in some patients
  3. Late symptoms occur in about one third of untreated patients in 10 to 30 years. The most important are neurological (atypical psychosis, paralytic dementia) and vascular symptoms (aortic aneurysm, valvular regurgitation).

Differential Diagnosis

• Primary syphilis
  • Genital herpes. Incubation time is short in primary infection, lesions occur in groups and they are painful. Lymphadenopathy is less pronounced; however, the nodes are tender.
  • Ulcus molle (soft chancre)
  • Infected coital or other traumas
• Secondary syphilis
  • Roseola may resemble pityriasis rosea, drug eruption, measles (rubeola), German measles (rubella), or scarlet fever (scarlatina).
  • Syphilids may resemble papular lichen ruber planus, psoriasis, scabies or infectious eczema of the feet (e.g., tinea). Condyloma latum may resemble condyloma acuminata.

Diagnosis

1. History of exposure (unprotected sex) and/or clinical picture.
2. Plain specimen. A dark field microscope may reveal spirochetes in lesion discharge and confirm the diagnosis.
3. Serology
   • The cardiolipin test becomes positive 3 to 4 weeks after infection. It is the primary test for screening. High titres (>16) are almost always specific. A low titre is in many cases a false positive result (pregnancy, connective tissue disease, infection) or a serological scar of an earlier treated infection or latent syphilis.
   • Determination of Treponema pallidum antibodies is a new specific and sensitive enzyme immunoassay screening test. It has been taken into use at antenatal clinics and in clinical work. The test is very sensitive and identifies Treponema antibodies also in previously treated or latent cases in which the cardiolipin test remains negative. A positive result must be verified with the Treponema pallidum haemagglutination test (TPHA) test.
   • TPHA is the test of choice for verifying syphilis. The result becomes positive slightly later than that of the cardiolipin test, but it is specific (almost 100%) and suitable for following up response to treatment.
   • Fluorescent treponemal antibody absorption test (FTA-abs) is a specific syphilis test used in special cases (neurosyphilis, suspicion of neonatal syphilis) as it detects also immunoglobulin M (IgM) antibodies.
   • Gene amplification methods are already being used for screening.

Treatment

• Procaine penicillin 1.2 million IU x 1 intramuscular (i.m.) for 10 days (primary and secondary syphilis; in latent syphilis treatment is received for three weeks), in neurosyphilis intravenous (i.v.) penicillin.
• For patients allergic to penicillin, ceftriaxone injections (1 g/day) are an alternative.

Follow-up and Identification of Partners

• After antibiotic therapy the cardiolipin and TPHA tests are performed at 3 and 6 months and one year. In primary stage infection, the tests become negative in most cases; in other recent infections the titre falls by at least two dilutions when the treatment has been successful.
• All sexual partners who have been exposed to infection should be screened with the cardiolipin test. If the result is negative, the test should be repeated after 3 months.

Related Resources

Refer to the original guideline document for related evidence, including Cochrane reviews and other evidence summaries.

None provided

Concise summaries of scientific evidence attached to the individual guidelines are the unique feature of the Evidence-Based Medicine Guidelines. The evidence summaries allow the clinician to judge how well-founded the treatment recommendations are.

• Appropriate use of clinical and serological tests for the verification of suspected syphilis
• Effective prevention and treatment of syphilis

A low titre of the cardiolipin test is in many cases a false positive result (pregnancy, connective tissue disease, infection) or a serological scar of an earlier treated infection or latent syphilis.

An implementation strategy was not provided.

Getting Better
Staying Healthy

Effectiveness

• Finnish Medical Society Duodecim. Syphilis. In: EBM Guidelines. Evidence-Based Medicine [Internet]. Helsinki, Finland: Wiley Interscience. John Wiley & Sons; 2008 Jun 6 [Various].

Not applicable: The guideline was not adapted from another source.

2001 Nov 22 (revised 2008 Jun 6)

Finnish Medical Society Duodecim - Professional Association

Finnish Medical Society Duodecim

Editorial Team of EBM Guidelines

Primary Author: Timo Reunala

Not stated

This is the current release of the guideline.

This guideline updates a previous version: Finnish Medical Society Duodecim. Syphilis. In: EBM Guidelines. Evidence-Based Medicine [Internet]. Helsinki, Finland: Wiley Interscience. John Wiley & Sons; 2006 Jul 25 [Various].

None available

None available

This summary was completed by ECRI on December 17, 2002. The information was verified by the guideline developer on February 7, 2003. This NGC summary was updated by ECRI on October 4, 2004 and on December 22, 2006. This summary was updated by ECRI Institute on October 3, 2007 following the U.S. Food and Drug Administration (FDA) advisory on Rocephin (ceftriaxone sodium). This NGC summary was updated by ECRI Institute on December 5, 2008.

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.