4.7 Article

Personalized Anatomic Modeling for Noninvasive Fetal ECG: Methodology and Applications

Journal

Publisher

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/TIM.2021.3069028

Keywords

Cardiac electrophysiology; fetal electrocardiography (FECG); forward problem; simulation; volume conductor model

Funding

  1. Austin Medical Research Foundation Grant
  2. Australian Government Research Training Program Scholarship at the University of Melbourne
  3. NHMRC Early Career Fellowship under NHMRC [1142636]
  4. Norman Beischer Clinical Research Fellowship

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This study presents an open-source method for modeling maternal body structure and fetal position changes in noninvasive fetal electrocardiography, with validation on specific fetal heart monitoring tasks and application in clinical scenarios.
Fetal cardiac monitoring is one of the cornerstones of modern obstetric care. Noninvasive fetal electrocardiography (NI-FECG) is an emerging modality for monitoring fetal well-being using electrical signals recorded from the maternal abdomen. However, the reliability of NI-FECG extraction techniques remains highly variable due to a range of technical and clinical factors, such as sensor placement and interindividual anatomic variations. In this work, we propose, develop, and validate an open-source method for modeling these variations, including changes in maternal body structure and fetal position using two clinical NI-FECG databases. To validate our model's accuracy, we first assess its performance in characterizing the fetal QRS (fQRS) complex amplitude in six private NI-FECG recordings with detailed anatomic information. To demonstrate its clinical utility, we next apply our model to predict an optimal sensor placement in a separate open-access database of 60 24-channel NI-FECG recordings. The optimal six sensor positions predicted by our model achieve similar reliability for fetal heart rate (FHR) monitoring compared to the entire 24-sensor array. The presented results indicate our model provides a suitable method for estimating the influence of anatomic variations on NI-FECG signals and optimizing sensor placement in a simulated setting. The code for the developed model has been made available under an open-source GPL license and contributed to the fecgsyn toolbox.

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