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McDonald criteria for diagnosis of Multiple Sclerosis

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The 2010 McDonald criteria for diagnosis of multiple sclerosis (MS)1

Clinical Presentation

Additional Data Needed

  • 2 or more attacks (relapses)
  • Objective clinical evidence of 2 or more lesions, or of 1 lesion with historical evidence of prior attacka
None; no additional tests required. However, additional evidence such as imaging or other test (for instance CSF) desirable and must be consistent with MS; if they are not, extreme caution is needed before making diagnosis of MS and alternative diagnosis must be considered.
  • 2 or more attacks
  • Objective clinical evidence of 1 lesion
Dissemination in space, demonstrated by:
  • Presence of 1 or more T2 lesions in at least 2 of 4 of the MS typical areas of the CNS: Periventricular, juxtacortical, infratentorial, or spinal cord;b
  • or: Await a further attack implicating a different CNS site.
  • 1 attack
  • Objective clinical evidence of 2 or more lesions
No longer a need to have separate MRIs run; dissemination in time, demonstrated by:
  • Simultaneous presence of asymptomatic gadolinium-enhancing and non-enhancing lesions at any time;
  • or: A new T2 and/or gadolinium-enhancing lesion(s) on follow-up MRI, irrespective of its timing with reference to a baseline scan;
  • or: Await a second clinical attack. [This allows for quicker diagnosis without sacrificing specificity, while improving sensitivity.]
  • 1 attack
  • Objective clinical evidence of 1 lesion (clinically isolated syndrome)
Dissemination in space and time, demonstrated by: For dissemination in space:
  • 1 T2 lesion in at least 2 of 4 MS-typical regions of the CNS (periventricular, juxtacortical, infratentorial, or spinal cord);
  • or: Await a second clinical attack implicating a different CNS site;and:

For dissemination in time:

  • Simultaneous presence of asymptomatic gadolinium-enhancing and non-enhancing lesions at any time;
  • or: A new T2 and/or gadolinium-enhancing lesion(s) on follow-up MRI, irrespective of its timing with reference to a baseline scan;
  • or: Await a second clinical attack.
  • Insidious neurological progression suggestive of MS (primary progressive MS)
One year of disease progression (retrospectively or prospectively determined) and 2 of the following criteria:b
  1. Evidence for dissemination in space in the brain based on 1 or more T2 lesions in the MS-characteristic regions (periventricular, juxtacortical, or infratentorial)
  2. Evidence for dissemination in space in the spinal cord based on 2 or more T2 lesions in the cord
  3. Positive CSF (isoelectrical focusing evidence of oligoclonal bands and/or elevated IgG index)

 

 

CNS = central nervous system; CSF = cerebrospinal fluid; MRI = magnetic resonance imaging

 

If the criteria are fulfilled and there is no better explanation for the clinical presentation, the diagnosis is ‘MS’; if suspicious, but the criteria are not completely met, the diagnosis is ‘possible MS’; if another diagnosis arises during the evaluation that better explains the clinical presentation, the diagnosis is ‘not MS’.

Attack (relapse; exacerbation): Patient-reported or objectively observed events typical of an acute inflammatory demyelinating event in the CNS, current or historical, with duration of at least 24 hours, in the absence of fever or infection.

a: Clinical diagnosis based on objective clinical findings for 2 attacks is most secure. Reasonable historical evidence for 1 past attack, in the absence of documented objective neurological findings, can include historical events with symptoms and evolution characteristics for a prior inflammatory demyelinating event; at least 1 attack, however, must be supported by objective findings.

b: Gadolinium-enhancing lesions are not required; symptomatic lesions are excluded from consideration in subjects with brainstem or spinal cord syndromes.

See also: 

Diagnosis of MS

Classification of MS

 

Reference:

1-  HSE (September 2012). The Multiple Sclerosis Specialist Nursing in Ireland: A Guide to Best Practice (2nd Edition). Chapter 2: Diagnosis. Available at: http://www.hse.ie/eng/about/Who/ONMSD/practicedevelopment/Multiple Sclerois Care/MS Guide to Best Practice2.pdf. Accessed 10/03/2014.


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