Neonatal Flashcards

1
Q

What is the difference between cephalhaematoma and caput succedaneum?

A
  • Both are non-concerning injuries causes by birthing trauma (instruments)
  • Caput succedaneum is associated with venous delivery and it extends across suture lines (like a cap). It is self-limiting (few days)
  • Cephalhaematoma is a subperiosteal bleed limited by suture lines (one side. Self limiting (couple of weeks-longer because bound by periosteum)
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2
Q

What is an example of a pathological, concerning head trauma associated with birthing injury?

A

If the birth is particularly traumatic it can cause Intraventricular haemorrhage (IVH):

  • Bleeding into the ventricles of the brain - as blood pools here it can clot and cause blockage to the drainage of CSF.
  • This can lead to hydrocephalus
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3
Q

What is the most common nerve palsy associated with traumatic delivery? Describe it and suggest management.

A

ERB’S PALSY - damage to C5, C6 nerve roots - associated with shoulder dystocia

  • The arm is flaccid, the forearm is pronated and the wrist flexed - WAITER’S TIP
  • Prognosis depends on damage (physio may resolve or may be there for life)
  • Important to get an x-ray of the clavicle to exclude fractures
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4
Q

What other nerve palsies can occur with traumatic delivery?

A

FACIAL NERVE PALSY - following pressure on the face from maternal ischial spines or forcept

  • FACIAL ASYMMETRY worse on crying
  • Majority will recovery within a week or 2 but they might need some ophthalmological input
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5
Q

What are some of the most common fractures for baby’s to get during a traumatic delivery and how should they be managed?

A

CLAVICLE - not uncommon with big babies, they need to be immobilised - have their arm inside their baby grow and usually have healed in a few weeks
AVULSION FRACTURES of the humeral or femoral epiphysis is also not uncommon
SKULL FRACTURES - slight risk with forceps - consider neuro r/v

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6
Q

What is the most common cause of birth asphyxia?

A

Drop in maternal blood flow during delivery

- Excessive haemorrhage

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7
Q

What sorts of problems might birth asphyxia cause?

A

Developmental delay
Intellectual delay
Physical problems e.g. spasticity - CEREBRAL PALSY

RISK OF HYPOXIC ISCHAEMIC ENCEPHALOPATHY (HIE)

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8
Q

What are some risk factors for birth asphyxia?

A
Elderly or young mothers 
Prolonged rupture of membranes 
Meconium stained fluid 
Multiple births 
Lack of antenatal care 
Low birth weight 
Malpresentation 
Use of oxytocin augmentation in labour 
APH 
Pre-eclampsia and eclampsia 
Anaemia
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9
Q

What causes HIE?

A

PERI-NATAL ASPHYXIA either due to poor pulmonary gas exchange in the newborn or poor placental perfusion in the mother
This leads to decreased cardio-respiratory effort> hypoxia> hypercapnia> metabolic acidosis>hypo perfusion>end organ ischaemia in the brain - HIE

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10
Q

What are the affects of HIE and what can we do to counter these?

A
  • Neurodisability as well as death in the infant
  • Immediate (primary) neuronal death from the hypoxic injury or further death of these tissues might occur when due to re-perfusion injury
  • We can try and protect/delay this secondary injury with THERAPEUTIC COOLING to induce hypothermia
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11
Q

What are some SPECIFIC causes of HIE?

A

What are some of the causes?
- Failure of gaseous exchange across the placenta
○ Placental abruption
○ Ruptured uterus
- Interruption of umbilical blood flow
○ Excessive or prolonged uterine contractions
○ Cord compression
○ Cord prolapse
○ Shoulder dystocia
- Inadequate maternal placental perfusion
○ Maternal hypotension or hypertension
○ This is often associated with intrauterine growth restriction
- Compromised fetus
○ Anemia
○ IUGR (intra uterine growth restriction)
○ Failure to breath at birth
- CAN BE CAUSES BY NEONATAL CONDITION
○ Inborn error of metabolism
Kernicterus

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12
Q

When and how will we know HIE has occurred (features)?

