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SYPHILIS
ā€œTHE GREAT PRETENDERā€
By
Dhananjay A. Desai
Research Scholar
Department of Microbiology
N. A. C. & Sc. College, Ahmednagar
dhananjayashokdesai@gmail.com
Overview
ā€¢ History of Syphilis.
ā€¢ Transmission pathogenesis and stages of syphilis.
ā€¢ Diagnostic tests.
ā€¢ Treatment and partner management.
ā€¢ Epidemiology.
The great pox
ā€¢ Epidemic in 15 century Europe.
ā€¢ Rapid spread and served symptoms in early stages.
ā€¢ Epidemic coincide with Columbus return from america in
1493.
ā€¢ Endemic but unrecognized.
ā€¢ A gift from new world.
Syphilis Discovery of its causes
ā€¢ 1903: Infection successfully transmitted to
monkeys.
ā€¢ 1905: Identification of the bacterium Treponema
pallidum.
ā€¢ 1906: Dark field microscopy.
Taxonomy
ā€¢ Domain: Bacteria
ā€¢ Phylum: Spirochaetes
ā€¢ Order: Spirocheteles
ā€¢ Family: Spirochetacae
ā€¢ Genus: Treponema
ā€¢ Species: pallidum
Characteristics
ā€¢ Helical, tightly coil, Mobile.
ā€¢ 5-10 Āµm in length and 0.1-0.4 Āµm diameter.
ā€¢ Pathogenic Treponema associated with ten Diseases.
ā€¢ Veneral syphilis- Pallidum
ā€¢ Endemic- Endemicum
ā€¢ YAWS- Pertenue
ā€¢ Pinta- Carateum
ā€¢ Obligatory parasite of human.
Epidemiology
and
Aspects of
Syphilis Prevention
Primary and secondary syphilis ā€” Rates by state:
United States and
outlying areas, 2007
Distribution of Reported STD in
World, 2008
Method of Infection
ā€¢ Viable bacteria from chancre enter through the fissure or
mucous membrane.
ā€¢ Bacteria multiply locally and causes painless chancre.
ā€¢ Spared via blood stream and lymphatic system.
ā€¢ Can almost infect many organ and tissue.
ā€¢ Continuous in vitro culture yet Not to be achieved.
Symptoms
(some have no symptoms for years)
ā€¢ 3 Stages:
ļƒ¼ Primary
ļƒ¼ Secondary
ļƒ¼ Late or latent
ā€¢ Congenital (passed from a mother to her child)
Pathogenesis
ā€¢ Multiple at the site of inoculation and form chancre.
ā€¢ Spread to local lymph nodes and then to blood
stream.
ā€¢ Can involve of many body organs.
ā€¢ Infection and inflammation of blood vessels.
Primary Stage
ā€¢ Appearance of a single sore or chancre (about 21 day
after infection).
ā€¢ Chancre lasts 3-6 weeks and heal by treatments.
ā€¢ If untreated disease progress to next stage.
Secondary stage
ā€¢ Occur as chancre is healing or few weeks after.
ā€¢ Skin rash developed on one or more areas.
ā€¢ appear like other disease (usually doesnā€™t cause itching).
ā€¢ Other symptoms: fever, swollen lymph gland, sore throat,
patchy hair loss, headaches, weight loss.
ā€¢ Without treatment disease progress to next late stage.
Late stage
(Hidden stage)
ā€¢ Person continues to have syphilis even through they
are no symptoms.
ā€¢ Disease can damage eyes, brain, nervous system,
liver, bones, joints.
ā€¢ Sign include: difficulty coordinating muscle
movement, paralysis, numbness, gradual blindness,
even death.
Diagnostic Tests
ā€¢ Dark field
ā€¢ PCR
ā€¢ VDRL/RPR
ā€¢ EIA
T. pallidum on Dark field
T. pallidum by DFA-TP
Syphilis Serology
ā€¢ Non-Treponema tests
ļƒ¼ VDRL (Venereal Disease
Research Laboratory)
ļƒ¼ RPR (Rapid Plasma Reagin)
ļƒ¼ TRUST (Toluidine Red
Unheated Serum Test)
ļƒ¼ USR (Unheated Serum
Reagin)
ā€¢ Treponema tests
ļƒ¼ TP-PA (Treponema Pallidum
Particle Agglutination)
ļƒ¼ FTA-abs (Fluorescent
Treponema Antibody -
Absorbed)
ļƒ¼ EIA (Enzyme Immunoassay)
Treponemal Tests
ā€¢ Specific for T. pallidum
ā€¢ Measure antibody (IgM & IgG) directed against T.
