Predicting major adverse cardiovascular events after orthotopic liver transplantation using a supervised machine

Jonathan Soldera1,2, Leandro Luis Corso3, Matheus Machado Rech4

  • 1Post Graduate Program at Acute Medicine and Gastroenterology, University of South Wales, Cardiff CF37 1DL, United Kingdom.

PubMed

Insights

A machine learning model accurately predicts major adverse cardiovascular events (MACE) after liver transplants (LT). This tool helps assess patient risk, improving clinical practice for liver transplant recipients.

Area of Science:

  • Cardiovascular Medicine
  • Hepatology
  • Machine Learning in Healthcare

Background:

  • Liver transplant (LT) recipients are increasingly older and sicker.
  • Major adverse cardiovascular events (MACE) and associated mortality are rising post-LT.
  • Traditional noninvasive cardiac stress testing has limitations in cirrhotic patients.

Purpose of the Study:

  • To evaluate the feasibility and accuracy of a machine learning model for predicting post-LT MACE.
  • To develop a predictive tool for major adverse cardiovascular events in liver transplant recipients.
  • To assess the performance of an extreme gradient boosting model in a regional cohort.

Main Methods:

  • Retrospective cohort study of 575 LT patients.
  • Developed an extreme gradient boosting (XGBoost) model using 83 features.
  • Addressed missing data using k-nearest neighbor imputation; model performance assessed by AUROC and Brier score.

Main Results:

  • The XGBoost model achieved an AUROC of 0.89 and excellent calibration (Brier score 0.07).
  • Key predictors included negative cardiac stress tests, beta-blocker use, bilirubin levels, and blood type.
  • The model demonstrated high accuracy (0.84), precision (0.85), recall (0.80), and F1-score (0.79).

Conclusions:

  • The XGBoost model is feasible and accurate for predicting post-LT MACE.
  • The model integrates cardiovascular and hepatic variables for robust risk assessment.
  • The study emphasizes the model's potential as a reliable clinical tool for post-LT MACE prediction.
Abstract

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