eMedicine Specialties > Dermatology > Bacterial Infections

Endemic Syphilis: Treatment & Medication

Author: Hassan I Galadari, MD, MBBS, Assistant Professor of Dermatology, Faculty of Medicine and Health Sciences, United Arab Emirates University
Coauthor(s): Ibrahim Galadari, MD, MB, BCh, MSc, Professor of Dermatology, Department of Internal Medicine, Faculty of Medicine and Health Sciences, United Arab Emirates University
Contributor Information and Disclosures

Updated: Feb 13, 2009

Treatment

Medical Care

  • Endemic syphilis responds well to penicillin and other treponemicidal drugs. Patients become noninfectious within 24 hours.
  • After successful treatment, the titer of nontreponemal tests shows a gradual decline and eventually becomes negative.
  • No vaccines for the disease are available.

Medication

The goals of pharmacotherapy are to eradicate the infection, to reduce morbidity, and to prevent complications.

Antibiotics

These agents have the capability to achieve a 100% cure rate. Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.


Penicillin G benzathine (Bicillin LA)

Effectively used to treat primary and secondary endemic syphilis. Tertiary endemic syphilis also responds to treatment but requires a longer time to achieve full effect.

Adult

1.2 million units IM once

Pediatric

<10 years: 50,000 U/kg IM once; not to exceed 1.2 million units/dose
>10 years: Administer as in adults

Probenecid can increase effects; coadministration of tetracyclines can decrease effects; may increase methotrexate toxicity; may decrease contraceptive efficacy; may interfere with immunological response to live typhoid vaccine; concurrent administration with aminoglycoside therapy may result in inactivation of aminoglycoside (amikacin appears to possess greatest stability in presence of penicillins; in treatment of severely ill patients requiring both penicillin and aminoglycoside therapy, amikacin is aminoglycoside of choice)

Documented hypersensitivity; patients with epilepsy (neurotoxicity is a common feature); patients predisposed to hemorrhage or those receiving anticoagulants

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in impaired renal function, preexisting seizure disorder, or patients with electrolyte abnormalities (contains 1.7 mEq of potassium per million U); can cause acute renal nephritis


Tetracycline (Sumycin)

Can be used in patients allergic to penicillin. Treats gram-positive and gram-negative organisms as well as mycoplasmal, chlamydial, and rickettsial infections. Inhibits bacterial protein synthesis by binding with 30S and possibly 50S ribosomal subunits.

Adult

500 mg PO qid for 15 d

Pediatric

<8 years: Not recommended
>8 years:
Bejel and Yaws: 25-50 mg/kg/d PO divided qid for 15 d

Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; may enhance agents with neuromuscular blocking effect; can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy; tetracyclines can increase hypoprothrombinemic effects of anticoagulants
Coadministration with retinoids can cause increased intracranial pressure (coadministration contraindicated); administer tetracycline at least 1 h before or 4-6 h after colestipol or cholestyramine; if tetracycline administered concurrently with digoxin, monitor digoxin levels (dosage adjustment for digoxin may be required; risk of interaction may be reduced if given with Lanoxicaps)

Documented hypersensitivity; severe hepatic dysfunction

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Pseudotumor cerebri has been associated with tetracyclines, therefore, possibility for permanent sequelae exists; photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (last half of pregnancy through age 8 y) can cause permanent discoloration of teeth; may cause falsely positive urine glucose measurements


Erythromycin (E.E.S., E-Mycin, Ery-Tab)

Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. For treatment of staphylococcal and streptococcal infections.
In children, age, weight, and severity of infection determine proper dosage. When bid dosing is desired, half-total daily dose may be taken q12h. For more severe infections, double the dose. Can be used in child <8 y.

Adult

Erythromycin estolate: 500 mg qid for 10 d
Erythromycin ethylsuccinate: 800 mg 6 times/d or 1600 mg tid for 10 d
Erythromycin stearate: 500 mg 6 times/d for 10 d or 1000 mg tid for 10 d

Pediatric

8 mg/kg PO qid for 15 d

May significantly alter metabolism of nonsedating antihistamines and cause serious adverse cardiovascular events; concurrent use of lovastatin and erythromycin may cause rhabdomyolysis in patients who are seriously ill; may increase serum theophylline levels and toxicity; concomitant administration of digoxin may result in elevated serum digoxin levels; coadministration can increase effects of anticoagulants; concurrent use with ergotamine or dihydroergotamine has been associated with acute ergot toxicity; may decrease clearance of triazolam and midazolam; in patients taking other drugs metabolized by cytochrome P-450 system, may be associated with elevations in serum concentrations of those drugs; has demonstrated QTc prolongation in combination with other drugs that prolong the QT interval

Documented hypersensitivity; hepatic impairment; concomitant therapy with astemizole, cisapride, pimozide, or terfenadine

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in liver disease; estolate formulation may cause cholestatic jaundice; GI adverse effects are common (give doses pc); discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occur; neurological symptoms can be potentiated in myasthenia gravis; elderly patients may experience increased susceptibility to torsades de pointes arrhythmias

More on Endemic Syphilis

Overview: Endemic Syphilis
Differential Diagnoses & Workup: Endemic Syphilis
Treatment & Medication: Endemic Syphilis
Follow-up: Endemic Syphilis
References

References

  1. Clyti E, dos Santos RB. [Endemic treponematoses in Maputo, Mozambique]. Bull Soc Pathol Exot. May 2007;100(2):107-8. [Medline].

  2. Parish JL. Treponemal infections in the pediatric population. Clin Dermatol. Nov-Dec 2000;18(6):687-700. [Medline].

  3. Sharma VK, Kumar B. Malignant syphilis or syphilis simulating malignancy. Int J Dermatol. Sep 1991;30(9):676. [Medline].

