Paeds 5B Flashcards

1
Q

List the median ages for vision and fine motor milestones.

A

6 weeks: follows moving object or face by turning head
4 months: reaches out for toys
4-6 months: palmar grasp
7 months: transfers toys from one hand to another
10 months: mature pincer grip
16-18 months: makes marks with a crayon, tower of 3
3 years: draws a circle

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2
Q

List the median ages for hearing, speech and language development.

A

3-4 months: vocalises alone or when spoken to, coos and laughs
7 months: turns to soft sound out of sight
10 months: sounds used discriminately to parents (mama/dada)
12 months: 2-3 words other than mama or dada
18 months: 6-10 words, shows two parts of the body
20-24 months: use 2 or more words to make simple phrases
2.5-3 years: talks constantly in 3-4 word sentences

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3
Q

List the median ages for social, emotional and behavioural development.

A

6 weeks: smiles responsively
6-8 months: puts food in mouth
10-12 months: waves bye bye, plays peek-a-boo
12 months: drinks from cup
18 months: uses spoon
18-24 months: symbolic play
2 years: dry by day
2.5-3 years: parallel play, takes turns

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4
Q

How is paracetamol overdose managed?

A

Measure plasma paracetamol concentration at 4 hours and plot on normogram
Treat with IV N-acetylcysteine if necessary

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5
Q

How is carbon monoxide poisoning treated?

A

Presents with headache, nausea, confusion and drowsiness
High-flow oxygen
Hyperbaric oxygen therapy may be considered

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6
Q

How is salicylate poisoning treated?

A

Presentation: vomiting, tinnitus, respiratory alkalosis
Measure plasma salicylate concentration at 2-4 hours
Alkalinisation of urine with sodium bicarbonate increases urinary excretion
Consider haemodialysis

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7
Q

How is TCA overdose treated?

A

Treat arrhythmias and give sodium bicarbonate
Support ventilation

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8
Q

How is ethylene glycol poisoning treated?

A

Presentation: intoxication, tachycardia, metabolic acidosis

Fomepizole inhibits the production of toxic metabolites (ethanol can also be used)

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9
Q

How is iron overdose treated?

A

Presentation: vomiting, diarrhoea, haematemesis, late drowsiness/coma/shock/hypoglycaemia

Serum iron level 4 hours after ingestion is the best measure of severity

IV desferoxamine chelates iron

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10
Q

How is organophosphorus pesticide poisoning treated?

A
Supportive 
Atropine (large dose)
Pralidoxime (reactivates actylcholinesterase) 

NOTE: presentation is mainly cholinergic features

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11
Q

What is a port wine stain?

A

Capillary malformation in the dermis that is present from birth and persists for life
If in the trigeminal nerve distribution, some children may have Sturge-Weber syndrome and should have an MRI

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12
Q

Describe the appearance and progression of cavernous haemangiomas.

A

Appears within the first month of life
Grows before shrinking and disappearing (before 5 years)

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13
Q

Describe the inheritance pattern of von Willebrand disease.

A

Type 1 and 2 = autosomal dominant
Type 3 = autosomal recessive

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14
Q

How should bladder outflow obstruction be investigatd?

A

MCUG

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15
Q

What are the two different types of polycystic kidney disease and how do they differ?

A

Autosomal Dominant - mainly in older children/adults, cysts are large

Autosomal Recessive - presents in childhood with bilateral renal masses, respiratory distress due to pulmonary hypoplasia and congenital hepatic fibrosis with pulmonary hypertension

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16
Q

What are the aspects of managing Duchenne muscular dystrophy?

A

Physiotherapy to prevent contractions
Exercise and psychological support
Surgery (e.g. tendoachilles lengthening)
CPAP for nocturnal hypoxia
Glucocorticoids may slow degeneration

17
Q

What’s the main difference between Duchenne and Becker muscular dystrophy?

A

Duchenne - no dystrophin - severe symptoms (LE: 20-30 years)
Becker - abnormal dystrophin - milder symptoms

18
Q

What are some consequences of neural tube defects?

A

Paralysis and muscle imbalance (needs physiotherapy)
Sensory loss (can lead to accidental damage)
Neuropathic bladder
Bowel denervation
Scoliosis
Hydrocephalus

19
Q

How is hydrocephalus treated?

A

Ventriculoperitoneal shunt

20
Q

Outline the management of idiopathic intracranial hypertension.

A

Eliminate causal factors
Weight-reduction
Low-sodium diet and fluid restriction
Acetazolamide
Analgesia
VP shunt

21
Q

List some clinical features of a child at high-risk of sepsis.

A

Behaviour:
• No response to social cues
• Appears ill
• Does not wake, or if roused does not stay awake
• Weak, high-pitched and continuous cry

Heart Rate:
• Tachycardia (different at different ages)
• < 60 bpm at any age

Respiratory Rate
• Tachypnoea (different at different ages)
• Grunting
• Apnoea
• SpO2 < 90% on air

Mottled or ashen appearance
Cyanosis of the skin, lips or tongue
Non-blanching rash
Aged < 3 months with temperature > 38 degrees
Temperature < 36 degrees

22
Q

Which investigations constitute a septic screen?

A

FBC
Blood culture
CRP
Urinalysis
LP
CXR

Also do a VBG

NOTE: if < 1 month, all children should have an LP

23
Q

Outline the role of a VBG in managing a child with moderate to high risk of sepsis.

A

> 2 mmol/L or evidence of AKI –> treat as high-risk
< 2 mmol/L = repeat assessment at least hourly, ensure review by senior clinician, identify a cause and manage it

24
Q

Outline the non-pharmacological steps taken in the management of high risk sepsis.

A

Immediate review by senior clinician
VBG (gas, glucose, lactate, FBC, U&E, creatinine, clotting)
Broad spectrum antibiotics immediately
Monitor continuously
Monitor mental state using GCS or AVPU

25
Q

Outline how the lactate guides treatment in high risk sepsis.

A

> 4 mmol/L = IV fluid bolus without delay, refer to critical care
2-4 mmol/L = IV fluid bolus without delay
< 2 mmmol/L = consider IV fluids