4.4 Article

Developing and internally validating a prognostic model (P Risk) to improve the prediction of psychosis in a primary care population using electronic health records: The MAPPED study

期刊

SCHIZOPHRENIA RESEARCH
卷 246, 期 -, 页码 241-249

出版社

ELSEVIER
DOI: 10.1016/j.schres.2022.06.031

关键词

First episode psychosis; Prediction; Electronic health records; Primary care

资金

  1. National Institute for Health Research (NIHR)
  2. School for Primary Care Research
  3. NIHR Biomedical Research Centre

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This study developed and validated a risk prediction model for psychosis using linked electronic health records. The model demonstrated good discrimination in identifying patients at high risk for developing psychosis based on various predictors such as consultations, diagnoses, and prescribed medications, as well as demographic factors including age, sex, and social deprivation.
Background: An accurate risk prediction algorithm could improve psychosis outcomes by reducing duration of untreated psychosis. Objective: To develop and validate a risk prediction model for psychosis, for use by family doctors, using linked electronic health records. Methods: A prospective prediction study. Records from family practices were used between 1/1/2010 to 31/12/ 2017 of 300,000 patients who had consulted their family doctor for any nonpsychotic mental health problem. Records were selected from Clinical Practice Research Datalink Gold, a routine database of UK family doctor records linked to Hospital Episode Statistics, a routine database of UK secondary care records. Each patient had 5-8 years of follow up data. Study predictors were consultations, diagnoses and/or prescribed medications, during the study period or historically, for 13 nonpsychotic mental health problems and behaviours, age, gender, number of mental health consultations, social deprivation, geographical location, and ethnicity. The outcome was time to an ICD10 psychosis diagnosis. Findings: 830 diagnoses of psychosis were made. Patients were from 216 family practices; mean age was 45.3 years and 43.5 % were male. Median follow-up was 6.5 years (IQR 5.6, 7.8). Overall 8-year psychosis incidence was 45.8 (95 % CI 42.8, 49.0)/100,000 person years at risk. A risk prediction model including age, sex, ethnicity, social deprivation, consultations for suicidal behaviour, depression/anxiety, substance abuse, history of consultations for suicidal behaviour, smoking history and prescribed medications for depression/anxiety/PTSD/OCD and total number of consultations had good discrimination (Harrell's C = 0.774). Identifying patients aged 17-100 years with predicted risk exceeding 1.0 % over 6 years had sensitivity of 71 % and specificity of 84 %.

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