Forecasting individual risk for long-term Posttraumatic Stress Disorder in emergency medical settings using biomedical data: A machine learning multicenter cohort study

K. Schultebraucks, M. Sijbrandij, I. Galatzer-Levy, J. Mouthaan, M. Olff, M. van Zuiden

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

The necessary requirement of a traumatic event preceding the development of Posttraumatic Stress Disorder, theoretically allows for administering preventive and early interventions in the early aftermath of such events. Machine learning models including biomedical data to forecast PTSD outcome after trauma are highly promising for detection of individuals most in need of such interventions. In the current study, machine learning was applied on biomedical data collected within 48 h post-trauma to forecast individual risk for long-term PTSD, using a multinominal approach including the full spectrum of common PTSD symptom courses within one prognostic model for the first time. N = 417 patients (37.2% females; mean age 46.09 ± 15.88) admitted with (suspected) serious injury to two urban Academic Level-1 Trauma Centers were included. Routinely collected biomedical information (endocrine measures, vital signs, pharmacotherapy, demographics, injury and trauma characteristics) upon ED admission and subsequent 48 h was used. Cross-validated multi-nominal classification of longitudinal self-reported symptom severity (IES-R) over 12 months and bimodal classification of clinician-rated PTSD diagnosis (CAPS-IV) at 12 months post-trauma was performed using extreme Gradient Boosting and evaluated on hold-out sets. SHapley Additive exPlanations (SHAP) values were used to explain the derived models in human-interpretable form. Good prediction of longitudinal PTSD symptom trajectories (multiclass AUC = 0.89) and clinician-rated PTSD at 12 months (AUC = 0.89) was achieved. Most relevant prognostic variables to forecast both multinominal and dichotomous PTSD outcomes included acute endocrine and psychophysiological measures and hospital-prescribed pharmacotherapy. Thus, individual risk for long-term PTSD was accurately forecasted from biomedical information routinely collected within 48 h post-trauma. These results facilitate future targeted preventive interventions by enabling future early risk detection and provide further insights into the complex etiology of PTSD.
Original languageEnglish
Article number100297
Pages (from-to)1-10
Number of pages10
JournalNeurobiology of Stress
Volume14
Early online date18 Jan 2021
DOIs
Publication statusPublished - May 2021

Bibliographical note

© 2021 The Authors.

Funding

The TraumaTIPS study was supported by ZonMw, the Netherlands Organization for Health Research and Development (grant # 62300038 ), the Hague, the Netherlands, and by Stichting Achmea Slachtoffer en Samenleving (SASS) , Aid to Victims, Zeist, the Netherlands. The current project was additionally supported by an Amsterdam Public Health Research Institute Alliance Grant, Amsterdam, the Netherlands , within the Mental Health Program. Katharina Schultebraucks was supported by the German Research Foundation (SCHU 3259/1-1 ). Mirjam van Zuiden was supported by a Veni grant from ZonMw, the Netherlands organization for Health Research and Development (# 91617037 ), the Hague, the Netherlands.. The funders were not involved in the collection, analysis and interpretation of data; in the writing of the report; and in the decision to submit the article for publication.

FundersFunder number
Netherlands Organization for Health Research and Development62300038
Stichting Achmea Slachtoffer en Samenleving
Deutsche ForschungsgemeinschaftSCHU 3259/1-1, 91617037
ZonMw

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