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PI Prob: A risk prediction and clinical guidance system for evaluating patients with recurrent infections

Primary immunodeficiency diseases represent an expanding set of heterogeneous conditions which are difficult to recognize clinically. Diagnostic rates outside of the newborn period have not changed appreciably. This concern underscores a need for novel methods of disease detection. We built a Bayesi...

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Published in:PloS one 2021-02, Vol.16 (2), p.e0237285-e0237285
Main Authors: Rider, Nicholas L, Cahill, Gina, Motazedi, Tina, Wei, Lei, Kurian, Ashok, Noroski, Lenora M, Seeborg, Filiz O, Chinn, Ivan K, Roberts, Kirk
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creator Rider, Nicholas L
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description Primary immunodeficiency diseases represent an expanding set of heterogeneous conditions which are difficult to recognize clinically. Diagnostic rates outside of the newborn period have not changed appreciably. This concern underscores a need for novel methods of disease detection. We built a Bayesian network to provide real-time risk assessment about primary immunodeficiency and to facilitate prescriptive analytics for initiating the most appropriate diagnostic work up. Our goal is to improve diagnostic rates for primary immunodeficiency and shorten time to diagnosis. We aimed to use readily available health record data and a small training dataset to prove utility in diagnosing patients with relatively rare features. We extracted data from the Texas Children's Hospital electronic health record on a large population of primary immunodeficiency patients (n = 1762) and appropriately-matched set of controls (n = 1698). From the cohorts, clinically relevant prior probabilities were calculated enabling construction of a Bayesian network probabilistic model(PI Prob). Our model was constructed with clinical-immunology domain expertise, trained on a balanced cohort of 100 cases-controls and validated on an unseen balanced cohort of 150 cases-controls. Performance was measured by area under the receiver operator characteristic curve (AUROC). We also compared our network performance to classic machine learning model performance on the same dataset. PI Prob was accurate in classifying immunodeficiency patients from controls (AUROC = 0.945; p
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Our model was constructed with clinical-immunology domain expertise, trained on a balanced cohort of 100 cases-controls and validated on an unseen balanced cohort of 150 cases-controls. Performance was measured by area under the receiver operator characteristic curve (AUROC). We also compared our network performance to classic machine learning model performance on the same dataset. PI Prob was accurate in classifying immunodeficiency patients from controls (AUROC = 0.945; p&lt;0.0001) at a risk threshold of ≥6%. Additionally, the model was 89% accurate for categorizing validation cohort members into appropriate International Union of Immunological Societies diagnostic categories. Our network outperformed 3 other machine learning models and provides superior transparency with a prescriptive output element. Artificial intelligence methods can classify risk for primary immunodeficiency and guide management. 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Diagnostic rates outside of the newborn period have not changed appreciably. This concern underscores a need for novel methods of disease detection. We built a Bayesian network to provide real-time risk assessment about primary immunodeficiency and to facilitate prescriptive analytics for initiating the most appropriate diagnostic work up. Our goal is to improve diagnostic rates for primary immunodeficiency and shorten time to diagnosis. We aimed to use readily available health record data and a small training dataset to prove utility in diagnosing patients with relatively rare features. We extracted data from the Texas Children's Hospital electronic health record on a large population of primary immunodeficiency patients (n = 1762) and appropriately-matched set of controls (n = 1698). From the cohorts, clinically relevant prior probabilities were calculated enabling construction of a Bayesian network probabilistic model(PI Prob). Our model was constructed with clinical-immunology domain expertise, trained on a balanced cohort of 100 cases-controls and validated on an unseen balanced cohort of 150 cases-controls. Performance was measured by area under the receiver operator characteristic curve (AUROC). We also compared our network performance to classic machine learning model performance on the same dataset. PI Prob was accurate in classifying immunodeficiency patients from controls (AUROC = 0.945; p&lt;0.0001) at a risk threshold of ≥6%. Additionally, the model was 89% accurate for categorizing validation cohort members into appropriate International Union of Immunological Societies diagnostic categories. Our network outperformed 3 other machine learning models and provides superior transparency with a prescriptive output element. Artificial intelligence methods can classify risk for primary immunodeficiency and guide management. 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subjects Application programming interface
Bioinformatics
Biology and Life Sciences
Children
Clinical decision making
Colon
Colon cancer
Computer and Information Sciences
Congestive heart failure
Data analysis
Decision making
Disease
Diseases
Drafting software
Editing
Evaluation
Health risks
Hospitals
Hypersensitivity
Immunology
Infectious diseases
Information services
Liver cancer
Liver diseases
Medical schools
Medicine
Medicine and Health Sciences
Patients
Pediatrics
Probability
Relapse
Streptococcus infections
title PI Prob: A risk prediction and clinical guidance system for evaluating patients with recurrent infections
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