Infections in pregnancy; Polyhydramnios Flashcards

1
Q

Describe the risk of infection of chickenpox during pregnancy [+]

A

Risk of Fetal varicella syndrome (FVS):
- skin scarring
- eye defects (microphthalmia) and cataracts
- scars and significant skin changes located in dermatomes
- limb hypoplasia
- microcephaly
- learning disabilities

Lecture notes:
- soft-tissue calcification
* polyhydramnios,
* limb defects and dermatomal skin scarring (due to fetal herpes zoster),
* soft-tissue calcification
* damage to the eyes and CNS.

Neurological defects include cortical atrophy, microcephaly, limb paresis, spinal cord atrophy, encephalitis, seizures and Horner’s syndrome.

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2
Q

What are the congenital TORCH infections? [5]

A

Toxoplasmosis
Others (syphilis, VZV, parvovirus B19, listeriorsis)
Rubella
CMV
Herpes Simplex V

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3
Q

severe neonatal varicella:
* if the mother develops rash between [] days before and [] days after birth there is a risk of neonatal varicella, which may be fatal to the newborn child in around 20% of cases

A

severe neonatal varicella:
- if the mother develops rash between 5 days before and 2 days after birth there is a risk of neonatal varicella, which may be fatal to the newborn child in around 20% of cases

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4
Q

How do you manage a patient who is unsure if they have previously had chickenpox? [1]

A

maternal blood should be urgently checked for varicella antibodies

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5
Q

Describe how you manage chickenpox exposure during pregnancy [1]

Describe how you manage chickenpox infection during pregnancy [1]

A

oral aciclovir (or valaciclovir) is now the first choice of PEP for pregnant women at any stage of pregnancy who are exposed to chickenpox
- antivirals should be given at day 7 to day 14 after exposure, NOT immediately

Infection:
- consensus guidelines (Health Protection Authority and RCOG) suggest oral aciclovir should be given if the pregnant women is ≥ 20 weeks and she presents within 24 hours of onset of the rash
- if the woman is < 20 weeks the aciclovir should be ‘considered with caution’

NB why wait: n a study evaluating the comparative effectiveness of 7 days course of aciclovir given either immediately after exposure or starting at day 7 after exposure to healthy children, the incidence and severity of varicella infection was significantly higher in those given aciclovir immediately (10/13 (77%) who received aciclovir immediately developed clinical varicella compared with 3/14 (21%) who started aciclovir at day 7

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6
Q

Rubella infection causing congenital rubella sydnrome is caused by maternal infection within the first [] weeks of pregancy.

When is there the highest risk? [1]

What is the clinical significance of this? [1]

A

First 20 weeks - but first 10 weeks poses highest risk

When primary infection occurs before 12weeks’ gestation, given the risk of fetal infection and the risk of an infected fetus developing severe abnormalities, it is reasonable to consider termination of pregnancy when appropriate

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7
Q

Describe the features of congenital rubella syndrome [5]

What is the clinical triad? [3]

A
  • Congenital deafness
  • Congenital cataracts
  • ‘Salt and Pepper’ chorioretinitis
  • Congenital heart disease (PDA and pulmonary stenosis)
  • Learning disability
  • Cerebral palsy

Triad:
- Microcephaly
- PDA
- Cataracts

Lecture:
- Hearing loss, learning disability, heart malformations and eye defects, neurodevelopmental delay, and endocrinopathies.

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8
Q

Describe how should vaccinate with regards to rubella and pregnancy? [1]

A

Women planning to become pregnant should ensure they have had the MMR vaccine.
- BUT should NOT recieve whilst pregnant as is a live vaccine

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9
Q

How do you manage non-immune mothers to MMR? [1]

A

non-immune mothers should be offered the MMR vaccination in the post-natal period
* MMR vaccines should not be administered to women known to be pregnant or attempting to become pregnant

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10
Q

Pregnant women are advised to avoid high-risk foods (e.g. blue cheese) and practice good food hygiene to prevent which infection? [1]

What is the clinical manifestation of having this infection in pregnancy? [1]

A

Listeria:
- Listeriosis in pregnant women has a high rate of miscarriage or fetal death.
- It can also cause severe neonatal infection.

