Congenital Flashcards

1
Q

Late sequelae- match

Hearing loss, minimal to severe brain dysfunction ( motor, learning, language, behavioural disorders)

Hearing, brain dysfunction, autism, diabetes, thyroid, precocious puberty, brain degeneration

Chorioretinitis, brain dysfunction, hearing loss, precocious puberty

Recurrent eye and skin infection, brain dysfunction

Subclinical hepatitis, fulminant hepatitis

A

CMV

Rubella

Toxoplasmosis

HSV

Hep B

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Most common symptoms in symptommatic CMV

A
SNHL (58%)
IQ<70 (55%)
Microcephaly (38%)
Seizures 
Chorioretinitis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Which congenital infection

CHD (PDA>PAS>AS>VSD)
Cataract, corneal opacities, glaucoma 
Microphthalmia 
Radiolucent brain lesions 
Thrombocytopenia 
HSM
Hepatitis
A

Rubella

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Rate of congenital HSV in primary maternal disease

Recurrent disease

A

30-50%

3-5%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What proportion of neonatal HSV cases will have visible skin lesions?

A

1/3rd

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What features would make one suspect HSV in unwell neonate?

A
Hx of 3rd trimester lesions 
Skin lesions suspicious
Seizures 
Abnormal LFTS 
Pleocytosis (lymphocytes)
Ill, irritability, hypothermia, lethargy, vomiting
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

6 weeks or 6 months of ganciclovir for congenital CMV ( symptomatic)

A

6 months improves hearing and neuro developmental outcome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Perinatal transmission

Hep B

Hep C

A

90%

5%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Congenital syphilis

Early manifestations in order of most common

A
Hepatomegaly (32%)
Skeletal abnormalities (29%)
Splenomegaly (18%)
LBW (16%)
Pneumonia 
Anaemia, hydrops
Skin lesions 
Hyperbilirubinemia
Snuffles, nasal discharge (9%)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Congenital syphilis

Late manifestations >2y

A

Orthopedic and teeth

Peg shaped teeth
Lytic bone lesions
Pseudo paralysis
Saddle nose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Toxoplasmosis transmission

1st

2nd

3rd
Trimester

A

25

50

65% in3rd trimester

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Congenital toxoplasmosis

Proportion symptomatic

Features

Risks if asymptommatic

A

10-30%

Chorioretinitis 
Microcephaly 
Seizures 
HSM
Intracranial calcification 

Chorioretinitis, hearing loss, developmental delay

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Treatment for toxoplasmosis

  • maternal infection only
  • maternal + fetal infection (amnio PCR positive)
  • infant
A

Spiramycin 3g/day
Doesn’t cross Placenta

Pyrimethamine plus Sulphadiazine
- supplement with folinic acid, monitor FBC

The same until 12 months of age

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Neonatal herpes simplex

3 main presentations
Treatment

Outcomes

What extra blood test is useful when working up the septic neonatal

A

CNS
Disseminated
Skin-eyes-mouth
IV acyclovir ? 6 months

30% mortality (disseminated)
70% neurological morbidity for CNS disease

LFTs: transaminitis rare in neonatal bacterial sepsis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Group B Streptococcus

% women colonised
Transmission occurs __
RFs (6)

Early onset presentations

Late onset presentations

A

40%
During labour
Preterm, PROM, maternal colonisation, fever, young age, ethnicity

Early- sepsis, pneumonia, meningitis (10%)

Late (>7 days) occult bacteraemia, meningitis (30%), bone and joint

Very late (>90) - prematurity and prolonged hospitalisation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Current rates of GBS sepsis

Early

Late

A
  1. 4 per 1,000

0. 27 per 1,000 (late)

17
Q

Syphilis

Transmission
Test which babies
What test

A

Anytime in pregnancy, any stage of disease

Mother untreated
Dx in last month of pregnancy
Inadequate fall in maternal non-treponemal antibody titre

TPPA- specific
RPR+ VDRL non specific

18
Q

Parvovirus

% women susceptible
Risk of transmission
First trimester- effect
Highest risk of hydrops when

A

40%
50% risk of transmission

First trimester- 10% excess fetal loss

Highest risk of hydrops between 9-20weeks

19
Q

Zika

Embryopathy

A

Microcephaly
Retinopathy
Intracranial calcification
Deafness

No HSM, CHD

20
Q

Parvovirus

Embryopathy
Risky time

A

1st trimester miscarriage (excess 10%)

Hydrops 9-20weeks

No prevention
Intrauterine transfusion