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A predictor model of treatment resistance in schizophrenia using data from electronic health records. | LitMetric

AI Article Synopsis

  • The study aimed to create a predictive tool for treatment-resistant schizophrenia (TRS) using data from mental health services across four London boroughs, analyzing a large diverse group of patients.
  • Data from clinical records of 1,515 patients revealed that 17% developed TRS, with the Cox LASSO survival model producing a Harrel's C index of 0.60, indicating a moderate predictive ability.
  • Key predictors of TRS included more inpatient days, increased face-to-face clinical contact prior to treatment, minor cognitive issues, and younger age at the first antipsychotic prescription; however, routine data alone may not be enough for accurate prediction.

Article Abstract

Objectives: To develop a prognostic tool of treatment resistant schizophrenia (TRS) in a large and diverse clinical cohort, with comprehensive coverage of patients using mental health services in four London boroughs.

Methods: We used the Least Absolute Shrinkage and Selection Operator (LASSO) for time-to-event data, to develop a risk prediction model from the first antipsychotic prescription to the development of TRS, using data from electronic health records.

Results: We reviewed the clinical records of 1,515 patients with a schizophrenia spectrum disorder and observed that 253 (17%) developed TRS. The Cox LASSO survival model produced an internally validated Harrel's C index of 0.60. A Kaplan-Meier curve indicated that the hazard of developing TRS remained constant over the observation period. Predictors of TRS were: having more inpatient days in the three months before and after the first antipsychotic, more community face-to-face clinical contact in the three months before the first antipsychotic, minor cognitive problems, and younger age at the time of the first antipsychotic.

Conclusions: Routinely collected information, readily available at the start of treatment, gives some indication of TRS but is unlikely to be adequate alone. These results provide further evidence that earlier onset is a risk factor for TRS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484642PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0274864PLOS

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