UKOM Sp.N (Neurology) flashcards
UKOM Sp.N (Neurology) · Build recall with a focused review session.
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- Corticospinal decussation
- Pyramidal fibers cross in the medulla; therefore a lesion above the decussation causes contralateral weakness, while a spinal cord lesion causes ipsilateral weakness below the level.
- Internal capsule blood supply
- Lenticulostriate branches of the middle cerebral artery supply the posterior limb; lacunar infarction here produces a pure motor hemiparesis without cortical signs.
- Broca versus Wernicke aphasia
- Broca aphasia is non-fluent with preserved comprehension; Wernicke aphasia is fluent with impaired comprehension. Both show impaired repetition, distinguishing them from conduction aphasia.
- Resting membrane potential
- Approximately −70 mV, determined largely by potassium permeability and the concentration gradient. The Nernst equation predicts the equilibrium potential for each ion.
- Cerebral blood flow thresholds
- Normal flow is about 50 mL/100 g/min. Flow below 20 mL causes EEG slowing and electrical failure; below 10 mL causes membrane failure and irreversible infarction.
- CSF production and volume
- The choroid plexus produces roughly 500 mL daily; total CSF volume is about 150 mL, so the compartment turns over three to four times per day.
- Upper versus lower motor neuron signs
- Upper motor neuron lesions cause spasticity, hyperreflexia, and Babinski sign. Lower motor neuron lesions cause flaccidity, atrophy, fasciculations, and areflexia.
- Sensory level localization
- A sensory level on the trunk localizes a spinal cord lesion to approximately one or two segments above the level of sensory loss.
- Red flags in headache
- New onset after age 50, thunderclap onset, fever, papilledema, focal deficit, cancer, immunosuppression, or positional change warrant urgent imaging and evaluation.
- Thrombolysis time window
- Intravenous alteplase or tenecteplase is indicated within 4.5 hours of last known well for disabling ischemic stroke after hemorrhage is excluded by imaging.
- Thrombectomy selection
- Mechanical thrombectomy is indicated for large-vessel occlusion within 6 hours, or 6 to 24 hours when perfusion imaging shows salvageable penumbra with a small core.
- Aneurysmal SAH management
- Secure the aneurysm by clipping or coiling, give nimodipine 60 mg every 4 hours for 21 days to reduce delayed ischemia, and monitor for hydrocephalus and hyponatremia.
- Status epilepticus treatment
- Give a benzodiazepine first, then a second-line agent such as levetiracetam, valproate, or phenytoin. Refractory cases require anesthetic infusion and EEG monitoring.
- Valproate pregnancy risk
- Valproate causes neural tube defects and neurodevelopmental harm and is contraindicated in pregnancy. It should be avoided in women of childbearing potential unless no alternative exists.
- Narcolepsy MSLT criteria
- The multiple sleep latency test shows a mean sleep latency under 8 minutes with at least two sleep-onset REM periods, alongside cataplexy or other characteristic features.
- Myasthenia gravis antibodies
- Anti-acetylcholine receptor antibodies are found in most generalized cases; anti-MuSK antibodies occur in a subset. Weakness is fatigable and often involves ptosis and diplopia.
- Guillain-Barré syndrome
- Ascending symmetric weakness with areflexia and albuminocytologic dissociation in CSF. Treat with IVIG or plasma exchange and monitor vital capacity for respiratory failure.
- Amyotrophic lateral sclerosis
- Combined upper and lower motor neuron signs with fasciculations and no sensory loss. Riluzole and edaravone offer modest benefit; noninvasive ventilation supports respiratory failure.
- Demyelinating versus axonal neuropathy
- Demyelinating neuropathy shows slowed conduction velocity, prolonged distal latency, and conduction block. Axonal neuropathy shows reduced compound muscle action potential amplitudes with preserved velocities.
- Neuropathic pain first-line drugs
- Gabapentin, pregabalin, duloxetine, and amitriptyline are first-line for neuropathic pain. Opioids are not recommended because of limited benefit and dependence risk.
