Neuro Acute 2 Flashcards

1
Q

metabolic disorder etiology of sezirues

A

Acidosis
Electrolyte imbalance
Hypoglycemia
Hypoxia
Alcohol or barbiturate withdrawal
Drug intoxication

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2
Q

prognosis of epilepsy/seizure is linked to?

A

underlying etiology of seizures

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3
Q

patients with primary epilepsy

A

can grow out of their seizure or may be well controlled on their medications

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4
Q

definition of status epilepticus

A

seizure activity persisting for more than 5 minutes

drug noncompliance, cns infection, metabolic disturbances, sleep deprivation, stroke, trauma, or encephalitis; with drawl of

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5
Q

what is the treatment for status epilepticus

A

check the sugar

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6
Q

initial drug of choice of status epilepticus

A

benzodizapem

pam,lam, dam

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7
Q

not iv access during a seizure

A

rectal or IM

IV is not that only route to go

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8
Q

if the benzos dont work during a seizure

A

fosphenytoin, valproic aic and or levetiracetam

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9
Q

compliacation of status epileptuicus

A

Hypertension
Lactic acidosis
Hyperthermia
Respiratory compromise
Pulmonary aspiration
Rhabdomylosis
Irreversible neurological damage

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10
Q

monroe kellie hypothesis

A

brain tissue, blood,

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11
Q

brain tumor globlastoma

A

most serious

4 % only survive

Commonly nonspecific, and complaints of increased ICP. As the tumor grows, focal deficits develop

Course is rapidly progressive with poor prognosis. Total surgical removal is usually not possible and response to radiation therapy is poor.

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12
Q

brain tumor meningioma

A

can be removed

Originates from the dura mater or arachnoid. Compresses rather than invades adjacent neural structures. Symptoms vary with tumor site. Tumor usually benign and readily detected by CT

Treatment is surgical. Tumor may recur if removal is incomplete. If removal incomplete, pts may undergo radiation to decrease the risk of recurrence.

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13
Q

brain tumor astrocytoma

A

slower growing

A glioma similar to glioblastoma multiforme, but its course is more protracted, often extending for several years.

Prognosis variable. By the time of diagnosis total excision is usually impossible; tumor often is not radiosensitive. In cerebellar astrocytoma, total surgical removal is often possible.

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14
Q

clinical manifestation of a brain tumor

A

H/A, N/V
Weakness, hemiparesis
Sensory disturbances
Altered mental status
Impaired gait
Aphasia, agraphia
Papilledema, diplopia, diminished visual acuity
Generalized or focal seizure activity (30%)

enlarged nerve, double vision, diminshed visual acuity

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15
Q

hydrocephalus

A

disturbance of csf formation, flow or absorption leading to an increase volume overload by the fluid in the central nervous system

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16
Q

how do you dx a brain tumor that is highly sensitive?

17
Q

hallmark manifestation for menigitis

A

Fever
Nuchal rigidity
Altered sensorium
Severe H/A
Photophobia
Chills,myalgias
Kernig’s sign
Brudzinski’s sign
N/V
Purpura or petechiae ( bacterial going into the blood stream)

bacterial meningitis*

18
Q

kernigs sign

A

k-knee cannot extent due to pain when hip flexed go 90 degrees

knee extension is painful

19
Q

brudzinskis sign

A

b-bend the neck hips and knees flex

neck flexion leads to knee flex

20
Q

dx of bacterial menigitis

A

lumbar puncture

inc icp? on ct very important********

21
Q

if they have inc icp on ct for a meningitis patient? the epidural cath can?

22
Q

lumbar puncture in bacterial meningitis

A

Appearance of CSF
Opening pressure- >180mmH2O (due to inflammation)
Cells (inc wbc)
Total protein (increased)
Glucose (will be decreased)
Culture

normally its clear, if its cloudy then bacterial

22
Q

lumbar puncture in viral meningitis

A

Appearance of CSF
Opening pressure
Cells (inc wbc)
Total protein (normal)
Glucose (normal)
Culture (normal)

23
Q

CT head is indicated for

A

pts with focal neurological signs or diminished loc.

Pt’s with s/s and csf findings typical of bacterial meningitis, but no organisms are found

24
classic features in GB syndrome
Paresthesia Diminished reflexes Symmetric limb weakness Symptoms preceded by infection Usually subside before weakness is apparent Resolves spontaneously in 80% of cases msyk-ASCENDING PARALYSIS
25
ASCENDING PARALYSIS FEET TO THE HIP WAIST AND THEN DIAPHRAGM
GB
26
treatment of MG
maintenance phase-Pyridostigmine (Mestinon) PO or IV Prednisone 1-1.5mg/kg/day or azathioprine 1-3mgkg/day or cyclosporine- immunmodulator when a patient has a immune response 2.5mg/kg bid Plasmapharesis Intravenous immunoglobulin G (IVIG) Surgical Thymectomy
27
treatment acute phase of MG
plasmapheresis and IVIG
28
Areas affected: optic nerve (usually 1st symptom), pyramidal tracts, brainstem nuclei, periventricular region of brain
MS
29
remission and relapse this myelin sheath disorder
MS
30
_________ shows the lesions and the plaques to dx MS
MRI
31
Third most common neurological disorder in older adults. DECREASE IN DOPAMINE PRODUCTION Dopamine production decreased resulting in excessive excitation and loss of control of voluntary movements.
excess acetycholine PARKINSONS
32
patient presentation of parkinsons
Tremor** resting Mask like facial expression Shuffling gait “pill rolling” Slow speech Drooling / difficulty swallowing Orthostatic hypotension Echolalia
33
pharmacological interventions of parkinsons
MAOB inhibitors-mild; selegiline, rasagiline inhibit dopamine and have more dopamine on board amantadine-mild anticholinergic symptom management dopamine agonist-ropinirole, pramiprezole levodopa-carbadopa; precurors helps inc dopamine on board (sinemet)
34
levodopa-carbidopa
efficacy is 5 years to assist with QOL
35
critical illness polyneuropathy occurs when?
Associated with sepsis and multi-organ failure in ICU (sepsis can cause nerve destruction) Limb weakness, flaccidity and ↓ reflexes May occur post neuromuscular blocker use (early mobilization) CK elevation: rhabdomyolsis, myoglobinuria EMG shows slow motor and sensory amplitude with preserved conduction velocity RX. Treat underlying disease
36
MG diagnosis
Tensilon Test Edrophonium- an acetylcholine receptor inhibitor.
37
tensilon test
Administer 10mg slowly IV. Atropine at bedside. An improvement in ptosis or muscular strength should be seen for the test to be considered positive