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Risk of repeat self-harm among individuals presenting to healthcare services: development and validation of a clinical risk assessment model (OxSET)
Department of Psychiatry, Warneford Hospital, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK.
Nuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, UK.
Department of Psychiatry, Warneford Hospital, University of Oxford, Oxford, UK; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
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2024 (English)In: BMJ Mental Health, E-ISSN 2755-9734, Vol. 27, no 1, article id e301180Article in journal (Refereed) Published
Abstract [en]

Background: A self-harm episode is a major risk factor for repeat self-harm. Existing tools to assess and predict repeat self-harm have major methodological limitations, and few are externally validated.

Objective: To develop and validate a risk assessment model of repeat self-harm up to 6 months after an episode of non-fatal self-harm that resulted in an emergency visit to hospital or specialised care.

Methods: Using Swedish national registers, we identified 53 172 people aged >= 10 years who self-harmed during 2008-2012. We allocated 37 523 individuals to development (2820 or 7.5% repeat self-harm incidents within 6 months) and 15 649 to geographic validation (1373 repeat episodes) samples, based on region of residence. In a temporal validation of people who self-harmed during 2018-2019, we identified 25 036 individuals (2886 repeat episodes). We fitted a multivariable accelerated failure time model to predict risk of repeat self-harm.

Findings: In the external validations (n=40 685), rates of repeat self-harm were 8.8%-11.5% over 6 months. The final model retained 17 factors. Calibration and discrimination were similar in both validation samples, with observed-to-expected ratio=1.15 (95% CI=1.09 to 1.21) and c-statistic=0.72 (95% CI=0.70 to 0.73) in the geographical validation. At 6 months and a 10% risk cut-off, sensitivity was 51.5% (95% CI=48.8% to 54.2%) and specificity was 80.7% (95% CI=80.1% to 81.4%) in geographic validation; corresponding values were 56.9% (95% CI=55.1% to 58.7%) and 76.0% (95% CI=75.5% to 76.6%) in temporal validation. Discrimination was slightly worse at the 1-month prediction horizon (c-statistics of 0.66-0.68).

Conclusions: Using mostly routinely collected data, simple risk assessment models and tools can provide acceptable levels of accuracy for repeat of self-harm.

Clinical implications: This risk model (OXford SElf-harm repeat tool) may assist clinical decision-making.

Place, publisher, year, edition, pages
BMJ Publishing Group Ltd, 2024. Vol. 27, no 1, article id e301180
Keywords [en]
Data Interpretation, Statistical, Suicide & self-harm
National Category
Psychiatry
Identifiers
URN: urn:nbn:se:oru:diva-116877DOI: 10.1136/bmjment-2024-301180ISI: 001337651900001PubMedID: 39414315Scopus ID: 2-s2.0-85206660149OAI: oai:DiVA.org:oru-116877DiVA, id: diva2:1906622
Funder
Wellcome trust, 202836/Z/16/ZSwedish Research Council, 2015-0028
Note

Funding: This research study was supported by grants from the Wellcome Trust (202836/Z/16/Z) to SF, NIHR Oxford Health Biomedical Research Centre (BRC-1215-20005) and the Swedish Research Council (2015-0028). TRF received funding from the NIHR Community Healthcare MedTech and In Vitro Diagnostics Co-operative at Oxford Health NHS Foundation Trust (MIC-2016-018) and the NIHR Applied Research Collaboration Oxford and Thames Valley at Oxford Health NHS Foundation Trust (grant number N/A). 

Available from: 2024-10-18 Created: 2024-10-18 Last updated: 2024-11-01Bibliographically approved

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