pallidum antigens by particulate agglutination (TP-
PA) or immunofluorescence (FTA-abs)
ā€¢ May remain positive after treatment
ā€¢ More sensitive and specific than non-trep. tests
ā€¢ More expensive and labour intensive
ā€¢ Can not quantitateā€¦not useful for following response
to treatment
FTA-ABS
Non-Treponemal Tests
ā€¢ VDRL and RPR are most commonly used.
ā€¢ Detect Abs against cardiolipin-lecithin-cholesterol
antigens; not specific for T. pallidum.
Uses of Non-Treponemal Tests
ā€¢ Screening.
ā€¢ Evaluation of patients with symptoms or possible re-
infection.
ā€¢ Follow-up assessment after treatment.
RPR Test for Syphilis
Non-Treponemal Tests
Advantages
ā€¢ Rapid & inexpensive compared to treponemal tests.
ā€¢ Easy to perform.
ā€¢ Quantitative (can be tittered)
ā€¢ Used to follow response to therapy.
ā€¢ Can evaluate possible reinfection.
Non-Treponemal Tests
Disadvantages
ā€¢ Biological false positive reactions (BFPs).
ā€¢ Viral illnesses including HIV, recent immunizations, IDU,
autoimmune and chronic diseases.
ā€¢ False negative reactions.
ā€¢ Prozone effect.
ā€¢ Early primary and late latent stages.
Sensitivity of Serologic Tests
According to Stage
ā€¢ Test 1 2 Latent Tertiary
ā€¢ VDRL/RPR 74-87% 100% 88-100% 37-94%
ā€¢ FTA-ABS 70-100% 100% 100% 96%
ā€¢ MHA-TP* 69-90% 100% 97-100% 94%
ā€¢ *MHA-TP and TP-PA probably perform equivalently.
Serologic Pitfalls
in the Diagnosis of Syphilis
ā€¢ Negative nontreponemal test may occur early in primary
or late in tertiary - check FTA-ABS or TP-PA.
ā€¢ Prozone phenomenon: false negative due to lack of
agglutination with high antibody levels.
ā€¢ Serofast: persistent, low-level positive titre after adequate
treatment.
Treatment
and
Partner Management
Treatment of Penicillin G
ā€¢ Intravenous or intramuscular injection of penicillin G
is the preferred drug for treatment of all stages of
syphilis
ā€¢ Benzathine penicillin G, aqueous procaine penicillin
or aqueous crystalline penicillin can be used
Syphilis Resistant to
Azithromycin?
ā€¢ In San Francisco, the frequency of azithromycin-resistant T. pallidum
isolates increased from 4% during 2000ā€“2002 to 37% during 2003.
ā€¢ San Francisco STD clinic discontinued use of azithromycin for treating
syphilis infection.
ā€¢ Notified San Francisco medical providers of azithromycin treatment
failures.
ā€¢ Recommendation to use Benzathine penicillin G.
ā€¢ Doxycycline as alternative in PCN-intolerant.
ā€¢ National notification via MMWR.
Syphilis: Treatment
in Pregnancy
ā€¢ Penicillin is the only adequate form of treatment for
syphilis in pregnancy.
ā€¢ Penicillin-allergic patients - Hospitalize, desensitize
& treat with penicillin.
ā€¢ Erythromycin is not accepted as alternative drug in
penicillin-allergic patients.
Management of Contacts
ā€¢ Contacts to primary, secondary or early latent syphilis.
ā€¢ Persons exposed within 90 days preceding the diagnosis
in a sex partner might be infected even if seronegative:
Treat presumptively.
ā€¢ Persons exposed >90 days before the diagnosis should be
treated presumptively if serologic tests are unavailable or
follow up is uncertain; if serologic tests are negative no
treatment is needed.
Chances Reduction
ā€¢ Abstain from sex until treatment is finished and until
partners have been evaluated and treated.
ā€¢ Use condoms consistently and correctly.
ā€¢ Avoid having sex with partners with genital ulcers/lesions
or rashes.
ā€¢ Get check-ups every 6 months if engaging in sex with
more than one sex partner.