- McDonald criteria
- Multiple sclerosis diagnosis requires dissemination in space and time demonstrated clinically or by MRI, with alternative diagnoses excluded. CSF oligoclonal bands can substitute for time dissemination.
- Neuromyelitis optica spectrum disorder
- Anti-aquaporin-4 antibodies cause longitudinally extensive transverse myelitis and optic neuritis. Attacks are treated with steroids and plasma exchange; maintenance uses rituximab or complement inhibitors.
- Anti-NMDAR encephalitis
- Presents with psychiatric symptoms, dyskinesias, seizures, and autonomic instability, often with an ovarian teratoma. EEG may show extreme delta brush; treat with immunotherapy and tumor removal.
- Bacterial meningitis CSF
- Neutrophilic pleocytosis with low glucose and high protein. Empiric ceftriaxone plus vancomycin, adding ampicillin when Listeria is possible in older or immunocompromised patients.
- HSV encephalitis treatment
- Temporal lobe hemorrhagic necrosis suggests herpes simplex encephalitis. Start intravenous aciclovir 10 mg/kg every 8 hours empirically for 14 to 21 days without waiting for PCR.
- Parkinson disease treatment
- Levodopa with carbidopa is the most effective symptomatic therapy. Motor fluctuations and dyskinesias emerge after several years and may require COMT or MAO-B inhibitors.
- Progressive supranuclear palsy
- Atypical parkinsonism with early falls, vertical supranuclear gaze palsy, and axial rigidity. It responds poorly to levodopa and progresses more rapidly than Parkinson disease.
- Cluster headache treatment
- High-flow oxygen and subcutaneous sumatriptan abort attacks. Verapamil is first-line prophylaxis; transitional steroids may be used while prophylaxis takes effect.
- Trigeminal neuralgia
- Lancinating unilateral facial pain in the second or third trigeminal division, often triggered by touch or chewing. Carbamazepine is first-line; microvascular decompression is definitive.
- Diffusion-weighted imaging
- DWI detects restricted diffusion within minutes of acute infarction and is the most sensitive MRI sequence. Restricted diffusion also occurs in abscess, prion disease, and highly cellular tumors.
- CT head in acute stroke
- Non-contrast CT excludes hemorrhage immediately and may show early ischemic change. It is the first-line imaging test before thrombolysis in acute stroke.
- Absence seizure EEG
- Generalized 3 Hz spike-and-wave discharges provoked by hyperventilation, with abrupt onset and offset of impaired awareness and no postictal confusion.
- EMG denervation signs
- Fibrillation potentials and positive sharp waves appear after denervation. Large, long-duration motor unit potentials indicate chronic reinnervation from collateral sprouting.
- Febrile seizure features
- Occurs between 6 months and 5 years with fever, lasting under 15 minutes without focal features. Routine EEG and imaging are not indicated for simple febrile seizures.
- West syndrome
- Infantile spasms with hypsarrhythmia on EEG and developmental arrest. Treatment includes adrenocorticotropic hormone or vigabatrin, especially when associated with tuberous sclerosis.
- Delirium assessment
- Acute fluctuating inattention and altered awareness, screened with the Confusion Assessment Method. Identify and treat the underlying cause; antipsychotics are reserved for severe agitation.
- Psychosis in Parkinson disease
- Reduce dopaminergic medication first. If symptoms persist, use quetiapine or clozapine; typical antipsychotics worsen motor symptoms and should be avoided.
- Enzyme-inducing antiepileptics
- Carbamazepine, phenytoin, and phenobarbital induce hepatic enzymes, reducing levels of oral contraceptives, warfarin, and other antiepileptic drugs.
- Lamotrigine titration
- Start low and titrate slowly to reduce the risk of Stevens-Johnson syndrome. Valproate inhibits lamotrigine metabolism, so the starting dose must be halved.
- Informed consent elements
- Valid consent requires capacity, adequate information about risks, benefits, and alternatives, and voluntary decision-making. Document the discussion in the medical record.
- Duty of candour
- When harm occurs, promptly disclose it to the patient, apologize, explain what happened, and offer support. This is a statutory professional obligation in the UK.