Description

Measurement of changes in the serum prolactin concentration can be used as supportive evidence for the diagnosis of an epileptic seizure.


 

The rise in prolactin is seen after generalized tonic-clonic or partial complex seizures. The peak level is seen 15-20 minutes after the event. The half-life of the prolactin is about 20 minutes, and there is a return to pre-ictal levels after 60 minutes.

 

Sample collection should be standardized for optimum usability:

(1) Ideally this would be 20-30 minutes after the episode. A sample more than 60 minutes after the seizure will likely be a false negative.

(2) Baseline level, either drawn more than 60 minutes after the seizure or on a day without seizure activity.

 

Criteria for elevations in serum prolactin seen in epileptic seizures:

(1) A level 2 times baseline levels (some use 3 times baseline).

(2) A level more than 3 standard deviations above the baseline.

 

Serum prolactin levels can help distinguish pseudoseizures from true seizures. However, this may be limited:

(1) by the prevalence of pseudoseizures in the population (see Table 2, page 1225, Yerby et al, 1987).

(2) in patients with concurrent epilepsy and pseudoseizures

 

The absence of a rise in prolactin does not exclude the diagnosis of epilepsy. Prolactin levels will not be elevated if (Sperling et al):

(1) the seizure was brief (< 10 seconds), or

(2) there was no loss of consciousness.

A sample drawn more than 60 minutes after the event will miss an elevated value.

 


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