Congenital, perinatal, neonatal infections Flashcards

1
Q

What are examples of congenital infections

A

Rubella
Cytomegalovirus (CMV)
Toxoplasma gondii
Parvovirus
Varicella zoster
Syphilis

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2
Q

What are the features of congenital rubella infection

A

Risk and extent of foetal damage are determined by gestational age at onset of maternal infection
<8 weeks gestation:
- Deafness
- Congenital heart disease
- Cataracts
13-16 weeks gestation:
- Impaired hearing
- Beyond 18 weeks, risk to the foetus is minimal

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3
Q

What investigations and treatment should be done for rubella

A

Seroconversion on screening serology
Blood serology for IgM
Amniocentesis or CVS
PCR
Infant urine testing

Prevention via the MMR programme (13-14 months and 3 years)

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4
Q

What are the features of congenital CMV

A

Most common congenital infection (0.5/1000 in the UK)
DNA virus from the herpes family (HHV-5)
90% will have a normal birth and develop normally
5% have clinical features at birth
- Hepatosplenomegaly
- Petechiae
- Jaundice ± blueberry muffin rash
- IUGR
- Chorioretinitis → cataracts
- Neurodevelopmental disabilities e.g. sensorineural hearing loss, cerebral palsy, epilepsy, cognitive impairment
- PERIVENTRICULAR calcifications
5% develop problems later e.g. sensorineural hearing loss

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5
Q

What investigations should be done for congenital CMV

A

Seroconversion on screening serology
Blood serology for IgM
Amniocentesis or CVS
Infant urine testing for PCR

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6
Q

What is the management for congenital CMV

A

Infants: Early antiviral therapy with oral valganciclovir for 6 months or IV ganciclovir

+ audiology follow up
+ ophthalmology follow up

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7
Q

What is Toxoplasma gondii and what are the causes

A

Protozoan parasite
Consumption of raw or undercooked meat and contact with faeces of infected cats
Increased risk of vertical transmission with increasing gestational age (5% 1st, 80% 3rd trimester)
- Infection in 1st trimester- most likely to cause foetal damage but transmission rate is LOW (10%)
- In 3rd trimester- risk of foetal damage is low (10%) but transmission MUCH higher (85%)
Risk of congenital toxoplasmosis reduced with increasing gestational age (60-80% 1st, 5% 3rd)

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8
Q

What are the clinical features of congenital toxoplasmosis

A

Most infected infants are asymptomatic, but 10% may have manifestations such as (The 4C’s):
- Retinopathy, an acute fundal chorioretinitis, which sometimes interferes with vision
- Cerebral scattered calcification (Tram-like)
- Hydrocephalus (microcephaly)
- Convulsions
+ hepatosplenomegaly/jaundice

Infants will usually have long-term neurological disabilities e.g. deafness, low IQ, microcephaly

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9
Q

What are the investigations for congenital toxoplasmosis

A

Not usually screened
Sabin Feldmann Dye test
Bloods: IgM (active), IgG(immunity)
US: foetal anomaly scan
Amniocentesis + PCR to detect foetal infection

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10
Q

What is the management for toxoplasmosis

A

Pyrimethamine and sulfadiazine + calcium folinate for 1 year

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

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11
Q

What are the features of parvovirus B19 infection

A

Up to 75% of women are immune to parvovirus B19
Infection is rare and usually uneventful
Can cause:
- Spontaneous miscarriage
- Stillbirth
- Hydrops fetalis (oedema and ascites from HF)

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12
Q

What is the management for antenatal parvovirus B19 infection

A

Infection identified → serial ultrasound monitoring to detect foetal anaemia and need for intrauterine transfusion

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13
Q

What are the features of congenital varicella zoster

A

<20 weeks
- Severe scarring of the skin
- Ocular damage
- Neurological damage
- Digital dysplasia

Last 4 weeks of pregnancy + 7 days after delivery - foetus is unprotected by maternal Abx
- Vesicular rash
- High mortality rate

