Maternal Infections in Pregnancy Flashcards

1
Q

Why is it important to know about maternal infections during pregnancy?

A

Some infections have the propensity for vertical transmission to the foetus despite mother being asymptomatic.

There is a potential for suboptimal management unless discussed with relevant expert colleagues.

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2
Q

Which viruses have the propensity to cause deleterious effects on the foetus?

A

Parvovirus

Cytomegalovirus

Varicella zoster virus

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3
Q

How can likelihood of infection be minimised?

A

Educate mothers/partners/doctors on infection transfer

Antenatal screening / preconception (rubella immunity, HBV sAg, HCV, HIV, syphilis, be especially rigorous with non-Australian born patients.

Active immunisation pre-conception against HBV, VZV, measles, mumps, rubella, HPV,

Passive immunisation (post exposure prohylaxis) involving IgG antibodies or normal human IgG if the former is not available.

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4
Q

When can pregnant women be vaccinated?

A

It is always fine provided the vaccine is not a live virus.

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5
Q

When is it best to administered a vaccine against whooping cough?

A

Last trimester of pregnancy i.e >16 weeks in

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6
Q

When is contact with rash illness during pregnancy a concern?

A

Only with direct contact. Otherwise, majority of cases are of no concern

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7
Q

What are the differential diagnoses for an infective rash?

A

Varicella-zoster virus

Parvovirus B19

Enteroviruses (coxsachie, echovirus, etc)

etc

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8
Q

When is rubella an issue during pregnancy?

A

Before 16 weeks it can be problematic, after 16 weeks it is harmless to the foetus.

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9
Q

How is diagnosis of viral infection conducted?

A

Serology for pre-existing immunity (IgG)

Serology for IgM, or IgG seroconversion (need 1 - 2 weeks to demonstrate)

Compare with booking antenatal sera (held for 12 months min)

IF of rash material: for VZV, herpes simplex but not perfect

PCR and/or culture

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10
Q

What percentage of pregnancies are estimated to be complicated by varicella? What should be considered?

A

10 - 60/year. Consider utero foetal or neonatal infection

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11
Q

What complications can arise from maternal varicella infection?

A

Causes morbidity in later pregnancy

Increase risk of viral pneumonitis

Risk factors for pneumonitis include smoking and >100 lesions.

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12
Q

What must be done if maternal varicella is diagnosed?

A

Antiviral therapy must be utilised early to maximise the benefit

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13
Q

What investigations should be done with mothers that have been exposed to chickenpox?

A

Attempt to confirm the index case (Check whether they’ve had VZV vaccination)

Determine mothers serostatus (95 to 99% of people who had chicken pox have detectable anti VZV IgG and are thus immune)

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14
Q

What percentage of people who do not report a history of chicken pox have anti VZV IgG?

A

60 to 93%

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15
Q

How many chickenpox vaccine shots need to be given to be considered immune to VZV?

A

2 doses.

If 1 dose immunity should be tested for via serology.

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16
Q

How is the maternal risk of VZV infection different to other adults (<20 weeks)?

A

Maternal risk for serious disease not increased over that of other non-pregnant adults.

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17
Q

How is congenital varicella zoster treated (if <20 weeks)?

A

Small risk of congenital varicella syndrome is ~1% and this should be treated with VZIG antibodies asap.

Consider acyclovir if chickenpox is developed.

No evidence that these methods work but it may do so

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18
Q

What are the risks associated with VZV exposure at >20 weeks?

A

Increased maternal risk of pneumonitis particularly if smoker.

Increased risk of shingles in infant (from birth to adolescence)

Scattered case reports of congenital abnormalities.

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19
Q

How is VZV infection treated if infected at >20 weeks of pregnancy?

A

VZIG for maternal protection/disease amelioration

Aciclovir prophylaxis if too late for VZIG.

Alternatively, aciclovir treatment at first sign

20
Q

Which antivirals are known to be safe in pregnancy?

A

Aciclovir and valaciclovir are safe in pregnancy.

Little data is known about famciclovir.

21
Q

What is the incidence in Australia of congenital varicella syndrome?

A

Estimated annual incidence in Australia is 1 to 4 cases.

22
Q

What stages of pregnancy is congenital varicella syndrome risk greatest?

A

Risk is ~0.4% if infected in the first 14 weeks, maximum 2% if infected from week 13 - 20.

No risk if >20 weeks

23
Q

How does congenital varicella syndrome present?

A

Cicatricial scarring, multidermatomal

Limb hyperplasia

Neurological defects

Ocular defects

Risk of infant death in first 2 years: ~15%

24
Q

When is the worst time for perinatal varicella infection?

A

Severe neonatal infection is associated with onset of maternal varicella 5 days before to 5 days after delivery. Mortality up to 30%

This is due to high maternal viral load without protective effect of maternal antibody.

25
Q

What is the incidence of lactational mastitis?

A

~ 10 - 20% of breast feeding women.

Most common during first month of breast feeding.