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11
Q

The features of congenital CMV are [5]

A

The features of congenital CMV are:
* ‘Blueberry muffin rash’
* Petachial rash
* Fetal growth restriction
* Microcephaly
* Hearing loss - this is the key one to remember
* Vision loss
* Learning disability
* Seizures

NB: With approximately 40,000 infected children per year, congenital CMV infection is the most common cause of congenital non-genetic hearing loss

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12
Q

How do you treat congenital CMV? [1]

A

IV ganciclovir / PO valganciclovir

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13
Q

Bilateral cataracts in a newborn would most likely indicate..[1]

A

Congential rubella infection

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14
Q

There is a classic triad of features in congenital toxoplasmosis.

What is it? [3]

A

Intracranial calcification
Hydrocephalus
Chorioretinitis (inflammation of the choroid and retina in the eye)

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15
Q

How do you treat listeriosis infection in pregnancy? [2]

A

Ampicillin and gentamicin

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16
Q

Fetal hydrops would indicate infection from..?[1]

A

Parvovirus B19

17
Q

Blueberry muffin rash has which 2 key ddx? [2]

A

CMV
Rubella

18
Q

Infections with parvovirus B19 in pregnancy can lead to several complications, particularly in the first and second trimesters. Complications are: [4]

A
  • Miscarriage or fetal death
  • Severe fetal anaemia
  • Hydrops fetalis (fetal heart failure)
  • Maternal pre-eclampsia-like syndrome
19
Q

What causes fetal anaemia from parvovirus B19 infection? [1]
What effect does this have? [1]

A

Fetal anaemia is caused by parvovirus infection of the erythroid progenitor cells in the fetal bone marrow and liver.
- This anaemia leads to heart failure, referred to as hydrops fetalis.

20
Q

What is the triad of seen in pregnant parvovirus b19 infection? [3]

A

It involves a triad of hydrops fetalis, placental oedema and oedema in the mother
- + hypertension and proteinuria.

21
Q

Women suspected of parvovirus infection need which tests? [3]

A
  • IgM to parvovirus, which tests for acute infection within the past four weeks
  • IgG to parvovirus, which tests for long term immunity to the virus after a previous infection
  • Rubella antibodies (as a differential diagnosis)
    *
22
Q

A baby born with congenital Zika syndrome which would [2]

A

Microcephaly
Fetal growth restriction
Other intracranial abnormalities, such as ventriculomegaly and cerebellar atrophy

23
Q

Define what is meant by polyhydramnios [1]

How does it present? [1]

A

Polyhydramnios is the presence of too much amniotic fluid in the uterus.
- Polyhydramnios may present with a uterus which feels tense or large for dates and it may be difficult to feel the foetal parts on palpation of the abdomen.

24
Q

How can the causes of polyhydramnios be split? [2]

A

Causes of polyhydramnios can be due to excessive production of amniotic fluid or insufficient removal of amniotic fluid.

25
Q

Causes of polyhydramnios can be due to excessive production of amniotic fluid or insufficient removal of amniotic fluid
.
Excess production can be due? [4]

Insufficient removal can be due to reduced foetal swallowing. Due to: [4]

A

Excess production can be due to increased foetal urination:
* Maternal diabetes mellitus
* Foetal renal disorders
* Foetal anaemia
* Twin-to-twin transfusion syndrome

Insufficient removal can be due to reduced foetal swallowing. Due to: [4]
* Oesophageal or duodenal atresia
* Diaphragmatic hernia
* Anencephaly
* Chromosomal disorders

26
Q

What are the maternal [4] complications of polyhydramnios?

A

Maternal:
- respiratory compromise due to increased pressure on the diaphragm
- Increased risk of urinary tract infections due to increased pressure on the urinary system
- Worsening of other symptoms associated with pregnancy such as gastro-oesophageal reflux, constipation, peripheral oedema and stretch marks
* Increased incidence of caesarean section delivery

27
Q

What are the foetal [4] complications of polyhydramnios?

