2013 Flashcards

(41 cards)

1
Q

חומצה ולפוראית

A

לטיפול בהתקף אפילפסיה כללי
יכול להיות טוב לכל התקף בתיאוריה

תל - השמנה, שחלות פוליציסטיות
pancreatitis
edema
hepatic dysfunction

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2
Q

קרבמזפין

Tegretol

A

treatment of epilepsy and neuropathic pain

טוב בעיקר להתקף פוקאלי
לא טרטוגני כל כך

idiosyncretic:
Skin rash
Blood dyscrasia
Hepatic dysfunction
Stevens-Johnson syndrome
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3
Q

כלונזפם

A

בנזודיאזפין
טוב לפרכוס אקוטי ולא לטיפול ארוך טווח
טוב לסטטוס אפילפטיקוס

סתם תופעות לוואי- בילבולף ירידה בחשק מיניף קוגניציה…

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4
Q

למיקטל
סוג התקף לטיפול
אוכלוסיה מועדפת לטיפול

A

נגד פרכוס פוקאלי או כללי טוני קלוני
טובה לצעירות בגלל טרטוגניות נמוכה ומעט אינטראקציות עם גלולות
מעט תופעות לוואי קוגנטיביות

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5
Q

קונטרא אינדיקציות ל TPA

A
חסר קטן וחולף
6 שעות ומעלה
185/110
INR 1.7
דימום
טראומה
היפוגליקמיה 50
טסיות מתחת 100 אלף
PTT גבוה
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6
Q

סוג אטקסיה בחוסר B12

A

פגיעה בעמודות האחוריות - בעיות של ש”מ ונפילות (אטקסיה).

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7
Q

DBS

A
#לא נציע לחולה עם ספק באבחנה או עם אבחנה של פרקינסון+
# טוב לצעירים עם מעט תופעות מנטליות ואפקטיביות
# טוב לכאלו שהגיבו לטיפול בדופה
#פותר בעיה מוטורית - מקטין און אוף, ממגר דיסקינזיה
# סיבוכים - זיהום, דימום, אלרגיה לאלקטרודה. ירידה קוגניטיבית ודיכאון
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8
Q

PMP22

A

AD
מאפיין מחלת צ’רקו מרי תוס
מחלה תורשתית חולשה ואטרופית שרירים דיסטאלים
יכול להיות פגיעה סנסורית - יותר בסוג 1 ולא בסוג 2

Hereditary neuropathy with liability to pressure palsies

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9
Q

PARKIN

A

juvenile Parkinson’s disease

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10
Q

PRNP

A

Familial CJD

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11
Q

genes associated with parkinson

Rarely, parkinsonism occurs on a familial basis.

A

AD - α-synuclein SNCA, LRRK2, UCHL1

early-onset, autosomal
recessive, and sporadic juvenile-onset parkinsonism.
- PARK2 and DJ1

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12
Q

Neurosarcoidosis

A

גרנולומטוזה של רקמת מוח
פגיעה עיקרית - עצבים קרניאלים
5-10% מהאנשים עם סרקואידוזיס באיבר אחר יהיו עם נוירוסרקואידוזיס
צריך ביופסיה בשביל לדעת באמת

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13
Q

alzhimer risk factors

A

age, female sex, APOE4 genotype.

less -
family history depression, low educational level, smoking, diabetes, HTN and fatty diet.

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14
Q

arnold chiari

A

obstructive hydrocephalus, brainstem compression, and
syringomyelia

Cerebellar ataxia - bilateral
Hydrocephalus - headache and vomiting.
brainstem compression - vertigo, nystagmus, and lower
cranial nerve palsies.

can be diagnosed by CT or MRI studies that demonstrate cerebellar tonsillar herniation

Communicating syringomyelia is often associated
spinothalamic tract

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15
Q

Modafinil

A

wakefulness-promoting agent

עוזר באופן לא רשמי לעייפות נוירולוגית של מולטיפל סקלרוזיס

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16
Q

Fingolimod (Gilenya)

A

immunomodulating for MS
reduced the rate of relapses

most common side effects of fingolimod have been head colds, headache, and fatigue.

some cases of PML, skin cancer,

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17
Q

Tolterodine

A

treatment of urinary incontinence

18
Q

Todd’s paresis

A

focal weakness in a part of the body after a seizure

19
Q

Todd’s paresis

A

focal weakness in a part of the body after a seizure

20
Q

pregabalin (Lyrica)

A

טיפול בכאב נוירופתי

טיפול פרכוסים פוקאלים

21
Q

Hepatic encephalopathy

Investigative Studies

A
  1. nearly invariable presence
    of hyperventilation with resultant respiratory alkalosis
  2. The CSF is usually normal but may appear yellow
  3. The diagnosis is confirmed by an elevated CSF glutamine concentration
    4.
22
Q

Hepatic encephalopathy

treatment

A
  1. controlling gastrointestinal bleeding or
    systemic infection
  2. decreasing protein intake
  3. lactulose - decreasing intracolonic pH
  4. Neomycin - bacteria may be reduced
    Rifaximin - reduces ammonia-forming bacteria in the colon
  5. FFP & vitamin K - reverse coagulopathy
23
Q

Hepaic encephalopathy

The most helpful neurologic sign

24
Q

topiramate (Topomax)

