Neurology and Development Flashcards

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1
Q

What is acute cerebellar ataxia and what are potential etiologies of it?

A
  • Focal encephalitis of the cerebellum that accounts for 50% of acute ataxia
  • Etiologies include post-vaccination, as well as post/para-infectious (VZV, staph, strep, other viruses)
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2
Q

What are sxs that would suggest acute cerebellar ataxia?

A

-truncal instability, ataxia, dysphagia, dysarthria, diplopia, tremor, past-pointing

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3
Q

Give a differential diagnosis for acute cerebellar ataxia

A

-infection, toxin, trauma, tumor, stroke, demyelinating conditions

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4
Q
  • What is the workup for acute cerebellar ataxia?

- How should it be treated?

A
  • Obtain an MRI/CT to rule out tumor, trauma, demyelinating conditions. Consider tox screen with concerning history. If AMS or meningeal signs obtain LP and full septic workup to r/o meningitis
  • Acute cerebellar ataxia requires only supportive care and most self resolve, however you should be ruling out other scary causes for a focal neurological change before hanging your hat on this diagnosis
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5
Q
  • What is ADEM?
  • What is its etiology?
  • How does it present?
A
  • Acute demyelinating encephalomyelitis-demyelinating condition of CNS white matter. Many of these patients go on to have a diagnosis of multiple sclerosis
  • usually para/post-infectious
  • Variable presentation depending on what is demyelinated-motor palsies, cerebellar findings, sensory losses, dysarthria, dysphagia, anything
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6
Q
  • What workup should be done for ADEM?
  • What will workup show that proves ADEM?
  • How is this condition treated?
A
  • Given the variable and acute onset w/u like any other neurological emergency-r/o toxin, stroke, infection, trauma, tumor, demyelinating conditions.
  • MRI will show multifocal CNS demyelination
  • Tx with IVIG and steroids
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7
Q
  • Describe how a patient with altered mental status should be managed when they enter the emergency department
  • What labwork should you consider?
  • What other ancillary tests should consider?
A
  • This is an emergency until proven otherwise!
  • Assess ABCDs and start PALs if needed, start IV access, put patient on monitor, start O2
  • Go through AEIOU TIPS pneumonic and obtain workup based on salient history
  • Labs to consider-loaded gas, CBC+diff, blood+urine+CSF cultures, BMP+hepatic, tox screen
  • other tests to consider-emergent head imaging, ekg
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8
Q
  • What physical exam findings need to be assessed for anyone presenting with altered mental status?
  • What score should you obtain?
A
  • pupil size, activity/tone, responsiveness, detailed neuro exam, presence of meningeal signs, presence of rashes, abdominal exam, pulm exam
  • Obtain a GCS score!
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9
Q
  • How is the GCS used and what do score ranges indicate for the degree of brain injury?
  • In what age group is pediatric GCS validated?
A
  • 15 point scale scored 3-15, 13-14 indicating mild brain injury; 9-12 indicating moderate brain injury; =8 indicating severe brain injury and a need to intubate
  • validated for age < 2yo
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10
Q

-What are the pediatric GCS scores?

A
  • eye opening (1-4)- 1=none; 2=to pain; 3=to sound; 4=spontaneous
  • verbal response (1-5)- 1=none; 2=moans to pain; 3=cries to pain; 4=cries, irritable; 5=age appropriate vocalizations
  • Motor response (1-6)- 1=none; 2=decerebrate (extended) posturing to pain; 3=decorticate (flexed) posturing to pain; 4=withdraws from pain; 5=localized pain; 6=spontaneous movements
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11
Q

What are the non-pediatric GCS scores?

A
  • For verbal patients >2yo
  • eye opening (1-4)- 1=none; 2=to pain; 3=to command; 4=spontaneous
  • verbal response (1-5)- 1=none; 2=incomprehensible sounds; 3=inappropriate words; 4=confused, disoriented; 5=oriented
  • Motor response (1-6)- 1=none; 2=decerebrate (extended) posturing to pain; 3=decorticate (flexed) posturing to pain; 4=withdraws from pain; 5=localizes pain; 6=spontaneous movements
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12
Q

What is the AEIOU-TIPS pneumonic for ddx for altered mental status?