A
  • Pre-term labour and delivery
  • Premature rupture of membranes
  • Placental abruption
  • Malpresentation of the foetus (the foetus has more space to “move” within the uterus)
  • Umbilical cord prolapse (polyhydramnios can prevent the foetus from engaging with the pelvis, thus leaving room for the cord to prolapse out of the uterus before the presenting part)
28
Q

Lecture notes

It causes up to 21% of all congenital hearing loss at birth and 10% of all cases of cerebral palsy

Refers to

CMV
VZV
Rubella
Parvovirus
Toxoplasmosis

A

Lecture notes

It causes up to 21% of all congenital hearing loss at birth and 10% of all cases of cerebral palsy

Refers to

CMV
VZV
Rubella
Parvovirus
Toxoplasmosis

29
Q
A
30
Q

Lecture

When is the greatest risk of transmission of CMV in pregnancy? [1]

When is the greatest risk of severe fetal infection? [1]

A

The risk of congenital infection appears to vary according to the point in gestation at which primary infection occurs, increasing from around 30% in the first trimester to 47% in the third trimester.

While the risk of viral transmission is lower in early pregnancy, the proportion of cases with a prenatal diagnosis of severe fetal infection is higher when infection occurs in the first compared with the third trimester of pregnancy.

31
Q

Which of the following best describes CMV in pregnancy

  • Infection is most likely in first trimester; biggest risk to baby in first trimester
  • Infection is most likely in first trimester; biggest risk to baby in third trimester
  • Infection is most likely in third trimester; biggest risk to baby in third trimester
  • Infection is most likely in third trimester; biggest risk to baby in first trimester
A
  • Infection is most likely in third trimester; biggest risk to baby in first trimester
32
Q

Describe how you dx CMV in pregnancy [2]

A

The diagnosis of primary CMV infection in pregnancy can be made following either:
the appearance of CMV-specific IgG in a woman who was previously seronegative; or
detection of CMV IgM antibody and low IgG avidity

33
Q

Lecture:

The main sequelae of congenital toxoplasma infection involve the CNS and eyes, and typically include [4]

A

The main sequelae of congenital toxoplasma infection involve the CNS and eyes, and typically include microcephaly, hydrocephalus, ventriculomegaly and chorioretinitis. These may lead to developmental delay, epilepsy and blindness.

34
Q

How do you treat TG infection:
- to prevent vertical transmission after maternal infection [1]
- If vertical transmission is confirmed [4]

A

Spiramycin (until the end of the pregnancy, in the absence of confirmed vertical transmission) should be used to prevent vertical transmission after maternal toxoplasma infection during pregnancy

If vertical transmission is confirmed:
- fetal infection should be treated by spiramycin only for 1 week, followed by pyrimethamine plus sulfadiazine plus folinic acid throughout the pregnancy and the infant treated for 1further year.

35
Q

Parvovirus

Fetal anaemia and fetal hydrops both visible on ultrasound. Anaemia can be assessed measuring at the how exactly? [1]

A

Fetal anaemia and fetal hydrops both visible on ultrasound. Anaemia can be assessed measuring at the Peak Systolic on Middle Cerebral artery (raised MCA-PSV).

36
Q

Describe how herpes simplex can impact new born? [3]

A

Can cause localised to skin, eye and/or mouth lesionsor local central nervous system (CNS) disease (encephalitis)

37
Q

How do you treat HSV infection in pregnancy? [2]

A

Treatment should not be delayed. Management of the woman should be in line with her clinical condition and will usually involve the use of oral (or intravenous for disseminated HSV) aciclovir in standard doses (400 mg three times daily, usually for 5 days). In the third trimester, treatment will usually continue with daily suppressive aciclovir 400 mg three times daily until delivery.

Caesarean section should be the recommended mode of delivery for all women developing first episode genital herpes in the third trimester, particularly those developing symptoms within 6 weeks of expected delivery, as the risk of neonatal transmission of HSV is very high at 41%

38
Q

Describe how you would deliver a patient with polyhydramnios:
- moderate [1]
- severe [1]
- what would do for baby afterwards birth [1]

A

Delivery:
* Risk of malpresentation / cord prolapse/ pre term labour
* Aim delivery around 37 weeks for severe polyhydramnios
* 38-40 weeks for moderate polyhydramnios
* Nasogastric tube postnatally to ensure there is no blockage in oesophgus/ tracheoesophageal fistula