Key Takeaways
Extended Takeaways
- In this claims cohort, baseline psychotic disorders were far more common before a hallucinogen-related admission than before other substance-related admissions (19.2% vs 6.3%), suggesting that outpatient psychosis history can materially change how postexposure risk is interpreted.
- The crude postadmission signal was substantial—16.4% vs 6.6% had ≥1 psychosis diagnosis and 9.3% vs 3.3% had ≥1 psychosis admission between 30 days and 6 months—but the association with psychosis diagnosis was no longer significant after full adjustment (HR=0.97 [0.95–1.00]).
- Baseline vulnerability markers outperformed hallucinogen exposure in adjusted models: baseline psychotic admissions showed HRs ranging from 1.28 to 1.35, stimulant use disorders HRs ranging from 1.27 to 1.32, and opioid use disorder HRs ranging from 1.28 to 1.32.
- Only 695/6,184 individuals with ≥1 hallucinogen-related admission had no other nonhallucinogen substance-related admission during enrollment, so clinicians should expect polysubstance use to be the rule rather than the exception when assessing acute psychosis risk in this population.
- The median age for hallucinogen-related admissions was 24 years [IQR=16], overlapping the usual age of onset for schizophrenia spectrum disorders; this makes prodromal illness a practical alternative explanation when psychosis emerges after hallucinogen-related care.
- Excluding people with prior psychosis admissions alone may miss many high-risk patients, because psychosis-related admissions represented only a subset of those with baseline psychotic disorders (10,719/18,131 people); outpatient diagnostic history added meaningful confounder control.