ID Flashcards

1
Q

C diff diagnosis

A

Enzyme immunoassay for glutamate dehydrogenase, toxins A and B
(EIA less sensitive)
And
Cell cytotoxin assay (labour intensive and expensive)

So EIA for GDH for screen then toxin EIA or cell cytotoxin assay

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2
Q

Treatment c diff (mild)

A

Watery diarrhea without systemic toxicity (<4 abn stool/d) = d/c precipitating antibiotic, follow up and reassess

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3
Q

C diff treatment initial episode moderate (or mild not responding to d/c abx)

A

Moderate (>4 abnormal stools/d) without systemic toxicity = flagyl 30 mg/kg/d divided 4 doses for 10-14 days

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4
Q

C diff treatment initial episode severe

A

Severe (evidence of systemic toxicity - rigours, high grade fever) = vanco 40mg/kg/d PO for 10-14 days

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5
Q

C diff treatment initial episode severe, complicated

A

Complicated (evidence of severe colitis, hypotension, shock, peritonitis, ileus, or megacolon) = vanco PO plus iv flagyl (same doses as above, 10-14 days. For ileus can give vanco PR.

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6
Q

C diff treatment for recurrence

A

First: Same treatment as first episode
Second: vancomycin in a tapered or pulsed regimen (40/kg/d divided 4 times daily for 10-14 days then 10 mg/kg twice daily for 7 days, the 10/kg once daily for 7 days, then every 2-3 days for 2-8 weeks)

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7
Q

C diff prevention

A

Hand hygiene
Identify and remove environmental sources of c diff
Chlorine containing sporicidal agents (alcohol doesn’t kill)
Contact precautions until 48 hours no diarrhea
Private rooms or cohorting and don’t retest stool, go based off of symptoms
Anti microbial stewardship

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8
Q

Toxoplasmosis classic triad + other symptoms and timing of infection

A
1st - most severe, fetal demise
2nd trimester - classic:
- intracranial calcifications
- hydrocephalus
- chorioretinitis 
\+ jaundice, HSM, anemia, hearing loss, microcephaly, developmental delay, LAD, visual problems  
3rd trimester: asyptomatic
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9
Q

Congenital toxo diagnosis

A

organism isolation from the placenta, serum, and cerebrospinal fluid (CSF)
ophthalmologic examination - chorioretinitis, CT head looking for calcifications, and
CSF - elevated protein and pleocytosis

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10
Q

congenital toxo treatment

A

pyrimethamine, sulfadiazine, and leucovorin for 1 year

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11
Q

Syphilis bug

A

gram-negative spirochete Treponema pallidum

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12
Q

Congenital Syphilis most common presentation:

A

majority of infants born with congenital syphilis are asymptomatic at birth

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13
Q

Congenital syphilis - early

A

1-2 months:
maculopapular rash, snuffles, generalized lymphadenopathy, hepatomegaly, thrombocytopenia, anemia, meningitis, chorioretinitis, pneumonia alba, and osteochondritis.

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14
Q

Congenital syphilis - late

A

Hutchinson/peg teeth (small teeth with an abnormal central groove), mulberry molars (bulbous protrusions on the molar teeth resembling mulberries), hard palate perforation, eighth nerve deafness, interstitial keratitis, bony lesions, and saber shins (due to chronic periosteitis)

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15
Q

Syphilis nontreponemal tests (2)

A

venereal disease research laboratory test and rapid plasma reagin are used for screening and monitoring treatment of the disease

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16
Q

Syphilis treponemal tests

A

fluorescent treponemal antibody absorption test or T pallidum particle agglutination are used to confirm diagnosis. Treponemal tests are not used alone due to false positives that may occur with other infections such as Lyme disease

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17
Q

Syphilis testing in newborn

A

same nontreponemal test as the mother if the mother has a nontreponemal titer that increased fourfold; had a positive treponemal test without documented treatment; had a positive treponemal test not treated with penicillin; had a positive treponemal test and was treated less than 1 month before delivery; or if the infant has signs of congenital syphilis.

