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Updated: Jul 6, 2026

Handwriting Analysis Indicates Spontaneous Dyskinesias in Neuroleptic Naïve Adolescents at High Risk for Psychosis
Published on: November 21, 2013
Tardive dyskinesia and new antipsychotics
Christoph U Correll1, Eva M Schenk
1The Zucker Hillside Hospital, North Shore Long Island Jewish Health System, Glen Oaks, NY 11004, USA. ccorrell@lij.edu
Second-generation antipsychotics show a lower tardive dyskinesia risk than first-generation antipsychotics. However, current incidence rates for tardive dyskinesia are higher than previously reported, necessitating further investigation.
Area of Science:
- Psychiatry and Neurology
- Pharmacology
- Clinical Trials
Background:
- Tardive dyskinesia (TD) is a potential side effect of antipsychotic medications.
- First-generation antipsychotics (FGAs) have been associated with higher TD risks compared to second-generation antipsychotics (SGAs).
- Recent data is needed to update understanding of TD rates with contemporary antipsychotic use.
Purpose of the Study:
- To update the incidence and prevalence rates of tardive dyskinesia (TD) in patients treated with FGAs versus SGAs.
- To analyze TD rates based on patient age groups (children, adults, elderly).
- To compare TD risk between FGAs and SGAs using recent study data.
Main Methods:
- Systematic review and meta-analysis of 12 trials including 28,051 patients.
- Analysis of annualized TD incidence and point prevalence rates.
- Stratification of TD rates by age group and antipsychotic generation.
Main Results:
- Annual TD incidence was 5.5% for FGAs and 3.9% for SGAs.
- Adults showed significantly higher TD rates with FGAs (7.7%) versus SGAs (2.98%).
- Adult TD prevalence was 32.4% for FGAs, 13.1% for SGAs, and 15.6% for antipsychotic-free patients.
Conclusions:
- Current evidence indicates a lower risk of tardive dyskinesia (TD) with second-generation antipsychotics (SGAs) compared to first-generation antipsychotics (FGAs).
- Observed TD incidence with SGAs is higher than previously reported, potentially due to study duration and diagnostic criteria.
- Further research is warranted to clarify TD risk with contemporary antipsychotic use.
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