Table Of Contents
Alcohol Withdrawal
- Treatment:
- Delirium Tremens (48 hours)3 B’s:
- Benzodiazepines
- Beta-Blocker
- Banana Bag (thiamine/folate)
- Delirium Tremens (48 hours)3 B’s:
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
- EEG
- 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
- admit to the hospital for observation and treatment
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)
- Short term:
- 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
- Muscle spasticity:
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
- Thymoma
- 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
- Pyridostigmine
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
- Acetazolamide
- Progressing Vision Loss:
- Surgical intervention with optic nerve sheath fenestration (ONSF) and/or a cerebrospinal fluid (CSF) shunting procedure
- Headache:
- Amitryptiline and naproxen
- Vision:
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)
- ABC
- 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
- Low grade astrocytoma (pilocytic astrocytoma/glioma)
- Ependymoma
- Medulloblastoma
- Craniopharyngioma and pituitary adenoma
- Ganglioglioma
- Pineal tumor
- Meningioma
Adults
- Glioblastoma multiforme (GBM)
- Meningioma
- Low grade astrocytoma
- Ependymoma
- Medulloblastoma
- Schwannoma
- Oligodendroglioma