Neuro Quick Management



Alcohol Withdrawal

  • Treatment:
    • Delirium Tremens (48 hours)3 B’s:
      • Benzodiazepines
      • Beta-Blocker
      • Banana Bag (thiamine/folate)

Benign positional paroxysmal vertigo

  • Presentation:
    • spinning with the head still
    • worsening with change positions
  • Diagnosis:
    • Dix-hallpike maneuver
  • Management:
    • Epley maneuver

Cerebrovascular Accident (stroke)

  • Types:
    • TIA
    • Ischemia
      • Thrombus
      • Embolus
    • Hemorrhage
      • Intracerebral hemorrhage
      • Subarachnoid hemorrhage
  • Diagnosis:
    • EKG – look for atrial fib or atrial flutter
    • 24-hour monitoring
    • CBC, Hgb, Hct WBC
    • Platelet count
    • PT, PTT, and INR
    • Serum lipids, Total, HDL, LDL, and Triglycerides
    • Blood glucose
    • Thrombin time and/or ecarin clotting time if patient is taking a direct thrombin inhibitor or a direct factor Xa inhibitor
  • Confirmatory: 
    • duplex ultrasound of the neck and transcranial Doppler (TCD) of the intracranial arteries
    • CT angiography (CTA) or MR angiography (MRA) of the neck and head arteries
    • transthoracic echocardiography (TTE) then transesophageal echocardiography (TEE) – a source of embolism
  • Steps:
    • Assess vital signs and stabilize airway, breathing, and circulation
    • CT, MRI, CT angiography or MRA
    • Managing volume depletion and electrolyte disturbances
    • Checking serum glucose.
      • Low serum glucose <60 mg/dL – corrected rapidly.
      • High serum glucose level >180 mg/dL – a goal of keeping serum glucose levels within a range of 140 to 180 mg/dL 
    • Assess swallowing and preventing aspiration
    • Optimizing head of bed position.
  • Management:
    • tPA (alteplase)
    • aspirin within 48 hours
    • pharmacologic VTE prophylaxis – subcutaneous low molecular weight (LMW) heparin – Enoxaparin 40 mg daily

Creutzfeldt Jacob Disease

  • Diagnosis:
    • MRI of brain
    • Brain biopsy (definitive)

Epilepsy

  • Differential Diagnosis:
    • Migraine HA
    • Stoke
    • Febrile seizure
    • Syncope
    • Psychogenic non-epileptic syndrome
  • Diagnosis:
    • EEG
      • absence seizures: 3 Hz spike and wave pattern
    • CT r/o tumor
    • MRI – focal abnormalities in the brain
    • CMP – r/o electrolyte abnormalities
    • CBC, Toxicology, AED levels
  • Management:
    • antiepileptic drugs not started if first seizure
    • EEG before starting a regimen
    • 5-7 day continuous video EEG
    • Absence seizures:
      • Ethosuximide
    • Simple or secondary generalized: 
      • Carbamazepine (best for prego pts)
      • Oxcarbazepine
      • Lamotrigine (steven johnson syndrome)
      • Topiramate
    • Generalized Epilepsy or Unclassified Epilepsy:
      • Valproate (teratogenic)

Guillain-Barre Syndrome

  • Path:
    • recent infection, diarrheal, URI or herpetic
  • Presentation:
    • ascending weakness/neuropathic sx. 
    • pain
    • weakness or paresthesias in the feet or weakness of the legs
    • loss of DTRs
  • Diagnosis:
    • routine labs normal
    • LP/CSF analysis – initial 
    • CSF – elevated protein, but no cells
    • EMG/ nerve conduction studies – most accurate test
  • Management:
    • admit to the hospital for observation and treatment
      • monitor vital capacity in pulmonary function test to check his respiratory diaphragm
    • plasma exchange or IVIG

