Rosen & Barkin's 5-Minute Emergency Medicine Consult (84 page)

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Authors: Jeffrey J. Schaider,Adam Z. Barkin,Roger M. Barkin,Philip Shayne,Richard E. Wolfe,Stephen R. Hayden,Peter Rosen

Tags: #Medical, #Emergency Medicine

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History
  • A careful history is essential since gait changes may be caused by pain, weakness, lightheadedness, vertigo, or incoordination
  • Onset:
    • Hours–days: Acute
    • Weeks–months: Subacute
    • Months–years: Chronic
  • Symmetric or focal symptoms
  • Presence of fever, mental status changes, weakness, sensory loss, or urinary incontinence
  • Recent viral illness or immunizations
  • History of trauma or toxic ingestion
  • Family history of movement disorder
Physical-Exam
  • Perform a complete physical exam, including neurological and gait testing
  • Assess for signs or symptoms of acute, life-threatening disorders such as hemorrhage, stroke, or CNS infection:
    • Altered mental status
    • Headache
    • Focal neurological deficits
    • Elevated intracranial pressure:
      • Bradycardia, HTN, abnormal respiratory pattern
      • Papilledema
      • Bulging fontanelles
    • Fever
    • Meningismus
    • Nystagmus
    • Nausea/vomiting
    • Examine ears and perform provocative testing for nystagmus (Dix–Hallpike)
  • Note the presence of intoxication or toxidromes in patients with suspected ingestion
ESSENTIAL WORKUP

A detailed history and physical exam will help determine which tests are necessary

