G40.812
BillableLennox-Gastaut syndrome, not intractable, without status epilepticus
HCC Category Mapping
What This Code Means
Lennox-Gastaut syndrome, a severe childhood epilepsy with multiple seizure types that can be controlled with medication, not currently in a prolonged seizure state.
Coding Tips
- •This syndrome typically presents in early childhood with developmental delay and multiple seizure types
- •Document the specific seizure types observed (tonic, atonic, absence) to support the diagnosis
Clinical Significance
Lennox-Gastaut syndrome without status epilepticus and not intractable represents a rare presentation where this severe epilepsy syndrome is adequately controlled with medication. LGS typically involves multiple seizure types, characteristic EEG patterns, and cognitive impairment. Even when seizures are controlled, these patients require ongoing comprehensive care for developmental and neurological needs.
Documentation Requirements
- ✓Confirmed Lennox-Gastaut syndrome diagnosis
- ✓Documentation of seizure types (tonic, atonic, atypical absence)
- ✓EEG findings showing slow spike-and-wave pattern
- ✓Confirmation seizures are controlled (not intractable)
- ✓Absence of status epilepticus at the encounter
- ✓Cognitive and developmental assessment
- ✓Current medication regimen with response documentation