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| Feature | Typical (First-Generation) | Atypical (Second-Generation) |
|---|---|---|
| Primary Mechanism | D2 receptor blockade | D2 and 5-HT2A receptor blockade |
| EPS Risk | High | Low to moderate |
| Tardive Dyskinesia Risk | Higher | Lower |
| Metabolic Effects | Lower | Higher (weight gain, diabetes) |
| Efficacy for Negative Symptoms | Limited | Better |
| Cost | Generally less expensive | Generally more expensive |
Antipsychotics used in elderly patients with dementia-related psychosis increase risk of death. These medications have a black box warning for this population.
Neuroleptic Malignant Syndrome is a medical emergency requiring immediate discontinuation of the antipsychotic, intensive supportive care, and possibly dantrolene or bromocriptine.
Remember the Abnormal Involuntary Movement Scale (AIMS) for assessing tardive dyskinesia:
Conduct AIMS assessment regularly for patients on long-term antipsychotic therapy.
For IM administration of olanzapine (Zyprexa), observe for at least 3 hours for signs of post-injection delirium/sedation syndrome, which can resemble an overdose.
A 32-year-old patient with schizophrenia reports feeling "jittery" and unable to sit still after starting haloperidol 5 mg twice daily three days ago. On assessment, the patient appears restless, constantly shifting position, and pacing. Vital signs are within normal limits.
Nursing Considerations:
| EPS Type | Timing | Symptoms | Management |
|---|---|---|---|
| Acute Dystonia | Hours to days | Muscle spasms, oculogyric crisis, torticollis | IM/IV anticholinergics (benztropine) |
| Akathisia | Days to weeks | Restlessness, inability to sit still | Beta-blockers, benzodiazepines, dose reduction |
| Parkinsonism | Weeks to months | Tremor, rigidity, bradykinesia | Oral anticholinergics, dose reduction |
| Tardive Dyskinesia | Months to years | Orofacial movements, choreiform movements | Prevention, switch to atypical, VMAT2 inhibitors |
| Feature | Antipsychotics | Anxiolytics (Benzodiazepines) |
|---|---|---|
| Primary Indication | Psychotic disorders, bipolar disorder | Anxiety disorders, insomnia |
| Mechanism | Dopamine/serotonin receptor blockade | GABA enhancement |
| Onset of Action | Full effect: 2-6 weeks | Rapid: minutes to hours |
| Key Side Effects | EPS, metabolic effects | Sedation, dependence, respiratory depression |
| Abuse Potential | Low | High |
| Feature | Neuroleptic Malignant Syndrome | Serotonin Syndrome |
|---|---|---|
| Causative Agents | Antipsychotics | SSRIs, SNRIs, MAOIs, other serotonergic drugs |
| Onset | Gradual (1-3 days) | Rapid (hours) |
| Temperature | Severe hyperthermia (>40°C) | Mild to moderate fever |
| Muscle Findings | Lead-pipe rigidity | Hyperreflexia, clonus, tremor |
| Treatment | Dantrolene, bromocriptine | Cyproheptadine, benzodiazepines |
Both NMS and Serotonin Syndrome are medical emergencies requiring immediate discontinuation of causative agents and supportive care. Mortality is higher with untreated NMS.
Remember "DANCE" for what typical antipsychotics cause more than atypicals:
Remember "COZQ" for metabolic risk from highest to lowest:
Remember "ABCS" for clozapine monitoring:
1. Which antipsychotic requires regular WBC monitoring due to risk of agranulocytosis?
2. What is the most appropriate initial nursing intervention for a patient experiencing acute dystonic reaction?
3. Which metabolic parameters should be monitored in patients taking atypical antipsychotics?
4. What is the cardinal symptom of akathisia?
5. Which antipsychotic side effect is characterized by involuntary movements of the face and tongue that may be irreversible?
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