Machine Learning for Prediction of Patients on Hemodialysis with an Undetected SARS-CoV-2 Infection.

COVID-19 SARS-CoV-2 artificial intelligence coronavirus dialysis end stage kidney disease machine learning prediction

Journal

Kidney360
ISSN: 2641-7650
Titre abrégé: Kidney360
Pays: United States
ID NLM: 101766381

Informations de publication

Date de publication:
25 03 2021
Historique:
received: 22 06 2020
accepted: 12 01 2021
entrez: 4 4 2022
pubmed: 13 1 2021
medline: 8 4 2022
Statut: epublish

Résumé

We developed a machine learning (ML) model that predicts the risk of a patient on hemodialysis (HD) having an undetected SARS-CoV-2 infection that is identified after the following ≥3 days. As part of a healthcare operations effort, we used patient data from a national network of dialysis clinics (February-September 2020) to develop an ML model (XGBoost) that uses 81 variables to predict the likelihood of an adult patient on HD having an undetected SARS-CoV-2 infection that is identified in the subsequent ≥3 days. We used a 60%:20%:20% randomized split of COVID-19-positive samples for the training, validation, and testing datasets. We used a select cohort of 40,490 patients on HD to build the ML model (11,166 patients who were COVID-19 positive and 29,324 patients who were unaffected controls). The prevalence of COVID-19 in the cohort (28% COVID-19 positive) was by design higher than the HD population. The prevalence of COVID-19 was set to 10% in the testing dataset to estimate the prevalence observed in the national HD population. The threshold for classifying observations as positive or negative was set at 0.80 to minimize false positives. Precision for the model was 0.52, the recall was 0.07, and the lift was 5.3 in the testing dataset. Area under the receiver operating characteristic curve (AUROC) and area under the precision-recall curve (AUPRC) for the model was 0.68 and 0.24 in the testing dataset, respectively. Top predictors of a patient on HD having a SARS-CoV-2 infection were the change in interdialytic weight gain from the previous month, mean pre-HD body temperature in the prior week, and the change in post-HD heart rate from the previous month. The developed ML model appears suitable for predicting patients on HD at risk of having COVID-19 at least 3 days before there would be a clinical suspicion of the disease.

Sections du résumé

Background
We developed a machine learning (ML) model that predicts the risk of a patient on hemodialysis (HD) having an undetected SARS-CoV-2 infection that is identified after the following ≥3 days.
Methods
As part of a healthcare operations effort, we used patient data from a national network of dialysis clinics (February-September 2020) to develop an ML model (XGBoost) that uses 81 variables to predict the likelihood of an adult patient on HD having an undetected SARS-CoV-2 infection that is identified in the subsequent ≥3 days. We used a 60%:20%:20% randomized split of COVID-19-positive samples for the training, validation, and testing datasets.
Results
We used a select cohort of 40,490 patients on HD to build the ML model (11,166 patients who were COVID-19 positive and 29,324 patients who were unaffected controls). The prevalence of COVID-19 in the cohort (28% COVID-19 positive) was by design higher than the HD population. The prevalence of COVID-19 was set to 10% in the testing dataset to estimate the prevalence observed in the national HD population. The threshold for classifying observations as positive or negative was set at 0.80 to minimize false positives. Precision for the model was 0.52, the recall was 0.07, and the lift was 5.3 in the testing dataset. Area under the receiver operating characteristic curve (AUROC) and area under the precision-recall curve (AUPRC) for the model was 0.68 and 0.24 in the testing dataset, respectively. Top predictors of a patient on HD having a SARS-CoV-2 infection were the change in interdialytic weight gain from the previous month, mean pre-HD body temperature in the prior week, and the change in post-HD heart rate from the previous month.
Conclusions
The developed ML model appears suitable for predicting patients on HD at risk of having COVID-19 at least 3 days before there would be a clinical suspicion of the disease.

Identifiants

pubmed: 35369017
doi: 10.34067/KID.0003802020
pii: 02200512-202103000-00009
pmc: PMC8786002
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

456-468

Informations de copyright

Copyright © 2021 by the American Society of Nephrology.

Déclaration de conflit d'intérêts

C. Monaghan, F. Maddux, H. Han, J. Larkin, L. Usvyat, S. Chaudhuri, and Y. Jiao are employees of Fresenius Medical Care in the Global Medical Office. E. Weinhandl, I. Dahne-Steuber, J. Hymes, K. Belmonte, K. Bermudez, and R. Kossmann are employees of Fresenius Medical Care North America. F. Maddux has directorships in the Fresenius Medical Care Management Board, Goldfinch Bio, and Vifor Fresenius Medical Care Renal Pharma. F. Maddux, I. Dahne-Steuber, J. Hymes, K. Belmonte, L. Usvyat, P. Kotanko, and R. Kossmann have share options/ownership in Fresenius Medical Care. L. Neri is an employee of Fresenius Medical Care Deutschland GmbH in the Europe, the Middle East, and Africa Medical Office. P. Kotanko is an employee of Renal Research Institute, a wholly owned subsidiary of Fresenius Medical Care; reports receiving honorarium from Up-To-Date; and is on the Editorial Board of Blood Purification and Kidney and Blood Pressure Research. All remaining authors have nothing to disclose.

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Auteurs

Caitlin K Monaghan (CK)

Fresenius Medical Care, Global Medical Office, Waltham, Massachusetts.

John W Larkin (JW)

Fresenius Medical Care, Global Medical Office, Waltham, Massachusetts.

Sheetal Chaudhuri (S)

Fresenius Medical Care, Global Medical Office, Waltham, Massachusetts.
Division of Nephrology, Maastricht University Medical Center, Maastricht, The Netherlands.

Hao Han (H)

Fresenius Medical Care, Global Medical Office, Waltham, Massachusetts.

Yue Jiao (Y)

Fresenius Medical Care, Global Medical Office, Waltham, Massachusetts.

Kristine M Bermudez (KM)

Fresenius Medical Care North America, Medical Office, Waltham, Massachusetts.

Eric D Weinhandl (ED)

Fresenius Medical Care North America, Medical Office, Waltham, Massachusetts.

Ines A Dahne-Steuber (IA)

Fresenius Medical Care North America, Medical Office, Waltham, Massachusetts.

Kathleen Belmonte (K)

Nursing & Clinical Services, Fresenius Kidney Care, Waltham, Massachusetts.

Luca Neri (L)

Fresenius Medical Care Deutschland GmbH, EMEA Medical Office, Bad Homburg, Germany.

Peter Kotanko (P)

Research Division, Renal Research Institute, New York, New York.
Division of Nephrology, Icahn School of Medicine at Mount Sinai, New York, New York.

Jeroen P Kooman (JP)

Division of Nephrology, Maastricht University Medical Center, Maastricht, The Netherlands.

Jeffrey L Hymes (JL)

Fresenius Medical Care North America, Medical Office, Waltham, Massachusetts.

Robert J Kossmann (RJ)

Fresenius Medical Care North America, Medical Office, Waltham, Massachusetts.

Len A Usvyat (LA)

Fresenius Medical Care, Global Medical Office, Waltham, Massachusetts.

Franklin W Maddux (FW)

Fresenius Medical Care AG & Co. KGaA, Global Medical Office, Bad Homburg, Germany.

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