Neonatology, preterm & low birth weight babies Flashcards

1
Q

Primary cause of death in preterm infants (<26wks)

A

RDS+-IVH+-Infection (29%) - down from 31% in 1995
Pulmonary insufficiency (22%) - down from 34% in 1995
Infection (16%) - up from 8% in 1995
NEC (12%) - up from 4% in 1995

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2
Q

Causes of Mortality in low birth weight infants

A

Prematurity – System immaturity or complications of prematurity
Small for gestational age – Underlying cause of prematurity or inadequate growth

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3
Q

Regulatory problems in preterm infants

A

Homeostasis - skin integrity, heat loss & energy use

Fluid Balance - skin integrity or renal immaturity

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4
Q

Respiratory problems in preterm infants

A

Apnoea/poor respiratory effort (central factors) or poor muscle bulk (peripheral)
Surfactant deficiency or bronchopulmonary dysplasia
Infections or air leak leading to pneumothorax

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5
Q

Respiratory/Hyaline distress syndrome (RDS)

A

Surfactant deficiency – common cause of death
Worse with: greater prematurity, boys, caucasians, second twins
Worsened by: Hypothermia, treatment delay, infection

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6
Q

Chronic lung disease of prematurity

A

A broad term used to describe ongoing respiratory symptoms at 36wks post-menstrual age most commonly in infants who have needed mechanical ventilation - used to be called chronic pulmonary dysplasia

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7
Q

Respiratory/Hyaline distress syndrome - management

A

Antenatal steroids to mature the lungs – reduces RDS and mortality by 50%
Surfactant replacement – reduces mortality & pneumothorax by 40%
Ventilation – CPAP, conventional ventilation, high frequency oscillation

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8
Q

Gastro-intestinal problems in preterm infants

A

Feed intolerance
Poor growth
Gastro-oesophageal reflux
Necrotising enterocolitis (NEC)

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9
Q

Causes of Chronic lung disease of prematurity (5)

A

Immature lungs, surfactant deficiency, ventilator induced lung injury (barotrauma, volutrauma, atelectotrauma)
Infection or inflammation

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10
Q

Breast milk in preterm babies

A

Better feeding tolerance and trophic to immature gut –> Reduces infection and NEC risk. Nutritionally matched to gestation
Possibly improves metabolic/endocrine adaptation to life ex-utero and promotes brain growth

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11
Q

Necrotising Enterocolitis (NEC)

A

4-8% of preterm babies, 10% of those under 1.5kg
Increased risk with increasing immaturity & IUGR
Pathogenesis –> Mucosal injury, bowel ischemia, presence of bacteria. 20-40% mortality

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12
Q

Intraventricular haemorrhage (IVH)

A

– 25% of VLBW babies
Post IVH - 15% Haemorrhagic parenchymal infarction (HPI)
- 14% Post-haemorrhagic hydrocephalus (PHH)

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13
Q

Periventricular leuomalacia

A

2-10% of VLBW babies – depending on maturity

Necrosis and coagulation of periventricular white matter

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14
Q

Risk of brain injury in premature infants is increased by?

A

Increasing immaturity. Infection. Ischaemia . Hypotension. Antenatal steroids are protective

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15
Q

Long term prognosis of brain injury in premature infants?

A

Cerebral palsy – spastic diplegia or hemiparesis. Cognitive impairments or learning difficulties. Visuospatial problems
Attention deficit and behavioural problems. Require multi-disciplinary support at home and at school

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16
Q

Retinopathy of prematurity

A

60-70% of VLBW babies – only 6% require treatment
untreated 50% will progress to retinal detachment and visual loss
Risk increased by prematurity, hypoxia and severe illness

17
Q

Retinopathy of prematurity – screening

A

All babies under 31wks or under 1500g

18
Q

Retinopathy of prematurity – treatment

A

Start at 6-7wks post-natal age

Use lasers for stage 3 and worse or for progressive disease

19
Q

Long term prognosis for respiratory disease

A

May require long term domiciliary oxygen
50% will have persistent wheeze or respiratory symptoms during infancy
50% will be rehospitalised for viral infections
The impact on lung function is still detectable at school age

