Development and Validation of a Dynamic Risk Prediction Model to Forecast Psychosis Onset in Patients at Clinical High Risk

Author:

Studerus Erich1,Beck Katharina12ORCID,Fusar-Poli Paolo3456,Riecher-Rössler Anita1

Affiliation:

1. Center for Gender Research and Early Detection, University of Basel Psychiatric Hospital, Wilhelm Klein-Strasse, Basel, Switzerland

2. Department of Psychology, Division of Clinical Psychology and Epidemiology, University of Basel, Basel, Switzerland

3. Early Psychosis: Interventions and Clinical-detection (EPIC) Lab, Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK

4. OASIS Service, South London and Maudsley National Health Service Foundation Trust, London, UK

5. Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy

6. National Institute of Health Research—Mental Health—Translational Research Collaboration—Early Psychosis Workstream, London, UK

Abstract

Abstract The prediction of outcomes in patients at Clinical High Risk for Psychosis (CHR-P) almost exclusively relies on static data obtained at a single snapshot in time (ie, baseline data). Although the CHR-P symptoms are intrinsically evolving over time, available prediction models cannot be dynamically updated to reflect these changes. Hence, the aim of this study was to develop and internally validate a dynamic risk prediction model (joint model) and to implement this model in a user-friendly online risk calculator. Furthermore, we aimed to explore the prognostic performance of extended dynamic risk prediction models and to compare static with dynamic prediction. One hundred ninety-six CHR-P patients were recruited as part of the “Basel Früherkennung von Psychosen” (FePsy) study. Psychopathology and transition to psychosis was assessed at regular intervals for up to 5 years using the Brief Psychiatric Rating Scale-Expanded (BPRS-E). Various specifications of joint models were compared with regard to their cross-validated prognostic performance. We developed and internally validated a joint model that predicts psychosis onset from BPRS-E disorganization and years of education at baseline and BPRS-E positive symptoms during the follow-up with good prognostic performance. The model was implemented as online risk calculator (http://www.fepsy.ch/DPRP/). The use of extended joint models slightly increased the prognostic accuracy compared to basic joint models, and dynamic models showed a higher prognostic accuracy than static models. Our results confirm that extended joint modeling could improve the prediction of psychosis in CHR-P patients. We implemented the first online risk calculator that can dynamically update psychosis risk prediction.

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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