A
1. Mild:
○ Responding excessively to stimulation 
○ Staring of the eyes 
○ Irritable 
○ Hyperventilation 
○ Impaired feeding 
2. Moderate:  ○ Marked abnormalities of tone and movement ○ Cannot feed  ○ May have seizures 

3. Severe:  ○ No normal spontaneous movements or responses to pain ○ Tone in the limbs may fluctuate between hypertonia and hypotonia ○ Seizures are prolonged and often not responsive to treatment ○Multi-organ failure is often present
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13
Q

How should we manage HIE?

A
  • Resuscitation and stabilisation
  • COOLING (32 degrees for 72 hours)
  • Respiratory support
  • EEG monitoring -identify seizures and encephalopathy
  • Treat seizures if they have
  • Fluid restriction because of renal impairment, prevent odema (40ml a day)
  • Moniter and treat electrolyte inbalance
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14
Q

What is the prognosis for babies with HIE?

A
  • Complete recovery can be expected if babies have MILD HIE
  • In some moderate cases there will be partial recovery in the first 2 weeks (although there is not likely to be any recovery after this time)
  • PERFORM MRI at day 4 and day 14 - if significant abnormalities exist bilaterally in the basal ganglia, thalamus and internal capsule (lack of myelin) then this is a strong predator of CEREBRAL PALSY
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15
Q

When should APGAR scoring be done?

A

1, 5 and 10 minutes

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16
Q

What are the categories in APGAR scoring and how are they scored?

A

Activity/Muscle tone

  • none=0
  • flexed arms and legs=1
  • active =2

Pulse
-absent=0
<100bpm=1
>100bpm=2

Grimace/Reflex irritability to stimuli
No response=0
Minimal response to stimuli=1
prompt response to stimuli=2

Appearance/Colour
Blue/pale=0
Pink centrally but with slightly blue peripheries =1
pink all over =2

Respiration
none=0
infrequent and irregular =1
normal (vigourous cry)=2

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17
Q

What is a normal APGAR score?

A

An ideally healthy baby should score 10, however scores of 7+ are normal

-Very often even health babies have slightly blue extremities, this loses them a point on appearance but is not often a cause for concern.

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18
Q

What is necrotising entircolitis (NEC)?

When and who does NEC usually occur?

A
  • Gut gets inflamed and starts to die

- In premature babies and it will often develop in the first few weeks of life. More common in cows milk fed babies

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19
Q

What are some features of NEC?

A
Stopping tolerating feeds 
Aspiration 
Vomit +/- bile stained 
Abdominal distension 
Fresh blood in the stool
SHOCKED - due to distension and pain
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20
Q

How should we investigate NEC?

A

AXR

  • Will see distended loops of bowel
  • Thickening of the bowel wall due to intra-mural gas
  • Gas in the portal tract
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21
Q

How should we treat NEC?

A
Stop oral feeding (TPN)
Broad spectrum abx (aerobic and anaerobic bacteria) 
Ventilatory support 
Cardiovascular support 
Danger of BOWEL PERF - refer to surgery
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22
Q

What can be offered antenatally to help prevent NEC?

A

Erythromycin

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23
Q

What is the prognosis in infants with NEC? Long-term complications?

A
-Mortality rate is about 20%
LONG TERM SEQUELAE: 
-Strictures
-Malabsorption
-Short bowel syndrome as consequence of surgery
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24
Q

What is the first thing you should do when resuscitating a newborn?

A

DRY THE BABY

Then assess breathing, heart rate and tone

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25
Q

Newborn resuscitation: After drying it what is the next stage in neonatal resuscitation?

A
  • Optimise airway (face parallel to surface)
  • Assess tone, resp and heart rate
  • ADMINISTER 5 RESCUE BREATHS
  • Repeat this, improving manoeuvres and considering intubation until the chest is seen to rise
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26
Q

Newborn resuscitation: Spontaneous ventilation has recovered what is the next stage in neonatal resuscitation?

A
  • Assess for heart beat and if there is none, or it is low (<60bpm) begin chest compression with compression:breath ratio of 3:1
  • Re-assess for heart beat every 30 seconds until heart rate is >60bpm
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27
Q

What would you expect of the saturations of a neonate?

A

THEY ARE VERY OFTEN VERY LOW and this is not always concerning - check them to see whether they recover

Neonates also very often have something called
TRANSIENT TACHYPNOEA OF THE NEWBORN (TTN) where grunting or occasional nasal flaring might occur
- monitor reps rate and sats and respond accordingly

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28
Q

What % of babies are jaundiced and is this always concerning?