Headache

Migraine
  • Presentation:
    • Bright lights, loud sound
    • sharp, pulsatile
    • radiates to the supraorbital
    • usually 6-8 severity
    • hours to days
  • Treatment:
    • Triptans
    • Topiramate used for prevention
Tension
  • Presentation:
    • Stress, insomnia, hunger, eye-strain
    • wrapping, tight
    • around the head
    • Usually < 6
    • hours to days
  • Treatment:
    • NSAID
Cluster
  • Presentation:
    • Usually random
  • Stabbing, squeezing
  • Supraorbital, temporal
  • Usually > 8
  • Minutes; multiple
  • Treatment:
    • 100% O2, triptans; CCB for prevention

Multiple Sclerosis

  • Presentation:
    • Optic Neuritis
    • Space and Time
  • Diagnosis:
    • MRI w and w/o contrast – white matter lesion
    • CSF – Oligoclonal bands
    • McDonald criteria
  • Management:
    • Short term:
      • IV methylprednisolone for 2-3 days followed by a taper of PO prednisone for 3-4 weeks.
    • Long term:
      • Injection therapy Interferon 1a, Interferon 1b, or glatiramer (safe during pregnancy)
      • Oral therapy with dimethyl fumarate, teriflunomide, fingolimod
      • Infusion monotherapy with natalizumab or ocrelizumab
    • Monitor outpatient disease-modifying therapy (DMT)
  • Manage various sxs:
    • Muscle spasticity:
      • Baclofen
      • Dantrolene
      • Diazepam (for PM use)
    • Fatigue and narcolepsy:
      • Amantadine
      • Modafinil
      • Methylphenidate
    • Pain:
      • Phenytoin
      • Carbamazepine
      • Pregabalin
    • Urinary Urgency:
      • Tolterodine
      • Oxybutinin

Myasthenia Gravis

  • Differentials:
    • Generalized fatigue
    • Amyotrophic lateral sclerosis (ALS)
    • Lambert-Eaton myasthenic syndrome
    • Miller Fisher
    • Guillain-Barré syndrome
    • Botulism
    • Autoimmune disorders
  • Diagnosis:
    • Ice Pact Test
    • AChR-Ab
    • or against a receptor-associated protein, muscle-specific tyrosine kinase (MuSK-Ab) 
    • or low-density lipoprotein receptor-related protein 4 (LRP4)
  • Confirmatory:
    • Repetitive nerve stimulation
    • Single-fiber electromyography 
  • Associated Conditions:
    • Thymoma
      • Imaging mediastinum with CT or MRI
  • Workup:
    • CBC
    • Thyroid function test
    • ANA 
    • RF
  • Management:
    • Pyridostigmine
      • Adults and older adolescents: 30 mg TID.
      • Children and younger adolescents: initial dose is 0.5 to 1 mg/kg every 4-6 hrs.
    • Plasma exchange
    • IVIG
    • Thymectomy

Pseudotumor Cerebri

  • Presentation:
    • Headache 
    • Papilledema
    • Diplopia
    • Obese and young childbearing age
  • Differential Diagnosis:
    • Intracranial mass lesions (tumor, abscess)
    • Obstruction of venous outflow (venous sinus thrombosis, jugular vein compression, neck surgery)
    • Obstructive hydrocephalus
    • Decreased CSF absorption (infectious meningitis, subarachnoid hemorrhage)
    • Increased cerebrospinal fluid (CSF) production (choroid plexus papilloma)
    • Malignant HTN
  • Diagnosis:
    • Papilledema
    • Normal neurologic examination, except for papilledema and cranial nerve abnormalities
    • MRI w and w/o contrast and postcontrast MR venography
    • Lumbar puncture > 250 mmH2O = elevated intracranial pressure
    • Normal CSF composition
    • Ophthalmologic exam/Ophthalmologic consult
  • Management:
    • Vision:
      •  Acetazolamide
        • Alternatives: Topiramate or other carbonic anhydrase inhibitors
        • add Furosemide
    • Progressing Vision Loss:
      • Surgical intervention with optic nerve sheath fenestration (ONSF) and/or a cerebrospinal fluid (CSF) shunting procedure
    • Headache:
      • Amitryptiline and naproxen

