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G40.811

Billable

Lennox-Gastaut syndrome, not intractable, with 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, currently experiencing a prolonged seizure state.

Coding Tips

  • Lennox-Gastaut is a specific, well-defined epilepsy syndrome; ensure diagnosis is confirmed before coding
  • Status epilepticus in this syndrome is particularly dangerous and requires emergency management

Clinical Significance

Lennox-Gastaut syndrome is a severe childhood-onset epilepsy characterized by multiple seizure types (tonic, atonic, atypical absence), slow spike-and-wave EEG pattern, and intellectual disability. Status epilepticus in LGS is particularly dangerous and may present as non-convulsive status. This syndrome carries significant lifelong morbidity and requires comprehensive multidisciplinary management.

Documentation Requirements

  • Confirmed diagnosis of Lennox-Gastaut syndrome by neurologist
  • Documentation of characteristic features: multiple seizure types, cognitive impairment, EEG findings
  • Active status epilepticus during the encounter
  • Statement that condition responds to medication (not intractable)
  • Current antiepileptic drug regimen
  • Emergency interventions for status epilepticus

Commonly Confused Codes

Code Hierarchy

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