Clinical high-risk for psychosis (CHR-P) criteria identify individuals with attenuated psychotic symptoms, brief, limited psychotic episodes, or genetic risk accompanied by functional decline.1 This state is associated with an elevated risk of transition to psychosis, which increases with time.1 The CHR-P population is heterogeneous, with many individuals experiencing persistent symptoms or functional impairment.1,2 Advances in detection, prognosis, and stage-specific interventions aim to reduce transition risk and improve overall clinical outcomes.2

APS= attenuated psychosis syndrome; BLIPS=brief limited intermittent psychotic symptoms; CAARMS=Comprehensive Assessment of At-Risk Mental States; GRD=genetic risk and deterioration; SIPS=Structured Interview for Psychosis-Risk Syndromes

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