A

A-alcohol, acidosis
E-encephalopathy, epilepsy, electrolytes, endocrine
I-ingestion, intussusception, infection, insulin
O-overdose
U-uremia
T-trauma, toxin, tumor
I-ischemia, ingestion, intracranial hemorrhage, ICP
P-psychosis, poisoning
S-stroke, sepsis, seizure

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13
Q

Define simple and complex febrile seizures.

A
  • Simple-generalized, age 6mo-6yr, febrile, and lasts <15minutes
  • Complex-focal, febrile, lasting >15mins, or recurrent seizure w/in 24 hours
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14
Q

How should febrile seizures be managed?

A

2 categories:

1) simple febrile seizure and patient back to neurological baseline-manage the underlying cause of fever, supportive care
2) complex febrile seizure or patient not back to neurological baseline-full workup, head imaging, rule out meningitis

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15
Q

What education should be given to parents about febrile seizures?

A
  • reassure parents that their child is at no increased risk of neuro complications, give return precautions, and advise that antipyretics have no benefit. Advise family to obtain quick PCP FU
  • only prescribe anticonvulsants in consultation with neurologist who will follow patient in outpatient setting.
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16
Q

How should a first time afebrile seizure be managed?

A
  • if generalized, short duration, patient back to neurological baseline patient can be discharged with return precautions and advice to FU w/PCP. <40% have recurrence
  • If focal, prolonged, continued AMS, recurrent, hx suspicious for NAT, or patient <1yo-obtain meningitis w/u and head imaging, admit this patient
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17
Q
  • What are the first line agents that can be given for status epilepticus?
  • How are these dosed?
  • what non-IV formulations exist?
  • When can first line agents be repeated and when should you move to 2nd line agents?
A

1) ativan-preferred as it has a 4 hour duration
- IV as 0.1mg/kg, max 4 mg
2) Versed-only lasts 20 minutes
- IV loading dose as 0.1mg/kg
- IM or IN at 0.2mg/kg
3) Diastat-rectal 0.5 mg/kg for 1st dose, 0.25 mg/kg 2nd dose

-1st line agents can be repeated after 5 minutes and you should move to 2nd line agents after the 2nd dose of 1st line agent

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18
Q
  • At what point should you be prepared to intubate for status epilepticus?
  • What sedative would you use for RSI?
  • What paralytic would you use for RSI?
A
  • if patient is vomiting/aspirating or you are giving your 2nd 1st line agent as the increased sedation can lead to problems protecting the airway.
  • Sedative-if hemodynamically stable use versed or propofol, if hypotensive use etomidate
  • Paralytic-succinylcholine, if contraindicated use rocuronium
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19
Q
  • What are the 2nd line agents that can be given for status epilepticus?
  • What should you be doing if administering a 2nd line agent?
  • How are these dosed?
  • what non-IV formulations exist?
  • When can 2nd line agents be repeated and when should you move to 3rd line agents?
  • What side effects should you be aware of?
A

1) Keppra-20-60mg/kg IV
2) Fosphenytoin-20mg/kg IV or IM
- draw up your 3rd line agent! 2nd line agents take 20 minutes to have effect, time is brain!
- 2nd loading dose of fosphenytoin can be given vs switching to keppra following 10 minutes.At least 2 doses of 2nd line agent should be given (Keppra x1+forpheny x1 vs fospheny x2) prior to switching to 3rd line agent
- fosphenytoin can cause hypotension

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20
Q
  • What are 3rd line agents that can be given for status epilepticus?
  • How are these dosed?
  • What should have already happened prior to giving a 3rd line agent?
A
  • Versed-continuous IV infusion of 0.05-2mg/kg/hr
  • pentobarbital-5-15 mg/kg bolus followed by 0.5-5mg/kg/hr continuous infusion
  • ketamine 0.5-2mg/kg/hr continuous infusion
  • propofol 2mg/kg bolus followed by 1-15mg/kg/hr continuous infusion
  • Before you give a 3rd line medication patient needs to be intubated
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21
Q
  • What are potential etiologies of seizure?

