epilepsy types and treatment Flashcards
Characterized by frequent brief episodes of unresponsiveness or staring, often with subtle motor features like eyelid fluttering. It’s most common in children.
Absence epilepsy:
The first-line treatments are Ethosuximide and Sodium Valproate. Sodium Valproate should be avoided in women and girls of childbearing age if possible due to risks to the unborn child.
Characterized by brief episodes of jerking movements, usually occurring after waking up.
Juvenile Myoclonic epilepsy:
Sodium Valproate is commonly used, though Levetiracetam and Lamotrigine are also considered.
Characterized by a combination of muscle stiffness and jerking movements. The person often loses consciousness.
Tonic-clonic seizures:
Sodium Valproate, Lamotrigine, and Levetiracetam are considered first-line treatments.
These start in one part of the brain and can present with a wide variety of symptoms, depending on the part of the brain affected. Symptoms can include motor symptoms, sensory symptoms, autonomic symptoms, or cognitive/psychic symptoms.
Focal seizures:
Carbamazepine, Lamotrigine, and Levetiracetam are commonly used.
This is a severe form of epilepsy beginning in infancy. Symptoms include prolonged seizures that may be triggered by fever or infection. First-line treatment typically includes
Dravet Syndrome:
Sodium Valproate, Stiripentol, or Clobazam.
This is a severe form of epilepsy characterized by multiple seizure types and cognitive decline. Treatment usually involves multiple medications, including
Lennox-Gastaut Syndrome:
Valproate, Lamotrigine, and Clobazam.
Characterized by brief episodes of spasms, often upon waking. First-line treatments include
Infantile Spasms (West syndrome):
hormonal therapy (such as prednisolone or tetracosactide) or Vigabatrin, especially if associated with tuberous sclerosis.