MUSCLE: Muscle Understanding through Synthetic Computation and Lesion Evaluation A Semi-Synthetic Dataset for Hamstring Injury Prediction Using Electrical Impedance

Abstract

Hamstring Injuries (HSIs) are common among athletes and necessitate extended rehabilitation before Return to Sport (RTS). Post-injury, athletes undergo physical examinations, which often fall short in assessing injury severity or guiding rehabilitation. Therefore, imaging techniques such as Magnetic Resonance Imaging (MRI) are used to evaluate the injury more comprehensively, aiding in the assessment of optimal rehabilitation and RTS timelines. Given the significant impact of HSIs on athletic careers, early prediction is essential. This article investigates the use of Electrical Impedance Tomography (EIT) for HSI prediction. EIT, a noninvasive method, involves injecting a current or voltage into the affected area to detect property changes, allowing for real-time monitoring and supporting its role in HSI prediction. A semi-synthetic dataset was created using MRI scans of patients with hamstring injuries. The dataset was developed by mapping the boundaries of the hamstring muscles (semimembranosus, semitendinosus, and biceps femoris) with Electrical Impedance Tomography and Diffuse Optical Tomography Reconstruction Software (EIDORS). EIDORS generated EIT voltage measurements by defining muscle boundaries and setting appropriate properties, forming the basis for the dataset. Machine Learning (ML) models were then employed to validate the dataset by distinguishing between injured and healthy hamstrings. The best-performing model, Random Forest (RF), achieved an accuracy of 98%, demonstrating the potential of EIT in predicting HSIs.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This work was supported by the Lebanese American University.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study used openly available human data that were originally located at:https://www.youtube.com/@dr.gayfirstlookmri The rest of the data is generated sythetically.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

留言 (0)

沒有登入
gif