CMV Flashcards

1
Q

Possible indications for antenatal testing

A
  1. History suggestive of CMV illness (90% are asymptomatic)
  2. Abnormalities on routine antenatal US
  3. Exposure to known CMV infected individual
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2
Q

Congenital CMV Incidence

A

3.85/10 000 live births
Leading cause of congenital infections

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3
Q

Cases of cCMV that occur in non-primary maternal infection

A

75%
In-utero transmission in non-primary infection is less likely but if infected the full range of features of cCMV is possible

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4
Q

Recommendations to women to reduce CMV infection

A
  1. Do not share food / utensils etc with children <3yrs
  2. Do not put child’s dummy in mouth
  3. Avoid kiss on lips / with saliva
  4. Hand hygiene esp with children
  5. Clean surfaces that come in contact with children
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5
Q

Major risk factors for maternal CMV

A

Frequent prolonged contact with young children
1. Day care workers
2. Parents with child in day care

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6
Q

Sensitivity and Specificity of Ultrasound in Detecting Fetal CMV

A

Sens <30-50%, Spec low

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7
Q

Features of cCMV on ultrasound

A
  1. Head: Microcephaly, Cerebral ventriculomegaly, intracranial calcification
  2. Abdomen: Ascites, Hepatomegaly, abdominal calcification, pseudomeconium ileus, hyperechoic bowel
  3. Chest: pleural or pericardial effusions
  4. General: oligo / polyhydramnios, IUGR, hydrops fetalis
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8
Q

Amniocentesis for CMV PCR <20 weeks

A

Sensitivity 45%, Specificity High

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9
Q

Amniocentesis for CMV PCR ≥21 weeks and ≥ 6 weeks after maternal infection

A

Sensitivity 80-95%
Specificity approaches 100%
PPV approaches 100%

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10
Q

Prevential of Fetal CMV Transmission

A
  1. CMV Hyperimmuneglobulin (HIG) no currently routinely recommended, consider case-by-case
  2. Data of valaciclovir emerging for use in first trimester
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11
Q

Intervention for CMV infected fetus

A
  1. Seek expert advice
  2. TOP is an option (however positive PCR is not predictive of fetal damage)
  3. CMV IgG can be considered (observational studies)
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12
Q

Risk of fetal transmission, fetal symptoms, fetal sequelae with primary CMV

A

~30%
- symptomatic cCMV 10-15%
—–> sequelae ~50%
- asymptomatic cCMV 85-90%
—–> sequelae 10-15%

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13
Q

Risk of fetal transmission, feteal symptoms, fetal sequelae with non-primary CMV (reinfection or reactivation)`

A

~1%
- symptomatic cCMV ≤1%
- asymptomatic cCMV ≥99%

—–> both have risk of sequelae ≤10%

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14
Q

Overall risk of long-term sequelae in a congenitally infected child (CMV)

A

~10-20%

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15
Q

Fetal transmission of CMV according to trimester

A
  1. Periconception (3 months before LMP) = 5.5%
  2. Periconception (4 weeks before, 6 weeks after LMP) = 21%
  3. First trimester = 36.5%
  4. Second trimester = 40.3%
  5. Third trimester = 66%
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16
Q

When is risk of severe adverse neurological outcomes greatest? (cCMV)

A

Primary infection in first trimester
(A fetus infected late in pregnancy is unlikely to have significant neurological sequelae

17
Q

Main concerns of symptomatic cCMV infection

A
  1. Early mortality 5-10%
  2. Neuro: microcephalic (35-50%), seizures (10%), chorioretinitis (10-20%), developmental delay (70%)
  3. Sensorineural hearing loss (25-50%) - can be late onset
18
Q

Main concerns of asymptomatic cCMV infection

A
  1. Senorineural hearing loss (~10%, can be late onset up to 2 years)
  2. Neurodevelopmental (maybe)
  3. Chorioretinitis 2%
19
Q

Period of paediatric follow-up for cCMV

A

6 years
- Audiology 6 mthly for 2 years then yearly
- Opthal yearly
- Paeds 3-6 mthly for 2 years than yearly
Normal development by 12 months is associated with higher likelihood of normal development long-term

20
Q

Neonatal examination at birth

A

≤21 days of age
- CMV PCR urine and saliva
- Newborn hearing screen
If PCR positive, ophthal review and head imaging
+/- antiviral therapy