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51 Cards in this Set
- Front
- Back
Metoclopromide can cause what kind of change in neuro exam?
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drug-induced extrapyramidal sx
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cauda equina syndrome
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serious neurologic disorder characterized by saddle anesthesia, bowel and bladder dysfunction, low back pain, and a variety of lower extremity findings.
Etiology, trauma, lumbar disk disease, malignancy, abscesses |
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Damage to lateral spinothalamic tracts will cause loss of pain and temp sensation to what level of lesion?
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Beginning at two levels below the level of the lesion
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pronator drift
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sensitive and specific for UMN dz.
UMN lesions cause a weakness in supination that results in the pronator muscles becoming dominant. As a result, when these pts close their eyes and extend their arms with the palms up, the affected arm will tend to pronate. |
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amaurosis fugax
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painloss loss of vision from emboli -> warning sign for an impending stroke. Most emboli occur from a carotid bifurcation; hence, a duplex U/S of the neck should be performed
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trigeminal neuralgia
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pain in the distribution of the branches of the fifth nerve: severe, intense, burning or electric shock-like
use carbamazepine |
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Migraine with N/V tx?
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IV antiemetics (chlorpromazine, prochlorperazine or metoclopramide) can be used as monotherapy for acute migraine attacks, particularly in patients with accompanying N/V
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torticollis
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focal dystonia of SCM
dystonia defined as sustained muscle contraction resulting in twisting, repetitive movements, or abnormal postures. medications commonly responsible include the typical antipsychotics, metoclopramide, and prochlorperazine |
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lacunar stroke
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principal cause is hypertension, which induces lipohyalinotic thickening of the small vessels. Lacunae are formed as a result of thrombotic occlusion of penetrating vessels, which are usually 0.5-0.8mm in diameter.
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heat stroke cause?
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occurs in otherwise healthy individuals undergoing conditioning in extreme heat and humidity due to thermoregulation failure.
look for altered mental status, high temp, hypotension, tachycardia, tachypnea |
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DLB
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dementia with lewy bodies: causes alterations in alertness, visual hallucinations, and extrapyramidal symptoms
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First line therapy for idiopathic benign intracranial hypertension (causing pseudotumor cerebri)
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acetazolamide
corticosteroids and repeated lumbar punctures may also be performed |
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Heat stroke definition
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core temp > 40C, altered mental status, tachycardia, and coagulaopathic bleeding after heavy work under direct sunlight (think epistaxis)
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How to distinguish between dementia and normal changes of aging?
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impairment of daily functioning essential in dementia
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Ulnar nerve syndrome
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decreased sensations over the 4th and 5th fingers and weak grip due to involvement of the interosseous muscles of the hand are characteristic.
Most common site of ulnar nerve entrapment is the elbow where the ulnar nerve lies at the medial epicondylar groove. Prolonged, inadvertent compression of the nerve by leaning on the elbows while working at a desk or table is the typical scenario. |
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areflexic weakness in the upper extremities and dissociated anesthesia in a cape distribution. Presence of cord cacvity is most characteristic feature
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syringomyelia
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ipsilateral ataxia, nystagmus, intention tremor, and loss of coordination
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cerebellar tumors
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myasthenia gravis patients have a 15% chance of having what?
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coexisting thymoma
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Hypokalemia manifestations of neurologic condition
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hypokalemia is a common electrolyte abnormality that causes weakness, fatigue, and muscle cramps. When severe, it can lead to paralysis and arrhythmia. ECG may show U waves, flat and broad T waves, and PVCs
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Huntington's dz pathophysiology
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atrophy of the caudate nucleus
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foot drop
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most commonly caused by peripheral neuropathy
also from trauma to common peroneal nerve or radiculopathy to any of the spinal roots that contribute to the common peroneal nerve (L4-S2) congenital: carcot marie tooth dz |
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distinguishing btw ruptured berry aneurysm and intracranial hemorrhage
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ICH: commonly involved sites include basal ganglia, thalamus, pons, cerebellum, and lobar (less common) cerebral lesions usually cause MOTOR DEFICITS OPPOSITE THE SITE OF THE LESION BUT GAZE DEVIATION TOWARD THE SITE OF THE LESION
focal eye and motor deficits not commonly observed in SAH |
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treatment of essential tremor if beta blockers contraindicated
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can also use anticonvulsants such as topiramate and primidone.
PRImidone CAN PRECIPITATE ACUTE INTERMITTENT PORPHYRIA, manifested as abdominal pain, neuro and psych anomalies (confusion, ha, hallucinations, and dizziness) alprazolam, but potential for dependence |
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diabetic mononeuropathy
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often involves CNIII -> down and out + ptosis
nerve damage is ischemic, and only somatic nerve fibers are affected. |
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most common hypertensive hemorrhages occur where?
