Before a client with syphilis can be treated, which issue must be addressed?

Syphilis is a systemic, bacterial infection caused by the spirochete Treponema pallidum. Due to its many protean clinical manifestations, it has been named the “great imitator and mimicker.” The origin of syphilis has been controversial and under great debate, and many theories have been postulated regarding this.

The pre-Columbian theory looked at findings on skeletal markers of syphilis before 1490. However, there is insufficient proof, as evidenced by the DNA and paleopathology findings, to support the existence of syphilis before 1492.

The Columbian and most accepted theory postulates that syphilis came from Europe in the 1490s when Columbus arrived in the New World (America). Syphilis spread when Christopher Columbus arrived in Naples (Italy). After Naples lost the battle to the French troops, this new disease spread across Europe.

Syphilis remains a contemporary plague that continues to afflict millions of people worldwide.

Nursing Diagnosis

  • Risk for transmission of infection to others

  • At risk for transmitting the infection to the fetus

Causes

German scientists identified Treponema pallidum as the agent that causes syphilis in 1905. One year later, a test to diagnose this infection was developed. Its genome was sequenced in 1998. Treponema genus is a spiral-shaped bacteria with a rich outer phospholipid membrane that belongs to the spirochetal order. It has a slow metabolizing rate, as it takes an average of 30 hours to multiply.

T. pallidum is the only agent that causes venereal disease. The other T. pallidum subspecies cause non-venereal disease that is transmitted via non-sexual contact: Treponema pertenue causes yaws, Treponema pallidum endemicum causes endemic syphilis, and Treponema carateum causes pinta. All the treponematoses have similar DNA but differ in their geographical distribution and pathogenesis.

The only host for the organisms is humans, and there is no animal reservoir. Syphilis is considered a sexually transmitted disease as most cases of syphilis are transmitted through vaginal, anogenital, and orogenital contact. The infection can rarely be acquired via non-sexual contact, such as skin-to-skin contact, or via blood transfer (blood transfusion or needle sharing). Vertical transmission occurs transplacentally, resulting in congenital syphilis.

Risk Factors

According to the Centers for Disease Control and Prevention (CDC) statistics, there were 88,042 reported new diagnoses of syphilis in 2016. Out of all syphilis cases, 27,814 were primary and secondary syphilis. In 2016, most syphilis cases occurred among gay, bisexual, and other men who have sex with men. Men aged 20 to 29 years have the highest rates of primary and secondary syphilis.

From 2008 to 2012, rates of congenital syphilis declined but increased by 38% 2012. During 2016, 628 cases of congenital syphilis were reported, with rates 8.0-times and 3.9-times higher among infants born to black and Hispanic mothers compared to White mothers.

Syphilis is endemic in the developing world and is especially common among poor people with limited access to health care. Promiscuity plays an important role in disease transmission as it is more common among people with multiple partners.

Syphilis is an important synergistic infection for HIV acquisition and has been closely linked with HIV infection.

Assessment

Primary syphilis appears 10 to 90 days after exposure to the infection and comprises a painless, indurated ulcer (chancre) at the site of inoculation with the T. pallidum. HIV patients usually develop multiple chancres. These lesions resolve without treatment in 3-6 weeks. Regional lymphadenopathy is common and consists of rubbery lymph nodes.

Secondary syphilis appears 2 to 8 weeks after the disappearance of the chancre and has multiple systemic manifestations that can involve any system and body part. The cutaneous manifestations are also varied  (condyloma lata, alopecia, mucous patches, palmar or truncal rash, papulosquamous rash), and because they contain a high load of spirochetes, these lesions are highly contagious.

Untreated primary or secondary syphilis is followed by an early latent phase (one year or less later) or late latent phase (over one year). It is characterized by positive serologic tests but negative clinical manifestations.

Tertiary syphilis is late symptomatic syphilis that can manifest months or years after the initial infection as cardiovascular syphilis (an aortic aneurysm, aortic valvulopathy), neurosyphilis (meningitis, hemiplegia, stroke, aphasia, seizures, tabes dorsalis), or gummatous syphilis (infiltration of any organ and its subsequent destruction).

Congenital syphilis results from transplacental transmission or contact with the infectious lesions during birth and can be acquired at any stage, causing stillbirth or neonatal congenital infection. There are many presentations of congenital syphilis, including nasal cartilage destruction (saddle nose), frontal bossing (Olympian brow), bowing of the tibia (saber shins), morbilliform rash, rhinitis (snuffles), sterile joint effusion (Clutton joints), peg-shaped upper central incisors (Hutchinson's teeth). Many of the neonates born with congenital syphilis are asymptomatic at birth.  

