🧠 McDonald Diagnostic Criteria Simulator
An interactive simulation of the McDonald 2017 diagnostic criteria based on MRI lesion distribution in space (DIS) and time (DIT), using parameters from MR lesions and oligoclonal bands in cerebrospinal fluid.
The Clinically Isolated Syndrome
A single demyelinating episode opens the diagnostic workup.
- 20–40: Typical age of onset (years, female-predominant)
- Optic neuritis: Common first symptom (or limb sensory loss)
- ~60–80%: CIS to MS conversion (over long-term follow-up)
- 2017: Criteria version used (McDonald revision)
What counts as a qualifying episode
Short placeholder: episode must reflect acute CNS demyelination, lasting >24 hours.
Why early diagnosis matters
Short placeholder: earlier treatment start correlates with better long-term outcomes.
Placeholder insight: the 2017 criteria let MS be diagnosed after just one attack.
Mapping Lesions Across Four CNS Regions
MRI screens four characteristic regions for demyelinating lesions.
- 4: Regions assessed (periventricular, cortical, infratentorial, cord)
- T2/FLAIR: Sequence used (plus gadolinium T1)
- ≥3 mm: Typical lesion size (ovoid, well-demarcated)
- 1.5–3T: Field strength (standard clinical MRI)
The four characteristic regions
Short placeholder: periventricular, cortical/juxtacortical, infratentorial, spinal cord.
Why region location matters
Short placeholder: distinct regions reflect disease spread through separate CNS pathways.
DIS — Lesions Across the CNS
DIS requires lesions in at least two of four regions.
- ≥2 / 4: DIS threshold (regions involved)
- Added 2017: Optic nerve status (as a fifth candidate region)
- Included: Symptomatic lesions (now count toward DIS)
- Improved: Sensitivity vs 2010 (earlier DIS detection)
Counting regions toward DIS
Short placeholder: one or more lesions per region qualifies that region.
Clinical significance of DIS
Short placeholder: DIS shows disease is spatially widespread in the CNS.
Placeholder insight: DIS alone is not sufficient — DIT is still required.
DIT — Evidence That Disease Evolves Over Time
DIT can be shown by new lesions, mixed enhancement, or CSF bands.
- New lesion: Path 1 (on follow-up MRI)
- Gd+/Gd−: Path 2 (simultaneous on one scan)
- CSF bands: Path 3 (oligoclonal bands substitute)
- Any time: Follow-up interval (no minimum interval required)
Three ways to satisfy DIT
Short placeholder: new T2 lesion, mixed enhancement, or CSF oligoclonal bands.
CSF oligoclonal bands as substitute
Short placeholder: bands allow earlier diagnosis without a second MRI.
Combining DIS and DIT Into a Diagnosis
Meeting both DIS and DIT confirms a diagnosis of MS.
- MS confirmed: DIS + DIT met (both criteria satisfied)
- CIS: One criterion met (clinically isolated syndrome)
- Insufficient: Neither met (continued monitoring advised)
- ~5–10%: Misdiagnosis rate (reported in MS clinics)
The final diagnostic decision rule
Short placeholder: DIS and DIT together, with no better explanation, confirm MS.
When criteria are not met
Short placeholder: patients are monitored clinically and with repeat imaging.
Placeholder insight: differential diagnoses must be excluded before confirming MS.
An interactive simulation of the McDonald 2017 diagnostic criteria based on MRI lesion distribution in space (DIS) and time (DIT), using parameters from MR lesions and oligoclonal bands in cerebrospinal fluid.
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