Peds Neuro Flashcards

1
Q

What are considered worrisome signs of Headaches

A

All indicate ICP

  1. Headache is so severe it wakes at night
  2. Exacerbated by coughing, bending or valsalva movements
  3. Progressive daily worsening of headache
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2
Q

What are migraines accommodated with?

What usually relieves them

A

accommodated with vomiting

relieved by rest/sleep

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3
Q

What are typical pediatric symptoms seen with Migraines in peds?

A

Frontal, bitemporal or unilateral throbbing for 2-72 hrs.

Symptoms are relieved by sleep

Possible visual aura

N/V, abdominal pain, phono/photophobia

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4
Q

What is a good way to eliminate migraine triggers?

A

HA DIARY!

Triggers- diet, menses, stress.

Increase exercise, sleep, routines

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5
Q

How are migraines in peds acutely treated?

A

NSAIDS,
APAP,
triptans (nasal sumitriptan approved >12 y/o),
antiemetics (Compazine-Benadryl-Toradol)

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6
Q

What are prophylactic treatments for migraines in children younger than 6 and older than 6?

What supplement can also be used for prevention

A

< 6 years old : cyproheptadine

> 6 years old propranolol, amitriptyline, topiramate, others

Non pharmacological options: Vitamin B12 (riboflavin) 25-400mg once daily (w/ food)

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7
Q

What is Idiopathic Intercranial Hypertension

A

Disorder defined as symptoms and signs isolated to those produced by increased intracranial pressure (eg, headache, papilledema, vision loss), elevated intracranial pressure with normal cerebrospinal fluid composition, and no other cause of intracranial hypertension

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8
Q

What do IIH not have?

What is the most common risk factor in getting these?

A

No space occupying lesion

obesity

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9
Q

What are signs associated with Idiopathic Intracranial Hypertension?

A
Headache 
Transient visual obscurations
Intracranial noises (pulsatile tinnitus) 
Diplopia
Back pain
Di
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10
Q

What diagnostic criteria must be met to diagnose IIH?

A
  • Papilledema OR sixth (abducens) nerve palsy (unilateral or bilateral)
  • Normal neurologic examination, except for papilledema and cranial nerve abnormalities
  • Neuroimaging shows normal brain parenchyma without evidence of hydrocephalus, mass, structural lesion, or meningeal enhancement
  • Normal cerebrospinal fluid (CSF) composition
  • Elevated lumbar puncture opening pressure
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11
Q

What is contraindicated when trying to diagnose IIH? Why?

What diagnostic test should be done further?

A

Lumbar puncture!
Increased ICP may cause cerebral herniation when LP is performed if obstructive hydrocephalus or mass

Imagine before LP!

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12
Q

What is the main complication seen in IHH/Pseudo Tumor Cerebri?

A

Vision loss

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13
Q

What is Cerebral Palsy?

A

Cerebral palsy (CP) refers to a heterogeneous group of conditions involving permanent non-progressive central motor dysfunction that affect muscle tone, posture, and movement-

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14
Q

What are postnatal causes of Cerebral Palsy?

A
Stroke
Kernicterus
Trauma
Near-drowning
Toxins
Hypoxic brain injury
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15
Q

What are prenatal causes of Cerebral Palsy

A

Prematurity
Intrauterine growth restriction
Intrauterine infection

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16
Q

What are the most common milestones not reached in kids with Cerebral palsy?

A

Not sitting by 8 mo
Not walking by 18mo
Early asymmetry of hand function (hand preference) before 1yr

17
Q

Most common classification of cerebral palsy?

What type of motor neuron lesion is this?

A

Spastic
(most common type, 70 – 80%)

features of an upper motor neuron syndrome

18
Q

Treatment goals of CP?

A

Social and emotional development and MORE ON SLIDE

19
Q

What is Spina bifida?

A

Neural tube disorder (NTD)= defective closure of the caudal neural tube early in gestation (about week 4)

20
Q

What spinal levels are seen with spina bifida?

A

May be just defect of L5 and S1 vertebral arch

21
Q

What is Meningomyelocele?

A

Meninges and spinal cord exposed;

22
Q

What is Meningocele

A

Spinal canal and meninges are exposed, underlying spinal cord is intact

23
Q

What is Spina bifida occulta?

A

Skin intact but underlying defects in bone and spinal canal present. May see sinus tract, dimple or tuft of hair.

24
Q

How is spina bifida prevented?

A

Folic acid?

25
Q

What two things need to be seen to diagnose Spina Bifida?

A

Routine screening w/ alpha-fetoprotein (AFP) level (16-18 w) in maternal serum

US (12-14 w & 18-20 w)

26
Q

How is Spina Bifida treated?

A

Surgical closure

VP shunt

27
Q

What is chiari malformations?

A

anatomic anomalies of the cerebellum, brainstem, and craniocervical junction, with downward displacement of the cerebellum, either alone or together with the lower medulla, into the spinal cana

28
Q

What spina bifida formations also tend to have chiari malformations?

A

myelomeningocele

29
Q

Difference between communicating and non-communicating hydrocephalus?

A

Communicating: CSF circulates through the ventricular system & into the subarachnoid space w/o obstruction

Non communicating: an obstruction blocks the flow of CSF w/in the ventricular system or blocks the egress of CSF from the ventricular system into the subarachnoid space

30
Q

What are signs and symptoms related to Hydrocephalus?

What are signs and symptoms seen in infants?

A

HA, vomiting, altered mental status, visual changes, ocular nerve palsies, and focal neurologic findings.

vomiting, lethargy, irritability, bulging fontanelle, or poor feeding, macrocephaly, excessive rate of head growth

31
Q

What are both temporary and surgical treatments for Hydrocephalus

A

Temporary: Loop diuretic and Acetazolamide

Surgery: remove obstruction or VP SHUNT