General pregnancy care Flashcards

1
Q

What is the infection rate if non immune and family contact with rubella

A

Almost 100%
30-50% casual contact

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2
Q

What are the symptoms of rubella?

A

Maculopapular rash
Fever
Arthralgia
Lymphadenopathy

Mostly asymptomatic

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3
Q

Rubella - Percentage risk of fetal infection first trimester and rate of congenital defects

A

80%
85%

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4
Q

Rubella: Risk of fetal infection / congenital defects by gestation

A

Risk of infection high initially, low in midtrimester and then 100% by term

Congenital defects - high risk first trimester, very rare from 17/40 onwards

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5
Q

congenital defects ass with rubella

A

Cataracts, IUGR, PTB, IUFD, deafness, developmental delay, cardiac disease, pneumonia, hepatsplenomegaly, blueberry muffin spots, developmental delay

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6
Q

What should you do if patient infected with rubella?

A

Rubella PCR / culture / fetal IgM with CVS or amnio. Can get false +ve PCR with CVS
First trimester: consider TOP
>20/40: rarely ass with congenital rubella syndrome.
No treatment options available
Ophthalmology, cardiac and hearing from birth to improve outcomes

VACCINATION pre pregnancy

If Re-infection with good hx of prev +ve serology then risk of fetal infection is <10%, rare for congenital rubella syndrome

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7
Q

How do you test for rubella after a possible contact

A

IgG / IgM testing
If IgG +ve and IgM +ve possible recent infection. REPEAT to confirm

If both negative repeat test if <3/52 since contqact or <7 days since illness

If IgG -ve but IgM +ve, repeat to check for seroconversion (if +ve then infected)

IgG +, IgM -ve = past infection or immunisation

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8
Q

What should you do at birth if fetus infected with rubella

A

Birth attendants must be immune

Infant
- IgM serology
PCR urine and throat
- IgG

If IgG > maternal IgG and IgM +ve and PCR +Ve and clinical features –> symptomatic infected infant - breast feeding okay, no specific management, ophthalmology and cardiac and hearing assessements and regular assessments. Infants can be infective for up to 12 months

No clinical features CRS but IgM + and PCR + - keep close eye as can have late onset disease

No clinical features and IgM -ve and PCR -ve –> reassure, reconfirm at 9/12 with IgG

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9
Q

What is the mortality rate of AFLP

A

2% maternal
11% perinatal

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10
Q

Clinical features AFLP

A

Presents after 30/40
Nausea, anorexia, malaise, severe vomiting, abdo pain, jaundice
Severe elevation transaminases
DIC
AKI
Lactic acidosis
Raised ammonia
Hepatic encephalopathy
Hypoglycaemia
Features of diabetes insipidus

(women with low BMI, multiple pregnancy get it)

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11
Q

What is swansea criteria

A

6 or more of
- Vomiting
- Abdo pain
- Hypoglycaemia
- Hyperuricaemia
- Coagulopathy
- DI
- Raised ammonia
- Enecephalopathy
- Leukocytosis
- Elevated transaminases
- AKI

(liver biopsy gold standard)

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12
Q

How do you manage
AFLP?

A

Expedite delivery
MDT
ICU
7% require ventilation
Coagulopathy - prolonged PT time - treat with FFP and vitamin K prior to delivery
10-50% dextrose for hypoglycaemia
Look for liver flap
Low threshold to start Abx as AFLP carries high risk fo sepsis (tazocin)
N-acetylcysteine - antioxidant
Can give desmopression if urine volumes are excessive

High recurrence rates!

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13
Q

Varicella:
What is the rash like and how long are they infectious?

A

Maculopapules - become vesicles and crust over
infectious up to 48 hours prior to rash

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14
Q

Is shingles and issue to the fetus

A

No

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15
Q

What are the maternal complications of varicella infection in pregnancy

A

Severe infections
Pneumonia
encephalitiis
death

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16
Q

Fetal complications of varicella

A

Risk of complication low
- <12/40 0.4%
12-20/40: 2%
>20/40: RARE

prematurity
LBW
Microcephaly / mental retardation
eye abnormalities - cataracts, chorioretinitis
skin scarring
limb hypoplasia
childhood zoster

17
Q

What is the management / treatment of varicella if exposed but no rash yet?

A

No treatment that prevents fetal transmission, just to prevent maternal morbidity / mortality
4-13% mortality rate if primary infection in pregnancy

Urgent VZV serology
if <96h since exposure: Passive immunisation with VZIG if IgG -ve
If >96h - consider oral aciclovir 800mg five x / day for 7/7. if high risk particularly (smoker, underlying lung disease, immunocompromised)
Seek medical attention immediately if rash develops or feeling unwell

18
Q

What is the management if expoed to varicella and have chickenpox lesions ?

A

No complications and ≤24h since onset of rash - give oral aciclovir

No complications and >24 hours since onset of rash - nothing

Complciation or immunocompromised: admit to hospital and give IV aciclovir. Do CS if fetal compromise, maternal resp failure

19
Q

What is the risk to the baby of varicella primary infection in pregnancy

A

<12/40 0.5%
12-28/40: 1.4%
>28/40 - 0%

Refer to MFM
Detailed scan for anomalies 5/52 post infection and then repeat USS until delivery. if abnormal could consider fetal MRI. Amnio not advised

Skin scarring
Eye abnormalities
limb abnormalities
prematurity / LBW
ID
Death

20
Q

Risk to BABY with maternal chickenpox in relation to time till delivery

A

> 7/7 before delivery: no issue. No isolation from mother, breast feeding encourages

7 /7 before to 2 days after delivery: ZIG immediately! should be given within 24h of birth, but can be up to 72h. No isolation of term infants from mother. BF required

> 2 - 28 days after delivery: ZIG required.
Give as soon as possible but cna be given up to 10/7 post rash.
No isolation from mother required. BF encouraged.