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14
Q

What is the management for congenital varicella zoster

A

Varicella zoster Immunoglobulin
Treatment with aciclovir

Foetus: VZIG + monitoring + aciclovir for signs of infection

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15
Q

What are the features of congenital syphilis

A

Gram-ve spirochete (Treponema pallidum)
Transmission is via sexual contact, vertically, or blood-bourne

Rash on the soles of the feet and hands
Bone lesions
Bloody rhinitis
Hepatosplenomegaly
Glomerulonephritis
“Hutchinson’s teeth” (small, widely spaced, notched)
Frontal bossing of skull, saddle-nose
“Saber’s shins” (anterior bowing)
“Clutton’s joints” (symmetrical knee swelling)

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16
Q

What investigations should be done for congenital syphilis

A

Microbiolgy: Dark-ground (from chancre)
PCR +ve
Infant TP syphilis IgM test

17
Q

What is the management for congenital syphilis

A

If mothers with syphilis identified on antenatal screening are fully treated 1 month or more before delivery, the infant does not require treatment and has an excellent prognosis
If there is any doubt about the adequacy of maternal treatment, the infant should be treated with penicillin.

IV benzylpenicillin

18
Q

What are the risk factors for neonatal infection

A

Mothers previously had baby with invasive GBS
Current GBS colonisation, bacteriuria or infection in current pregnancy
Prelabour rupture of membranes
Intrapartum temperature ≥ 38oC or suspected chorioamnionitis
Rupture of membranes ≥ 18 hours
Premature (< 37 weeks)
Suspected or confirmed infection in another baby in case of multiple pregnancy

19
Q

Why are preterm infants at an increase risk of infection

A

IgG is mostly transferred across the placenta in the last trimester, with no IgA or IgM transfer
Infection in or around the cervix is also a cause of preterm labour
Higher risk of nosocomial infection, often associated with indwelling catheters of mechanical ventilation

Contributes to bronchopulmonary dysplasia, brain injury and later disability

20
Q

What are the causes of early neonatal sepsis

A

Early-onset (<72h after birth)
- Group B Strep
- E. Coli
- Klebsiella
- Pseudomonas
- listeria monocytogenes
Vertical exposure from ascending infection or exposure to high bacterial load during birth, after ROM

21
Q

What are the causes of late-onset sepsis

A

Late-onset (>72h)
- Coagulase-negative staphylococcus (CONS) - staph. epidermis
- Staph aureus
- Enterococcus faecalis
- E. Coli
- Pseudomonas
- Klebsiella

Transmission from contamination by staff, ventral venous catheters, invasive procedures and tracheal tubes

22
Q

What are the signs of neonatal sepsis

A

Respiratory distress: Tachypnoea (>60), Intercostal recessions, Grunting, Cyanosis
Temperature instability (hypothermia to hyperthermia)
Poor feeding, irritability, lethargy, drowsiness
Vomiting
Apnoea and bradycardia
Abdominal distension
Shock
Jaundice
Seizures

Meningitis: tense or bulging fontanelle, head retraction (opisthotonos)

23
Q

What are the red flags for neonatal sepsis and what should be done if they are present

A

RR >60 min-1 or >5 below normal, or grunting
Oxygen needed to maintain saturations >92 %
Pale/mottled or non-blanching (purpuric) rash
Prolonged capillary refill >5 seconds
Hypotension
AVPU = V, P or U
Abnormal behaviour*
Blood lactate >2mmol/L

→ immediate sepsis 6 pathway

24
Q

What is the management for neonatal sepsis

A

Admit
A-E
Involve seniors
Initiate sepsis 6 (Within 1 hours):
1. Administer high flow oxygen
2. Gain IV or IO access and order:
- Blood cultures (BEFORE Abx)
- Blood glucose, lactate (VBG/ABG), FBC, CRP, U&Es, Creatinine, Clotting screen
3. Administer broad-spectrum antibiotic* within one hour of sepsis recognition + monitor response by using CRP
4. Measure Fluids
- Given in hypotension or lactate >4mm/l
- Initial minimum 20ml/kg crystalloid 0.9% NaCl bolus over 5-10 minutes
- Vasopressors for hypotension that does not respond to fluid resuscitation
- Measure urine output
5. Involve seniors
6. Consider inotropic support