20
Q

Long term prognosis for gastrointestinal disease

A

Persistent growth restriction and poor nutrition
Poor feeding due to: aversion, reflux, respiratory compromise, neurological problems, malabsorption after intestinal surgery

21
Q

IUGR

A

Due to placental insufficiency (illness or smoking)
Have general problems from being small (temp control or hypoglycaemia) and specific issues (NEC, HIE, haematological problems)
Can lead to preterm birth

22
Q

Physiological changes at birth

A

Cry in response to trauma –> fluid in the alveoli is rapidly absorbed
Clamping the cord –> removes low pressure umbilical circulation increasing systemic blood pressure

23
Q

Perinatal asphyxia

A

1 in 10 term babies need assistance – 1% need prolonged resuscitation – 30% of these have multi-organ hypoxia
Biggest risk is HIE

24
Q

Sarnat classification of HIE

A

Grade 1 – Mild (irritable, hyperalert)
Grade 2 – Moderate (lethargy, hypotonia, seizures)
Grade 3 – Severe (stuporous, absent reflexes, reduced background EEG activity)

25
Q

Neonatal sepsis

A

Before 7 days old implies vertical transmission (Group B strep or E coli)
clinical signs are subtle and non-specific - insidious onset
Beware meningitis

26
Q

Risk factors for neonatal sepsis

A

PROM >24hrs
Prematurity or low birth weight
Maternal GBS or infection, intrapartum pyrexia
Confirmed chorioamnionitis

27
Q

Group B strep (GBS) (6)

A

Most common cause of neonatal sepsis at term (within 24hrs) – very sensitive to penicillin. From the genital tract of asymptomatic mother
Rapid respiratory deterioration – lead to pulmonary HTN and possible shock or DIC. Can also have late (4-6wks) insidious onset with a poor prognosis

28
Q

Neonatal hypoglycaemia

A

Glucose below 2.6mmol/L – give 10% IV dextrose
Only need to test at risk babies – increased demand (macrosomia, polycythemia, infection, asphyxia) or decreased supply (poor feeding, IUGR, preterm, hypothermia)

29
Q

Neonatal jaundice

A

Common (60%) of term babies – if early (<48hrs) indicates infection or haemolysis and should be investigated
Can be conjugated (biliary atresia) or unconjugated

30
Q

Causes of unconjugated neonatal jaundice (4)

A

Isoimmunisation (ABO, rhesus or anti-C)
RBC defects – G6P deficiency or spherocytosis/epllipocytosis
Infection
Sequestered blood - cephalohematoma, large IVH, subdural

31
Q

Spherocytosis

A

A haemolytic anaemia where a autosomal dominant defect in the cytoskeleton of RBCs causes them to be spherical leading to splenic destruction and osmotic fragility – this causes chronic haemolytic anaemia. Northern european descent. Can also have gallstones, splenomegaly, chronic symptoms through haemolytic crises can be triggered by infection.

32
Q

Treatment for neonatal jaundice

A

Milk – increases bile excretion
Adequate hydration
phototherapy
Rarely exchange transfusions are required.

33
Q

Breast feeding jaundice vs breast-milk jaundice

A

Breast feeding jaundice is an early onset jaundice due to poor milk supply from first time mothers causing mild dehydration
Breast-milk jaundice is late onset where maternal hormones in breast milk slow bilirubin metabolism

34
Q

Common neonatal viral infections

A

Herpes simplex (local or disseminated)
CMV – most common
Varicella – should be protected by maternal IgG
Also – rubella, hepatitis A, B ,C and HIV

35
Q

Risks of maternal HIV

A

Maternal screening and treatment will reduce risk
Vertical transmission reduced with – keeping maternal viral load low, prevent PROM but early elective C-section
Post natal AZT therapy for 4 weeks and avoid breast feeding