Community paediatrics Flashcards

1
Q

What is cerebral palsy?

A

Group of permanent non progressing motor disorders affecting muscle tone, posture and movement.
Is acquired due to insult to developing brain in prenatal, perinatal or postnatal early infancy.

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2
Q

What are the RF of cerebral palsy?

A
  • Low birth weight and prematurity
  • Perinatal hypoxic ischaemic injury
  • Congenital abnormalities
  • Multiple births
  • Stroke and intracerebral haemorrhage
  • Intrauterine infection
  • Maternal factors - seizure disorder, thyroid
  • Genetic factors
  • Postnatal event eg. sepsis, trauma, kernicterus
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3
Q

How does prematurity contribute to CP development?

A

Cerebral injury due to under perfusion can cause periventricular leukomalacia = damage to white matter, this area normally controls motor func and tone

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4
Q

How can perinatal hypoxic ischaemic injury cause CP?

A

Causes - placental abruption, ruptured uterus, amniotic fluid embolus
Hypoxic ischaemic event = neonatal encephalopathy:
- Reduced conc
- Seizures
- Tone and reflex abnorm
- Apnoea and aspiration
these infants may develop CP.

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5
Q

What are some early features of CP?

A
  • Abnormal movement - paucity, asymmetrical, fidgety
  • Abnormal tone - floppy/hypotonic, spastiticty/stiff, dystonia = abnormal muscle contraction
  • Retained or exaggerated developmental reflexes
  • Feeding difficulties
    Red flag milestones - not sitting by 8m, not walking by 18m, early hand preference
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6
Q

What are the different subtypes of CP?

A

Spastic - features of upper motor neurone weakness - increased tone, weak, hyperreflexia, clonus (most common type)
Dyskinetic - involuntary movement - choreoathetosis, dystonia
Ataxic - abnormal coordination, rare

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7
Q

What are some conditions associated w CP?

A
  • ID
  • Pain
  • Visual impairment
  • Epilepsy
  • Speech and lang disorders
  • Bladder control problems
  • Drooling
  • Feeding difficulties
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8
Q

What are the types of spastic weakness in CP?

A

Spastic diplegia - lower limbs predominately affected, scissoring gait, hips flexed and adducted, int rotation
Spastic hemiplegia - only on side affected, arm more than leg, shoulder adducted, elbow flexed, hand closed and wrist flexed
Spastic quadriplegia - all limbs affected, severely handicapped

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9
Q

Chorea vs athetosis

A

Chorea - rapid, irreg, unpredictable muscle contractions - face, bulbar muscles, proximal muscles
Athetosis - slow, smooth, writhing movements - distal muscles

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10
Q

What is the medical management of CP?

A
  • Anti cholinergics for drooling
  • Laxatives eg. movicol for constipation
  • PEG for nutrition
  • Anti epileptics
  • Anti spasmodics for spasticity eg. baclofen, botox injections
  • Analgesia
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11
Q

What is the surgical management for CP?

A

For sx that don’t respond to conservative and medical therapyies.
Ortho - hip dysplasia, severe contractures
ENT - disabling drooling

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12
Q

What is the prognosis of CP?

A
  • Non progressive
  • Life expectancy reduced, more severe = shorter life expectancy
  • Aspiration pneumonia is most common cause of death
  • If child can’t sit or roll at 2 years old, unlikely to walk unaided
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13
Q

What are different types of developmental delay?

A

Develop arrest - child develops normally and then can’t develop new skills
Develop regression - develops normally and then looses prev acquired skills - red flag
Neurodevelop disorder - deficits in develop and impairment in normal func eg. ADHD, ASD
Learning disability - reduced intellectual ability in all aspects, sig impairment in social or adaptive func
Learning difficulty - specific problem eg. dyslexia, intellectual ability not affected

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14
Q

What are some antenatal causes of develop delay?

A
  • Genetic disorders - Down’s, Fragile X syndrome, Chromosomal abnormalities
  • Structural brain disorders - microcephaly, hydrocephalus
  • Vascular
  • Infections - rubella, CMV, toxoplasmosis
  • Drugs and toxins
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15
Q

What are some perinatal causes of develop delay?

A
  • Prematurity
  • FGR
  • Intraventricular haemorrhage
  • Perinatal asphyxia - hypoxic ischaemic encephalopathy
  • Hypoglycaemia
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16
Q

What are some post natal causes of develop delay?

A
  • Anoxia - suffocation, near drowning, seizures
  • Trauma
  • Malnutrition
  • Metabolic - electrolyte disturb, hypoglycaemia
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17
Q

What are the ix into develop delay?

A
  • History, exam, assess milestones
  • 1st line - bloods, genetic testing, TORCH screen
  • 2nd line - genetic or metabolic disorder, BRI brain or LP if possible structural problem
18
Q

What are some causes of global develop delay?

A
  • Down’s
  • Fragile X syndrome
  • Fetal alc syndrome
19
Q

What are some causes of gross motor delay?

A
  • CP
  • Ataxia
  • Spina bifida
  • Hypermobility
  • Myopathy
20
Q

What are some causes of fine motor delay?