- How are these treated?

A

1) Hypoglycemia-tx with rule of 50
2) Hyponatremia-tx with 5mL/kg of 3%NS over 20 minutes, do not correct more than 8 mEq in 24 hours to avoid central pontine myelinosis
3) hypocalcemia-tx with 10% calcium gluconate 0.3mL/kg over 5-10 minutes
4) Isoniazid toxicity-give pyridoxine (Vit B6) 70 mg/kg max 5g
5) Miscellaneous-NAT, toxin (B blocker), metabolic abnormality

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22
Q
  • How do afebrile seizures in neonates present?

- How should these be managed?

A
  • non-specific motor/neuro signs as their nervous system isn’t well developed yet-repetitive lip smacking, bicycling, eye twitching, abnormal vital signs
  • perform a full sepsis workup, obtain a head CT and admit
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23
Q

Give some red flags that a headache may be 2/2 brain tumor.

A
  • headache/vomiting in the middle of the night or morning
  • papilledema
  • ptosis
  • focal neuro deficits
  • torticollis
  • occipital headache
  • recent confusion or behavioral changes
  • lack of photo/phonophobia consistent with migraine or lack of family hx of migraine
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24
Q

What are sxs of low level carbon monoxide exposure?

A

dyspnea on exertion, difficulty concentrating

25
Q

What are sxs of moderate carbon monoxide exposure?

A

ataxia, confusion, PVCs, syncope

26
Q

What are sxs of high carbon monoxide exposure?

A

seizure, coma, encephalopathy, HA

27
Q

What are late findings of carbon monoxide poisoning?

A

retinal hemorrhages and cherry red skin

28
Q
  • Who will be most severely affected in a household by carbon monoxide poisoining?
  • How should CO poisoning be managed?
A
  • kids and pets! (the small ones)

- Give O2 immediately as it reduces the half life and consider hyperbaric O2 if patient has severe sxs, remove exposure!

29
Q
  • Give the 3 typical presentations of sinusitis
  • What symptoms are common?
  • How should this be treated?
A

1) URI sxs x10 days that aren’t resolving
2) severe URI sxs x3-4 days associated with high fever
3) Recurrence of URI sxs day 5-6 after initial improvement
- foul breath, pain with palpation, nocturnal cough
- Give augmentin and intranasal steroids

30
Q
  • Give the diagnostic criteria for migraine

- What other sxs are common?

A
  • 5+ headaches w/out other explainable source lasting 1-72 hours with at least 2 of the following characteristics:
    1) bifrontal, bitemporal, or unilateral
    2) pulsating/throbbing quality
    3) moderate-severe pain
    4) aggravated by activity
  • N/V and photo/phonophobia also common
31
Q

How should migraine be treated in the ER?

A
  • 1st trail NSAID/tylenol
  • 2nd give sumatriptan if not contraindicated
  • 3rd trial compazine
  • last measure discuss with neurology about inpatient admission for DHE
32
Q

What are contraindications for giving sumatriptan for migraine?

A
  • Triptan used more than once in past week
  • Sickle cell disease
  • CAD, dysrhythmia (WPW), or
  • congenital heart disease
  • CNS vasculitis/moya-moya
  • Zofran within last 24 hours
  • Recent MAO-I use
33
Q
  • What are sxs of infantile botulism?
  • What complications can it lead to?
  • How is it treated?
A
  • Sxs-constipation, lethargy, decreased tone, poor feeding, eye paralysis, cranial nerve findings
  • Complications-respiratory arrest
  • Tx-patient to be admitted for ventilatory support and botulism IG
34
Q

Give a ddx for pediatric stroke

A

-todd’s paralysis, demyelinating conditions, meningitis, meningococcemia, trauma, tumor, migraine, hypoglycemia, inborn error of metabolism, intoxication

35
Q
  • What are etiologies for hemorrhagic strokes?

- What modalities for treatment should be considered?

