Infections in pregnancy - finish! Flashcards

1
Q

what is the pathophysiology of rubella in pregnancy?

A

In first 8-10 weeks risk of damage to fetus is as high as 90%

  • Congenital rubella syndrome → rubella togavirus in first 20 weeks of pregnancy
  • transmission through respiratory droplets or aerosols
  • risk highest before 10 weeks gestation
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2
Q

what is the significance of the vaccine in rubella?

A
  • check rubella antibodies
  • vaccinatedwith two doses of the MMR, three months apart
  • pregnant women should not receive MMR as live vaccine
  • non-immune → offer after birth
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3
Q

what are some clinical features of rubella?

A
  • fever
  • coryza
  • arthralgia
  • rash which begins on face and moves to trunk
  • lymphadenopathy: post auricular
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4
Q

how do you investigate and manage rubella?

A

*serological testing: rubella-specific IgM or significant risk in rubella specific IgG

  • supportive
  • isolate to prevent spread
  • discuss with local health protection unit
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5
Q

what are some features of congenital rubella?

A
  • Congenital sensorineural deafness
  • Congenital cataracts
  • Congenital heart disease (PDA and pulmonary stenosis)
  • Growth retardation
  • Learning disability
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6
Q

what is the pathophysiology of chicken pox?

A

varicella zoster virus (VZV)

  • incubation period for the virus is10-21 days
  • woman is infectious from 48 hours prior to the rash to until the vesicles have crusted
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7
Q

what is the significance of exposure during pregnancy?

A
  • safe if previously had
  • When they are not sure about their immunity, test the VZV IgG levels. If positive, they are safe
  • When they are not immune, they can be treated withIV varicella immunoglobulinsas prophylaxis against developing chickenpox
    • This should be given within ten days of exposure.
  • Infection is associated with pneumonia, hepatitis, and encephalitis – accounting for the2% mortalityin mother
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8
Q

how do you manage a suspected contact?

A

less than 20 weeksgestation, the woman should receivevaricella zoster immunoglobulin (VZIG)within 10 days of the contact, and before the onset of rash

more than 20 weeks gestation, the woman can receive eitherVZIG, or alternativelyAciclovircan be given from days 7 to 14 following exposure

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9
Q

how do you manage maternal chicken pox?

A
  • aciclovir within 24h of rash at >20w, consider in those <20 w
  • counselled about the symptoms ofpneumonia, neurological signs and haematological rash - attend hosp
  • fetal medicine specialist, withserial ultrasound examinationsbeginning at 5 weeks post infection to identify any fetal abnormalities
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10
Q

what are some complications for mother and baby in chicken pox?

A
  • More severe cases in the mother, such asvaricellapneumonitis,hepatitisorencephalitis
  • Fetal varicella syndrome
  • Severeneonatal varicella infection(if infected around delivery)
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11
Q

what is the route of infection for the newborn?

A

transplacental, vaginal, direct contact after birth

mx: varicella-zoster immunoglobulin (VZIG) ± aciclovir

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12
Q

what is congenital varicella syndrome?

A
  • reactivation of the virus in utero as herpes zoster - fetus is infected by maternal varicella before 20 weeks gestation
  • Fetal growth restriction
  • Microcephaly, hydrocephalus and learning disability
  • Scars and significant skin changes located in specificdermatomes
  • Limbhypoplasia(underdeveloped limbs)
  • Cataracts and inflammation in the eye (chorioretinitis)
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13
Q

what is the pathophysiology of parvovirus infection?

A
  • Parvovirus B19 virus - ‘fifth disease, slapped cheek syndrome, erythema infectiosum’
    • self limiting, rash and sx fade over 1-2w
  • infectious 7 to 10 days before rash
    • not once rash
  • significant exposure → 15 min in same room, face to face contact
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14
Q

how does parvovirus present?

A
  • non-specific viral
  • 2-5 days later rash
    • quite rapidly as a diffuse bright red rash on both cheeks
    • few days later - reticular(net-like) mildly erythematous rash affecting the trunk and limbs appears, which can be raised and itchy
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15
Q

how is parvovirus investigated and managed?