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putamen -> the internal capsule that lies adjacent to the putamen is almost always involved, leading to contralateral dense hemiparesis
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most common organisms in brain abscess
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aerobic and anaerobic streptococci and bacteroides species (anaerobes)
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wallenberg syndrome
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occurs due to occlusiono f hte posterior inferior cerebellar or vertebral artery.
pts develop loss of pain and temp over the ipsilateral face and contralateral body, ipsilateral bulbar muscle weakness, vestibulocerebellar impairment (vertigo, nystagmus), and horner's syndrome. motor funciton of the face and body is typically spared due to LATERAL MEDULLARY INFARCT |
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bell's palsy vs stroke
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bell's: sudden onset unilateral facial paralysis. inability to raise eyebrow or close the eye, drooping of mouth corner, and disappearance of the nasolabial fold. may also have decreased tearing, hyperacusis, and/or loss of taste sensation over the anterior 2/3 of the tongue.
Lesions in CNS occuring above the facial nucleus will typically cause a contralateral lower facial weakness that spares the forehead. |
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multiple system atrophy
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always consider this when a pt with Parkinsonism experiences orthostatic hypotension, impotence, incontinence, or other autonomic sx
qid 4130 |
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tPa therapy indications
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recommended in pts with acute ischemic stroke if it is initiated within 3-4.5 hours of sx onset (unless contraindicated)
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restless leg syndrome tx
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dopamine agonists (pramiprexole) OR alpha 2 delta ca channel ligands (gabapentin)
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CJD
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rapidly progressive dementia, myoclonus and sharp, triphasic, synchronous discharges on EEG!!!! know all of these
spongiform encephalopathy caused by prion. most pts die within one year of sx onset. |
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alzheimer's dementia: histopathologic findings
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amyloid plaques, neurofibrillary tanles, and selectivel oss of cholinergic neurons
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craniopharyngiomas
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signs of hypopituitarism, headaches, and bitemporal blindness
extremely high yield! benign tumor of rathke's pouch bimodal age distribution -> children and 55-65yo in children, retarded growth is more prominent whereas sexual dysfunction more prominent in adults |
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GBS: how to adequately monitor respiratory function
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serial measurements of bedside vital capacity
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pt develops serious bleeding (eg ICH) due to excess anticoagulation with warfarin. next step in mgmt?
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ffp!
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pseudotumor cerebri complications
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shunting or optic nerve sheath fenestration may be performed to prevent BLINDNESS
most significant complication of otherwise benign disorder |
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antipsychotics vs bzd for agitation of older adults
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better to use antipsychotics. bzd typiocally not recommended bc older pts tend to metabolize these drugs slowly, making their effects verrry long lasting.
plus, in elderly, bzd often worsen confusion. finally elderly at increased risk for all adverse events a/w bzd including withdrawal, dependence, and motor impairment |
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causes of idiopathic intracranial hypertension
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most common in obese young women.
growth hormone, tetracyclines (minocycline, doxy), and excessive vitA and its derivatives (isotretinoin, all trans retinoic acid) can cause IIH. withdrawal of these meds lead to sx resolution |
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hemi-neglect syndrome
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characterized by ignoring the left side of a space, and involves the right (nondominant) parietal lobe
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three treatment options for myasthenia gravis
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acetylcholinerase inhibitors (anticholinesterases), immunosuppressive agents and thymectomy
immunosuppressives (prednisone, azathioprine and cyclosporine which are used with poor response to anticholesterases) and thymectomy may induce remission |
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ALS
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characterized by preence of both upper (spasticity, bulbar sx, hyperreflexia) and lower (fasciculations) motor neuron lesions
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bulbar
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muscles of mouth and throat responsible for speech and swallowing
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eaton lambert syndrome
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a/w small cell carcinoma of hte lung, results from autoantibodies against voltage gated ca channels in the presynaptic motor nerve terminal
electrophysiological studies show muscle response to motor nerve stimulation should increase with repetitive stimulation! treatment consists of plasmapharesis and immunosuppressive drug therapy |
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cerebral salt wasting syndrome
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may occur in pts with SAH
pathology involves 1) inappropriate secretion of vasopressin, and 2) increased secretion of atrial/brain natriuretic peptide, which causes cerebral salt wasting. |
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brain death criteria
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total loss of brain fxn and is a legally acceptable definition of death
criteria include: absent CN reflexes, fixed and dilated pupils, no spontaneous breaths, and agreement of two physicians |
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approved tx for ALS
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riluzole (gluamate inhibitor)
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cerebellar hemorrhage sx
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ataxia, vomiting, occipital HA, gaze palsy, and facial weakness
no hemiparesis |
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BPPV
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triggered by changes in head position, dx confirmed with Dix Hallpike maneuver
pathophys: semicircular canal dysfunction! |
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hallmark of prolonged seizures
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cortical laminar necrosis! -> can lead to persistent neuro deficits and recurrent seizures
lasting greater than 5min |
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NPH: pathophys
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decreased CSF absorption or transient increases in ICP that cause permanent ventricular enlargement w/o chronically increasing ICP
characterized by gait disturbance, urinary incontinence, and dementia treated with serial LP and if successful ventriculoperitoneal shunt |