Paeds ILAs - 5 and 6 Flashcards

1
Q

Developmental milestones at 6 months

A

GM

  • Head control
  • Sits unsupported - Arched back

VFM

  • Palmar grasp
  • Passes objects from one hand to the other

HSL

  • Babbles
  • Turns in response to sound

Social

  • Puts objects in mouth
  • Shakes rattle
  • Reaches for bottle
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2
Q

Developmental milestones at 12 months

A

GM
- Cruises for 10 metres

VFM

  • Refined pincer grip
  • Puts blocks in a cup

HSL

  • Knows and responds to name
  • Knows 2/3 words

Social
- Drinks from a cup with both hands

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3
Q

Primitive reflexes and significance

A

Moro reflex - Sudden loss of support

  1. Arm abduction
  2. Arm adduction
  3. Crying

Persisting after 4 months - Sign of UMN lesion

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4
Q

What is cerebral palsy

A

Non-progressive disorder of movement and position
Occurs in the developing brain

Symptoms may appear to change over time - This is because as the child gets older the things they cannot do become more apparent

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5
Q

Cerebral palsy aetiology

A

Antenatal - 80%

  • Infection
  • Genetics
  • Vascular occlusion

Intrapartum

  • HIE
  • Asphyxia
  • Trauma

Post-partum

  • Trauma
  • Meningitis
  • Periventricular leukomalacia
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6
Q

Cerebral palsy early features

A

Poor feeding

Delayed motor milestones
Asymmetrical hand function < 12 months
Persistent primitive reflexes

Abnormal tone
Abnormal gait

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7
Q

Spastic cerebral palsy

A

80-90% - Damage to motor cortex - UMN signs

Hemiplegic

  • Arm and leg
  • Face sparing
  • Tip toe walk
  • Asymmetrical hand

Diplegic - Periventricular leukomalacia
- Knock-kneed gait

Quadriplegic

  • All 4 limbs
  • Extensor posturing
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8
Q

Dyskinetic cerebral palsy

A

Problem in the basal ganglia - Extrapyramidal tracts

Associated with HIE and kernicterus

Chorea
Athetosis
Dystonia

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9
Q

Ataxic cerebral palsy

A

Lesion in the cerebellum

Broad gait
Hypotonia
Poor balance

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10
Q

Cerebral palsy MDT

A
Occupational therapy 
S/L
School 
Paediatrician 
Neurologist 
Social worker 
Physiotherapy
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11
Q

Cerebral palsy risk factors

A

Twins
Prematurity
Maternal infections
Difficult delivery

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12
Q

Cerebral palsy associations

A
Learning difficulties 
Epilepsy 
Squint 
Deafness 
Poor feeding - Poor growth
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13
Q

Cerebral palsy investigations

A
MRI 
Cytogenetic 
Metabolic profile 
Biopsy and histopathology 
EEG
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14
Q

Absence seizure presentation

A

Child stops what they’re doing
Remains conscious

Can occur with hyperventilation

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15
Q

Absence seizure investigations

A

EEG 3Hz
Hearing test
ADHD assessment

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16
Q

Absence seizure management

A

Valproate

Ethosuximide

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17
Q

Juvenile myoclonic epilepsy presentation

A

Teenage girls

Myoclonic jerks - Suddenly throwing things

History of absence seizures

18
Q

JME investigations and management

A

Investigations - EEG - Polyspike and wave

Management - Valproate

19
Q

Types of strabismus (squint)

A

Paralytic

  • Nerve palsy
  • Can only move the eye in certain directions

Non-paralytic

  • Misalignment
  • Can move the eye in all directions

Manifesto - Always present
Latent - Comes and goes

20
Q

Strabismus investigations

A

ONLY IF PARALYTIC

Cover test

  1. Ask the child to focus on an object
  2. Cover one eye
  3. Observe movement of uncovered eye
  4. Cover other eye and repeat
21
Q

Strabismus management and complications

A

Management - Patching

Complications - Amblyopia

22
Q

RDS presentation

A

Tachypnoea
Intercostal recession
Expiratory grunting
Cyanosis

23
Q

RDS risk factors

A

Prematurity

  • 26-28 weeks - 50%
  • 30-31 weeks - 25%

Maternal diabetes
CS
Male
Second born of premature twins

24
Q

RDS prevention

A

Dexamethasone

Delayed cord clamping - 45 seconds

25
RDS investigations
CXR - Ground glass
26
RDS management
O2 CPAP Surfactant therapy - Through ET tube
27
RDS complications
Pneumothorax BPD Retinopathy Renal failure
28
BPD
Chronic lung disease Occurs due to mechanical ventilation and oxygen supplementation Requires long-term oxygen therapy
29
BPD investigations
O/E - Crackles and wheeze CXR - Round radiolucent areas - Fibrosis CT - Mosaic lunch parenchyma
30
BPD management
Dexamethasone Palivizumab O2
31
Neonatal jaundice < 24 hours
BAD ``` Rhesus incompatibility ABO incompatibility Hereditary spherocytosis G6PD Infection Sepsis ```
32
Neonatal jaundice | 24 hours - 2 weeks
NORMAL Dehydration Infection Physiological Bleeding
33
Neonatal jaundice > 2 weeks
BAD High conjugated bilirubin = Biliary atresia! ``` Cystic fibrosis Congenital hypothyroidism Pyloric stenosis Hepatitis Infection ```
34
Neonatal jaundice investigations
Conjugated bilirubin Unconjugated bilirubin Coombs test Blood film FBC U/E LFT TFT Urinalysis
35
Kernicterus
Deposition of unconjugated bilirubin in the basal ganglia Presentation - Arching of back - Seizures - Comas Complications - Learning difficulties - Sensorineural deafness - Cerebral palsy
36
Necrotising enterocolitis
Bacterial infection of ischaemic bowel wall Inflammatory bowel necrosis due to premature GI tract Risk factors - Cow's milk
37
NEC presentation
Bilious vomiting Distended abdomen - Tense, shiny and red Blood in stool Decreased bowel sounds Palpable abdominal mass Shock
38
NEC investigations - AXR
Intramural gas Distended bowel Thickening of the bowel Perforation - Pneumoperitoneum Rigler sign - Air inside and outside the bowel wall Football sign - Air outlining the falciform ligament
39
NEC investigations - Bloods
Thrombocytopenia Neutropenia Acidosis
40
NEC management
Broad spectrum abx Cefotaxime Vancomycin Gentamicin NG tube - Decompress Surgery - Bowel resection
41
NEC complications
Perforation Peritonitis Short bowel syndrome - Following surgery