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Aripiprazole (abilify) and tardive dyskinesia
P & T : a Peer-Reviewed Journal for Formulary Management
|September 15, 2009
Summary
Second-generation antipsychotics, like aripiprazole, can cause tardive dyskinesia (TD) even when used off-label. This case highlights the ongoing risk of TD, emphasizing the need for continued monitoring in patients.
Area of Science:
- Psychiatry
- Pharmacology
- Neurology
Background:
- Second-generation antipsychotics (SGAs) are widely prescribed for their favorable side effect profiles regarding extrapyramidal symptoms (EPS) and tardive dyskinesia (TD).
- Metabolic adverse effects have become a significant focus in clinical practice and research concerning SGAs.
- Off-label use of SGAs is common, expanding their application beyond approved indications.
Observation:
- A case report details a patient who developed tardive dyskinesia (TD).
- The patient was treated with aripiprazole, an atypical antipsychotic, as an off-label augmentation strategy.
- The indication for aripiprazole was treatment-resistant depression.
Findings:
- Aripiprazole, despite its lower risk of EPS/TD compared to older antipsychotics, can still induce tardive dyskinesia.
- This case demonstrates that TD remains a potential adverse effect even with newer antipsychotic agents.
- The development of TD occurred in the context of off-label use for treatment-resistant depression.
Implications:
- Clinicians must remain vigilant for tardive dyskinesia (TD) in patients using second-generation antipsychotics, including off-label.
- Despite the focus on metabolic risks, the potential for neurological side effects like TD persists.
- Ongoing monitoring for TD is crucial for all patients treated with atypical antipsychotics, regardless of indication.
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