A

60% babies jaundiced - very often this is physiological

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29
Q

Should you be concerned about jaundice in the first 24h of life??

A

YES - jaundice in the first 24h of life is ALWAYS PATHOLOGICAL

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30
Q

Describe why physiological jaundice occurs?

A

When babies are born they have

  • high levels of RBC
  • high turnover rate
  • low liver maturity so cant congegate (build up of uncongegated bilirubin that cannot be excreted)
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31
Q

When will physiological jaundice occur? and when will it go?

A

Physiological jaundice will happen in the first 2-3 days of life and it should disappear after 10 days as the liver matures

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32
Q

What should we do if a baby (older than 24 hours) has jaundice?

A

Reassure parents

  • very common and harmless
  • self limiting should go away after ten days
  • more common in pre term and breast fed babies

Investigations
-look at bilirubin levels (bilirubinometer) to to see whether it reaches the threshold for treatment (use a bilirubin threshold graph specifically for gestational age)
-DIrect antiglobin Coombs test
-FBC and blood film TFT LFT Us&Es
-Urine dipstick (glucose and infection-do a culture)
particularly common in breast-fed babies (might be slightly dehydrated)

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33
Q

What are some causes of early jaundice/heamolytic disease of newborn

A

Causes of early jaundice
-Sepsis
-ABO incompatibility and Rh disease (heamolytic anaemia)
-Polycythemia (IDM)
-RBC deformities (G6DP (mainly males)/Hereditary spherocytosis)
-Cephalohematoma
SHOULD INVESTIGATE FOR ALL OF THESE

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34
Q

When do we deem it prolonged jaundice?

A
  • Once it has lasted for longer than 2 weeks (14 days)

- OR longer than 3 weeks (21 days) in a pre-term baby

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35
Q

What are some causes of prolonged jaundice?

A
  • Biliary atresia (increased congegated-surgical emergency)
  • Breast-milk jaundice (should investigate for liver disease extensively before just calling it this)
  • Breast milk failure
  • G6PD deficiency
  • Gilberts disease (reduced production of liver enzymes)
  • Crigler-najjar syndrome
  • Galactosemia
  • Congenital hypothyroidism
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36
Q

If you do some blood tests and find the bilirubin to be conjugated what does this mean?

A

This suggests that the cause is LIVER DISEASE (either biliary atresia (surgical emergency) or neonatal hepatitis)
- OBSTRUCTIVE JAUNDICE (pale stools and dark urine)

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37
Q

What tests/investigations should we consider in early jaundice within 24 hours?

A

Sepsis or heamolysis until proven otherwise

• SEPTIC SCREEN

  • Blood cultures
  • Urine cultures
  • CSF-lumbar puncture

• Screen for HEAMOLTYIC ANEMIA

  • Maternal group and antibodies
  • Group and Coombs test (direct) -if clumping its positive for rhesus
  • FBC (heamatocrit may show heamolysis. Also sepsis)
  • Blood film (Bite and blister cells in G6PD/Spherocytes in hereditory spherocytosis
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38
Q

How do we decide what treatment we need to give and when we need to give it in neonatal jaundice?

A
  • Take their bilirubin levels and plot it on a chart against their age (specific one for <38 weeks)
  • See if they reach the treatment threshold for phototherapy or even transfusion
39
Q

How often should we check bilirubin levels in neonates with jaundice?

A

Every 12h if not concerned or every 6-8 if more worried.

40
Q

What are some complications of neonatal jaundice?

A
  • bilirubin deposition in the brain leading to a form of cerebral injury called KERNICTERUS
  • Unconjugated bilirubin collecting in the basal ganglia
41
Q

What are some symptoms of kernicterus?

A
Poor feeding
irritable
high-pitched cry
lethargy
apnoea
hypotonia
seizures 
muscle spasms
42
Q

How does phototherapy work in the treatment of jaundice?

A
  • 450nm wavelength of light given
  • Converts bilirubin into water soluble pigment that can be excreted in the urine (lumirubin)
  • Cover infants eyes and take bilirubin levels every 4-6hrs
  • breaks every 30 mins (feeding, bonding, changing)
43
Q

Why does respiratory distress occur in the newborn?

