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Neurology

2010 Revised McDonald Criteria for Multiple Sclerosis calculator

Enter the published formula inputs below to calculate and interpret this score.

Clinical inputs

Onset
Attacks

Count attacks typical of inflammatory demyelination.

Objective clinical lesions

Objective clinical evidence of lesions.

Result

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Clinical inputs

  • A better explanation than multiple sclerosis
  • Onset
  • Attacks
  • Objective clinical lesions
  • Reasonable historical evidence of a prior attack at another site
  • Periventricular T2 lesion
  • Juxtacortical T2 lesion
  • Infratentorial T2 lesion
  • Spinal cord T2 lesion
  • Clinical dissemination in space
  • MRI dissemination in time
  • A second clinical attack
  • Positive cerebrospinal fluid
  • One year of progression
  • Two or more spinal T2 lesions

Primary source

Polman CH et al. Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria. Ann Neurol. DOI: 10.1002/ana.22366. PMID: 21387374. Table 1: dissemination in space is at least one T2 lesion in at least two of four areas (periventricular, juxtacortical, infratentorial, spinal cord). Gadolinium enhancement is not required. A symptomatic brainstem or spinal cord lesion is excluded from the count. Table 2: dissemination in time is a new T2 or gadolinium-enhancing lesion on follow-up, whatever the timing of the baseline scan, or simultaneous asymptomatic gadolinium-enhancing and nonenhancing lesions. Table 3: primary progressive disease needs one year of progression plus two of brain dissemination (≥1 T2 lesion in at least one of periventricular, juxtacortical, or infratentorial), ≥2 spinal T2 lesions, and positive CSF (oligoclonal bands on isoelectric focusing and/or an elevated IgG index). Table 4: two attacks with two objective lesions, or one objective lesion plus reasonable historical evidence of a prior attack, meet the diagnosis with no further data. Two attacks and one objective lesion need dissemination in space or a later attack in a different site. One attack and at least two objective lesions need dissemination in time or a second attack. One attack and one objective lesion need both dissemination in space and dissemination in time. A better explanation is not multiple sclerosis. Suspicious disease that does not meet the table is possible multiple sclerosis. Positive CSF does not replace dissemination in time after an attack. (2011)

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