Paediatric Revision Lecture - part 2 Flashcards

(27 cards)

1
Q

Septic arthiritis vs transient synovitis

A

Septic:
* Unable to weight bear
* Looks unwell
* Fever - moderate/high
* Pain at rest

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2
Q

How long does JIA have to be there for to have as differential?

A

For more than 6 weeks
If systemic - get salmon pink rash with fever

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3
Q

Organism causing croup

A

Parainfluenza

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4
Q

Cut off for O2 in bronchiolitis

A

If under 92%

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5
Q

Inv for croup

A

Nasopharyngeal aspirate
Nose swab

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6
Q

Cause of bronchiolitis

A
  • Respiratory syncytial virus
  • Rhinovirus
  • Adenovirus
  • Influenza
  • Coronavirus
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7
Q

Cause of acute wheeze

A
  • Virus
  • Bronchiolitis
  • Pneumonia - mycoplasma, chlamydia
  • Foreign body
  • Anaphylaxis
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8
Q

Laryngomalacia presentation

A
  • Mild - stridor when feeding/crying - will resolve likely by 12-18 months
    If problems with growth, choking or feeding problems will need surgery
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9
Q

Pierre robin sequence

A
  • Micrognathia - hypoplasia of mandible
  • Cleft palate
  • Tongue tends to prolapse backwards causing obstruction
  • If mild - will resolve as chin grows, support with feeding.
  • If very severe - tracheostomy to maintain airway
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10
Q

Adverse effect of prostaglandin (given to prevent duct closure)

A
  • Not really - very safe drug
    High doses can lead to apnoea but rare
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11
Q

Management constipation in children

A
  • Paediatric Movicol - osmotic
  • If not controlled - add stimulant laxative eg senna or sodium picosulfate
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12
Q

Most common cause early vomitting baby

A
  • Amniotic fluid gastritis
  • Posseting
  • GORD or CMPA (allergy likely to have faltering growth)
  • Pyloric stenosis - do a CBG (hypoChlor hypoKal metabolic alkalosis)
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13
Q

Management of GORD

A
  • New position during feeds - 30 degrees head up
  • Smaller feeds
  • Milk thickener for formula
  • Gaviscon (not with thickener)
  • PPI
  • Erythromycin as a prokinetic
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14
Q

CMPA management

A
  • Extensively hydrolysed formula
  • Amino acid based formula
  • Refer to dieticians - likely resolve by 1 yr, need milk ladder trials
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15
Q

2 causes of short stature

A
  • Familial short stature
  • Constitutional growth delay - takes more time, then grow to expected height

Do x-ray of non-dominant hand and get bone age

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16
Q

Predicted height for children

A
  • Mother + fathers height divided by 2
  • Add 7cm for boys, minus 7cm for girls
17
Q

Craniofacial features of down syndrome

18
Q

Other anomalies of down syndrome

19
Q

Clinical features of Turner syndrome

20
Q

Infantile spasms(west syndrome) EEg

A

Hypsarrythmia - even when not seizing

21
Q

Childhood adolesence epilepsy EEG

A

3 hz spike and wave - even when not seizing

22
Q

Where does spinal muscular atrophy arise from?

A

Anterior horn cell

23
Q

3 features of muscular dystrophy

A
  • Delayed motor milestones
  • Gower sign
  • Hypertrophic calf
24
Q

Inv for ?ITP - bloods

A

FBC - if more than 1 cell line involved - COULD THIS BE LEUKAEMIA- follow up
Blood film

25
Management of oromucosal bleed in ITP
* Oral steroids * If severe - IVIG
26
Prophylaxis for nephrotic syndrome
* Penicilln V * VTE prophylaxis
27
Differentials for nephrotic syndrome
* Protein losing enteropathy * R sided heart failure - feet and face