Status epilepticus

  • Differential Diagnosis:
    • Delirium tremens
    • Neuroleptic malignant syndrome
    • Drug ingestion
  • Diagnosis:
    • CMP (metabolic derangements)
    • CBC, cultures, LP (Infection)
    • CT, MRI (structural lesions)
    • CT (trauma)
    • Toxicology, hx (drugs)
  • Management:
    • ABC
      • Vitals – monitor oxygen saturation
      • High flow oxygen
      • EKG monitoring
    • Establish IV access
    • CBC, CMP, toxicology, AED levels
    • Hypoglycemia
      • CANNOT check levels – assume hypoglycemia – administer 50mL of D50 with Thiamine
    • Administer 1st round of Benzos:
      • IV lorazepam (diazepam, midazolam) (T=5 mins)
      • IV lorazepam (T=10mins)
      • Fosphenytoin (watch for hypotension) (T=15 mins)
        • prepare for impending mechanical intubation
        • call anesthesia, intensivist
      • IV phenobarbital (T=20 mins)
        • Insert Foley catheter, IV fluids
        • prepare rapid sequence intubation and propofol (anesthesiologist)
  • Post status epilepticus:
    • Rhabdomyolysis
    • Aspiration pneumonitis
    • Arrhythmia

Vertigo

Vestibular Neuronitis
  • Path:
    • acute, peripheral vertigo associated with URI
  • Presentation:
    • Vertigo, nausea, vomiting
  • Diagnosis:
    • + Romberg’s test
    • abnormal caloric vestibular stimulation test
  • Management:
    • Rehydration
    • Antiemetics: diphenhydramine, Phenergan, metoclopramide
    • Anticholinergics/vestibulosuppressants: meclizine, scopolamine

Labyrinthine Concussion
  • Path:
    • acute, peripheral vertigo associated with head injury or trauma to the ear
  • Presentation:
    • vertigo, nausea, and vomiting
  • Diagnosis:
    • + Romberg’s sign
    • signs of head injury or ear injury on otoscopic exam
    • examine head and neck for injury
    • Trauma to head = Head CT (r/o cranial bleed)
  • Management:
    • supportive
    • vestibulosuppressants: Meclizine
    • consult ENT if medical fails

Meniere’s disease
  • Path:
    • Recurrent, peripheral vertigo associated with constant tinnitus and progressive hearing loss. 
    • unilateral increase in perilymphatic volume
  • Presentation:
    • MC older adults
    • women > men
    • feeling of fullness in one ear
    • ringing
  • Diagnosis:
    • Imaging to r/o acoustic neuroma (NF)
    • abnormality in hearing
    • unilateral conductive hearing loss
  • Management:
    • Supportive (gentle diuretics)
    • ENT surgical therapy

Normal Pressure Hydrocephalus

  • Treatment:
    • Ventriculoperitoneal or Ventriculoatrial shunt

Perilymphatic Fistula
  • Path:
    • Recurrent, peripheral vertigo caused by rupture of the bony capsule in the inner ear, leakage of perilymph into the middle ear
  • Presentation:
    • Pop associated with an increase in middle ear pressure (Valsalva maneuver, straining, coughing, sneezing)
  • Diagnosis:
    • differential from Meniere’s disease
  • Management:
    • Supportive
    • ENT surgery

Wallenberg’s Syndrome
  • Path:
    • stroke of PICA
    • infarct of the lateral inferior medulla
  • Presentation:
    • acute, central vertigo
    • n/v, facial hemianesthesia, contralateral body hemianesthesia, dysphagia, dysarthria
    • horner syndrome (ptosis, miosis, anhidrosis)
    • Medical emergency
  • Diagnosis:
    • Non-contrast CT
  • Management:
    • Stroke protocol (tPA if within 3 hours of sx)

Tumors of Nervous system


Children
  1. Low grade astrocytoma (pilocytic astrocytoma/glioma)
  2. Ependymoma
  3. Medulloblastoma
  4. Craniopharyngioma and pituitary adenoma
  5. Ganglioglioma
  6. Pineal tumor
  7. Meningioma
Adults
  1. Glioblastoma multiforme (GBM)
  2. Meningioma
  3. Low grade astrocytoma
  4. Ependymoma
  5. Medulloblastoma
  6. Schwannoma
  7. Oligodendroglioma