Acute flaccid paralysis

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Background

Epidemiology

  • In Canada, 27 to 51 cases nationally every year
  • Enterovirus D68 May have a biennial pattern with peaks every 2 years

Clinical Presentation

  • Defined as sudden onset of muscle weakness or paralysis
    • Flaccid or hypotonic, rather than hypertonic
    • No other obvious cause, such as trauma
  • Excludes transient weakness
  • In acute flaccid myelitis, there are changes seen on MRI of the spinal cord

Differential Diagnosis

Guillain-Barré Syndrome and Paralytic Poliomyelitis

Guillain-Barré syndrome Paralytic poliomyelitis
Fever afebrile febrile with myalgias
Progression subacute, days to weeks acute, peaks at 2-4 days
Neurological deficits ascending, symmetric muscle weakness with decreased DTRs asymmetric weakness with increased DTRs; proximal more than distal, and legs more than arms
Sensory changes mild disturbances or paresthesias none
CSF findings minimal or no pleocytosis, but elevated protein (albuminocytologic dissociation) pleocytosis with elevated protein, normal glucose (aseptic meningitis)

Exhaustive List

Investigations

  • CBC
  • Imaging: CT head, MRI brain
  • CSF for routine, and especially for virology
  • Viral (especially enteroviral) PCR from CSF, nasopharyngeal swab, and/or stool
    • Stool sample is sent in unpreserved, simple sterile container
    • If Enterovirus PCR is positive, can request specific PCR or sequencing for poliovirus, EV D68, and EV A71

Management

  • All cases of acute flaccid paralysis are reportable in Ontario