A
  • ruptured AVM, trauma, coagulopathy, tumor, cavernous hemongioma
  • treat the ICP with mannitol, hypertonic saline, treat coagulopathy and consider seizure prophylaxis
36
Q

Describe risk factors for ischemic stroke

A

1) infection
2) arteriopathy (posterior palate trauma–>carotid dissection, moyamoya, lupus/rheumatologic)
3) cardiac dz-congenital malformation
4) hematologic disease-platelet disorder vs sickle cel disease
5) Drugs-meth, cocaine, chemotherapy, radiation

37
Q

How should ischemic stroke be managed?

A
  • discuss with a neurologist or stroke expert as data is limited.
  • If arteriopathy consider heparin, aspirin, plavix (clopidogrel)
  • Discuss tPA if clot demonstrated on an emergent MRI
  • If patient has sickle cell obtain stat H/O consult for exchange transfusion
38
Q
  • What is transverse myelitis?
  • What sxs does it present with?
  • How should it be managed?
A
  • post/parainfectious focal spinal cord demyelination usually following a VZV or EBV infection
  • sxs of bilateral motor/sensory loss at a specific dermatome and urinary retention, back pain, loss of deep tendon reflexes
  • mgmt by getting MRI and neuro consult. If focal spinal demyelination seen give high dose steroids and plasmapheresis
39
Q
  • What is Guillain-Barre Syndrome and how does the Miller Fischer variant differ?
  • What are the sxs?
  • How is it treated?
A
  • typically ascending paralysis 2/2 an autoimmune response following a campylobacter, flu infection or rarely flu vaccine. The Miller-Fischer variant is descending paralysis
  • Sxs-progressive weakness, sensory loss, or decreased deep tendon reflexes
  • respiratory support, IVIG, plasmapheresis
40
Q

At what age does modesty develop in children?

A

Modesty develops between 4 to 6 years of age

41
Q

At what age do children gain a visual preference for the human face?

A

newborn period

42
Q

At what age do children begin smiling responsively?

A

1 month

43
Q

At what age do children begin climbing onto furniture?

A

2yo

44
Q

At what age do children have the ability to balance on 1 foot?

A

6yo

45
Q

At what age can children visually follow a moving object?

A

1mo

46
Q

At what age can children stand momentarily on one foot?

A

3yo

47
Q

When do most babies begin crawling by?

A

9mo

48
Q

At what age do most babies have a pincher response by?

A

1 yo

49
Q

At what maximum rate can fosphenytoin be given?

A

3mg/min

50
Q

What are risk factors for febrile seizure recurrence?

A

Risk factors for febrile seizure recurrence include:

  • age less than 12 months with onset of febrile seizures
  • temperature less than 40C with febrile seizure
  • family history of febrile seizures
51
Q

What is the dosing of diazapam for status epilepticus?

A
  • rectal: 0.5mg/kg

- IV:0.2-0.3mg/kg

52
Q

What common pathogen for gastroenteritis is associated with seizures?

A

Shigella!

53
Q
  • What is the drug of choice for neonatal seizures?

- What is the dosing?

A

Phenobarbital-20 mg/kg; maximum dose: 1,000 mg/dose

54
Q

When can children do tandem gait on a neurologic exam?

A

5 years

55
Q

When is an upgoing plantar reflex normal?

A

Up to 1yo

56
Q

What are some early signs of hypertonicity in a child who is fighting you?

A

Scissoring and truncal hypertonicity. Babies who are trying to kick you away can seem surprisingly strong. While they are resting, holding their legs crossed in a “scissors position” is frequently abnormal. Also, when you turn the baby from back to front by pulling on one arm, he/she should move in sections- chest first, then abdomen, then diaper area. If they roll over all at once, like a log, this is abnormal.

57
Q

When should the moro reflex stop?

A

6 months

58
Q

When do the palmar and plantar grasps stop?

A

4 months