Congenital Syphillis Flashcards

1
Q

What population/demographic accounts for most cases of syphilis in Canada?
What 2 provinces have highest incidence?

A

Heterosexual transmission in inner city populations
(previously men who have sex with men)

Highest incidence in BC & Alberta

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2
Q

Most recent incidence of congenital syph in Canada?

A

10 cases per year

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3
Q

How is syphilis usually transmitted? What are rarer mechanisms of transmission?

A

Usually - sex with person infected with syphilis within the past year

Rarely - blood transfusion, oral secretions, needle sharing, direct contact with infected lesion

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4
Q

Why are all pregnant women assumed to be at risk?

A

Many infected pts are asymptomatic

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5
Q

What is the risk of vertical transmission if:

(1) Untreated primary or secondary syph during pregnancy
(2) Early latent syph
(3) Late latent syph

A

(1) Untreated primary/secondary - 70-100%
(2) Early latent - 40% (at risk for reactivation)
(3) Late latent - 10%

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6
Q

When are fetuses infected with syphilis?

A

In utero, after 4 months gestation

but can occur as early as 9 weeks OR with during birth with active lesion

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7
Q

When should syphilis serology be done on pregnant patients?

When should rescreening be done and what population?

A
  • Syph serology at first prenatal visit

- Rescreen at 28-32 weeks + at delivery for high risk women (i.e. high incidence of syph in country of origin)

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8
Q

What if maternal serologies not done before delivery?

A

Do not discharge newborn until maternal serologies drawn and f/u arranged

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9
Q

What are the different types of syphilis serology tests for screening vs confirmation?

A

Nontreponemal tests for screening:

  • RPR (rapid plasma reagin)
  • VDRL (venereal disease research lab)

Treponemal test for screening:
- EIA (enzyme immunoassay)

Treponemal test for confirmation:

  • florescent treponemal antibody absorption (FTA-ABS)
  • T pallidum particle agglutination (TP-PA)
  • Line blot immunoassay (INNO-LIA)
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10
Q

If RPR negative, TP-PA negative, FTA positive – what is the most likely condition?

A

Primary syphilis

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11
Q

If RPR positive, TP-PA positive, FTA-ABS positive – what is the most likely condition?

A

Any of:

  • Any stage of syphilis
  • Old treated syphilis/being treated
  • Pt from endemic country
  • Lyme disease/yaws/pinta

**If both confirmatory tests+ and RPR+, CAN be active syphilis (along with other possibilities). RPR- means not most active syphilis.

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12
Q

If RPR negative but TP-PA/FTA positive – what is the most likely condition?

A

Any of:

  • Old treated syphilis
  • Early infection (early primary)
  • Late latent/tertiary syphilis
  • Persons from endemic countries
  • Lyme disease/yaws/pinta
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13
Q

If RPR positive, TP-PA/FTA negative – what is the most likely condition?

A

False positive

Some reasons for this:

  • collagen vascular diseases
  • pregnancy
  • IVDU
  • Lyme disease
  • Test technique
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14
Q

If RPR negative (and conf tests not performed) – what is the most likely condition?

A

Not syphilis!

Repeat serology if at risk

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15
Q

EIA indeterminate
RPR negative
Confirmation test neg/indeterminate

What is the most likely condition?

A

May be in early serovonversion
Needs repeat serology
(if repeat same, not syphilis!)

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16
Q

EIA indeterminate
RPR negative
Confirmation test positive

What is the most likely condition?

A

Any of:

  • Early primary
  • Late latent
  • Previously treated
  • Endemic country
  • Lyme disease
17
Q

EIA positive
(RPR positive OR negative)
Confirmation test negative

A

False positive

18
Q

EIA positive + RPR positive

Confirmation test indeterminate

A

Repeat serology
(if conf test + – any stage of syphilis or treated syphilis or endemic person)
(if unchanged - false positive)

19
Q

EIA positive
RPR negative
Confirmation test indeterminate

A

Repeat serology
(if conf test + – any stage of syphilis or treated syphilis or endemic person)
(if unchanged - false positive)

20
Q

EIA positive
RPR negative
Conf test positive

A

Early primary, late latent, or previously treated; endemic person, Lyme disease
- just not the most active syph*

21
Q

EIA positive
RPR positive
Conf test positive

A

Any stage of syphilis
(more likely to be infectious if RPR titre 32 dilutions+)

  • Includes old treated syphilis, being treated
  • Endemic persons
  • Lyme/yaws/pinta/bejel
22
Q

What is the usual screening approach for syphilis in Canada?

A

RPR initial screen
Treponemal test to confirm

  • Others use EIA as initial screen (more sens and spec than RPR)
  • Still need to obtain RPR titres if EIA positive – RPR used for staging of infection
23
Q

How long with treponemal tests remain reactive for after treatment?

A

Usually for life, unless tx started v early in course of infection

24
Q

How do you monitor for adequacy of maternal syphilis tx?

A

Decline in RPR titres!

25
Q

What is the expected RPR titre decline in tx of maternal syphilis (primary) at:

  • 6 months
  • 12 months
  • 24 months
A

6 months - 4-fold drop
12 months - 8-fold drop
24 months - 16-fold drop

26
Q

What is the expected RPR titre decline with tx of maternal syphilis (secondary) at:

  • 6 months
  • 12 months
A

6 months - 8 fold drop

12 months - 16 fold drop

27
Q

What is the expected RPR titre decline with tx of maternal syphilis (early latent) at:
- 6 months

A

6 months - 4 fold drop

28
Q

If RPR serofasts (reverts to nonreactive) after tx, what next?

A

Still need to repeat RPR at regular intervals is reinfection thought to be a risk

29
Q

If treponemal test reactive (and RPR nonreactive) during pregnancy – no history of treatment and no evidence of early primary syphilis… what should be done?

A

Treat as late latent syphilis

Assume there is some risk of vertical transmission

30
Q

How do you manage a neonate with maternal treponemal test+ but inadequately treated?

What is the definition of early congenital syphilis?

A

Infant at risk for congenital syphilis!

Early congenital syphilis = diagnosis within first 2 years of life

31
Q

What are the H+N manifestations of congenital syphilis?

A

Rhinitis - in 40% of cases; often first manifestation at birth

Hutchison’s teeth - upper central and lateral incisors widely spaced, look like screwdrivers

Mulberry molars - first molars have dwarfing of cusps; hypertrophy of enamel around cusp (looks like a berry)

32
Q

Neurologic and MSK manifestations of congenital syphilis?

A

Neurosyphilis - present at birth or delayed; in 50% of cases (but usually asymptomatic)

CN8 impairment - onset 10-40 years, SNHL

Osteochondritis or perichondritis

  • 25% seen initially on XR within 2 weeks
  • pseudoparalysis can occur
  • later changes: frontal bossing, poorly developed maxilla, saddle nose, winged scapula, sabre shins

Recurrent arthropathy/painless knee effusions (Clutton’s joints)
- occurs after 2 yo

33
Q

Abdominal and skin manifestations of congenital syphilis?

A

HSM - onset in first 8 weeks; occurs in 20% of cases; may persist for many years

Rash - onset in first 8 weeks; 50% of cases; diffuse MP rash typically
(can also have just desquamation or vesicles or bullae or mucosal lesions)

Necrotizing funisitis - present at birth; umb cord looks like barbershop pole (rare by pathognomonic!)

34
Q

% of congenital syph cases presenting as SA/stillbirth/hydrops fetalis?

A

40% if syphilis acquired during pregnancy – highest risk if first trimester infection