A
  • Occurs in prem babies when there has not been sufficient surfactant production to provide the tension necessary to keep the alveoli open
  • Alveoli collapse leading to poor ventilation of the lung and inadequate gaseous exchange
44
Q

What is done to prevent RDS?

A

-Giving corticosteroids in the likely event of premature delivery

45
Q

If RDS occurs in the newborn how do we treat it?

A
  • Give artificial surfactant down ET tubes in prem babies (often done anyway)
  • Oxygen therapy and positive airway pressures (careful monitoring to prevent retrolental fibroplasia and blindness.
46
Q

How does RDS present?

What would you see in a CXR of RDS?

A

Might not present straight away but within 4 hours of birth:

  • TACHYPNOEA (>60)
  • Laboured breathing (recession, tracheal tug, nasal flaring)
  • Expiratory grunting
  • Cyanosis if severe

CXR: A CXR is striking and characteristic with BILATERAL PNEUMOTHORACES
• Diffuse ground glass lungs with low volumes and a bell-shaped thorax
• Lung whiteout in severe cases

47
Q

What are some complications of RDS in the newborn?

A

the extensive oxygen therapy that is given can lead to RETINOPATHY OF PREMATURITY (overgrowth of vessels)
RENAL FAILURE

48
Q

What heart defect is common in RDS?

A

PDA

  • increased pulse pressure
  • systolic impulses are audible
49
Q

What are some common reasons for IUGR babies?

A
Smoking 
Pre-eclampsia 
Maternal drug or alcohol use 
Could be constitutionally small 
Genetic abnormalities 
HTN 
Cardiovascular or renal disease of mother 
Multiple pregnancy

placental insufficiency is leading cause so babies should grow okay after birth

50
Q

What would you see in asymmetrical IUGR? When does this happen?

A

Expect to see Head-Sparing effect in the baby (asymmetrical)

  • the head circumference and overall length will be normal while all other parameters are low
  • better prognosis

Causes are later in pregnancy:

  • Pre-eclampsia
  • Malnutrition
  • Chronic hypoxia (maternal smoking)
  • Multiple pregnancy
51
Q

What does a symmetrically small (small across all parameters) baby indicate? Whats the prognosis?

A

Symetrical IUGR is associated with:

  • TORCH infections
  • Chromosomal abnormalities
  • Chronic maternal drug or alcohol abuse

Poorer prognosis

52
Q

What two measurements are most likely used to diagnose IUGR?

A

AC AND EFW (estimated fetal weight)

53
Q

If the baby in utero is found to be growth restricted what investigations should be done?

A

USS Scan and fetal doppler
Karyotyping
Screening for CMV and toxoplasmosis

54
Q

How often should testing be repeated in a woman who is found to have an IUGR baby and what should this testing involve?

A

USS and umbilical artery doppler every 2 weeks - do BFP (biophysical profile: AC, HC, FL, CRL etc.)
Consider CTGs in these appointments as well (although should NOT be used alone)
Assess amniotic fluid volume

55
Q

At what age should we delivery IGUR babies?

A

If the IUGR is found before 32 weeks gestations then consider delivery at 32 weeks after giving steroids and assuming umbilical artery doppler is normal until then

IF FOUND AFTER 32 weeks then consider delivery NO LATER than 37w

56
Q

What immediate concerns do we have following the delivery of an IUGR baby?

A

Hypothermia - they need to be kept very warm. they will have thin skin and very little sub-cutaneous fat
Hypoglycaemia - this is again because of their lack of fat and their use of their hepatic glycogen stores in utero
Hypocalceamia
Polycythaemia

57
Q

What are some features of fetal alcohol syndrome?

A
Absent or small philtrum 
Small head 
Short palpebral fissures 
Epicanthal folds 
Mild ear abnormalities 
Flat nasal bridge 
Thin upper lip
Small chin (micrognathia)
58
Q

THE BABY CHECK: what questions should you ask before beginning?

A

Baby checks usually happen at 6-8 weeks…
Is the baby smiling?
Is the baby fixing and following?
Is the baby starting to try support their own head?
H+S - check the RED BOOK for the hearing assessment

Ask mother questions about birth, neonatal period, pregnancy, birth weight (putting on since?)

59
Q

What things do you need to look for on the head of the new born?

