Common Postnatal Problems Flashcards

1
Q

what are the different types of problems that may occur in newborns?

A
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2
Q

what changes to the skin may you notice and what ca they signify?

A
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3
Q

Skin colour - Plethora

what is it?

A

One twin get more blood form placenta than other

Red colour

Take a FBC to look at haematocrit

If blood flow can cause end organ damage

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4
Q

Skin colour - what cyanosis should you be worried about?

A

Blue peripheries is common in new borns

Central cyanosis needs investigation with oxygen saturations

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5
Q

skin colour - is jaundice common?

A

Very common

physiological jaundice occurs in almost all new borns especially pre terms

Increased red cell turnover and also immaturity of hepatic enzymes that process bilirubin

This causes unconjugated hyperbilirubinaemia

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6
Q

what causes jaundice in 1st 24hrs?

A
  • Haemolytic ( Rh incompatibility, other antibodies, hereditary anaemias e.g. G6PD deficiency, spherocytosis )
  • Sepsis

In first 24 hours is always pathological and always needs investigation

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7
Q

what causes jaundice in 2nd day – 2nd/3rd wk ?

A
  • Physiological
  • Dehydration/poor feeding
  • Breast milk
  • Sepsis
  • Polycythaemia
  • Bruiding e.g. cephalohaematoma
  • Haemolytic
  • Crigler-Najjar Syndrome
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8
Q

what causes jaundice in Prolonged jaundice (>2 weeks term, >3 weeks preterm)?

A
  • Breast milk
  • Sepsis
  • Haemolytic
  • Hypothyroidism

•Cholestasis e.g. biliary atresia

Prolonged jaundice needs investigation, most of these babies will have breast milk jaundice, but do need to exclude other causes

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9
Q

how do you treat jaundice?

A

Treat underlying cause

Hydrate

Phototherapy – NICE guideline charts (convers the unconjugated bilirubin to water soluble isomers that can be excreted through the normal pathways)

Exchange transfusion

Immunoglobulin

(Exchange transfusion and immunoglobulin are more extreme treatments)

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10
Q

what is Erythema toxicum? how common is it? how is it treated?

A
  • maculo-papular rash
  • 30 – 70% of normal term neonates
  • very rare in the pre-term
  • rash fades by end of 1st wk
  • no Rx is required
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11
Q

what are Mongolian blue spots?

A
  • blue-grey pigmentations (Can be mistaken with bruising)
  • often : lower back + buttocks
  • accumulation of melanocytes
  • very common : races with pigmented skin
  • less obvious as skin darkens

Simple birth marks and nothing needs to be done about them apart form reassurance

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12
Q

what are Capillary vascular malformations - Stork marks?

A

•Naevus simplex

  • light colour capillary dilatation
  • commonly at back of neck
  • Maybe along midline of face
  • Gradually fade
  • within the 1st 2 yrs
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13
Q

what are Capillary vascular malformations - Port Wine Stain?

A
  • Naevus flammeus
  • Present at birth, flat or slightly raised.
  • Caused by dilated, mature capillaries in the superficial dermis
  • These do not regress

Associations: Sturge Weber, Klippel-Trenaunay

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14
Q

what are Capillary haemangioma - Strawberry naevus?

A
  • a cluster of dilated capillaries which appears within the first month after birth.
  • Raised and bright red, with discrete edges, occurring in any part of the body.
  • Usually regresses after one year of age
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15
Q

how are babies vulnerable to hypothermia?

A

The large body surface area in relation to weight and the relative lack of subcutaneous fat make preterm infants at risk for hypothermia (body temperature below 36.5°C), especially in the first few hours after birth

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16
Q

Resuscitation and Cold Stress - how should it be done?

A

Dry quickly

Remove wet linens

Use warm towels/blankets

Provide radiant warmer heat

Use heated/humidified oxygen

Key message – always keep newborns warm

17
Q

Hypoglycaemia = blood sugar <2.0 mmol/l

what babies are at risk?

A

Limited glucose supply - Premature babies, Perinatal stress

Hyperinsulinism - Infants of diabetic mothers

Increased glucose use - Hypothermia, Sepsis

18
Q

how can we test for hypoglycaemia?

A

Bedside testing can be inaccurate:

  • At low or high levels
  • When there is poor perfusion
  • When there is polycythaemia (high Hct)

Check a lab sample if there are concerns - Glucose on a blood gas machine is also just as accurate as the lab sample and will give you an immediate result so I recommend to use this

19
Q

what are the symptoms of hypoglycaemia?

