The Specialist Forum May 2017 | Page 34

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NEUROLOGY
Epilepsy statistics
» Epilepsy affects one in every 100 people in South Africa , i . e . approximately half a million South Africans based on a total estimated population of 52 million .
» If every person with epilepsy has four immediate family members , at least another two million South Africans are affected by the condition .
» There are approximately 50 million people with epilepsy worldwide .
» Since 2004 SUDEP ( Sudden Unexpected Death in Epilepsy ) has increased by more than 100 % in South Africa .
» The overall risk of a child having unprovoked seizures is between 1 and 2 % of the general population . However , this increases to approximately 6 % if a parent has epilepsy .
» 75 % of people with epilepsy will experience their first seizure before the age of 20 .
» Up to 80 % of people with epilepsy will be able to control their seizures with medication .
» 1 in 20 people will have a seizure at some time in their lives . However , this does not mean that they have epilepsy ( which requires a specific diagnosis ).
» Slightly more men than women have epilepsy . for an epileptogenic zone is the finding that most often suggests increased risk for seizure recurrence . Diffuse abnormalities , such as hydrocephalus , may increase the risk by injuring the cerebral cortex ,” Ko said .
Abnormalities on an EEG may include any of the following :
» Epileptiform discharges
» Focal slowing
» Diffuse background slowing
» Intermittent diffuse intermixed slowing .
Epileptiform abnormalities and focal slowing are the EEG findings associated with the highest risk of seizure recurrence . Nevertheless , even a normal EEG does not eliminate recurrence risk .
The risk of recurrence in a person with one generalised tonic-clonic seizure , a normal EEG , a normal brain MRI , and no evidence of focal onset is about 15 %; in this case , the patient is not treated . If a patient has all risk factors , the risk is approximately 80 %, and the patient is treated .
“ The major unresolved question is how to treat patients with one abnormality , whose recurrence risk is 30- 50 %. One approach is to base the decision on a discussion with the patient that includes the risk of seizure recurrence , the risk of toxic effects from the anticonvulsant , and the benefits of avoiding another seizure .
“ The clinician should also describe seizure precautions , including not driving for a specific time . Treatment with anticonvulsants does not alter the natural history of seizure
Active ingredient Epilepsy / seizure type Side effects
Carbamazepine Simple and complex partial seizures , generalised tonic-clonic seizures .
Clobazam ‘ Add-on ’ in tonic-clonic , myoclonic and partial epilepsies . Effective in catamenial epilepsy ( menstrual seizures ).
Clonazepam Second or third choice for myoclonic seizures . Effective “ add- on ” for tonic-clonic and absence seizures . May be used in status epilepticus .
Diazepam
Drug of choice in status epilepticus ( rectally or intravenously ). Rarely used in regularly in tablet form .
Ethosuximide First or second choice for typical absence seizures . May be effective in myoclonic seizures . Not effective in generalised tonic-clonic seizures .
Dose related : Nausea , double vision , unsteadiness . Allergic : Rash , reduced white blood cells count , increased appetite ( rarely ), no obvious effect on concentration , memory or behaviour .
Dose related : Drowsiness and lethargy . Drug loses effect over time despite increasing dosage .
Dose related : Drowsiness , lethargy , drooling and hyperactivity in children . Drug loses effect over time . May cause inflammation of the veins .
Dose related : Drowsiness , lethargy , drooling and hyperactivity in children .
Dose related : Drowsiness , nausea , vomiting , headache , irritability . Allergic : Rashes .
Gabapentin
‘ Add-on ’ therapy in partial seizures .
Dose related : Drowsiness , lethargy , nausea .
Lamotrigine
‘ Add-on ’ and ( in patients over 12 years ) monotherapy in generalised tonic-clonic seizures ( possible second choice after sodium valproate ). Effective in absences with myoclonic seizures and partial seizures .
Dose related : Sedation , unsteadiness and possibly worsening of seizures . Allergic : Rashes may occur in 10 % of patients , particularly if sodium valproate is taken simultaneously . To avoid rashes the drug must be introduced very gradually .
Oxcarbazepine
Primary generalised tonic-clonic seizures and partial seizures .
Similar to carbamazepine , but less severe .
Phenobarbitone
Phenytoin
Effective in generalised tonic-clonic , myoclonic and partial seizures . Effective in status epilepticus .
Second or third choice in generalised tonic-clonic seizures . Effective in partial and myoclonic seizures . Drug of choice in status epilepticus .
Sodium valproate First choice in primary generalised tonic-clonic seizures , typical absence , atonic and myoclonic seizures and photosensitive epilepsy . Effective in partial seizures ( second choice after carbamazepine ).
Topiramate
Prescribed for partial seizures with or without secondarily generalised seizures , inadequately controlled by conventional first-line drugs .
Valproic acid Similar to sodium valproate Similar to sodium valproate
Dose related : Drowsiness , lethargy , unsteadiness . Chronic use : Tolerance and impairment of concentration and memory , slowness in activities . Withdrawal seizures if discontinued too quickly .
Dose related : Nausea , vomiting , unsteadiness , slurred speech . Allergic : Rash , hepatitis ( inflammation of the liver ), swelling of lymph glands . Chronic use : Gum , swelling , acne , hairiness ( face and body ), folate deficiency , involuntary movements , rickets .
Dose related : Tremor , sedation , restlessness , increased appetite . Allergic : Stomach irritation , inflammation of liver and pancreas . Chronic use : Hair loss ( usually transient ), weight gain , low platelets in blood ( may cause excessive bleeding Should not be taken during pregnancy .
Dose related : Drowsiness . Loss of appetite and weight may occur .
34 | May 2017
The Specialist Forum | Vol . 17 No . 4