A

GENERAL INSPECTION (colour, crying, tone etc., birth marks, blue spots)

  1. Feel for suture lines and fontanelles (bulging, sagging)
  2. Measure the head circumference
  3. Look in the baby’s eyes for RED REFLEX
  4. Check inside the baby’s mouth for tongue tie, cleft palate and sucking reflex (GLOVED FINGER)
  5. Check the face for any dysmorphic features
60
Q

What things do we need to look for on the chest and torso during a baby check?

A

Look for breathing movements (symmetrical, any chest wall deformities)
Check the cap refill centrally
LISTEN to the heart and to the breathing (might want to do this earlier so baby doesn’t cry)
- Normal HR is 110-160 - listen for added sounds

Finally feel the babies abdomen, can sometimes feel liver edge and tip of spleen but not massively
ASK ABOUT MECONIUM AND POOING

61
Q

What do you feel for in the groin and hips?

A
  1. FEMORAL PULSES - are they present and equal
  2. Check SCROTUM for testicles present - if not feel up and try and find then in inguinal region, if found them here can you manipulate them down
  3. DDH - Barlow’s (push back and down) and Ortolani’s (pull back in)
  4. Check ANUS for patency
62
Q

What should you be looking for in the limbs and peripheries in the baby check?

A
  1. Check for number of fingers and toes

2. Check for tone in the limbs (moving regularly and symmetrically)

63
Q

What should you check for on the spine and neck and how should you do this?

A

Lie the baby on its front (on your hand) and see if it is attempting to hold up its own head
Also feel down the spine for any abnormalities, skin dimpling or lumps

***to further check for baby’s tone can try pull them up to sitting by their hands to check for head lag?

64
Q

What age would we expect babies to fully be able to support their own head?

A

3-4 months so some head lag on baby check is normal

65
Q

In which babies is DDH more common?

A
Girls 
First born 
Breech 
FH
Multiple pregnancy 
Oligohydramnios 

If any of these risk factors USS at birth
Pavlik harness to fix flex and slightly abduct

66
Q

What are the two types of talipes?

A

TALIPES EQUINOVARUS - feet are hyper-introverted

TALIPES CALCANEOVALGUS - ankles are hyper flexed

67
Q

What does talipes equinovarus appear like?

A
  • The feet are inverted and supinated and forefoot is adducted
  • Often bilateral and calf muscle is thinner
68
Q

What is talipes equinovarus associated with?

A
  • Oligohydramnios
  • Male sex
  • Spina bifida
  • DDH
69
Q

How is talipes equinovarus managed?

A

Bracing and casting immediately - PONSETTI METHOD

  • Usually effective and if not consider surgery
  • Also make sure to differentiate from the much rarer congenital condition VERTICAL TALUS where the foot is much stiffer and rocker-bottom in shape (Memory: rocks are vertical)
70
Q

What is talipes calcaneovalgus?

A

Foot is DORSIFLEXED and EVERTED

71
Q

How should talipes calcaneovalgus be managed?

A
  • Usually self-limiting and has just occurred due to the shape of the uterus
  • Sometimes mum can be given passive foot exercises to do
  • Association with DDH
72
Q

What is the average and minimal birth weight for a normal baby?

A

3.5kg is average

We are not concerned with any baby that is 2.5kg and above

73
Q

What is the average length of a full term baby?

A

36.5-50cm

74
Q

What might the skin of the newborn look like and what should we tell mum about this?

A

Dusky pink
Can have lanugo (body hair, will go)
Will be covered in VERNIX (almost creamy covering babies have) - NORMAL
BABY ACNE is very common in the neonatal period - this is normal. Tell mum to just wash baby with soap and water and it will go
Can have small, hard bumps called MILIA - these resolve themselves
Baby’s skin can also go PEELY - again this is normal

75
Q

When would we normally expect the baby to have passed meconium and when does it become concerning if the baby hasn’t yet passed it?

A

Normally would expect within 24 hours

Concerning if baby hasn’t passed within 48 hours - consider bowel obstruction or meconium ileum (CF)

76
Q

What changes does the fetal circulation undergo at birth?

A

Ductus venosus closes
Ductus arteriosus closes
Foramen ovale closes

DA might not close for 6-8 weeks - takes a while for the arterial pressure to build up sufficiently to close this hole.

