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Published on: November 21, 2013
Clinical High-Risk for Psychosis in Adolescents: Updated Meta-analysis on Transition Rates and Antipsychotic
Andrea Raballo1, Michele Poletti2, Raffaele Lavalle3
1University of Southern Switzerland, Lugano, Switzerland; Cantonal Sociopsychiatric Organisation, Repubblica e Cantone Ticino, Mendrisio, Switzerland.
The clinical high-risk for psychosis (CHR-P) criteria are valid in youth, with transition rates around 16-17% in adolescents. Baseline antipsychotic (AP) use increases psychosis transition risk, highlighting its prognostic significance.
Area of Science:
- Child and Adolescent Psychiatry
- Psychosis Risk Research
- Mental Health Prognostics
Background:
- The clinical high-risk for psychosis (CHR-P) paradigm is used in youth mental health.
- Prognostic validity of CHR-P in minors requires further investigation.
- Antipsychotic (AP) exposure is a potential factor influencing CHR-P outcomes.
Purpose of the Study:
- To conduct an updated meta-analysis of psychosis transition rates in children and adolescents meeting CHR-P criteria.
- To evaluate the impact of baseline antipsychotic (AP) exposure on transition outcomes in this population.
Main Methods:
- Systematic review and meta-analysis adhering to PRISMA guidelines.
- Searched PubMed/MEDLINE and Cochrane Library up to August 30, 2025.
- Included studies with participants ≤18 years or mean age <18 years, using validated CHR-P instruments and reporting longitudinal transition data.
- Pooled transition prevalences using random-effects models and conducted subgroup analyses for AP exposure.
Main Results:
- Included 32 independent cohorts with 2951 CHR-P individuals, predominantly adolescents.
- Overall transition rates were ~16-17% in studies restricted to minors and ~23% in broader samples including young adults.
- Baseline AP exposure was associated with a significantly higher risk of transition (risk ratio ≈1.5).
Conclusions:
- CHR-P criteria show prognostic validity in developmental populations, with adolescent transition rates comparable to young adults.
- Baseline AP use is a significant negative prognostic factor, increasing transition risk.
- Future research should expand prognostic focus to include remission, persistence, and functional outcomes.
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