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Clinical Pharmacology and Therapeutics

A Textbook of Clinical Pharmacology and ... - clinicalevidence

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134 ANTI-EPILEPTICS<br />

Is it true epilepsy?<br />

Yes<br />

No<br />

No<br />

Is it secondary to an<br />

underlying CNS or<br />

generalized abnormality?<br />

No<br />

Are these reversible or<br />

precipitating factors?<br />

Yes<br />

Yes<br />

Consider underlying<br />

disorder<br />

– brain tumour<br />

– brain abscess<br />

– stroke<br />

– alcohol withdrawal<br />

– other<br />

Investigate for other<br />

disorder<br />

– Syncope<br />

– dysrhythmia<br />

– pseudo-epilepsy<br />

– metabolic disturbance<br />

(e.g. hypoglycaemia)<br />

– drug withdrawal<br />

– other<br />

Are seizures frequent<br />

<strong>and</strong>/or likely to present<br />

risk to patients?<br />

Yes<br />

No<br />

Address these:<br />

– flashing lights<br />

– stress<br />

– alcohol/alcohol withdrawal<br />

– drugs<br />

Drug treatment No drug treatment<br />

(see Table 22.1)<br />

Figure 22.1: Pathway for the management of epilepsy.<br />

• Are there remediable or reversible factors that aggravate<br />

the epilepsy or precipitate individual attacks?<br />

• Is there a clinically important risk if the patient is left<br />

untreated?<br />

• What type of epilepsy is present?<br />

The ideal anti-epileptic drug would completely suppress<br />

all clinical evidence of epilepsy, while producing no immediate<br />

or delayed side effects. This ideal does not exist (the British<br />

National Formulary currently lists 23 anti-epileptic drugs),<br />

<strong>and</strong> the choice of drug depends on the balance between efficacy<br />

<strong>and</strong> toxicity <strong>and</strong> the type of epilepsy being treated. Table<br />

22.1 summarizes the most common forms of seizure <strong>and</strong> their<br />

drug treatment.<br />

Control should initially be attempted using a single drug<br />

which is chosen on the basis of the type of epilepsy. The dose is<br />

increased until either the seizures cease or the blood drug concentration<br />

(see Chapter 8) is in the toxic range <strong>and</strong>/or signs of<br />

toxicity appear. It should be emphasized that some patients<br />

have epilepsy which is controlled at drug blood concentrations<br />

below the usual therapeutic range, <strong>and</strong> others do not manifest<br />

toxicity above the therapeutic range. Thus, estimation of drug<br />

plasma concentration is to be regarded as a guide, but not an<br />

Table 22.1: Choice of drug in various forms of seizure<br />

Form of seizure First line Second line<br />

Partial seizures with Valproate Phenytoin<br />

or without secondary Carbamazepine Topiramate<br />

generalized tonic–clonic Lamotrigine Tiagabine<br />

seizures<br />

Generalized seizures<br />

Primary (tonic–clonic) Valproate Clonazepam/<br />

Lamotrigine<br />

clobazam<br />

Topiramate<br />

Phenytoin<br />

Absence seizures Ethosuximide Lamotrigine<br />

Valproate<br />

Clobazam/<br />

clonazepam<br />

Myoclonic jerks Valproate Lamotrigine<br />

Clonazepam<br />

Other anti-epileptics not listed above may be useful. Refer to National<br />

Institute for <strong>Clinical</strong> Excellence (NICE) guidelines.

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