NOW TOPIC OPEN FOR DIOSCUSSION

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Syphilis : An Introduction

  • 1. SYPHILIS ā€œTHE GREAT PRETENDERā€ By Dhananjay A. Desai Research Scholar Department of Microbiology N. A. C. & Sc. College, Ahmednagar dhananjayashokdesai@gmail.com
  • 2.
  • 3. Overview ā€¢ History of Syphilis. ā€¢ Transmission pathogenesis and stages of syphilis. ā€¢ Diagnostic tests. ā€¢ Treatment and partner management. ā€¢ Epidemiology.
  • 4. The great pox ā€¢ Epidemic in 15 century Europe. ā€¢ Rapid spread and served symptoms in early stages. ā€¢ Epidemic coincide with Columbus return from america in 1493. ā€¢ Endemic but unrecognized. ā€¢ A gift from new world.
  • 5. Syphilis Discovery of its causes ā€¢ 1903: Infection successfully transmitted to monkeys. ā€¢ 1905: Identification of the bacterium Treponema pallidum. ā€¢ 1906: Dark field microscopy.
  • 6. Taxonomy ā€¢ Domain: Bacteria ā€¢ Phylum: Spirochaetes ā€¢ Order: Spirocheteles ā€¢ Family: Spirochetacae ā€¢ Genus: Treponema ā€¢ Species: pallidum
  • 7. Characteristics ā€¢ Helical, tightly coil, Mobile. ā€¢ 5-10 Āµm in length and 0.1-0.4 Āµm diameter. ā€¢ Pathogenic Treponema associated with ten Diseases. ā€¢ Veneral syphilis- Pallidum ā€¢ Endemic- Endemicum ā€¢ YAWS- Pertenue ā€¢ Pinta- Carateum ā€¢ Obligatory parasite of human.
  • 9. Primary and secondary syphilis ā€” Rates by state: United States and outlying areas, 2007
  • 10. Distribution of Reported STD in World, 2008
  • 11. Method of Infection ā€¢ Viable bacteria from chancre enter through the fissure or mucous membrane. ā€¢ Bacteria multiply locally and causes painless chancre. ā€¢ Spared via blood stream and lymphatic system. ā€¢ Can almost infect many organ and tissue. ā€¢ Continuous in vitro culture yet Not to be achieved.
  • 12.
  • 13. Symptoms (some have no symptoms for years) ā€¢ 3 Stages: ļƒ¼ Primary ļƒ¼ Secondary ļƒ¼ Late or latent ā€¢ Congenital (passed from a mother to her child)
  • 14. Pathogenesis ā€¢ Multiple at the site of inoculation and form chancre. ā€¢ Spread to local lymph nodes and then to blood stream. ā€¢ Can involve of many body organs. ā€¢ Infection and inflammation of blood vessels.
  • 15. Primary Stage ā€¢ Appearance of a single sore or chancre (about 21 day after infection). ā€¢ Chancre lasts 3-6 weeks and heal by treatments. ā€¢ If untreated disease progress to next stage.
  • 16. Secondary stage ā€¢ Occur as chancre is healing or few weeks after. ā€¢ Skin rash developed on one or more areas. ā€¢ appear like other disease (usually doesnā€™t cause itching). ā€¢ Other symptoms: fever, swollen lymph gland, sore throat, patchy hair loss, headaches, weight loss. ā€¢ Without treatment disease progress to next late stage.
  • 17. Late stage (Hidden stage) ā€¢ Person continues to have syphilis even through they are no symptoms. ā€¢ Disease can damage eyes, brain, nervous system, liver, bones, joints. ā€¢ Sign include: difficulty coordinating muscle movement, paralysis, numbness, gradual blindness, even death.