A
  • Dyspraxia
  • CP
  • Muscular dystrophy
  • Visual impairment
21
Q

What are some causes of lang delay?

A
  • Hearing impairment
  • Language barrier/multiple languages
  • ID
  • Neglect
  • Autism
  • CP
22
Q

What are the red flags of milestones?

A
  • Not smiling by 10w
  • Not sitting unsupported by 12m
  • Not walking by 18m
  • Hand preference before 12m - early = stroke?
  • Speech and lang - not knowing 2-6 words by 18m
23
Q

What is Down’s syndrome and what are the RF?

A
  • Increasing maternal age = most significant RF for DS
  • Trisomy 21 = additional copy of 21st chromosome
24
Q

What dysmorphic features are seen in people w DS?

A
  • Bracycephaly - flat back of head
  • Epicanthal folds
  • Up slanting eyes
  • Flat face and nose
  • Small open mouth w protruding tongue
  • Small, low set ears
  • Short neck
  • Single transverse palmar crease
  • Hyperflexibility
25
Q

What are the other CF of Trisomy 21?

A
  • ID - lots of variability, common to have develop delay
  • Early onset Alzheimer’s
  • ~50% have congenital heart disease
  • Males unlikely to be fertile
  • Increased risk of haematological cancers
  • Hearing impairment
  • Visual impairment
  • OSA more common
  • Obesity
26
Q

How do you ix a newborn w Trisomy 21?

A
  • Karyotyping
  • FBC - check for haem issues
  • CHD screen = echo
  • Neonatal hearing screen
  • Eye check - cataracts
27
Q

What are some indicators that an injury is non accidental?

A
  • Child <2 years
  • Presentation delay
  • Changing narratives and not matching up w severity or type of injury
  • Unwitnessed injury
  • Drug or alc use in household
28
Q

What are some common non accidental injuries?

A
  • Burns eg. cigarette burn
  • Bruises on arms, legs or face - gripping, if most on legs can maybe rule out
  • Subconjunctival or retinal haemorrhage
  • Bite marks
  • Rib fractures
  • Skull fractures/cranial bleeds - shaken baby
  • Metaphyseal corner fracture - pull or twist limb
  • Finger or clavicle fractures
29
Q

What is the management of non accidental injury?

A
  • Inform senior and safeguarding lead
  • Admit child, ensure other children at home are safe, contact social care
  • Manage injuries
  • Document !!
30
Q

What are some complications of shaken baby syndrome?

A
  • Blindness
  • Develop delays, ID
  • Seizure disorders
  • CP
31
Q

What is a dysmorphic child?

A

Child w an abnormal difference in body structure, most commonly genetic

32
Q

What are some causes of dysmorphic child?

A
  1. Down syndrome
  2. Turner syndrome - fat feet and hands
  3. Fragile X syndrome
  4. Fetal alc syndrome
  5. Neurofibromatosis
  6. Achondroplasia
33
Q

What are the CF of ADHD in children?

A
  • Short attention span
  • Quickly losing interest in a task and moving from activity to another
  • Constantly moving
  • Fidgety
  • Impulsive
  • Disruptive and rule breaking
34
Q

What is the management of ADHD in children?

A

1st line - behavioural techniques, extra support at school, educational psychologist
2nd line - methyphenidate w monitoring of height and weight, also dexamgetamine and atomoxetine
Healthy diet and exercise improves sx, eliminate triggers.

35
Q

What are features of autism that affect social interaction?

A
  • Lack of eye contact
  • Delay in starting to smile
  • Avoid physical contact
  • Not able to read non verbal cues
  • Difficulty w friendhsips
  • Not displaying a desire to share attention
36
Q

What are some communication features of autism?

A
  • Delay, absence or regression in lang develop
  • Lack of appropriate non verbal cues eg. smiling, eyecontact, sharing interest
  • Difficulty w imaginative or imative behaviour
  • Repetitive use of words or phrases
37
Q

What are some features of autism that affect behaviour?

A
  • Restrictive interests
  • Stereotypical movements - stimming
  • Repetitive behaviour and fixed routine
  • Anxiety and distress when routine changes
  • Sensory issues - noise, food, texture
38
Q

What is the management of autism?

A
  • CAMHS
  • SALT
  • Dietician
  • Social workers
  • Educational psychologist
39
Q

What are some ADHD screening tools?

A

Conners questionnaire
Dundee Difficult Times of Day Scale
SNAP-IV
Strengths and difficulties questionnaire

40
Q

What are some conditions associated w Down’s?

A
  • Leukaemia
  • Cardiac defromities
  • Subfertility in females, males often infertile = impaired spermatogenesis
  • Learning difficulties
  • Short stature
  • Repeated respiratory infections (+hearing impairment from glue ear)
  • Acute lymphoblastic leukaemia
  • Hypothyroidism
  • Alzheimer’s disease
  • Atlantoaxial instability
41
Q

What is included in a TORCH screen?

A

Toxoplasmosis
Other - HIV, EBV, parvovirus, syphilis, hep B, mumps, measles
Rubella
CMV
HSV