Abstract

BackgroundPsychotic disorders affect about 3% of the population worldwide and are associated with high personal, social and economic costs. They tend to have their first onset in adolescence. Increasing emphasis has been placed on early intervention to detect illness and minimise disability. In the late 1990s, criteria were developed to identify individuals at high risk for psychotic disorder. These are known as the at-risk mental state (ARMS) criteria. While ARMS individuals have a risk of psychosis much greater than the general population, most individuals meeting the ARMS criteria will not develop psychosis. Despite this, the National Institute for Health and Care Excellence recommends cognitive behavioural therapy (CBT) for all ARMS people.Clinical prediction models that combine multiple patient characteristics to predict individual outcome risk may facilitate identification of patients who would benefit from CBT and conversely those that would benefit from less costly and less intensive regular mental state monitoring. The study will systematically review the evidence on clinical prediction models aimed at making individualised predictions for the transition to psychosis.MethodsDatabase searches will be conducted on PsycINFO, Medline, EMBASE and CINAHL. Reference lists and subject experts will be utilised. No language restrictions will be placed on publications, but searches will be restricted to 1994 onwards, the initial year of the first prospective study using ARMS criteria. Studies of any design will be included if they examined, in ARMS patients, whether more than one factor in combination is associated with the risk of transition to psychosis. Study quality will be assessed using the prediction model risk of bias assessment tool (PROBAST). Clinical prediction models will be summarised qualitatively, and if tested in multiple validation studies, their predictive performance will be summarised using a random-effects meta-analysis model.DiscussionThe results of the review will identify prediction models for the risk of transition to psychosis. These will be informative for clinicians currently treating ARMS patients and considering potential preventive interventions. The conclusions of the review will also inform the possible update and external validation of prediction models and clinical prediction rules to identify those at high or low risk of transition to psychosis.Trial registrationThe review has been registered with PROSPERO (CRD42018108488).

Highlights

  • Psychotic disorders affect about 3% of the population worldwide and are associated with high personal, social and economic costs

  • Growing calls for improving the routine clinical management of people with at-risk mental state (ARMS) are likely to result in an additional strain on resources and an urgent need to develop better systems to identify ARMS individuals that might be at the highest risk of developing psychosis and might benefit from receiving evidence-based preventive interventions

  • Selection criteria Study design The review will include any prospective or retrospective studies, with participants meeting the ARMS criteria, which have developed, compared, or validated a prediction model, or clinical prediction rule based on a model, combining multiple prognostic factors to predict the risk of transition to psychosis

Read more

Summary

Methods

Selection criteria Study design The review will include any prospective or retrospective studies (i.e. cohort studies as well as randomised controlled trials of preventive interventions), with participants meeting the ARMS criteria, which have developed, compared, or validated a prediction model, or clinical prediction rule based on a model, combining multiple prognostic factors to predict the risk of transition to psychosis. Data extraction related to clinical prediction models will include the final model (its specification, included factors, values of regression coefficients and standard errors), how it was developed and any internal or external validation performance statistics for discrimination (such as the c-statistics or area under the curve) or for calibration (such as the expected/observed events ratio), together with their associated measures of spread. This will be informed by the Critical Appraisal and Data Extraction for Systematic Reviews of Prediction Modelling Studies (CHARMS) checklist which helps frame the review question, design the review and extract the relevant items from the reports of the primary prediction modelling studies [20]. Analysis of subgroups or subsets If there are sufficient relevant prediction models available, subgroup analyses will synthesise calibration and discrimination statistics for studies conducted in different settings (countries) or different types of studies (prospective studies vs randomised studies vs randomised trials) or different model types (logistic vs survival analysis)

Discussion
Background
Findings
Availability of data and materials Not applicable
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call