  • 18. Diagnostic Tests ā€¢ Dark field ā€¢ PCR ā€¢ VDRL/RPR ā€¢ EIA
  • 19. T. pallidum on Dark field
  • 20. T. pallidum by DFA-TP
  • 21. Syphilis Serology ā€¢ Non-Treponema tests ļƒ¼ VDRL (Venereal Disease Research Laboratory) ļƒ¼ RPR (Rapid Plasma Reagin) ļƒ¼ TRUST (Toluidine Red Unheated Serum Test) ļƒ¼ USR (Unheated Serum Reagin) ā€¢ Treponema tests ļƒ¼ TP-PA (Treponema Pallidum Particle Agglutination) ļƒ¼ FTA-abs (Fluorescent Treponema Antibody - Absorbed) ļƒ¼ EIA (Enzyme Immunoassay)
  • 22. Treponemal Tests ā€¢ Specific for T. pallidum ā€¢ Measure antibody (IgM & IgG) directed against T. pallidum antigens by particulate agglutination (TP- PA) or immunofluorescence (FTA-abs) ā€¢ May remain positive after treatment ā€¢ More sensitive and specific than non-trep. tests ā€¢ More expensive and labour intensive ā€¢ Can not quantitateā€¦not useful for following response to treatment
  • 24. Non-Treponemal Tests ā€¢ VDRL and RPR are most commonly used. ā€¢ Detect Abs against cardiolipin-lecithin-cholesterol antigens; not specific for T. pallidum.
  • 25. Uses of Non-Treponemal Tests ā€¢ Screening. ā€¢ Evaluation of patients with symptoms or possible re- infection. ā€¢ Follow-up assessment after treatment.
  • 26. RPR Test for Syphilis
  • 27. Non-Treponemal Tests Advantages ā€¢ Rapid & inexpensive compared to treponemal tests. ā€¢ Easy to perform. ā€¢ Quantitative (can be tittered) ā€¢ Used to follow response to therapy. ā€¢ Can evaluate possible reinfection.
  • 28. Non-Treponemal Tests Disadvantages ā€¢ Biological false positive reactions (BFPs). ā€¢ Viral illnesses including HIV, recent immunizations, IDU, autoimmune and chronic diseases. ā€¢ False negative reactions. ā€¢ Prozone effect. ā€¢ Early primary and late latent stages.
  • 29. Sensitivity of Serologic Tests According to Stage ā€¢ Test 1 2 Latent Tertiary ā€¢ VDRL/RPR 74-87% 100% 88-100% 37-94% ā€¢ FTA-ABS 70-100% 100% 100% 96% ā€¢ MHA-TP* 69-90% 100% 97-100% 94% ā€¢ *MHA-TP and TP-PA probably perform equivalently.
  • 30. Serologic Pitfalls in the Diagnosis of Syphilis ā€¢ Negative nontreponemal test may occur early in primary or late in tertiary - check FTA-ABS or TP-PA. ā€¢ Prozone phenomenon: false negative due to lack of agglutination with high antibody levels. ā€¢ Serofast: persistent, low-level positive titre after adequate treatment.
  • 32. Treatment of Penicillin G ā€¢ Intravenous or intramuscular injection of penicillin G is the preferred drug for treatment of all stages of syphilis ā€¢ Benzathine penicillin G, aqueous procaine penicillin or aqueous crystalline penicillin can be used
  • 33. Syphilis Resistant to Azithromycin? ā€¢ In San Francisco, the frequency of azithromycin-resistant T. pallidum isolates increased from 4% during 2000ā€“2002 to 37% during 2003. ā€¢ San Francisco STD clinic discontinued use of azithromycin for treating syphilis infection. ā€¢ Notified San Francisco medical providers of azithromycin treatment failures. ā€¢ Recommendation to use Benzathine penicillin G. ā€¢ Doxycycline as alternative in PCN-intolerant. ā€¢ National notification via MMWR.
  • 34. Syphilis: Treatment in Pregnancy ā€¢ Penicillin is the only adequate form of treatment for syphilis in pregnancy. ā€¢ Penicillin-allergic patients - Hospitalize, desensitize & treat with penicillin. ā€¢ Erythromycin is not accepted as alternative drug in penicillin-allergic patients.
  • 35. Management of Contacts ā€¢ Contacts to primary, secondary or early latent syphilis. ā€¢ Persons exposed within 90 days preceding the diagnosis in a sex partner might be infected even if seronegative: Treat presumptively. ā€¢ Persons exposed >90 days before the diagnosis should be treated presumptively if serologic tests are unavailable or follow up is uncertain; if serologic tests are negative no treatment is needed.
  • 36. Chances Reduction ā€¢ Abstain from sex until treatment is finished and until partners have been evaluated and treated. ā€¢ Use condoms consistently and correctly. ā€¢ Avoid having sex with partners with genital ulcers/lesions or rashes. ā€¢ Get check-ups every 6 months if engaging in sex with more than one sex partner.
  • 37.
  • 38. NOW TOPIC OPEN FOR DIOSCUSSION