Early signs can manifest up to 48 months as rash, hepatosplenomegaly, fever, bulging fontanels, seizures, or cranial nerve palsies. Those untreated neonates enter a latent period. Routine screening is recommended at the first prenatal visit and during the third trimester and delivery in high-risk women.

Evaluation

Testing strategies for syphilis consist of dark-field microscopy and serological tests.

Dark-field examination by microscope allows for direct examination of spirochetes from the mucosal lesion and thus offers an immediate diagnosis.

The serological tests are classified as non-treponemal and treponemal. The non-treponemal tests (venereal disease research laboratory tests, rapid plasma reagin test) are screening tests that detect antibodies to cardiolipin in blood. The VDRL and RPR tests are only positive after the development of the primary chancre.

Positive non-treponemal tests are confirmed with treponemal tests (fluorescent treponemal antibody absorption assay, T. pallidum particle agglutination assay) that detect antibodies to the T. pallidum in blood. Syphilis is a reportable disease.

Patients with neurologic symptoms should undergo a cerebrospinal (CSF) examination.

Reverse sequence screening is an increasingly used algorithm across US laboratories that use treponemal tests as the initial screening to identify those patients with treated, untreated, or incompletely treated syphilis.  Because of a lack of validation of the reverse algorithm, higher rates of false-positive results can be seen, leading to difficulty interpreting these tests and the need for second confirmatory treponemal tests.

Medical Management

Treatment depends on the disease stage.

Primary, secondary, or early latent syphilis is treated with a single dose of intramuscular (IM) penicillin G benzathine 2.4 million units. Alternative therapies include doxycycline 100 mg orally (PO) twice daily for 14 days or ceftriaxone 1 to 2 gm IM or intravenously (IV) daily for 10 to 14 days or tetracycline 100 mg PO 4 times daily for 14 days.

Late latent syphilis is treated with IM penicillin G benzathine 2.4 million units once weekly for three weeks. Alternative therapies include doxycycline 100 mg PO twice daily for 28 days or tetracycline 100 mg PO four times daily for 28 days.

Tertiary syphilis is treated with IM penicillin G benzathine 2.4 million units once weekly for three weeks.

Neurosyphilis is treated with IV penicillin G aqueous 18-24 million units daily for 10 to 14 days.

Patients with a high titer of secondary syphilis can develop Jarisch-Herxheimer reaction, which is an immune-mediated self-limited reaction that occurs within 2 to 24 hours of treatment and is characterized by high fever, headache, myalgias, and rash.

Nursing Management

  • Educate patient on safe sex practice

  • Encourage the use of condoms

  • Encourage treatment of a partner

  • Administer benzathine penicillin

  • Educate the patient on avoiding sex with an infected partner

  • Listen to the heart for the murmur of aortic regurgitation

  • Check the chest x-ray report (syphilis can cause aortic aneurysms)

  • Assess neurologic and mental status (rule out tertiary syphilis)

  • Assess genitals to ensure healing has occurred

When To Seek Help

If nursing staff encounter exam findings that deviate from the norm or are unsure of any aspects of the patient's sexual or social history, they should alert the clinician for further assessment.

Outcome Identification

The outlook for most patients who comply with treatment is good, but those who delay or fail to comply with treatment can develop life-threatening complications.

Monitoring

Post-treatment, patients need to be followed at 3, 6, 9, 12, and 24 months with serial non-treponemal tests. A 4-fold decline in these tests indicates successful treatment.

Coordination of Care

Once the diagnosis of syphilis has been made, the management is with a multidisciplinary team since the infection can affect almost every organ in the body. These patients need close follow-up by the cardiologist, neurologist, dermatologist, internist, ophthalmologist, obstetrician, and infectious disease expert. The patient must be followed by the infectious disease nurse to ensure that the treatment is working and the patient is compliant with therapy. The patient's partner has to be investigated and treated if positive. If the patient with syphilis is pregnant, close follow-up with an obstetrician is highly recommended.

Health Teaching and Health Promotion

Nurses are responsible for education regarding safe sex practices, treatment compliance, risks to unborn children, and answering any questions the patient may have.

