» Articles » PMID: 35694657

Left Ventricular Pressure Estimation Using Machine Learning-Based Heart Sound Classification

Overview
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: A method to estimate absolute left ventricular (LV) pressure and its maximum rate of rise (LV dP/dtmax) from epicardial accelerometer data and machine learning is proposed.

Methods: Five acute experiments were performed on pigs. Custom-made accelerometers were sutured epicardially onto the right ventricle, LV, and right atrium. Different pacing configurations and contractility modulations, using isoflurane and dobutamine infusions, were performed to create a wide variety of hemodynamic conditions. Automated beat-by-beat analysis was performed on the acceleration signals to evaluate amplitude, time, and energy-based features. For each sensing location, bootstrap aggregated classification tree ensembles were trained to estimate absolute maximum LV pressure (LVPmax) and LV dP/dtmax using amplitude, time, and energy-based features. After extraction of acceleration and pressure-based features, location specific, bootstrap aggregated classification ensembles were trained to estimate absolute values of LVPmax and its maximum rate of rise (LV dP/dtmax) from acceleration data.

Results: With a dataset of over 6,000 beats, the algorithm narrowed the selection of 17 predefined features to the most suitable 3 for each sensor location. Validation tests showed the minimal estimation accuracies to be 93% and 86% for LVPmax at estimation intervals of 20 and 10 mmHg, respectively. Models estimating LV dP/dtmax achieved an accuracy of minimal 93 and 87% at estimation intervals of 100 and 200 mmHg/s, respectively. Accuracies were similar for all sensor locations used.

Conclusion: Under pre-clinical conditions, the developed estimation method, employing epicardial accelerometers in conjunction with machine learning, can reliably estimate absolute LV pressure and its first derivative.

Citing Articles

Machine learning: a new era for cardiovascular pregnancy physiology and cardio-obstetrics research.

Ricci C, Crysup B, Phillips N, Ray W, Santillan M, Trask A Am J Physiol Heart Circ Physiol. 2024; 327(2):H417-H432.

PMID: 38847756 PMC: 11442027. DOI: 10.1152/ajpheart.00149.2024.

References
1.
Martirosyan M, Caliskan K, Theuns D, Szili-Torok T . Remote monitoring of heart failure: benefits for therapeutic decision making. Expert Rev Cardiovasc Ther. 2017; 15(7):503-515. DOI: 10.1080/14779072.2017.1348229. View

2.
Bordachar P, Labrousse L, Ploux S, Thambo J, Lafitte S, Reant P . Validation of a new noninvasive device for the monitoring of peak endocardial acceleration in pigs: implications for optimization of pacing site and configuration. J Cardiovasc Electrophysiol. 2008; 19(7):725-9. DOI: 10.1111/j.1540-8167.2008.01105.x. View

3.
Delnoy P, Marcelli E, Oudeluttikhuis H, Nicastia D, Renesto F, Cercenelli L . Validation of a peak endocardial acceleration-based algorithm to optimize cardiac resynchronization: early clinical results. Europace. 2008; 10(7):801-8. PMC: 2435018. DOI: 10.1093/europace/eun125. View

4.
Vos T, Flaxman A, Naghavi M, Lozano R, Michaud C, Ezzati M . Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012; 380(9859):2163-96. PMC: 6350784. DOI: 10.1016/S0140-6736(12)61729-2. View

5.
Whinnett Z, Francis D, Denis A, Willson K, Pascale P, van Geldorp I . Comparison of different invasive hemodynamic methods for AV delay optimization in patients with cardiac resynchronization therapy: implications for clinical trial design and clinical practice. Int J Cardiol. 2013; 168(3):2228-37. PMC: 3819984. DOI: 10.1016/j.ijcard.2013.01.216. View