77
Q

What condition might you consider when there is prolonged neonatal jaundice and hepatomegaly?

A

NEONATAL HEPATITIS

78
Q

What causes neonatal hepatitis?

A
Congenital infection (TORCH)
Inborn errors of metabolism 
Alpha-1 antitrypsin 
Galactoseamia 
Tyrosinaemia 
Errors of bile acid synthesis 
Progressive familial intra-hepatic cholestasis 
Cystic fibrosis
79
Q

What is one of the differentials for prolonged jaundice in the newborn and what is a useful feature to differentiate between these two?

A

Biliary atresia - common cause
Babies who have neonatal hepatitis will usually be a normal weight at birth however babies with biliary atresia will usually be low birth weight
**also hepatomegaly will usually be present from birth

80
Q

How is alpha-1 antitrypsin inherited and where around the body does it commonly affect?

A

Autosomal recessive

Affects the lungs as well as liver

81
Q

What is the pathophysiology of alpha-1 anti-trypsin?

A

A1AT is a protease inhibitor and when it is deficient the protease is more active and starts to break down vital proteins around the body

82
Q

Aside from the prolonged neonatal jaundice what is another key symptom of A1AT deficiency?

A

Bleeding - as the liver starts to fail clotting factors aren’t produced as effectively
Because bile isn’t produced as well there is poor absorption of the fat-soluble vitamin K

83
Q

What is one of the most concerning things to look for in the newborn from a mother that had diabetes mellitus during pregnancy?

A

HYPOGLYCAEMIA of the newborn - babies are used to being in very glucose rich environments and so have not adapted to managing normal concentrations of glucose

84
Q

What other cases of hypoglycaemia in the neonatal period are there?

A
Sepsis 
Prematurity 
IGUR 
Hypothermia 
Maternal labetalol
Inborn errors of metabolism 
Nesidoblastosis 
Beckwith-Weideman syndrome (overgrowth and cancer at birth)
85
Q

Explain RHESUS incompatibility?

What can be done to prevent?

A

Cause of isoimmune haemolytic anaemia (and jaundice)

  • Mother is Rh negative (moody)
  • Baby is Rh positive (second child- the mum creates IgG antibodies which can cross placenta)
  • Affected infants are usually identified antenatally and anti D IG given - Rho(D) immune globulin (RhoGAM) IM SO MOODY GOT TO TAKE ANTI D
  • If not identified early then children can be born with anaemia, hydrops and hepatosplenomegaly
86
Q

What is ABO incompatibility?

What can be done to prevent?

A
  • mOther O
  • bABy=A or B

-ABO normally has fewer other severe symptoms compared to RHESUS

87
Q

What are risk factors of respiratory distress syndrome?

A

RDS risk factors

   - Prematurity 
    - maternal diabetes
- Male
- Cesarian section 
- Hypothermia 
- Perinatal asphyxia 
- +ve family history
88
Q

What other respiratory system abnormalities can occur int the pre-term baby and when will these stop?

A

Episodes of bradycardia and apnoea
Will occur up to 32 weeks gestation
Child stops breathing for 20-30s

89
Q

define prematurity?

A

< 37 weeks

90
Q

How do we treat mum to prevent prematurity complications?

A

Maternal prevention (<37 week delivery)

  • Magnesium sulphate to protect neuro
  • Steroid injection (beclamethasone/dexamethasone) to protect lungs)
91
Q

Treatment for pre-term babies?

A
  • Keep them warm and deliver in a bag (lose water through skin)
  • Curosurf and intubate
  • Umbilical venous and arterial lines (UVC/UAC)
  • Don’t give too much oxygen- retinopathy of prematurity
  • Normal CO2- If its too low-vasoconstriction- problem with head (cranial USS)
  • Don’t feed too much -necrotizing enterocolitis
  • Caffeine- up to 34 weeks given for apnoeas to stimulate breathing and reduce long term problems
92
Q

Will Coomb’s test be positive or negative in a case of blood group incompatibility?

A

positive

93
Q

How can we tell that the anaemia in the newborn is haemolytic?

A

Increased reticulocyte count
Increase in inconjugated bilirubin due to excessive break down of blood cells and liver not being able to keep up
Jaundice
Consider DAT - COOMB’S (LDH)