Infections in Pregnancy Flashcards

1
Q

What are the TORCH infections

A

Toxoplasmosis
Other (syphilis, parvovirus B19, hep B/C, listeriosis, VZV, HIV, GBS)
Rubella
CMV
HSV

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2
Q

What is toxoplasmosis and how is it transmitted

A

Protozoan toxoplasma gondii with reservoir in the domestic cat
Indigestion of raw or undercooked meat containing cysts
Infectious oocytes presented in contaminated water/soil
Increased risk of vertical transmission with increasing gestational age (5% 1st, 80% 3rd trimester)
Risk of congenital toxoplasmosis reduced with increasing gestational age (60-80% 1st, 5% 3rd)
Only seroconversion places risk to the foetus, occurring in 2 weeks
IgG detectable 1-2 weeks after infection

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3
Q

What are the clinical features of toxoplasmosis in the mother and foetus

A

Mother: asymptomatic or fever, malaise, arthralgia

Child:
60% asymptomatic at birth → deafness, low IQ, microcephaly
- Chorioretinitis (→ cataracts)
- Convulsions
- Hydrocephalus (microcephaly)
- Intracranial (‘tram-like’) calcifications - Scattered throughout the brain (unlike CMV, which is peri-ventricular)
- Hepatosplenomegaly/jaundice

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4
Q

What investigations should be done for toxoplasmosis

A

Bloods: Sabin Feldmen Dye test, IgM and IgG serology
Other:
- US foetal anomaly scan: FGR, microcephaly, ventriculomegaly, ascites
- Amniocentesis and PCR

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5
Q

What is the management for toxoplasmosis

A

Prevention: Mother should avoid eating raw/rare meat and handling cats and cat litter

Toxoplasmosis PCR +ve in mother, -ve in baby→ Spiramycin (3-week course, 2-3g/day) - prevents vertical transmission

Toxoplasmosis PCR +ve in mother, +ve in baby → Pyrimethamine + Sulfadiazine
- Treat baby for up to 1 year after delivery (if no TOP)

Adjunct: Prednisolone

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6
Q

What is rubella and how is it transmitted

A

RNA virus from togaviridae family
Outbreaks from migrants where vaccination programmes do not exist
Vertical infection during maternal varicaemia 5-7d post exposure
90% chance of virus being passed to the foetus if Rubella infection is in early pregnancy - multiple defects are most likely when infection occurs in the first 16 weeks

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7
Q

What are the features of congenital rubella

A

Eye defects e.g. cataracts
Hearing impairment
Cardiac abnormalities e.g. patent ductus arteriosus and pulmonary artery stenosis
CNS defects e.g. microencephaly, mental and psychomotor retardation, progressive panencephalitis
IUGR
Autism
Endocrine abnormalities e.g. diabetes mellitus, thyroid dysfunction

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8
Q

What investigations should be done for rubella in pregnancy

A

Oral fluid sample or throat swab for viral culture
Rubella-specific IgM serum antibody for capture ELISA

US: Normal OR
FGR
Microphthalmia
Hepatosplenomegaly
Cardiac defects

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9
Q

What is the management for rubella in pregnancy

A

Notify the local health protection team (HPT) as it is a notifiable disease
Symptomatic relief: paracetamol, fluids, isolate for 5 days

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10
Q

How is CMV transmitted

A

1st and 2nd trimester vertical transmission 40% and foetal damage in 10%
3rd trimester vertical transmission 80%

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11
Q

What are the features of congenital CMV

A

Mortality (6%)
Prematurity
Petechiae, thrombocytopenia, haemolysis
Hepatosplenomegaly
Conjugated hyperbilirubinaemia/jaundice
Microcephaly, hypotonia, seizures
Intracranial calcifications (periventricular)

Long term:
- Psychomotor delay
- Sensorineural hearing loss
- Ocular abnormalities (Chorioretinitis → cataracts)

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12
Q

What are the features of congenital HSV

A

SEM disease
CNS ± SEM disease
Disseminated disease

Chorioretinitis → cataracts
Vesicular lesions [SKIN, EYES, MOUTH]
CNS signs
Disseminated infection signs
Microcephaly, microphthalmia, LBW

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13
Q

What is the management for HSV in pregnancy

A

<28w first genital herpes: start antiviral medication from 36w until birth, vaginal delivery allowed
>28w first genital herpes: continue antivirals until baby is born, may require ELCS
Recurrent genital infection → can deliver vaginally

Treatment: IV Aciclovir

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14
Q

What are the clinical features of congenital parvovirus B19 infection

A

Severe haemolytic anaemia → heart failure → oedema → Hydrops fetalis
Thrombocytopenia → petechial rash

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15
Q

What is the management for congenital Parvovirus B19 infection

A

FBS and intrauterine blood transfusion if severe foetal anaemia and hydrops in USS.
Risk of 1% foetal loss due to this procedure.