A

Jitteriness

Temperature instability

Lethargy

Hypotonia

Apnoea, irregular respirations

Poor suck / feeding

Vomiting

High pitched or weak cry

Seizures

Asymptomatic - Can be asymptomatic so important in babies with identified risk factors for low sugars that we do some routine monitoring of the bed side blood sugars to detect any hypoglycaemia

20
Q

Promote breast feeding

what are tongue ties? and how are they managed?

A

◦Short +/- thickened frenulum

◦Attached anteriorly = base of the tongue

◦Mostly: no treatment necessary (If no impact on feeding then they don’t need treatment)

◦Restriction of tongue protrusion beyond the alveolar margins AND feeding is affected = frenotomy

21
Q

what are some common gastrointestinal problems?

A

Bilious vomiting is important not to miss as it is bowel obstruction until proven otherwise

Yellow vomiting is not bilious vomiting as can just be partially digested milk

22
Q

Respiratory distress is one of the commonest reasons for admission to NNU

what things should you evaluate?

A

Respiratory rate

Increased effort - Grunting, Retractions, Nasal flaring

Colour

Oxygen saturations

23
Q

Absent/weak femoral pulses - what may they indicate?

A

Very important that the femoral pulses are palpated during the newborn examination

Absent/weak femoral pulses can indicate coarctation of the aorta

Cyanotic and congenital heart disease

24
Q

what is Cleft lip?

A

70% of cases also have cleft palate

Can be incomplete (small gap in lip) or complete (continue into the nose)

Can be unilateral (left sided unilateral is most common) or bilateral (85% have palatal involvement)

Maxillary and medial nasal processes fail to merge, usually around 5 weeks gestation

Guidance about cleft palate detection had become important as delay in detection can adversely affect growth and development and the timely medical and surgical management of these cases

25
Q

Cleft lip/palate issues - what issues may it cause?

A

Feeding issues - Special bottles and teats, Can still attempt breast feeding

Airway problems

Associated anomalies - Need hearing screen, Need cardiac echo, Remember trisomies

26
Q

Ophthalmology - whats important to watch out for?

A

Always check red reflexes

Cataracts

  • lens opacification
  • If undetected early could lead to blindness
  • May require no treatment
  • May require lens removal and artificial lens

Important to pick up cataracts as vision development is incomplete at birth and is dependant on light coming in and stimulating the retina

Retinoblastoma:

  • Rare eye cancer which can be successfully treated if picked up early
  • Laser therapy, chemo, surgical removal of eye

White red reflex

27
Q

what are spinal dimples?

A

Can reveal a more serious abnormality involving the spine and/or spinal cord, such as spina bifida occulta which is the least serious form of spina bifida +/- tethered cord

If the dimple is large, off midline, high or with other cutaneous maker (e.g. hairy tuft) = spinal imaging

28
Q

what are Cephalohaematomas?

A

Localised swelling over one or both sides of the head

becomes maximal in size by the 3rd to 4th day of life

Soft, non translucent swelling

limits are those of one of the cranial bones – usually parietal bone

haemorrhage is beneath the pericranium

Limited by the sutures so wont spread out with that region

Bleeding associated with traumatic process of birth

29
Q

how are Cephalohaematomas managed?

A

no treatment is required and resolution occurs in 3-4 weeks

occasionally, if the haematoma is very large, the increased haemolysis results in increased or prolonged neonatal jaundice

no association with intracranial bleeding

30
Q

Talipes (Club foot) - what is it and how is it managed?

A

Medial (varus) or lateral (valgus) deviation of the foot is often positional and requires no treatment other than physiotherapy

Fixed talipes requires more vigorous manipulation, strapping, casting or possibly surgery

Babies with significant talipes may also have developmental dysplasia of the hips

Positional – when an otherwise normal foot is help in a incorrect position in the womb and on examination the foot is flexible instead of rigid and will correct itself with time but sometimes physio therapy may be needed

31
Q

what is Developmental Dysplasia of the Hip (DDH)?

A

Developmental dysplasia of the hip (DDH) is a condition where the “ball and socket” joint of the hip does not properly form in babies and young children

socket is shallow and not develop properly so the hip slips out and becomes dislocated

Check movements

32
Q

what tests can be done for DDH?

A
33
Q

what is DDH treatment?

A

Goal - Relocate head of femur to acetabulum so hip develops normally

Pavlik harmess

Surgical reduction

34
Q

what are the effects of trisomy 21?

A

Dysmorphism - Low set ears, upward slanting palpebral fissures, epicanthic folds, single palmar creases, wide sandal gap

Hypotonia

Cardiac defects

Learning problems

Haematological problems

Thyroid problems

35
Q

Take home messages:

A good newborn examination is crucial

Know the range of normal and reassure

Signs of acute illness may be subtle

Some findings require investigation

This can prevent permanent disability e.g. DDH, cataracts, hypoglycaemia

A