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 optica spectrum disorder (NMOSD) . 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