DIAGNOSIS TESTS & NTERPRETATION
Lab
  • Blood glucose level
  • Serum electrolytes
  • Toxicology screen:
    • Standard panels may not include the drugs of interest in the ataxic patient
  • Thyroid function testing
  • Target additional testing to likely exposures, such as anticonvulsants
Imaging
  • CT:
    • Head CT can identify mass, hemorrhage, subacute infarct, or hydrocephalus
    • Consider CT with and without IV contrast if mass suspected
    • CT angiography can be performed to evaluate for vascular disease
  • MRI:
    • Excellent study to evaluate for acute ischemia, mass, demyelinating lesions, and vascular abnormalities
    • Superior for imaging the posterior fossa
    • MR angiography of head/neck may be indicated if vascular abnormality is suspected
  • EKG:
    • Not indicated as part of ataxia workup, but may be useful in evaluation of nonspecific dizziness
Diagnostic Procedures/Surgery
  • Lumbar puncture:
    • Indicated if infection or Guillain–Barré suspected
DIFFERENTIAL DIAGNOSIS
  • Acute symmetric ataxia:
    • Head trauma
    • Drug use/toxic ingestion:
      • Alcohol
      • Lithium
      • Phenytoin
      • Barbiturates
      • Carbamazepine
      • Phenobarbital
      • Valproic acid
      • Benzodiazepines
      • Diphenhydramine
      • Dextromethorphan
    • Acute viral cerebellitis
    • Meningitis/encephalitis
    • Hydrocephalus
    • Postinfectious syndrome
    • Hypoglycemia
    • Hyponatremia
    • Severe heat stroke
  • Acute focal ataxia:
    • Posterior circulation infarction
    • Anterior cerebral artery syndrome
    • Vertebrobasilar insufficiency (VBI)
    • Cerebellar hemorrhage
    • Subdural hematoma
    • Cerebellar abscess
    • Acute disseminated encephalomyelitis
    • Complicated migraine
    • Atypical seizure
  • Subacute symmetric ataxia:
    • Drug use/toxic ingestion:
      • Mercury
      • Lead
      • Hydrocarbons
      • Glue sniffing
      • Cytotoxic chemotherapy
      • Organophosphates
    • Vitamin B
      1
      or B
      12
      deficiency
    • Paraneoplastic syndromes:
      • Breast/ovarian cancer
      • Hodgkin lymphoma
      • Neuroblastoma
    • Lyme disease
    • Toxoplasmosis
    • Creutzfeldt–Jakob disease
  • Subacute focal ataxia:
    • Cerebellar glioma
    • Metastatic tumors
    • Lymphoma
    • Multiple sclerosis
    • Guillain–Barré syndrome
    • AIDS-related progressive multifocal leukoencephalopathy
    • Syringomyelia
    • Cervical spondylosis
  • Chronic ataxia:
    • Alcohol-related cerebellar degeneration
    • Stable gliosis
    • Inherited disorders:
      • Spinocerebellar ataxias
      • Friedreich ataxia
      • Ataxia telangiectasia
      • Niemann–Pick disease
    • Hypothyroidism
    • Vitamin E deficiency
    • Tabes dorsalis
    • Congenital malformation:
      • Arnold—Chiari
      • Dandy–Walker
  • Disease states that cause peripheral vertigo can mimic the gait findings in ataxia:
    • Benign paroxysmal positional vertigo
    • Acute labyrinthitis
    • Méniére disease
Pediatric Considerations
  • May present with a refusal to walk
  • Acute ataxia in children is usually a benign, self-limited process:
    • 60% of cases caused by acute cerebellar ataxia or drug ingestion
  • Acute cerebellar ataxia:
    • Postinfectious cerebellar demyelination
    • Usually occurs in children 2–5 yr old
    • Onset 1–3 wk after triggering illness
    • Over 1/4 of cases occur after varicella, but linked to many viral infections and immunizations
    • Normal mental status
    • No fever, focal deficits, or seizures
    • Mild cases may be managed at home, but require injury prevention counseling
    • Most children recover completely within 3 mo without intervention
  • Drug/toxic ingestions:
    • Expect mental status changes
    • Assess access to medications and order appropriate toxicological testing
  • Guillain–Barré syndrome:
    • 15% present with sensory ataxia
    • Miller-Fisher variant: Clinical triad of ataxia, areflexia, and ophthalmoplegia
  • Neoplasm:
    • More than 50% of childhood brain tumors occur in the brainstem or cerebellum
    • Opsoclonus-myoclonus-ataxia syndrome:
      • Paraneoplastic autoimmune syndrome affecting cerebellum
      • Over 50% due to neuroblastoma
  • Stroke:
    • Rare in children, but can occur in patients with sickle cell disease or hypercoagulable states
Geriatric Considerations
  • Gait disorders in the elderly are often multifactorial
  • Underlying cognitive deficits may make it difficult to distinguish presyncope, weakness, vertigo, and incoordination
  • Posterior circulation cerebrovascular syndromes, like VBI and stroke, are more common in the elderly and may present with vague symptoms, like dizziness
  • Evaluate for signs of orthostasis or extrapyramidal disorders, like Parkinsonism
TREATMENT
PRE HOSPITAL
ALERT
  • Acute onset of ataxia may be due to stroke or hemorrhage
  • Deterioration in mental status may warrant field endotracheal intubation
INITIAL STABILIZATION/THERAPY
  • ABCs
  • IV access
  • Supplemental oxygen
  • Cardiac monitor
  • Fingerstick blood glucose:
    • Administer dextrose if hypoglycemic
    • Consider thiamine in alcoholics and malnourished patients
ED TREATMENT/PROCEDURES
  • Institute fall precautions
  • Treatment must be tailored to the patient’s presentation and underlying pathology
  • Cerebellar infarction can lead to significant edema with mass effect and herniation:
    • Neurosurgery consultation may be needed for decompressive craniectomy
MEDICATION
  • Dextrose: D
    50
    W 1 amp (50 mL or 25 g) (peds: D
    25
    W 2–4 mL/kg) IV
  • Thiamine (vitamin B
    1
    ): 100 mg IV
FOLLOW-UP
DISPOSITION
Admission Criteria
  • Acute and subacute ataxia, particularly if a benign etiology cannot be established
  • Patients who cannot ambulate safely
  • Admit patients with cerebellar hemorrhage or mass effect to the ICU
Discharge Criteria
  • Reversible or mild symptoms
  • Normal mental status
  • Able to ambulate safely
FOLLOW-UP RECOMMENDATIONS

Follow up with primary care or neurology depending on likely etiology of symptoms

PEARLS AND PITFALLS
  • Failure to distinguish true ataxia from other causes of gait instability
  • Failure to note trauma in intoxicated patients
  • Failure to realize the limitations of CT scan in evaluating the posterior fossa
  • Failure to recognize the risk of herniation in cerebellar lesions, including stroke
ADDITIONAL READING
  • Friday JH. Ataxia. In: Fleisher GR, Ludwig S, Henretig FM, et al., eds.
    Textbook of Pediatric Emergency Medicine.
    5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:189–192.
  • Manto M, Marmalino D. Cerebellar ataxias.
    Curr Opin Neurol.
    2009;22:419–429.
  • Mariotti C, Fancellu R, Di Donato S. An overview of the patient with ataxia.
    J Neurol.
    2005;252:511–518.
  • Savitz SI, Caplan LR. Vertebrobasilar disease.
    N Engl J Med
    . 2005;352(25):2618–2626.
CODES

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