Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Oct;14(3):322-32.
doi: 10.1002/wps.20250.

At risk or not at risk? A meta-analysis of the prognostic accuracy of psychometric interviews for psychosis prediction

Affiliations

At risk or not at risk? A meta-analysis of the prognostic accuracy of psychometric interviews for psychosis prediction

Paolo Fusar-Poli et al. World Psychiatry. 2015 Oct.

Abstract

An accurate detection of individuals at clinical high risk (CHR) for psychosis is a prerequisite for effective preventive interventions. Several psychometric interviews are available, but their prognostic accuracy is unknown. We conducted a prognostic accuracy meta-analysis of psychometric interviews used to examine referrals to high risk services. The index test was an established CHR psychometric instrument used to identify subjects with and without CHR (CHR+ and CHR-). The reference index was psychosis onset over time in both CHR+ and CHR- subjects. Data were analyzed with MIDAS (STATA13). Area under the curve (AUC), summary receiver operating characteristic curves, quality assessment, likelihood ratios, Fagan's nomogram and probability modified plots were computed. Eleven independent studies were included, with a total of 2,519 help-seeking, predominately adult subjects (CHR+: N=1,359; CHR-: N=1,160) referred to high risk services. The mean follow-up duration was 38 months. The AUC was excellent (0.90; 95% CI: 0.87-0.93), and comparable to other tests in preventive medicine, suggesting clinical utility in subjects referred to high risk services. Meta-regression analyses revealed an effect for exposure to antipsychotics and no effects for type of instrument, age, gender, follow-up time, sample size, quality assessment, proportion of CHR+ subjects in the total sample. Fagan's nomogram indicated a low positive predictive value (5.74%) in the general non-help-seeking population. Albeit the clear need to further improve prediction of psychosis, these findings support the use of psychometric prognostic interviews for CHR as clinical tools for an indicated prevention in subjects seeking help at high risk services worldwide.

Keywords: Psychosis; high risk services; prevention; prognostic accuracy; psychometric interviews.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Meta-analytical summary receiver operating characteristic (SROC) curve of clinical high risk (CHR) psychometric interviews. Se – sensitivity, Sp – specificity, AUC – area under the curve, 1 – Klosterkötter et al (52), 2 – Yung et al (45), 3 – Riecher-Rössler et al (11), 4 – Woods et al (20), 5 – Addington et al (48), 6 – Liu et al (49); 7 – Simon et al (50), 8 – Lee et al (44), 9 – Schultze-Lutter et al (46), 10 – Kotlicka-Antczak et al (47), 11 – Spada et al (51)
Figure 2
Figure 2
Meta-analytical probability modifying plot, illustrating the relationship between pre-test probability (PreTP) (9 to 24% psychosis risk at 38 months in subjects seeking help at early detection services) and post-test probability (PostTP) (psychosis risk at 38 months in help-seeking subjects based on clinical high risk psychometric interviews), computed as the likelihood of a positive (above diagonal line; LR+) or negative (below diagonal line, LR−) test result over the 0-1 range of PreTP
Figure 3
Figure 3
Fagan’s nomogram illustrating the meta-analytical clinical value (post-test probability) of clinical high risk (CHR) psychometric interviews in the general population in order to predict risk of psychosis at 38 months, given an assumed psychosis risk (pre-test probability) of 3.27%, as reported in a nationally representative sample of general population subjects aged 30-44 years (see 53)

Similar articles

Cited by

References

    1. Insel TR. Rethinking schizophrenia. Nature. 2010;468:187–93. - PubMed
    1. McGorry PD. Early clinical phenotypes, clinical staging, and strategic biomarker research: building blocks for personalized psychiatry. Biol Psychiatry. 2013;74:394–5. - PubMed
    1. Arbyn M, Verdoodt F, Snijders P, et al. Accuracy of human papillomavirus testing on self-collected versus clinician-collected samples: a meta-analysis. Lancet Oncol. 2014;15:172–83. - PubMed
    1. Michel C, Schultze-Lutter F, Schimmelmann BG. Screening instruments in child and adolescent psychiatry: general and methodological considerations. Eur Child Adolesc Psychiatry. 2014;23:725–7. - PubMed
    1. Tabak AG, Herder C, Rathmann W, et al. Prediabetes: a high-risk state for diabetes development. Lancet. 2012;379:2279–90. - PMC - PubMed

LinkOut - more resources