| Literature DB >> 31681029 |
Paolo Fusar-Poli1,2,3,4, Andrés Estradé1,5, Tom J Spencer2,6, Susham Gupta7, Silvia Murguia-Asensio8, Savithasri Eranti9, Kerry Wilding10, Olivier Andlauer7,11, Jonathan Buhagiar7, Martin Smith2, Sharon Fitzell2, Victoria Sear2, Adelaide Ademan8, Andrea De Micheli1,2, Philip McGuire4,6.
Abstract
Background: The empirical success of the Clinical High Risk for Psychosis (CHR-P) paradigm is determined by the concurrent integration of efficient detection of cases at-risk, accurate prognosis, and effective preventive treatment within specialized clinical services. The characteristics of the CHR-P services are relatively under-investigated. Method: A Pan-London Network for psychosis prevention (PNP) was created across urban CHR-P services. These services were surveyed to collect the following: description of the service and catchment area, outreach, service users, interventions, and outcomes. The results were analyzed with descriptive statistics and Kaplan Meier failure function.Entities:
Keywords: at risk mental state; prevention; psychosis; risk; schizophrenia; structured interview for psychosis-risk syndromes
Year: 2019 PMID: 31681029 PMCID: PMC6798006 DOI: 10.3389/fpsyt.2019.00707
Source DB: PubMed Journal: Front Psychiatry ISSN: 1664-0640 Impact factor: 4.157
Figure 1Pan-London Network for Psychosis-Prevention (PNP). Luton and Bedfordshire services were not included. K&C, Kensington and Chelsea; H&F Hammersmith and Fulham.
Figure 2Pan-London crude predicted incidence of psychosis per 100,000 person-year (16-35 years). aNational average calculated from the PsyMaptic Psychosis LAD v1-0 xlsx file available at: http://www.psymaptic.org/prediction/psychosis-incidence-data/.
Sociodemographic characteristics of the PNP.
| OASIS Lambeth and Southwark | OASIS Croydon and Lewisham | THEDS | HEADS UP | NEIS | ||
|---|---|---|---|---|---|---|
| Sample size | 419 | 159 | 104 | 31 | 36 | |
| CHR-P assessment | CAARMS | CAARMS | SIPS | CAARMS | CAARMS | |
| Yearly caseload | 80 | 55 | 50 | 25 | 10 | |
| Age mean (SD) | 22.84 (4.93) | 22.01 (4.76) | 22.02 (4.02) | 23.35 (4.88) | 22.33 (3.66) | |
| Age range | 14-35 | 13-36 | 17-26 | 17-33 | 18-31 | |
| Gender | ||||||
| % males | 54.65 | 57.14 | 69.23 | 58.06 | 69.44 | |
| % females | 45.35 | 42.86 | 30.77 | 41.94 | 30.56 | |
| Ethnicity | ||||||
| White | 48.55 | 40.76 | 23.11 | 58.06 | 22.22 | |
| Asian | 6.04 | 10.19 | 59.24 | 9.68 | 52.78 | |
| Black African | 9.42 | 6.37 | 8.20 | 9.68 | 0 | |
| Black Caribbean | 6.76 | 6.37 | 1.56 | 9.68 | 0 | |
| Black British | 16.43 | 19.75 | 0 | 0 | 25.00 | |
| Other | 12.8 | 16.56 | 7.89 | 12.9 | 0 | |
| Employment | ||||||
| % unemployed | 57.87 | 68.59 | 51.25 | 29.03 | 75.00 | |
| % students or employed | 42.13 | 31.41 | 48.75 | 70.97 | 25.00 | |
| Marital status | ||||||
| % married/with a partner | 21.52 | 16.13 | 6.5 | 22.58 | 5.56 | |
| % single | 78.48 | 83.87 | 93.5 | 77.42 | 94.44 | |
| Any substance misuse | ||||||
| % yes | NA | NA | 40.00 | 45.16 | 27.78 | |
| % no | NA | NA | 60.00 | 54.84 | 72.22 | |
| CHR-P subgroup | ||||||
| % APS | 80 | 75.72 | NA | 51.61 | 55.56 | |
| % BLIPS/BIPS | 19.59 | 19.65 | NA | 32.26 | 25.00 | |
| % GRD | 0.41 | 4.62 | NA | 16.13 | 19.44 | |
Additional 38 CHR-P individuals were detected in the Luton and Bedfordshire services; CAARMS, comprehensive assessment of at-risk mental states;
SIPS, structured interview for psychosis-risk syndromes; APS, attenuated psychosis syndrome; BLIPS, brief and limited intermittent psychotic symptoms;
BIPS, brief intermittent psychotic symptoms; GRD, genetic risk and deterioration syndrome; CHR-P, clinical high risk for psychosis.
Figure 3Cumulative risk of psychosis onset (failure function) in 787 CHR-P individuals from the Pan-London Network for Psychosis-Prevention (PNP). There were 503 individuals at-risk at year 1, 283 individuals at-risk at year 2, 192 individuals at-risk at year 3, 158 individuals at-risk at year 4, 139 individuals at-risk at year 5, 113 individuals at-risk at year 6, 110 individuals at-risk at year 7, 72 individuals at-risk at year 8, 42 individuals at-risk at year 9, and 29 individuals at-risk at year 10. The function was truncated at 4081 days of follow-up when 10 individuals were still at-risk for psychosis.