26
Q

What are the potential consequences of lactational mastitis?

A

Infrequent/missed feeds

Poor latching

Nipple damage, fissures

27
Q

What are the signs and symptoms of lactational mastitis?

A

Erythema - oedema

Tenderness

Fever

Malaise

28
Q

What are the causative organisms of lactational mastitis?

A

Ordered by commonness:

Staph aureus

Staph epidermidis

Group B strep

E. coli

Candida

29
Q

How is mastitis diagnosed?

A

Breast milk culture

Diagnostic ultrasound to localise collection

+/- aspirate pus

30
Q

How is mastitis treated?

A

Most important thing is to treat milk stasis (heat before feeds, massage during feeds, manual expression or pump)

Analgesia (Ibuprofen/paracetamol)

Antibiotics (Usually given if inflammatory symptoms have not resolved over 12 - 24 hours): Particularly anti staph antibiotics.

In infrequent cases should be admitted to hospital for IV antibiotics.

Potentially could need surgical aspiration/drainage

Continuation of breast feeding should always be actively encouraged

31
Q

What is the risk of maternal antibiotics to neonate like?

A

Relative infant dose is a % of weight adjusted maternal dose. This is expressed by the ratio of milk dose to plasma dose: Milk/plasma ratio (is 0.01 - 0.05 for amoxycillin/cephalexin)

32
Q

What are the neonatal effects of antibiotics used for mastitis?

A

Proportion absorbed into infant blood is unknown

Modification of bowel flora can lead to possible associated symptoms in infant

Modulation of mucosal and systemic immune response by gut flora.

Possible inhibition of septic screen cultures if baby is febrile.

33
Q

Should antibiotics be continued by the mother while she is breastfeeding?

A

All current recommendations are to continue breastfeeding in setting of mastitis +/- concurrent antibiotics

34
Q

What kinds of bacteria are present in post partum genital tract infections?

A

Opportunistic infections arising from normal vaginal flora. (genital tract specimens are contaminated with normal vaginal flora)

Anaerobes outnumber aerobes 10 - 100:1 and include:

Peptococcus/peptostreptococcus

Clostridium species

Bacteriodes species

Aerobes:

Group B strep (S. agalactiae)

Group A strep (S.pyogenes)

Enterococci

Enteric Gram -ve rods (E.coli, klebsiella, etc)

35
Q

What are potential complications of post partum genital tract infections?

A

Bacteraemia

Septic shock / pelvic thrombophlebitis

36
Q

How are post partum genital tract infections diagnosed?

A

Investigate fever and non-specific symptoms immediately

Cultures (blood, urine, woulnd/genital tract swabs)

37
Q

How are post partum genital tract infections treated?

A

Depends on likely cause, most are polymicrobial thus:

Antibiotic combinations are used or broad spectrum antibiotics to cover several features of the bacteria (eg aerobic capacity)

Amoxycillin + Gentamicin + Metronidazole

38
Q

How can post partum genital tract infections be prevented?

A

Good antenatal care

Operative delivery based on accepted indications

Skillful technique

High standard infection control

ANTIBIOTIC PROPHYLAXIS FOR ALL C-SECTIONS

39
Q

What do group B streptococci infections cause besides post partum infections?

A

Skin/soft tissue infections 35 - 40%

Bacteraemia with no identifiable focus 30%

Urosepsis 15%

Osteomyelitis 5%

Foreign body infections

Pneumonia

Peritonitis

40
Q

What is the fatality rate of Group B strep infections in adults?

A

30% of cases (usually elderly with co-morbidities)

41
Q

Where are group B strep located normally?

A

They are normal commensals in the gut and the vagina. (means detected GBS in culture is not necessarily an infection caused by GBS)

42
Q

What type of disease does GBS result in mother?

A

Choriamnionitis

Endometritis

Bacteraemia and secondary complications

43
Q

What type of disease does GBS result in neonate?

A

Early onset EOGBS (first week of life): fatal in 25% preterm and 5% term and causes:

Pneumonia

Septicaemia

Meningitis

Late onset LOGBS (day 7 and beyond): fatal in 10% preterm and 1% term and causes:

Meningitis mainly

44
Q

How can we prevent perinatal group B strep infection?

A

Controversy over prevention strategies since emergence of GBS in late 1970s

Australian hospitals first to introduce routine antenatal screening for maternal GBS carriage and intrapartum antibiotic chemoprophylaxis for those with it. This has been shown to be effective in relation to neonatal sepsis rates.

Debate still ranges over most effective prevention strategy

45
Q

What are the 4 main methods for prevention of perinatal GBS disease?

A

1) Intrapartum chemoprophylaxis to at risk women:

Those either found to have GBS on screening

OR

Those who enter labour with risk factors present (preterm labour, prolonged rupture of membranes, intrapartum fever, GBS at any stage of pregnancy)

2) Postnatal penicillin prophylaxis to newborn babies
3) Vaginal disinfectants-chlorhexidine
4) GBS polysaccharide-protein conjugate vaccines.