Risk factors for 1‐year allograft loss in pediatric heart transplant patients using machine learning: An analysis of the pediatric heart transplant society database

Author:

Wisotzkey Bethany L.1ORCID,Jaeger Byron2ORCID,Asante‐Korang Alfred3ORCID,Brickler Molly4,Cantor Ryan S.5ORCID,Everitt Melanie D.6ORCID,Kirklin James K.5ORCID,Koehl Devin5ORCID,Mantell Benjamin S.7ORCID,Thrush Philip T.8,Kuhn Micheal9ORCID

Affiliation:

1. Division of Cardiology Phoenix Children's Center for Heart Care, University of Arizona College of Medicine Phoenix Arizona USA

2. Biostatistics and Data Science, Division of Public Health Sciences Wake Forest University School of Medicine Winston‐Salem North Carolina USA

3. Division of Cardiology Johns Hopkins All Children's Hospital St. Petersburg Florida USA

4. Department of Pediatrics, Section of Cardiology, Medical College of Wisconsin The Herma Heart Institute, Children's Wisconsin Milwaukee Wisconsin USA

5. Kirklin Solutions Birmingham Alabama USA

6. Division of Cardiology Children's Hospital Colorado, University of Colorado Colorado Aurora USA

7. Department of Pediatrics, Division of Pediatric Cardiology Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

8. Division of Cardiology Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine Chicago Illinois USA

9. Division of Cardiology Loma Linda University Children's Hospital and Medical Center Loma Linda USA California

Abstract

AbstractBackgroundPediatric heart transplant patients are at greatest risk of allograft loss in the first year. We assessed whether machine learning could improve 1‐year risk assessment using the Pediatric Heart Transplant Society database.MethodsPatients transplanted from 2010 to 2019 were included. The primary outcome was 1‐year graft loss free survival. We developed a prediction model using cross‐validation, by comparing Cox regression, gradient boosting, and random forests. The modeling strategy with the best discrimination and calibration was applied to fit a final prediction model. We used Shapley additive explanation (SHAP) values to perform variable selection and to estimate effect sizes and importance of individual variables when interpreting the final prediction model.ResultsCumulative incidence of graft loss or mortality was 7.6%. Random forests had favorable discrimination and calibration compared to Cox proportional hazards with a C‐statistic (95% confidence interval [CI]) of 0.74 (0.72, 0.76) versus 0.71 (0.69, 0.73), and closer alignment between predicted and observed risk. SHAP values computed using the final prediction model indicated that the diagnosis of congenital heart disease (CHD) increased 1 year predicted risk of graft loss by 1.7 (i.e., from 7.6% to 9.3%), need for mechanical circulatory support increased predicted risk by 2, and single ventricle CHD increased predicted risk by 1.9. These three predictors, respectively, were also estimated to be the most important among the 15 predictors in the final model.ConclusionsRisk prediction models used to facilitate patient selection for pediatric heart transplant can be improved without loss of interpretability using machine learning.

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology and Child Health

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