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Published on: November 21, 2013
Antipsychotic-induced extrapyramidal syndromes in psychiatric practice: a case-control study
I Schillevoort1, R M C Herings, G W K Hugenholtz
1Department of Pharmacoepidemiology & Pharmacotherapy, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands.
This study found low potency antipsychotics carry a lower risk of extrapyramidal side effects (EPS). However, atypical antipsychotics did not show a reduced EPS risk compared to clinical trials, possibly due to dosing differences.
Area of Science:
- Pharmacology
- Clinical Pharmacy
- Psychiatry
Background:
- Atypical antipsychotics are generally considered to have a lower risk of extrapyramidal side effects (EPS) compared to classical antipsychotics.
- However, this finding is not universally accepted, prompting further investigation into comparative EPS risks.
Purpose of the Study:
- To compare the risk of extrapyramidal side effects (EPS) among different subgroups of antipsychotic medications.
- To investigate potential discrepancies in EPS risk between real-world data and previous clinical trial findings.
Main Methods:
- Utilized automated dispensing records from a large psychiatric hospital in The Netherlands.
- Identified cases as first-time users of anticholinergic antiparkinson drugs and controls as non-users of such medication.
- Compared previous antipsychotic use and relevant co-factors between cases and controls.
Main Results:
- Antipsychotic users were significantly more likely to require anticholinergic antiparkinson medication (OR: 10.1).
- Low potency antipsychotics showed a lower odds ratio for EPS (3.0) compared to high potency ones (10.8).
- Both classical and atypical antipsychotics demonstrated comparable odds ratios for EPS (10.0 and 8.0, respectively), with lower equivalent doses than in prior trials.
Conclusions:
- Low potency antipsychotics are associated with a substantially lower risk of EPS.
- The expected reduced EPS risk with atypical antipsychotics was not observed, potentially due to the high and non-equivalent doses of classical antipsychotics used in previous studies.
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