If baby gets chickenpox from mother
- Preterm or <1000g - admit to NICU and give IV aciclovir
- Term infant - admit to paeds unit and give ZIG and only IV aciclovir if resp symptoms develop or severe disease.

21
Q

What is polymorphic eruption of pregnancy?

A

Common pregnancy dermatosis
1/200 incidence
Stretching of the skin elicits an immune response - connect tissue damage
Onset is usually 3rd trimester - mean GA 34/40
More common in primips, multiple pregnancies
On striae, umbilical sparing
Pruiritic, urticarial papules, often red with pale halo around each papule. Lesions on breast rare
No effects for fetus

22
Q

How should you treat PUPPS

A

Menthol (1%) aqueous cream
Hydrocortisone 1%
Sedative antihistamine
No sedating antihistamines
Systemic steroids only occ used for severe pruritis

23
Q

What is pemphigoid gestationis

A

Rare but serious
Occurs anywhere from 9 weeks gestation to 1/52 PP
Rarely presents with trophoblastic tumours
Distribution: abdomen (with umbilicus), spreads to limbs, palms, soles
Eruption: intensely pruritic, urticarial erythematous papules and plaques, target lesions and annular wheals . After variable delay (usually 2 weeks), vesicles and large tense bullae form
Autoimmune process, possibly related to fetal antigens. Binding of circulating complement fixing IgG Ab to a protein in the basement membrane of teh skin - triggers and immune response
Exacerbating and remitting course
Lesions usually rsolve weeks to months after delivery, rarely can persist for years.

Ass with other autoimmune conditions: Graves, vitiligo, type 1 diabetes, RA

24
Q

How do you diagnose pemphigoid gestationis?

A

skin biopsy - shows completment deposition in basement membrane.

25
Q

What are the fetal considerations in pemphigoid gestationis?

A

low birthweight, preterm delivery, stillbirth
Infant can have bullous eruption (10%, usually mild and transient)

26
Q

What is the treatment of pemphigoid gestationis?

A

Relieve itch, prevent blisters, avoid secondary infection
- Potent topical steroids
- Most require systemic prednisone (40-60mg / day)
- Oral antihistamines for itch
- If unresponsive to oral steroids can use azathioprine, cyclosporin, IV IG, plasmapheresis

27
Q

Recurrence rate of pemphigoid gestationis?
What contraception should you avoid?

A

Usually recurs - usually earlier onset and severe course
May recur with COC

28
Q

How is parvovirus transmitted?

A

Resp secretion and saliva

29
Q

What issues does parvovirus cause?

A

Cytotoxic for erythroid progenitor cells - decreased survival of red cells (anaemia)
supression of bone marrow

30
Q

Who is at risk of parvovirus?

A

Childcare workers
School teachers
People with young children

31
Q

What is the risk of parvovirus transmission from mother to fetus?

A

50% (less if exposed at school rather than at home)

32
Q

What is the risk of fetal demise if confirmed parvovirus fetal infection?

A

10% <20/40
<1% >20/40

3% risk hydrops if infected before 20/40
- 30% spontaneously resolve
20% die without IUT
20% die with IUT

33
Q

What symptoms does parvovirus cause?

A

Rash - slap cheek sometimes
Arthralgia
Non specific viral illness

34
Q

How do you check for parvovirus?

A

IgM and IgG
(if both negative, or igg neg but igm +ve, repeat serology 2-4 weeks)
If IgM and IgG +ve then have infection

if confirmed maternal infection do ultrasound weekly to fortnightly until 10-12 weeks post infectino, if no issues then routine cares. if fetal anaemia - refer MFM for IUT

35
Q

What is alloimmune thrombocytopenia?

A

Fetal disorder - caused by feto-maternal incompatibility for platelet antigens

No maternal symptoms
Mother is NOT thrombocytopenic
Condition develops in utero, affects all children, including the first born but is usually diagnosed after birth

Hx: previously affected child - symptoms, severity (bruising, bleeding, ICH)

Need to rule out other causes: e.g. if mother has thrombocytopenia - autoimmune causes such as ITP, SLE etc

36
Q

How do you diagnose / investigate for alloimmune thrombocytopenia?

A

Confirm dx with prev affected infant
Confirm presence of anti-HPA autoantibodies against platelets in maternal serum
- Then do paternal genotype and check whetehr heterozygote or homozygote
If heterozygote could do NIPT, CVS, amnio
- Cross match maternal serum with paternal platelets, both untreated and chloroquine treated (removes HLA antigens that may cause a “false positive”)

37
Q

What are the risks to the baby if previous baby was affected with NAIT?

A

7% if prior child had thrombocytopenia but no ICH
75% if prior child had ICH
No prior affected pregnancies 15%

60-65% of babies do well
20% die
15% have neurological damage

38
Q

How should you treat someone at risk of NAIT?

A

If no prev baby affected with ICH - IVIG from 28/40 and IOL 38/40
If prior baby affected IVIG from 12-18/40 and elective deliveyr 38/40
Regular USS with MFM

This treatment decreases risk of ICH but doesn’t guarantee no adverse outcomes