syhpilis Flashcards

1
Q

rubella IgM positive

A

distinguish between primary infection & reinfection with rubella vaccine virus by IgG avidity assay in pregnant women

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2
Q

avidity

A

strength in which a multivalent Ab binds a multivalent Ag

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3
Q

ulcerative infections

A

-syphilis does not hurt
-herpes does hurt
-both genital ulcers

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4
Q

frequency of genital ulcer infections

A

HSV > syphilis > chancroid
-chancroid is rare

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5
Q

herpesviruses

A

large, enveloped DNA viruses

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6
Q

HSV

A

-common cold sores
-can be neonatal or congenital
-risk of transmission is with primary maternal infection at the time of delivery
-risk smaller with recurrent herpes at time of delivery

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7
Q

VZV

A

chickenpox & shingles

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8
Q

HHV-6

A

-primary target of infection is T cells

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9
Q

prevention of neonatal herpes

A

-recognition
-elective section in primary herpes at term of <4 hours after membrane rupture
-elective selection when recurrent genital herpes is present at term

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10
Q

syphilis infection

A

-treponema pallidum (spirochete)
-sexually transmitted
-placental transmission >6 weeks gestation (mostly second half of pregnancy). mom with primary or secondary syphilis more likely to transmit

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11
Q

syphilis neonatal clinical manifestations

A

fetal: still birth, neonatal death, hydrops fetalis
-intrauterine death 25%
-perinatal mortality in 25-30% if untreated

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12
Q

early congenital syphilis manifestation

A

-1st 5 weeks
-cutaneous lesions (palms/soles)
-HSM
-jaundice
-anemia
-snuffles
-periostitis & metaphysical dystrophy (bone abnormality)
-funisitis

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13
Q

late congenital syphilis manifestations

A

-frontal bossing
-short maxilla
-high palatal arch
-hutchinson teeth (sharp)
-8th nerve deafness
-saddle nose
-perioral fissures

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14
Q

RPR/VDRL

A

nontreponemal test
-sensitive but not specific
-quantitative, can follow up to monitor treatment treatment
-all pregnant women get screened early & at term

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15
Q

MHA-TP/FTA-ABS

A

specific treponemal
-confirmatory testing
-qualitative, once positive always positive

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16
Q

CDC definition of congenital syphilis

A

confirmed if T. pallidum identified in skin lesions, placenta, umbilical cord or at autopsy

17
Q

latent syphilis

A

-seroreactivity without other evidence of primary, secondary or tertiary disease

18
Q

manifestation of primary syphilis

A

chancre:
-painless, but tender
-indurated
-highly contagious
-rapid dissemination
congenital

19
Q

manifestation of secondary syphilis

A

-diffuse maculopapular rash: non pruritic, lesions on palms & soles
-mucous membrane lesions/patches
-fever
-jaundice
-scleral icterus

20
Q

stages of syphilis

A

-primary: painless sores (chancre) at inoculation site
-secondary: rash, fever, lymphadenopathy, malaise
-tertiary/latent: CNS invasion, organ damage

21
Q

syphilis microbiology

A

-labile spiral bacterium with axial filaments
-non-cultivable: rely on dark field microscopy for diagnosis
-gram neg

22
Q

RIT

A

rabbit infectivity test:
-high sensitivity & specificity
-long TAT
-limited to research setting

23
Q

dark field microscopy

A

-primary infection
-expertise required

24
Q

immunostaining

A

direct fluorescent Ab or silver stain

25
Q

PCR

A

research only

26
Q

non-treponemal assays (RPR/VDRL)

A

-t. pallidum infections leads to production of reagin
- reagin react with cardiolipin

27
Q

reagin

A

Abs to substances released from cells damaged by T. pallidum

28
Q

cardiolipin

A

phospholipid component of certain eukaryotic & prokaryotic membranes

29
Q

non-treponemal advantages

A

-rapid TAT
-inexpensive
-no specialized instrumentation needed
-usually revert to negative following therapy
-monitor response to therapy
-successful treatment: 4 fold decrease in RPR titer

30
Q

non-treponemal limitations

A

-results are subjective
-non-specific (false pos)
-limited sensitivity in early/late infection
-low throughput
-prozone effect: high levels of Ab inhibit agglutination, dilute sample

31
Q

treponemal assays

A

-infection leads to production of specific Abs directed against t. pallidum
-detect IgG (or total IgM/IgG) Abs against T. pallidum
-multiplex flow immunoassay

32
Q

serologic treponemal assays for syphilis

A

-MHA
-FTA-ABS
-TP-PA
-EIA
-MFI

33
Q

treponemal limitations

A

-remain positive despite treatment (not used to monitor therapy)
-conventional methods (subjective interpretation)
-newer methods (expensive)

34
Q

traditional syphilis algorithm

A
  1. RPR
    NR = neg for syphilis
    R = treponemal test (FTA)
  2. FTA
    R = syphilis
    NR = no syphilis
35
Q

traditional algorithm advantages

A

-good correlation with disease state
-rapid & cheap
-approved by CDC
-good for small labs
-refluxed confirmation test leads to clear results

36
Q

traditional algorithm disadvantages

A

-manual & subjective
-non-specific & leads to false +
-not good for high volume labs
-lower sensitivity in early/late syphilis

37
Q

reverse syphilis algorithm

A
  1. treponemal (EIA)
    R = step 2
    NR = no syphilis
  2. RPR
    R = syphilis
    NR = step 3
  3. second treponemal (TP-PA)
    R = probable syphilis
    NR = no syphilis
38
Q

reverse algorithm advantages

A

-automated treponemal assays
-objective interpretation
-results from EIA or MFI can be interfaced with LIS
-specific screening for T. pallidum Abs
-increased detection of early syphilis

39
Q

reverse algorithm disadvantages

A

-high cost
-higher assay complexity
-increased detection of patients with + screen, RPR -