Pearls and Other issues

Syphilis can cause a gamut of systemic manifestations, and for this reason, it has been called the “great mimicker.” Despite its discovery centuries ago, it remains a significant public health problem. Because of its varied manifestations, diagnosis can be challenging. Physicians need to maintain an increased suspicion index for screening high-risk populations, such as men who have sex with men, pregnant women with syphilis, and HIV-infected patients. Penicillin remains the primary treatment based on the stage of infection and whether CNS involvement occurs. Treated patients must be followed up with non-treponemal antibody titers to evaluate treatment response.

Figure

Syphilis. Contributed by DermNetNZ

Figure

This photograph shows a close-up view of keratotic lesions on the palms of this patient’s hands due to a secondary syphilitic infection. Syphilis is a complex sexually transmitted disease (STD) caused by the bacterium Treponema pallidum. It has (more...)

Figure

Fundoscopic image, effect of late neuro-ocular syphilis on the optic disk and retina, Pathology, Severe optic nerve atrophy, chorioretinitis, inflammation of the choroidal and neural layers of the retina. Contributed by Susan Lindsley, The Centers for (more...)

Figure

Syphilis gummas lesion. Contributed by The Centers for Disease Control and Prevention (CDC)

Figure

Primary Syphilis Chancre. Contributed by Dr. Shyam Verma, MBBS, DVD, FRCP, FAAD, Vadodara, India

References

1.

Anteric I, Basic Z, Vilovic K, Kolic K, Andjelinovic S. Which theory for the origin of syphilis is true? J Sex Med. 2014 Dec;11(12):3112-8. [PubMed: 25187322]

2.

Peeling RW, Hook EW. The pathogenesis of syphilis: the Great Mimicker, revisited. J Pathol. 2006 Jan;208(2):224-32. [PubMed: 16362988]

3.

Hook EW. Syphilis. Lancet. 2017 Apr 15;389(10078):1550-1557. [PubMed: 27993382]

4.

Flamm A, Parikh K, Xie Q, Kwon EJ, Elston DM. Histologic features of secondary syphilis: A multicenter retrospective review. J Am Acad Dermatol. 2015 Dec;73(6):1025-30. [PubMed: 26464219]

5.

Mattei PL, Beachkofsky TM, Gilson RT, Wisco OJ. Syphilis: a reemerging infection. Am Fam Physician. 2012 Sep 01;86(5):433-40. [PubMed: 22963062]

6.

Cohen SE, Klausner JD, Engelman J, Philip S. Syphilis in the modern era: an update for physicians. Infect Dis Clin North Am. 2013 Dec;27(4):705-22. [PubMed: 24275265]

7.

Tipple C, Taylor GP. Syphilis testing, typing, and treatment follow-up: a new era for an old disease. Curr Opin Infect Dis. 2015 Feb;28(1):53-60. [PubMed: 25485649]

8.

Clement ME, Okeke NL, Hicks CB. Treatment of syphilis: a systematic review. JAMA. 2014 Nov 12;312(18):1905-17. [PMC free article: PMC6690208] [PubMed: 25387188]

9.

Hollier LM, Harstad TW, Sanchez PJ, Twickler DM, Wendel GD. Fetal syphilis: clinical and laboratory characteristics. Obstet Gynecol. 2001 Jun;97(6):947-53. [PubMed: 11384701]

10.

Dhakal A, Sbar E. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Apr 28, 2022. Jarisch Herxheimer Reaction. [PubMed: 32491752]

11.

Hawkes S, Matin N, Broutet N, Low N. Effectiveness of interventions to improve screening for syphilis in pregnancy: a systematic review and meta-analysis. Lancet Infect Dis. 2011 Sep;11(9):684-91. [PubMed: 21683653]

12.

Rac MW, Bryant SN, Cantey JB, McIntire DD, Wendel GD, Sheffield JS. Maternal titers after adequate syphilotherapy during pregnancy. Clin Infect Dis. 2015 Mar 01;60(5):686-90. [PubMed: 25414264]

13.

Pham MN, Ho HE, Desai M. Penicillin desensitization: Treatment of syphilis in pregnancy in penicillin-allergic patients. Ann Allergy Asthma Immunol. 2017 May;118(5):537-541. [PubMed: 28477786]

14.

Wendel GD, Sheffield JS, Hollier LM, Hill JB, Ramsey PS, Sánchez PJ. Treatment of syphilis in pregnancy and prevention of congenital syphilis. Clin Infect Dis. 2002 Oct 15;35(Suppl 2):S200-9. [PubMed: 12353207]

15.

Shann S, Wilson J. Treatment of neurosyphilis with ceftriaxone. Sex Transm Infect. 2003 Oct;79(5):415-6. [PMC free article: PMC1744761] [PubMed: 14573840]

16.

