International panel for NMO diagnosis criteria

The 2015 International Panel for NMO Diagnosis criteria are, as the name implies, a set of criteria used to diagnose neuromyelitis optic spectrum disorder (NMOSD) 1. They are based on a combination of clinical, laboratory, and neuroimaging findings.

Criteria

Diagnostic criteria for NMOSD with AQP4-IgG +
  • at least one core clinical characteristic
  • positive AQP4-IgG test
  • exclusion of alternative diagnoses
Diagnostic criteria for NMOSD without AQP4-IgG + or NMOSD with an unknown AQP4-IgG status
  • at least 2 core clinical characteristics following one or more clinical episodes and meeting all the following requirements
    • at least one of the core clinical characteristic is: optic neuritis, acute myelitis with longitudinally extensive transverse myelitis (LETM) or area postrema syndrome
    • dissemination in space (two or more different core clinical characteristics)
    • fulfillment of additional MRI requirements, as applicable 
  • negative AQP4-IgG test or testing unavailable
  • exclusion of alternative diagnoses
Core clinical characteristics
  • optic neuritis
  • acute myelitis
  • area postrema syndrome
  • acute brainstem syndrome
  • symptomatic narcolepsy or acute diencephalic clinical syndrome with NMOSD-typical diencephalic lesions on MRI
  • symptomatic cerebral syndrome with NMOSD-typical brain lesions
Additional imaging (MRI) requirements for NMOSD without AQP4-IgG + and NMOSD with an unknown AQP4-IgG status
  • acute optic neuritis
  • acute myelitis
    • requires associated intramedullary MRI lesion extending over more than 3 contiguous segments (LETM) or more than 3 contiguous segments of focal spinal cord atrophy in patients with a history compatible with acute myelitis
  • area postrema syndrome
    • requires associated dorsal medulla/area postrema lesions
  • acute brainstem syndrome
    • requires associated periependymal brain lesions
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Article information

rID: 59315
Synonyms or Alternate Spellings:
  • IPND criteria

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