25
Q

What are the antibiotic regimens for neonatal sepsis

A

Early onset
- IV Benzylpenicillin + Gentamicin
- Stop after 36-48h if cultures and CRP are negative
Late onset
- First line: Abx - flucloxacillin + gentamicin
- Second line: specific Abx (e.g. vancomycin for CONS/enterococci) or *broad-spectrum Abx e.g. meropenem

26
Q

Describe transmission of congenital HIV

A

present in vaginal fluid, semen, blood, breast milk → transmission through sexual contact, BB, vertical
Less transmission through vaginal mucosa than through anal mucosa
HIGHEST risk of transmission if mother is newly diagnosed at the beginning of pregnancy or near delivery (as viral load is extremely high in acute phase of infection)

27
Q

what are the signs and symptoms of congenital HIV

A

Recurrent and severe infection
Unusual rash
Hepatosplenomegaly

28
Q

What is the management for congenital HIV

A

Decision to treat with PEP based on guidelines (i.e. only ‘considered’ if penetrative vaginal intercourse)
Cord clamped as soon as possible and baby bathed immediately after birth
Zidovudine monotherapy for 2-4w (low/medium risk) OR 4w PEP combination (high risk/confirmed)
Women not to breastfeed
Give all immunisations including BCG (unless a moderate-high risk of transmission)
Confirm or deny diagnosis of HIV in the neonate with direct viral amplification by PCR
(normally carried out at birth, on discharge, 6 weeks, and 6 months)

29
Q

What is the management for babies born to mothers with viral hepatitis

A

Hep B: HBV IVIG within 12h of birth + vaccinate at birth, 1 month, 6 months + serological test at 12 months
Hep A: resolves within 6 months
± phototherapy/exchange therapy

30
Q

What are the signs and symptoms of congenital HSV

A

Microcephaly
Encephalomalacia
Hydranencephaly and/or intracranial calcification
Scarring, active lesions, hypo- and hyperpigmentation
Microphthalmia, retinal dysplasia, optic atrophy and/or chorioretinitis

31
Q

What are the signs and symptoms of neonatal HSV infection

A

Skin/eye/mouth (SEM) disease: blistering vesicular rash, chorioretinitis
CNS disease ± SEM:
- Seizures
- Lethargy
- Presents 10d-4w postpartum
- Irritability
- Poor feeding
- Temperature instability
- Bulging fontanelle
Disseminated infection: encephalitis, CNS, hepatitis, pneumonitis, no skin lesions, DIC

32
Q

What is the management for congenital HSV infection

A

IV aciclovir to child (14d if SEM disease  21d if CNS or disseminated)

+ monitor neutrophil count

33
Q

What is the aetiology of neonatal GBS

A

Commensal bacterium of vagina and rectum carried by 25% women
Majority of babies who come into contact are not affected (some become colonised, minority become ill)
This is particularly dangerous if acquired around the time of delivery
Transmission occurs between the time of rupture of membranes to delivery
It is the most common cause of severe early-onset (within 7 days of delivery) infection in newborns 

34
Q

What is the management for GBS

A

Postpartum – new-borns with:
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

35
Q

Describe listeriosis

A

Found in soil, decayed matter and animals
People with reduced cell-mediated immunity (i.e. pregnant women, neonates) are most at risk
Faecal-oral transmission (soft cheese, pate, unpasteurised dairy products, unwashed salads)
Vertical (transplacental or during delivery (ascending route through the cervix))

36
Q

What are the signs and symptoms of neonatal listeriosis

A

fever
Lethargy
Irritability
Diarrhoea
poor feeding
Vomiting
respiratory distress
skin rash - widely spread, small, pale nodules (granulomatosis infantiseptica)

37
Q

What is the management for neonatal listeriosis

A

IV ampicillin 2 g hourly for 14 days (or IV amoxicillin 6g/day) + gentamicin