  4. Antal GM, Lukehart SA, Meheus AZ. The endemic treponematoses. Microbes Infect. Jan 2002;4(1):83-94. [Medline].

  5. Blount JH, Holmes KK. Epidemiology of syphilis and the non-venereal treponematoses. In: Johnson RC, ed. The Biology of Parasitic Spirochetes. New York, NY: Academic; 1976:157-76.

  6. Cutler JC. Endemic syphilis, yaws, and pinta. In: Johnson RC, ed. The Biology of Parasitic Spirochetes. New York, NY: Academic; 1976:365-73.

  7. Engelkens HJ, Niemel PL, van der Sluis JJ, Meheus A, Stolz E. Endemic treponematoses. Part II. Pinta and endemic syphilis. Int J Dermatol. Apr 1991;30(4):231-8. [Medline].

  8. Falabella R. Nonvenereal treponematoses: yaws, endemic syphilis, and pinta. J Am Acad Dermatol. Dec 1994;31(6):1075. [Medline].

  9. Farnsworth N, Rosen T. Endemic treponematosis: review and update. Clin Dermatol. May-Jun 2006;24(3):181-90. [Medline].

  10. Kanan MW, Kandil E. Bejel or non-venereal endemic syphilis. Br J Dermatol. May 1971;84(5):461-4. [Medline].

  11. Knox JM, Musher D, Guzick ND. The pathogenesis of syphilis and the related treponematoses. In: Johnson RC, ed. The Biology of Parasitic Spirochetes. New York, NY: Academic; 1976:249-59.

  12. Koff AB, Rosen T. Nonvenereal treponematoses: yaws, endemic syphilis, and pinta. J Am Acad Dermatol. Oct 1993;29(4):519-35; quiz 536-8. [Medline].

  13. Meheus A, Antal GM. The endemic treponematoses: not yet eradicated. World Health Stat Q. 1992;45(2-3):228-37. [Medline].

  14. Morand JJ, Simon F, Garnotel E, Mahe A, Clity E, Morlain B. [Overview of endemic treponematoses]. Med Trop (Mars). Feb 2006;66(1):15-20. [Medline].

  15. Nsanze H, Lestringant GG, Ameen AM, Lambert JM, Galadari I, Usmani MA. Serologic tests for treponematoses in the United Arab Emirates. Int J Dermatol. Nov 1996;35(11):800-1. [Medline].

Further Reading

Keywords

nonvenereal syphilis of children, sibbens, radseyege, siti, therlijevo, njovera, frenjak, Treponema pallidum subsp endemicum, T pallidum subsp endemicum, nonvenereal endemic syphilis Bejel, non-venereal endemic syphilis Bejel

Contributor Information and Disclosures

Author

Hassan I Galadari, MD, MBBS, Assistant Professor of Dermatology, Faculty of Medicine and Health Sciences, United Arab Emirates University
Hassan I Galadari, MD, MBBS is a member of the following medical societies: American Academy of Dermatology, American Medical Association, American Medical Student Association/Foundation, and American Society for Dermatologic Surgery
Disclosure: Nothing to disclose.

Coauthor(s)

Ibrahim Galadari, MD, MB, BCh, MSc, Professor of Dermatology, Department of Internal Medicine, Faculty of Medicine and Health Sciences, United Arab Emirates University
Ibrahim Galadari, MD, MB, BCh, MSc is a member of the following medical societies: American Academy of Dermatology
Disclosure: Nothing to disclose.

Medical Editor

Craig A Elmets, MD, Director of Dermatology, Departments of Dermatology, Pathology, and Environmental Health Sciences; Professor, The Kirklin Clinic, University of Alabama at Birmingham
Craig A Elmets, MD is a member of the following medical societies: American Academy of Dermatology, American Association of Immunologists, American College of Physicians, American Federation for Medical Research, and Society for Investigative Dermatology
Disclosure: Palomar Medical Technologies Stock None; Merck Consulting fee Independent contractor; Tronox Consulting fee Independent contractor; Amgen Consulting fee Review panel membership; Astellas Consulting fee Review panel membership; Massachusetts Medical Society Salary Employment

Pharmacy Editor

Michael J Wells, MD, Associate Professor, Department of Dermatology, Texas Tech University Health Sciences Center
Michael J Wells, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American Medical Association, and Texas Medical Association
Disclosure: Nothing to disclose.

Managing Editor

Paul Krusinski, MD, Director of Dermatology, Professor, Department of Internal Medicine, Fletcher Allen Health Care, University of Vermont
Paul Krusinski, MD is a member of the following medical societies: American Academy of Dermatology, American College of Physicians, and Society for Investigative Dermatology
Disclosure: Nothing to disclose.

CME Editor

Catherine Quirk, MD, Clinical Assistant Professor, Department of Dermatology, Brown University
Catherine Quirk, MD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Dermatology
Disclosure: Nothing to disclose.

Chief Editor

Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center
Dirk M Elston, MD is a member of the following medical societies: American Academy of Dermatology
Disclosure: Nothing to disclose.

 
 
HONcode

We subscribe to the
HONcode principles of the
Health On the Net Foundation

All material on this website is protected by copyright, Copyright© 1994- by Medscape.
This website also contains material copyrighted by 3rd parties.

DISCLAIMER: The content of this Website is not influenced by sponsors. The site is designed primarily for use by qualified physicians and other medical professionals. The information contained herein should NOT be used as a substitute for the advice of an appropriately qualified and licensed physician or other health care provider. The information provided here is for educational and informational purposes only. In no way should it be considered as offering medical advice. Please check with a physician if you suspect you are ill.