MI: Viral Infections in Pregnancy Pt.1 Flashcards

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1
Q

What are the three times at which viral infections can be transmitted from the mother to the baby?

A
  • In utero
  • Perinatally (from vaginal secretions and blood during labour)
  • Postnatally (from breast milk and other sources)
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2
Q

What are the potential viral causes of rashes during pregnancy?

A
  • VZV (chicken pox and shingles)
  • EBV
  • HSV
  • CMV
  • Parvovirus B19
  • Enterovirus
  • Measles
  • Rubella
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3
Q

What type of virus is rubella?

A
  • RNA virus
  • Togaviridae family
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4
Q

How is rubella transmitted?

A
  • Via respiratory droplets (therefore ISOLATE in suspected cases)
  • Virus replicates in lymphoid tissue of URT then spreads haematogenously
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5
Q

What are the symptoms of rubella infection?

A

20-50% subclinical

  • Prodrome (1-5 days pre rash) - coryza, sore throat, headache, low-grade fever
  • Fine macular rash - mildy pruritic, starts on face and spreads to trunk/limbs within hours
  • Lymphadenopathy - tender, postauricular/cervical/suboccipital
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6
Q

What is the classic triad of congenital rubella syndrome?

A
  • Sensorineural hearing loss
  • Congenital cardiac defects (mainly PDA)
  • Eyes - cataracts, retinopathy, microphthalmia
  • Other: mental retardation, meningoencephalitis, microcephaly, hepatosplenomegaly, thrombocytopaenic purpura
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7
Q

Describe the relationship between gestation at which rubella infection occurs and the risk of congenital abnormalities.

A
  • Highest risk from 0-12 weeks
  • Low risk from 13-20 weeks
  • Very low risk >20 weeks

If infected before 10 weeks, 90% incidence of foetal defects

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8
Q

Describe some tests that are used in the diagnosis of rubella.

A
  • Serology - IgG, IgM
  • Detection of virus (PCR) - blood, urine, tissues
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9
Q

What is the role of pre-natal diagnosis of rubella?

A

All cases of symptomatic rubella infection in the 1st trimester should be considered for termination of pregnancy without prenatal diagnosis

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10
Q

What type of vaccine is the MMR?

A

Live attenuated vaccine

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11
Q

What is the definition of congenital CMV infection?

A

Detection of CMV from bodily fluids (normally urine and saliva) or tissues within the first 3 weeks of life

NOTE: it is the MOST COMMON congenital viral infection

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12
Q

How is CMV transmitted?

A

Infectious bodily fluids: saliva, respiratory droplets, urine, blood, breastmilk

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13
Q

What are the main symptoms of CMV infection?

A

Largely asymptomatic

  • Maculopapular rash
  • Infectious mononucleosis-like illness
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14
Q

Describe the risk of transmission from primary vs non-primary infection

A
  • Primary infection - 30% transmit virus across placenta
  • Non-primary infection - 1% transmit virus across placenta

Non-primary infection far more common than primary infection due to high CMV seroprevalence rates

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15
Q

What is the term used to describe congenital changes that occur as a result of CMV infection? List some features.

A

Cytomegalic inclusion disease

  • CNS - microcephaly, ventriculomegaly, encephalitis, peri-ventricular calcifications
  • Eye - chorioretinitis
  • Ear - sensorineural deafness
  • Liver - hepatosplenomegaly, jaundice
  • Thrombocytopaenia

NOTE: late sequelae include hearing defects, mental retardation, and epilepsy

CMV associated with periventricular calcifications, whereas toxoplasmosis associated with diffuse intracranial calcifications

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16
Q

What is the risk of CMV non-primary compared to primary CMV infection to the foetus?

A

Lower risk of foetal abnormalities

17
Q

What proportion of cases of congenital CMV infection are asymptomatic at birth?

A

90%

18
Q

What is the most common neurodevelopment abnormality causes by congential CMV?

A

Sensorineural deafness

19
Q

Outline some tests used in the diagnosis of CMV infection.

A
  • PCR of urine/saliva/amniotic fluid/tissue
  • Serology - IgG, IgM
20
Q

How is suspected antenatal maternal CMV infection investigated?

A
  • If maternal CMV infection is suspected then check serology (compare booking to repeat sample)
  • If seroconversion suspected (i.e. infection during pregnancy) then refer to fetal medicine unit for USS +/- amniocentesis for CMV PCR
  • No treatment available
  • Neonates are investigated – urine and saliva CMV PCR within 1st 21 days.
21
Q

Describe how foetal CMV infection is diagnosed

A

Amniotic fluid PCR at 21 weeks gestation

22
Q

How is congenital CMV infection treated?

A
  • There is NO vaccine
  • Congenital CMV with significant organ disease
    • Valganciclovir or ganciclovir for 6 months
    • Audiology follow-up until age 6 years
    • Ophthalmology review
23
Q

How are HSV 1 and 2 transmitted?
What are the incubation periods between oro-facial infection and genital infection?

A
  • Transmitted via direct contact with infected lesions
  • Oro-facial incubation - 2-12 days
  • Genital incubation - 4-7 days
24
Q

What are the symptoms of HSV 1 and 2 infection?

A

Can be asymptomatic

  • Painful vesicular rash
  • Lymphadenopathy
  • Fever
25
Q

What is the difference between primary, non-primary, and recurrent HSV infection?

A
  • Primary infection - first occurrence of gential HSV. No pre-existing HSV1 or HSV2 antibodies.
  • Non-primary infection - 1st episode of gential HSV but only has antibodies to the other HSV type
  • Recurrent infection - current HSV infection with pre-existing antibodies. Infection may previously have been asymptomatic or symptomatic.
26
Q

How can HSV be transmitted to foetus and neonate?

A

Foetal infection - ascending infection in PROM

Neonatal infection:

  • Direct contact with infected secretions during delivery
  • Kiss baby with oral herpes