Toward Predicting Peripheral Artery Disease Treatment Outcomes Using Non-Clinical Data

Abstract

Peripheral Artery Disease (PAD) significantly impairs quality of life and presents varying degrees of severity that correctly identifying would help choose the proper treatment approach and enable personalized treatment approaches. However, the challenge is that there is no single agreed-on measure to quantify the severity of a patient with PAD. This led to a trial-and-error approach to deciding the course of treatment for a given patient with PAD. This study uses non-clinical data, such as biomechanical data and advanced machine-learning techniques, to detect PAD severity levels and enhance treatment selection to overcome this challenge. After analyzing biomechanical data from 42 healthy controls and 65 patients with PAD before and after treatment and correlating it with other measures such as quality of life questionnaires, our findings reveal that ground reaction forces (GRF) features emerged as robust indicators of PAD severity. The GRF Propulsive Peak, in particular, demonstrated high accuracy (0.909) in quantifying PAD severity and is used to develop a straightforward metric for assessing PAD severity. This severity metric is used to gauge the outcome of a specific PAD treatment by comparing the severity before and after the treatment. Machine-learning models were then developed to predict such post-treatment outcomes effectively from the patient non-clinical data before treatment. This approach showed promise in predicting the effectiveness of a treatment for a patient with PAD before performing it, highlighting the potential of machine learning models in revolutionizing PAD treatment strategies. Our findings lay the groundwork for a more data-driven, patient-centric approach to PAD management, optimizing treatment strategies for better patient outcomes.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

The data used are collected from multiple NIH R01 grants

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:

Biomechanics data for this study were sourced from research approved by the Institutional Review Boards at the University of Nebraska Medical Center and the Nebraska-Western Iowa Veteran Affairs Medical Center

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

Data Availability

Data is available per request and after approval

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