If the infant’s nontreponemal titer is more than fourfold higher than the mother’s or if there is any clinical finding consistent with congenital syphilis, the infant must be treated and undergo a venereal disease research laboratory test of CSF, liver function tests, complete blood count, and long bone radiographs.

18
Q

Syphilis treatment

A

Pen G

19
Q

Mom HBsAg + treatment and tests

A

–> HBV vaccine and hepatitis B immune globulin within 12 hours of birth!
These infants should then complete the HBV vaccine series with two more additional immunizations per the CDC’s recommended schedule, as well as undergo HBsAg and anti-HBs testing after 9 months of age.

20
Q

Mom Hep B status unknown at delivery

A

Test mom immediately

Baby gets Hep B vaccine within 12 hours and if mom is positive Hep B IG within 7 days

21
Q

Maternal VZV

A

Treat baby with VZV IG if mom develops varicella 5 days before or 2 days after delivery

22
Q

Maternal HIV - who gets a c/s

A

viral load > 1000 copies/mL

23
Q

Baby to HIV + mom - when to test

A

HIV-1 DNA or RNA PCR should be analyzed at: 14 to 21 days after birth, 1 to 2 months of age, and 4 to 6 months of age

24
Q

HIV + mom - when is baby considered uninfected?

A

1) two negative HIV-1 DNA or RNA assays, one obtained after 1 month of age and the other at 4 months of age or older, or
2) two negative HIV-1 antibody tests from separate specimens obtained at 6 months of age or older.
Some practitioners may follow antibodies until after 18 months of age because maternally derived antibodies rarely persist beyond this age

25
Q

HIV + mom - treatment for baby

A

6 weeks of zidovudine. If confirmed infection then continue long term ARV

26
Q

Parvo virus B19 baby risk

A

hydrops, pleural/pericardial effusion, IUGR, death

infection during 1st half of preg has greatest risk

27
Q

Parvo virus B19 baby treatment

A

supportive care

IVIG may be helpful

28
Q

Congenital rubella (german measles)

A

blueberry muffin rash (extramedullary hematopeoisis), radiolucent bone disease, IUGR, interstistial pneumonitis, LAD, HSM, thrombocytopenia, cataract
endocrinopathies - DM

29
Q

Congenital rubella eye findings

A

cataract! also glaucoma, microphthalmos, pigmentary retinopathy

30
Q

Congenital rubella cardiac findings

A

Pulmonic stenosis, PDA

31
Q

Congenital rubella CNS s/e

A

developmental delay, encephalitis, SNHL

32
Q

Congenital rubella diagnosis

A

infant rubella IgM
rising rubella IgG
virus isolated from CSF, serum, oral/nasal secretions

33
Q

Most common congenital infection

A

CMV (0.5-1%)

34
Q

CMV presentation

A

most are asymptomatic!

SNHL, HSM, jaundice, thrombocytopenia, periventricular calcifications, retinitis, IUGR, microcephaly

35
Q

Congenital CMV diagnosis

A

CMV in urine or pharyngeal secretions in first 3 weeks - culture or PCR
Antibodies not helpful (IgG doesn’t tell you when mom got it, IgM not sens/specific)

36
Q

Cong CMV treatment

A

Ganciclovir to improve SNHL and neurodevelopment

37
Q

Maternal HSV highest risk

A

primary infection late in preg (3rd trimester)

38
Q

Congenital HSV age of presentation

A

birth-6 weeks

39
Q

How often is there a maternal Hx of HSV in infants with congenital HSV?

A

12.5%

40
Q

HSV classification (3)

A
  • primary skin, eyes, mucosa
  • primarily CNS
  • disseminated with multiple organ involvement
41
Q

Best test for HSV CNS

A

PCR (sensitivity 75-100%)

42
Q

Best test for HSV skin lesions

A

viral culture of skin lesion