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
. 2022 Dec;31(12):1943-1951.
doi: 10.1007/s00787-021-01817-3. Epub 2021 Jun 18.

National record-linkage study of hospital admissions for schizophrenia in childhood and adolescence in England

Affiliations

National record-linkage study of hospital admissions for schizophrenia in childhood and adolescence in England

Olena Seminog et al. Eur Child Adolesc Psychiatry. 2022 Dec.

Abstract

Background: There is a lack of information on changes in hospital admission rates for childhood-onset schizophrenia (COS), or on patient characteristics, to inform clinical research and health service provision.

Aims: To report age- and sex-specific incidence rates of hospital admissions and day patient care for schizophrenia (ICD-10 F20) and non-affective psychosis (ICD-10 F20-29), by year of occurrence and age, in childhood and adolescence.

Methods: Population-based study using person-linked data for England (available 2001-2016); time-periods in single years and 4-year groups.

Results: Hospitalised incidence for schizophrenia increased with increasing age, from 0.03 (95% confidence interval (CI) 0.02-0.05) and 0.01 (0-0.01) per 100,000 in, respectively, males and females aged 5-12 years, to 3.67 (3.44-3.91) in males and 1.58 (1.43-1.75) in females aged 13-17 years. There was no gender difference in hospitalised incidence rates in children aged 5-12, but in 13-17 years old, there was a male excess. Rates for schizophrenia were stable over time in 5-12 years old. In ages 13-17, rates for schizophrenia decreased between 2001-2004 and 2013-2016 in males, from 6.65 (6.04-7.31) down to 1.40 (1.13-1.73), and in females from 2.42 (2.05-2.83) to 1.18 (0.92-1.48). The hospitalisation rates for schizophrenia and non-affective psychosis, combined, in 13-17 years old decreased in males from 14.20 (13.30-15.14) in 2001-2004 to 10.77 (9.97-11.60) in 2013-2016, but increased in females from 7.49 (6.83-8.20) to 10.16 (9.38-11.00).

Conclusions: The study confirms that childhood-onset schizophrenia is extremely rare, with only 32 cases identified over a 15-year period in the whole of England. The incidence of schizophrenia and non-affective psychosis increased substantially in adolescence; however, the marked reduction in the proportion of those diagnosed with schizophrenia in this age group suggests a possible change in diagnostic practice.

Keywords: Childhood onset; Children; Electronic records; Epidemiology; Schizophrenia.

PubMed Disclaimer

Conflict of interest statement

Authors have no conflicts of interest to disclose.

Figures

Fig. 1
Fig. 1
Age distribution of schizophrenia cases in individual years, 2001–2016, males and females
Fig. 2
Fig. 2
Age distribution of non-affective psychosis cases in individual years of age, 2001–2016, males and females

References

    1. Rapoport JL, Giedd JN, Gogtay N. Neurodevelopmental model of schizophrenia: update 2012. Mol Psychiatry. 2012;17(12):1228–1238. doi: 10.1038/mp.2012.23. - DOI - PMC - PubMed
    1. Clemmensen L, Vernal DL, Steinhausen HC. A systematic review of the long-term outcome of early onset schizophrenia. BMC Psychiatry. 2012;12:150. doi: 10.1186/1471-244X-12-150. - DOI - PMC - PubMed
    1. Eggers C, Bunk D. Early development of childhood-onset schizophrenia. Fortschr Neurol Psychiatr. 2009;77(10):558–567. doi: 10.1055/s-0028-1109737. - DOI - PubMed
    1. NICE. Psychosis and schizophrenia in children and young people: recognition and management. www.nice.org.uk/CG1552013.
    1. Goldacre MJ, Simmons H, Henderson J, Gill LE. Trends in episode based and person based rates of admission to hospital in the Oxford record linkage study area. Br Med J (Clin Res Ed) 1988;296(6621):583–585. doi: 10.1136/bmj.296.6621.583. - DOI - PMC - PubMed