CMV Flashcards

1
Q

High risk groups for cmv

A

Daycare workers
Parents w kids in daycare
Health care workers

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2
Q

CMV negative

A

Igg and igm negative

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3
Q

Igg+

Igm -

A

Past cmv

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4
Q

Igg -

Igm+

A

Possible infection -test avidity igg
Low avidity recent primary infection
High avidity past infection

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5
Q

Fetal dx through amino

A

Needs to be after 21/40
80-100% specific, high specificity
Done 6/52 after primary infection (but >21/40)

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6
Q

Uss features of cmv

A
Microcephalic
Ascites 
Oli or poly
Abdo calc
Hydrocephalus 
Intracranial calc
Hydrops 
Pseudomeconium ileus 
Iugr
Pleural or pericardial effusions
Hepatomegaly
Hyperechogenic bowel
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7
Q

Tx

A

Top
Antenatal cmv immunoglobulin (IVIG)
Valcyclovir 500mg BD form 34/40

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8
Q

Neonatal

A
CMV PCR of saliva or urine within first 3 weeks of life - distinguish congenital from neonatal
Opthal
Hearing screen
Uss or mri head
Neurodevelopmental assessment

Ok to BF

Need to be followed up 3-6 monthly for 2 years

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9
Q

Advice to pregnant women

A

Assume all kids under 3 have cmv in saliva and urine
Throughly wash hands
Do not share food
Do not kiss kid on the mouth
Don’t sleep in the same bed
Do not put dummy/soother in mouth
Clean toys, countertops and other surfaces that come into contact with children’s urine or saliva

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10
Q

Clinical feature of symptomatic CMV neonate

A
Stillbirth, neonatal death
Neurological abnormality (hearing loss, developmental delay, microcephalic,, seizures, chorioretinitis
Thrombocytopenia
Hepatosplenomegaly
Petechiae, outputs
IUGR
Myocarditis
Pneumonitis
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11
Q

Risk of infection and damage with primary CMV

A

30-35% chance of fetal infection
30-35% chance of fetus being affected
(10-15% chance of fetus being damaged (90% asymptomatic)

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12
Q

Tx of neonate

A

CMV nuclei acid test from urine (PCR)
Hancock our or valganciclovir for babies with moderate to severe disease
No tx if asymptomatic

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13
Q

What’s in a TORCH screen

A

Toxo
Rubella
CMV
Herpes

Request also syphilis,, Zika and Parvo

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14
Q

CMV make up

A

Herpetoviridae family
DNA virus
Several strains
Serologic testing can’t differentiate strain

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15
Q

Incidence

A

1% all live births
3.85/100000
Most frequent cause mental retardation and sensory neural hearing loss

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16
Q

Pathogenesis

A

Replication t-helper cells
Endothiolel cells and PML are main cells infected, followed by haematogenous spread
Placenta and amnion infection causes vascular remodeling and change in protein expression- villous hypoplasia

Indirect or direct contact

17
Q

Investigations with active infection

A

USS- CNS signs, hydrops, echogenic bowel IUGR
MRI - microcephalic with abnormal gyral patterns (28 if first trimester infection and 34 weeks if late infection)
Amniocentesis- after 8 weeks of suspected infection and >21 weeks gestation (otherwise high false negative rate)

18
Q

Treatment of woman

A

If immunocompromised :

An I lovin, valganciclovir, valaciclovir

19
Q

Cytomegalic inclusion disease

A
CNS abnormalities
Choroidretinitis
Sensorineural deafness
Hepatosleponmegaly
Pneumonitis
Myocarditis
Haemolytic anaemia
Reduced intelligence
20
Q

Neonatal manifestations

A

CP
Sensorineural hearing loss
Visual impairment
Delayed psychomotor development