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G40.812

Billable

Lennox-Gastaut syndrome, not intractable, without status epilepticus

HCC Category Mapping

V28HCC 201Seizure Disorders and Convulsions
0.262
V24HCC 79Seizure Disorders and Convulsions
0.244
ESRDHCC 79Seizure Disorders and Convulsions
0.000
RxHCCHCC 164Seizure Disorders, Non-Intractable Epilepsy
0.000

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

Commonly Confused Codes

Code Hierarchy

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