A

treat epilepsy in children and adults,
migraine

idiosyncratic:
Renal stones
Glaucoma

25
Gerstmann syndrome
Destruction to the inferior parietal lobule (dominant (usually left) hemisphere): 1. Dysgraphia 2. Dyscalculia 3. Finger agnosia: inability to distinguish the fingers on the hand 4. Left-right disorientation brain lesions, stroke.
26
lesion at the facial colliculus in the right dorsal pons.
paralysis of the entire right side of the face: the right lower face droops, the patient cannot tightly close the right eye and cannot wrinkle the forehead on the right. inability to abduct the right eye.
27
LP CONTRAINDICATIONS
1. Suspected intracranial mass lesion. (can hasten incipient transtentorial herniation.) 2. Local infection overlying the site of puncture. 3. Coagulopathy. Clotting-factor deficiencies and thrombocytopenia (platelet count below 50,000/μL 4. Suspected spinal cord mass lesion. (fluid removal can produce a pressure differential above and below the block, which can increase the degree of spinal cord compression)
28
MYOGLOBINURIA causes lab treatment
1. Excessive unaccustomed exercise 2. Crush injuries 3. Muscle infarction 4. Prolonged tonic-clonic convulsions 5. Polymyositis 6. Chronic potassium depletion 7. An acute alcoholic binge 8. Certain viral infections associated with muscle weakness and pain 9. Hyperthermia 10. Metabolic myopathies (eg, muscle glycogen phosphorylase deficiency [McArdle disease]) serum CK elevated myoglobin in urine treatment : severe - dialysis non severe - hydration, monitor potassium levels
29
גידול פרונטלי | פגיעות
פגיעה מוטורית פוקאלית קושי בהתחלת תנועה בריחת שתן ללא בושה!!! סטיית מבט לצד הגידול - אין בעיה בתנועת עקיבה עם העיניים שינוים התנהגותיים הופעת רפלקסים פרימיטיבים - כמו פאלמר מנטל, רוטינג או גראספ פגיעה בברוקה עצבים קרניאלים - 1,2 עצב 2 - foster kenedy - אופטיק אתרופי ופפילאדמה בעין השניה שלא נלחצת על ידי הגידול
30
b12 deficiency anemia
combined degeneration of the posterior and lateral columns Onset of subacute combined degeneration is with #DISTAL PARAESTHESIS# and #WEAKNESS# in the extremities (involvement of the hands occurs relatively early), followed by the development of #SPASTIC PARAPERESIS#,with #ATAXIA# from the impairment of postural sensation in the legs. #LHERMITTE SIGN# may be present, and examination reveals a combined posterior column (vibration and joint position sense) and pyramidal deficit in the legs. Plantar responses are extensor, but tendon reflexes may be increased or depressed, depending on the site and severity of the involvement. Signs of cord involvement can be accompanied by centrocecal scotoma or optic atrophy from optic (II) nerve involvement, by behavioral or psychiatric changes (Chapter 4), or by peripheral neuropathy. The neurologic manifestations are often accompanied by #MACROCYTIC ANEMIA# but this is not invariably present.
31
Hemiballismus
unilateral chorea . vascular disease in the contralateral subthalamic nucleus
32
Alzheimer treatment
MEMANTINE- NMDA-type glutamate receptor antagonist drug, may produce modest improvement in patients with moderate or severe Alzheimer disease. tacrine, donepezil, rivastigmine, and galantamine, Acetylcholinesterase inhibitors, Antipsychotic drugs, antidepressants, and anxiolytics
33
Charcot-Marie-Tooth
weakness and wasting of distal muscles in the limbs, with or without sensory loss; pes cavus and reduced or absent tendon reflexes also occur
34
Guillain–Barré syndrome | Required for diagnosis
Progressive weakness of more than one limb Distal areflexia with proximal areflexia or hyporeflexia #Supportive of diagnosis: Progression for up to 4 weeks Relatively symmetric deficits Mild sensory involvement Cranial nerve (especially VII) involvement Recovery beginning within 4 weeks after progression stops Autonomic dysfunction No fever at onset Increased CSF protein after 1 week CSF white blood cell count ≤10/μL Nerve conduction slowing or block by several weeks
35
Guillain–Barré syndrome | Against diagnosis
Markedly asymmetric weakness Bowel or bladder dysfunction (at onset or persistent) CSF white blood cell count >50 or PMN count >0/μL Well-demarcated sensory level Excluding diagnosis: Isolated sensory involvement
36
Sydenham chorea
``` #children and adolescents #streptococcal GAS complication #most common cause of chorea developing acutely in children. #may recur during pregnancy #may be accompanying behavioral changes, #30% of cases there is evidence of cardiac ``` #diagnosis is supported by the presence of other manifestations of rheumatic fever Cerebral MRI or CT findings are usually normal. PET and SPECT studies show reversible basal ganglia hypermetabolism. ``` #treatment : bed rest, sedation, and prophylactic antibiotic therapy - penicillin chorea can be treated with valproic acid, risperidone, corticosteroids may be effective. ```
37
Ropinirole indication MOA
treatment: Parkinson's disease and restless legs syndrome MOA: dopamine receptor agonis
38
AMANTADINE indications MOA
treatment: mild parkinsonism alone or in combination with an anticholinergic MOA: blockade of NMDA preferring glutamate and muscarinic cholinergic receptors and stimulation of dopamine release.
39
Carbidopa | MOA
inhibits dopa decarboxylase, the enzyme responsible for the breakdown of levodopa to its active metabolite, dopamine. does not cross BBB
40
rasagiline | MOA
parkinson | moaB inhibitor
41
TORSION DYSTONIA
dystonic movements and postures and an absence of other neurologic signs inherited can begin in childhood (340)