Prediction of Suicide-Related Events by Analyzing Electronic Medical Records from PTSD Patients with Bipolar Disorder

被引:8
|
作者
Fan, Peihao [1 ]
Guo, Xiaojiang [1 ]
Qi, Xiguang [1 ]
Matharu, Mallika [2 ,3 ]
Patel, Ravi [4 ]
Sakolsky, Dara [5 ]
Kirisci, Levent [6 ]
Silverstein, Jonathan C. [7 ]
Wang, Lirong [1 ]
机构
[1] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Computat Chem Genom Screening Ctr, Pittsburgh, PA 15206 USA
[2] Univ Pittsburgh, Sch Arts & Sci, Dept Stat, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Sch Arts & Sci, Dept Econ, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Sch Pharm, Dept Pharm & Therapeut, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA 15213 USA
[6] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15213 USA
[7] Univ Pittsburgh, Sch Med, Dept Biomed Informat, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
PTSD; bipolar disorder; machine learning; random forest; suicide-related events; model decomposition; POSTTRAUMATIC-STRESS-DISORDER; PREVENTION STRATEGIES; SPECTRUM DISORDER; RISK-FACTORS; PREVALENCE; SCHIZOPHRENIA; ALGORITHM; LIFETIME;
D O I
10.3390/brainsci10110784
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Around 800,000 people worldwide die from suicide every year and it's the 10th leading cause of death in the US. It is of great value to build a mathematic model that can accurately predict suicide especially in high-risk populations. Several different ML-based models were trained and evaluated using features obtained from electronic medical records (EMRs). The contribution of each feature was calculated to determine how it impacted the model predictions. The best-performing model was selected for analysis and decomposition. Random forest showed the best performance with true positive rates (TPR) and positive predictive values (PPV) of greater than 80%. The use of Sertraline, Fentanyl, Aripiprazole, Lamotrigine, and Tramadol were strong indicators for no SREs within one year. The use of Haloperidol, Trazodone and Citalopram, a diagnosis of autistic disorder, schizophrenic disorder, or substance use disorder at the time of a diagnosis of both PTSD and bipolar disorder, predicted the onset of SREs within one year. Additional features with potential protective or hazardous effects for SREs were identified by the model. We constructed an ML-based model that was successful in identifying patients in a subpopulation at high-risk for SREs within a year of diagnosis of both PTSD and bipolar disorder. The model also provides feature decompositions to guide mechanism studies. The validation of this model with additional EMR datasets will be of great value in resource allocation and clinical decision making.
引用
收藏
页码:1 / 30
页数:27
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