A
  • IgM to parvovirus → acute infection within the past four weeks
  • IgG to parvovirus → long term immunity to the virus after a previous infection
  • Rubella antibodies (as a differential diagnosis)
  • supportive
  • Women with parvovirus B19 infection need a referral tofetal medicineto monitor for complications and malformation
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16
Q

what are some complications of parvovirus in pregnancy?

A
  • miscarriage or foetal death
  • severe foetal anaemia
  • hydros fetalis
  • mirror syndrome
17
Q

what is the pathophysiology of zika?

A
  • zika virus spread by host Aedes mosquitoes
  • also spread by sex with someone infected with virus
18
Q

what is the presentation of congenital zika syndrome?

A
  • microcephaly
  • foetal growth restriction
  • other - ventriculomegalyandcerebellar atrophy
19
Q

what is the pathophysiology of CMV in pregnancy?

A
  • Cytomegalovirus virus infection during pregnancy
    • herpesvirus family
  • spread via infected saliva or urine of asymptomatic children
  • most cases do not cause congenital CMV
20
Q

how does CMV present?

A
  • mild flu-like illness
  • Alternatively, in some patients, it can cause amononucleosis syndrome(similar to Epstein-Barr)
    • resulting in fever, splenomegaly and impaired liver function
21
Q

what is congenital CMV?

A
  • Fetal growth restriction
  • Hepatosplenomegaly
  • Microcephaly
  • Hearing loss
  • Vision loss - chorioretinitis
  • Learning disability
  • Seizures
22
Q

what are some complications of congenital CMV?

A

*20-30% mortalityin this symptomatic group, often due to disseminated intravascular coagulation (DIC), hepatic dysfunction, bacterial superinfection

<aside>
🤰🏽 Babies born without symptoms of CMV infection have a 10-15% chance of developing sequelae of the infection within**2 years,**

- Sensorineural hearing loss
- Psychomotor development delay
- Visual impairment
</aside>

23
Q

how is CMV managed?

A
  • maternal
    • immunocompetent no tx
    • anti-CMV drugs have teratogenic effects
  • foetal
    • diagnosed prenatally viaamniocentesisand PCR
      • after 21 weeks gestation as kidneys need to be developed to excrete virus in amniotic fluid
    • no effective therapy, andtermination of pregnancycan be offered
    • trials - IV CMV specifichyperimmune globulin
24
Q

how prevalent is HIV and pregnancy in the UK?

A

*increasing in numbers

in london as high as 0.4% of pregnant women

25
Q

what are some factors that reduce the risk of vertical transmission?

A
  • maternal antiretrovirals
  • mode of delivery - CS
  • neonatal antiretroviral therapy
  • infant feeding (bottle)
26
Q

what is the role of screening in pregnant women for HIV?

A

screening is offered to all pregnant women, ideally at booking
*considered an opt-out rather than opt-in test

*reoffer screening at 20w if declined previously

27
Q

what are some risk factors to consider a pregnant woman high risk for HIV?

A
  • IVDU, them or partner
  • women or partner lived in areas of HIV endemic
  • women who have had treatment abroad from high prevalence area
  • blood transfusion abroad or pre-1985
  • partner known or suspected as bisexual
28
Q

what areas of the world are considered as “HIV endemic”?

A
  • sub-saharan africa
  • far east
  • south east asia
29
Q

what would you do in a scenario where a woman presents, in labour unbooked?

A

give rapid HIV testing kit!!
- finger prick test with results available in 20min

*available in delivery suite and MAU

30
Q

how is HIV tested for?

A

fourth generation HIV antibody assays

A confirmatory blood sample must be sent to virology marked as urgent for
HIV testing and screening for Hep B, Syphilis

31
Q

how are pregnant women manages if found to be HIV positive?

A
  • psychosocial
  • MDT
  • confidentiality maintained, encourage partner and children testing
  • antiretroviral therapy!! cART
  • vaginal delivery if viral load less than 50 copies/ml at 36w
  • otherwise CS with zidovudine infusion before
  • monitor as required: DM
  • no breastfeeding
32
Q

how is a neonate managed for HIV?

A

*zidovudine orally if maternal load <50

*triple ART otherwise

*continue for 4-6w

33
Q
A