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16
Q

What are the features of congenital varicella

A

Chorioretinitis → cataracts
Microcephaly
Limb hypoplasia
IUGR
Cutaneous scarring

17
Q

What is the management for congenital varicella

A

Aciclovir

18
Q

What are the features of congenital HIV

A

Congenital immunodeficiency
Recurrent infections
Presents at 6m – diarrhoea, failure to thrive, fevers, lymphadenopathy, etc.

19
Q

What is group B streptococcus

A

Gram positive streptococcus characterised by presence of Group B Lancefield antigen – streptococcus agalactiae
Gram +ve cocci in chains

20
Q

What are the risk factors for GBS infection

A

GBS in a previous baby
Prematurity
Rupture of membranes >24 hours before delivery
Pyrexia during labour
Positive test for GBS in the mother
Mother diagnosed with a UTI found to be GBS during pregnancy

21
Q

What are the symptoms of GBS infection

A

Often asymptomatic and found incidentally
UTI: frequency, nocturia, dysuria
Chorioamnionitis
Endometritis

22
Q

What investigations should be done for GBS

A

Bedside: high vaginal swab, urine dip and MC&S, rectal swab
Bloods: FBC, CRP, U&Es, G&S, Blood cultures, ABG/VBG, coagulation screen, HIV screen
Other: CTG

23
Q

What is the screening procedure for GBS in pregnancy

A

Universal screening is not offered and maternal request is not indication
Previous GBS → intrapartum antibiotic prophylaxis (IAP) OR testing in late pregnancy
Swab for GBS 35-37 weeks or 3-5 weeks prior to delivery date

24
Q

What are the indications for GBS prophylaxis

A

Intrapartum fever
Prolonged rupture of membranes >18 hours
Prematurity <37 weeks
Previous infant with GBS
GBS bacteriuria

25
Q

What is the management for a positive vaginal or rectal swab for GBS

A

Antibiotics during labour
Antenatal prophylactic treatment NOT indicated (does not reduce likelihood of GBS colonisation at time of delivery)
(IV benzylpenicillin, alt: vancomycin)

26
Q

What is the management for urine infection with GBS

A

Antibiotics before and during labour (IV benzylpenicillin, alt: vancomycin)

27
Q

What is the management for a previous pregnancy with GBS

A

Previous foetal GBS: Abx in labour
No foetal infection: IV ABx in labour or swab at 35-37 weeks
(IV benzylpenicillin, alt: vancomycin)

28
Q

What is the management for SROM in a woman who is known GBS positive

A

Offer IOL immediately

29
Q

What is the management for preterm labour in a woman with GBS

A

IV Abx in labour (IV benzylpenicillin, alt: vancomycin)

30
Q

What is the management for GBS in a woman for ELCS

A

No Abx prophylaxis required

31
Q

What is the follow up advice after GBS in pregnancy

A

Full term + antibiotics > 4 hours before delivery → no indication for prolonged neonatal monitoring
Full term + antibiotics < 4 hours before delivery → Neonatal vitals need monitoring
High risk of foetal infection → Monitoring for at least 12 hours
Previous foetal GBS infection → monitoring for at least 12 hours

32
Q

What monitoring should be done for children in women with GBS

A

1 risk factor → remain in hospital for at least 24 hours for observations
≥2 risk factors or one red flag → sepsis ABx + septic screen ( )
GOSH ABx in neonate <72 hours = cefotaxime + amikacin + ampicillin

33
Q

How is HIV in pregnancy treated

A

Start on combination antiretroviral therapy (cART) asap
Viral load <50 → vaginal delivery recommended
>50 → ELCS recommended
Post-exposure prophylaxis for the baby → zidovudine monotherapy or cART
Breastfeeding not recommended but may be supported if on ongoing therapy