Automated Identification of Immunocompromised Status in Critically Ill Children

Author:

Kandaswamy Swaminathan1,Orenstein Evan W.12,Quincer Elizabeth3,Fernandez Alfred J.2,Gonzalez Mark D.4,Lu Lydia2,Kamaleswaran Rishikesan5,Banerjee Imon6,Jaggi Preeti3

Affiliation:

1. Department of Pediatrics, Emory University, Atlanta, Georgia, United States

2. Division of Hospital Medicine, Children's Healthcare of Atlanta, Atlanta, Georgia, United States

3. Division of Infectious Diseases, Department of Pediatrics, Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia, United States

4. Department of Pathology, Children's Healthcare of Atlanta, Atlanta, Georgia, United States

5. Department of Biomedical Informatics, Emory University, Atlanta, Georgia, United States

6. Department of Radiology, Mayo Clinic, Phoenix, Arizona, United States

Abstract

Abstract Background Easy identification of immunocompromised hosts (ICHs) would allow for stratification of culture results based on host type. Methods We utilized antimicrobial stewardship program (ASP) team notes written during handshake stewardship rounds in the pediatric intensive care unit (PICU) as the gold standard for host status; clinical notes from the primary team, medication orders during the encounter, problem list, and billing diagnoses documented prior to the ASP documentation were extracted to develop models that predict host status. We calculated performance for three models based on diagnoses/medications, with and without natural language processing from clinical notes. The susceptibility of pathogens causing bacteremia to commonly used empiric antibiotic regimens was then stratified by host status. Results We identified 844 antimicrobial episodes from 666 unique patients; 160 (18.9%) were identified as ICHs. We randomly selected 675 initiations (80%) for model training and 169 initiations (20%) for testing. A rule-based model using diagnoses and medications alone yielded a sensitivity of 0.87 (08.6–0.88), specificity of 0.93 (0.92–0.93), and positive predictive value (PPV) of 0.74 (0.73–0.75). Adding clinical notes into XGBoost model led to improved specificity of 0.98 (0.98–0.98) and PPV of 0.9 (0.88–0.91), but with decreased sensitivity 0.77 (0.76–0.79). There were 77 bacteremia episodes during the study period identified and a host-specific visualization was created. Conclusions An electronic health record–based phenotype based on notes, diagnoses, and medications identifies ICH in the PICU with high specificity.

Funder

National Institute of Health

1998 Society

Publisher

Georg Thieme Verlag KG

Subject

Health Information Management,Advanced and Specialized Nursing,Health Informatics

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