TABLE 16-1 - Neuroleptic lnduced Movement Disorders
| Disorder | Risk Factors | Onset | Treatment |
| Dystonia | High-potency antipsychotics Young men |
First few days of therapy | IM/IV benztropine or diphenhydramine Severe laryngospasm may require intubation |
| Akathisia | Recent increase/onset of medication dosing | First month of therapy | Propanolol, lorazepam (maybe anticholinergics) |
| EPS | High-potency antipsychotics Elderly Prior episode of EPS |
First few weeks of therapy | Anticholinergic Lower antipsychotic dosage or change to lower-potency antipsychotic |
| NMS | High-dose anti psychotics, rapid dose escalation, or IM injection of anti psychotics Agitation, dehydration Prior episode of NMS |
Usually within first few weeks; can occur at any point in antipsychotic therapy | Discontinue antipsychotic medication Supportive symptom management Dantrolene, bromocriptine May require intensive care |
| Tardive dyskinesia | Elderly Long-term antipsychotic treatment Female African American Mood disorders |
Usually after years of treatment | Lower dosage of antipsychotic Change antipsychotics Change to clozaril |
The DSM-IV classification for these disorders defines them as neuroleptic-induced movement disorders. The term neuroleptic generally refers to typical antipsychotics (see Chapter 11). Exceptions include risperidone, which is classified as an atypical antipsychotic but can cause all the above disorders; SSRls, which are not neuroleptic drugs but can clearly produce akathisia; and clozaril, which does not appear to produce dystonia, akathisia, EPS, or tardive dyskinesia but may cause NMS.