Trubiano JA, Thursky KA, Stewardson AJ, Urbancic K, Worth LJ, Jackson C, Stevenson W, Sutherland M, Slavin MA, Grayson ML, Phillips EJ. Impact of an Integrated Antibiotic Allergy Testing Program on Antimicrobial Stewardship: A Multicenter Evaluation. Clin Infect Dis. 2017 Jul 01;65(1):166-174. [PMC free article: PMC5849110] [PubMed: 28520865]

17.

Chen JR, Tarver SA, Alvarez KS, Tran T, Khan DA. A Proactive Approach to Penicillin Allergy Testing in Hospitalized Patients. J Allergy Clin Immunol Pract. 2017 May-Jun;5(3):686-693. [PubMed: 27888034]

18.

Shenoy ES, Macy E, Rowe T, Blumenthal KG. Evaluation and Management of Penicillin Allergy: A Review. JAMA. 2019 Jan 15;321(2):188-199. [PubMed: 30644987]

19.

Coyle M, Depcinski S, Thirumoorthi M. Prevention of congenital syphilis using ceftriaxone in a woman with Stevens-Johnson syndrome reaction to penicillin: A case report. Case Rep Womens Health. 2022 Oct;36:e00446. [PMC free article: PMC9441298] [PubMed: 36072694]

20.

Bettuzzi T, Jourdes A, Robineau O, Alcaraz I, Manda V, Molina JM, Mehlen M, Cazanave C, Tattevin P, Mensi S, Terrier B, Régent A, Ghosn J, Charlier C, Martin-Blondel G, Dupin N. Ceftriaxone compared with benzylpenicillin in the treatment of neurosyphilis in France: a retrospective multicentre study. Lancet Infect Dis. 2021 Oct;21(10):1441-1447. [PubMed: 34051142]

21.

Lang R, Shalit I, Segal J, Arbel Y, Markov S, Hass H, Fejgin M. Maternal and fetal serum and tissue levels of ceftriaxone following preoperative prophylaxis in emergency cesarean section. Chemotherapy. 1993 Mar-Apr;39(2):77-81. [PubMed: 8458249]

22.

Bourget P, Fernandez H, Quinquis V, Delouis C. Pharmacokinetics and protein binding of ceftriaxone during pregnancy. Antimicrob Agents Chemother. 1993 Jan;37(1):54-9. [PMC free article: PMC187604] [PubMed: 8431018]

23.

Patel IH, Kaplan SA. Pharmacokinetic profile of ceftriaxone in man. Am J Med. 1984 Oct 19;77(4C):17-25. [PubMed: 6093513]

24.

Garcia MR, Leslie SW, Wray AA. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Oct 8, 2022. Sexually Transmitted Infections. [PubMed: 32809643]

25.

Ha T, Tadi P, Dubensky L. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Jul 4, 2022. Neurosyphilis. [PubMed: 31082023]

26.

Hussain SA, Vaidya R. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Oct 2, 2022. Congenital Syphilis. [PubMed: 30725772]

27.

Koundanya VV, Tripathy K. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Aug 22, 2022. Syphilis Ocular Manifestations. [PubMed: 32644383]

28.

Bhandari J, Thada PK, Ratzan RM. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Aug 10, 2022. Tabes Dorsalis. [PubMed: 32491814]

29.

Jaan A, Rajnik M. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Oct 13, 2022. TORCH Complex. [PubMed: 32809363]

30.

Rockwood N, Nwokolo N. Syphilis the great pretender: when is cancer not cancer? Sex Transm Infect. 2018 May;94(3):192-193. [PubMed: 29519910]

31.

Zhou HY, Di Y, Ye JJ, Xu HY. [The ocular manifestations of human immunodeficiency virus and syphilis coinfection]. Zhonghua Yan Ke Za Zhi. 2019 Apr 11;55(4):267-272. [PubMed: 30982288]

32.

Forrestel AK, Kovarik CL, Katz KA. Sexually acquired syphilis: Historical aspects, microbiology, epidemiology, and clinical manifestations. J Am Acad Dermatol. 2020 Jan;82(1):1-14. [PubMed: 30986477]

33.

Del Re F, Falcetta GS, Pratali S, Belgio B, Pucci A, Bortolotti U. Syphilitic Aortic Aneurysm in the Third Millennium. Aorta (Stamford). 2018 Oct;6(5):118-119. [PMC free article: PMC6443384] [PubMed: 30934107]

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