Development and validation of high definition phenotype-based mortality prediction in critical care units

Author:

Sun Yao1,Kaur Ravneet2,Gupta Shubham2,Paul Rahul2,Das Ritu2,Cho Su Jin3,Anand Saket4,Boutilier Justin J5,Saria Suchi678,Palma Jonathan9,Saluja Satish10,McAdams Ryan M11,Kaur Avneet12,Yadav Gautam13,Singh Harpreet2ORCID

Affiliation:

1. Division of Neonatology, Department of Pediatrics, University of California San Francisco, San Francisco, California, USA

2. Research and Development, Child Health Imprints (CHIL) Pte. Ltd., Singapore

3. Department of Pediatrics, College of Medicine, Ewha Womans University Seoul, Seoul, Korea

4. Department of Computer Science, Indraprastha Institute of Information Technology, New Delhi, India

5. Department of Industrial and Systems Engineering, University of Wisconsin–Madison, Wisconsin, USA

6. Machine Learning and Healthcare Lab, Johns Hopkins University, Baltimore, Maryland, USA

7. Department of Applied Math & Statistics, Johns Hopkins University, Baltimore, Maryland, USA

8. Department of Health Policy & Management, Johns Hopkins University, Baltimore, Maryland, USA

9. Department of Pediatrics, Stanford University, Stanford, California, USA

10. Department of Neonatology, Sir Ganga Ram Hospital, New Delhi, India

11. Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA

12. Department of Neonatology, Apollo Cradle Hospitals, New Delhi, India

13. Department of Pediatrics, Kalawati Hospital, Rewari, India

Abstract

Abstract Objectives The objectives of this study are to construct the high definition phenotype (HDP), a novel time-series data structure composed of both primary and derived parameters, using heterogeneous clinical sources and to determine whether different predictive models can utilize the HDP in the neonatal intensive care unit (NICU) to improve neonatal mortality prediction in clinical settings. Materials and Methods A total of 49 primary data parameters were collected from July 2018 to May 2020 from eight level-III NICUs. From a total of 1546 patients, 757 patients were found to contain sufficient fixed, intermittent, and continuous data to create HDPs. Two different predictive models utilizing the HDP, one a logistic regression model (LRM) and the other a deep learning long–short-term memory (LSTM) model, were constructed to predict neonatal mortality at multiple time points during the patient hospitalization. The results were compared with previous illness severity scores, including SNAPPE, SNAPPE-II, CRIB, and CRIB-II. Results A HDP matrix, including 12 221 536 minutes of patient stay in NICU, was constructed. The LRM model and the LSTM model performed better than existing neonatal illness severity scores in predicting mortality using the area under the receiver operating characteristic curve (AUC) metric. An ablation study showed that utilizing continuous parameters alone results in an AUC score of >80% for both LRM and LSTM, but combining fixed, intermittent, and continuous parameters in the HDP results in scores >85%. The probability of mortality predictive score has recall and precision of 0.88 and 0.77 for the LRM and 0.97 and 0.85 for the LSTM. Conclusions and Relevance The HDP data structure supports multiple analytic techniques, including the statistical LRM approach and the machine learning LSTM approach used in this study. LRM and LSTM predictive models of neonatal mortality utilizing the HDP performed better than existing neonatal illness severity scores. Further research is necessary to create HDP–based clinical decision tools to detect the early onset of neonatal morbidities.

Funder

Child Health Imprints (CHIL) Pte. Ltd.

Child Health Imprints India Private Limited

Publisher

Oxford University Press (OUP)

Subject

Health Informatics

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