Neonatology pt 2 Flashcards

1
Q

Pathophysiology of respiratory distress syndrome?

A

Inaqequate surfactant leading to high surface tension within alveoli. This causes atelectasis leading to hypoxia, hypercapnia and distress.
CXR shows ground glass appearance.

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2
Q

What is the management of respiratory distress dyndrome?

A

Antepartum maternal steroids if preterm labour is suspected/confirmed.
Neonates may need intubation and ventilation, endotracheal surfactant, CPAP and supplimentary O2.

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3
Q

What are the complications of respiratory distress syndrome?

A

Short term - pneumothorax, infection, apnoea, intraventricular haemorrhage, pulmonary haemorrhage, necrotising entercolitis.

Long term - Chronic lung disease of prematurity, retinopathy of prematurity, neurological, hearing and visual impairment.

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4
Q

what are the causes of hypoxic-ischaemic encephalopathy?

A

Anything that leads to asphyxia to the brain, eg,
Maternal shock, intrapartum haemorrhage, prolapsed cord, nuchal cord.

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5
Q

Management of HIE?

A

Supportive care
Theraputic hypothermia - cooling blankets/hat. Aim for temp of 33-34. Continued for 72 hours. This reduced inflammation and neuronal loss after a hypoxic injury. reduces risk of cerebral palsy, developmental delat, learning disibilities and death

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6
Q

What is necrotising enterocolitis and its risk factors?

A

Disorder in neonates where part of bowel becomes necrotic - can lead to perforation.
Risk factors - very low birth weight or prematurity, formula feeds, respiratory distress, sepsis, congenital heart disease

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7
Q

Presentation of necrotising enterocolitis?

A

Intolerance to feeds,
Vomiting - green bile,
Distended, tender abdomen,
Absent bowel sounds.
Blood in stool

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8
Q

Investigations for necrotising enterocolitis?

A

Bloods: FBC, CRP, capillary blood gas, blood cultures.
Abdominal x-ray (ix of choice) - dilated bowel loops, bowel wall oedema, pneumatosis intestinalis (intramural gas), pneumoperitoneam, football sign

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9
Q

Management of necrotising enterocolitis?

A

NBM
IV fluids
TPN
Abx,
NG tube to drain fluid/gas.
Immediate referral to surgical team.

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10
Q

Complications of necrotising enterocolitis?

A

Perforation and peritonitis,
Sepsis,
Death,
Strictures,
Abscess formation,
Recurrance,
long term stoma
Short bowel syndrome

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11
Q

Describe features of meconium aspiration syndrome?

A

Respiratory distress due to meconium in trachea.
More common in postnatal deliveries.
Ix: Assess amniotic fluid for presence of meconium and CXT for assessment of lungs.
Rx: Immediate suctioning after birth, O2 therapy and antibiotics

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12
Q

Describe features of meconium ileus

A

Thickening of meconium causing obstruction in neonatal bowel. Early indicator of CF.
Symptoms: bilious vomiting, distended abdomen and failure to pass meconium.
Ix: Abdo X ray/US for diagnosis and sweat test for CF.
Rx: Surgery to remove obstruction

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13
Q

Risk factors for neonatal sepsis?

A

Vaginal GBS colonisation.
GBS in previous baby.
Maternal sepsis, chorioamnionitis or fever > 38 degrees.
Prematurity.
PPROM.

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14
Q

Clinical features of neonatal sepsis

A

Fever - not a reliable sign as can vary from elevated, normal or low.
Reduced tone and activity,
Poor feeding,
Resp distress or apnoea,
Vomiting,
Tachycardia or bradycardia,
Hypoxia,
Jaundice within 24hr,
Seizures,
Hypoglycaemia.

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15
Q

Causes of early/late onset sepsis in the neonate?

A

Early - GBS.
Late - commonly coagulase negative staph (S. epidermidis) or gram negative bacteria eg, pseudomonas aeruginosa, klebsiella or enterobacter.

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16
Q

Investigations for neonatal sepsis?

A

Blood cultures
FBC
CRP
Blood gases
Urine M,C&S
LP

17
Q

Management of neonatal sepsis?

A

IV benzylpenicillin with gentamicin.
CRP should be remeasured at 24h
Blood cultures remeasured at 36hr.
Consider stopping abx if baby is clinically well, blood cultures negative and CRP < 10.

18
Q

Types of spina bifida?

A

Spina bifida occulta - incomplete fusion of vertebrae but no herniation of spinal cord.
Meningocele - incomplete fusion of vertebra with herniation of meningeal sac containing CSF
Myelomeningocele - incomplete fusion of vertebrae with herniation of meningeal sac containing CSF and spinal cord
Managed with surgery

19
Q

Clinical manifestations of spina bifida

A

Neurological - motor deficits, sensory deficits, neurological bladder/bowel, hydrocephalus, seizures.
MSK - Increased risk of hip subluxattion, scoliosis and contractures.

20
Q

What is Talipes and the two types?

A

‘Clubfoot’ - fixed, abnormal ankle position present at birth.
Talipes equinovarus - plantar flexion and supination.
Talipes calcaneovalgus - dorsiflextion and pronation

21
Q

Talipes assocations?

A

Spina bifida,
Cerebral palsy,
Edward syndrome,
oligohydramnios,
Arthrogryposis

22
Q

Management of talipes?

A

Conservative methods eg, Ponseti method - manipulation and progressive casting starting soon after birth.
Achilles tenotomy performed at some point.
Brace used to hold feet in place until child is age 4 years old.