Key result
Olanzapine linked to highest rate of EEG abnormalities at ~35% versus other antipsychotics.
Why the study?
EEG abnormalities associated with different antipsychotics and their comparison with healthy subjects were not previously investigated electrophysiologically.
Do different antipsychotics (quetiapine, olanzapine, haloperidol) increase the risk of EEG abnormalities compared to healthy subjects?
Observational (n=111)
Single-blind
Do different antipsychotics (quetiapine, olanzapine, haloperidol) increase the risk of EEG abnormalities compared to healthy subjects?
Olanzapine and haloperidol are associated with significantly higher rates of EEG abnormalities compared to quetiapine and healthy controls.
Quetiapine linked to fewer EEG abnormalities than olanzapine or haloperidol; leaves open relevance for seizure risk in vulnerable patients.
In this study the effects of the atypical antipsychotics quetiapine and olanzapine, and the typical antipsychotic haloperidol on EEG patterns were retrospectively investigated in 81 patients under stable monotherapy with either drug (quetiapine: n=22, olanzapine: n=37, haloperidol: n=22). These three subgroups were compared with a control group of healthy subjects (n=30) which were matched regarding sex and age. Diagnoses of patients were schizophrenia (DSM-IV 295.xx, n=61), brief psychotic disorder (DSM-IV 298.8, n=9), schizoaffective disorder (DSM-IV 295.70, n=8) and delusional disorder (DSM-IV 297.1, n=3). There were no statistically significant differences regarding demographic characteristics between the groups. Digital EEG recordings were retrieved from a database and visually assessed by two independent investigators, and one blinded regarding medication. One patient from the quetiapine group (5%), 13 olanzapine patients (35%), five of the haloperidol patients (23%) and two subjects of the control group (7%) had an abnormal EEG. Epileptiform activity was observed in four patients (11%) of the olanzapine group, and none in the others. EEG abnormalities were statistically significantly increased with dose in the olanzapine group, in contrast to patients treated with haloperidol, quetiapine or healthy subjects. In conclusion, EEG abnormalities seem to occur rarely in patients treated with quetiapine comparable to the control group, but significantly more often with haloperidol and olanzapine, possibly due to different receptor profiles of these substances. To our knowledge, this is the first electrophysiological investigation comparing the new atypical antipsychotics quetiapine, haloperidol, olanzapine with healthy subjects.
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Amann et al. (2003) conducted an observational in Psychotic disorders (n=111). Antipsychotics (quetiapine, olanzapine, haloperidol) vs. Healthy subjects was evaluated on Abnormal EEG. EEG abnormalities occurred in 35% of patients on olanzapine, 23% on haloperidol, and 5% on quetiapine, compared to 7% of healthy controls.
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