Accurate detection of 3D pelvic-floor-muscle strength for reforming clinical diagnosis and treatment of women's pelvic floor dysfunction

Abstract

Accurate and comprehensive evaluation of three-dimensional (3D) pelvic-floor-muscle (PFM) strength distributions are highly expected to play a crucial role in clinical early diagnosis and physiotherapy precise treatment of women’s pelvic-floor-dysfunction (PFD). However, clinically existing PFM-evaluating methods merely assess a rough and synthetical PFM strength from the whole vagina muscle tunnel, seriously restricting the development of PFD-related diagnostic methodologies and therapeutic interventions. Here, 3D complex female PFM-strength distributions have been accurately detected by developing a portable multi-channel PFM-pressure dynamic measuring system. Clinical trials demonstrate the superiority in high PFM-strength sensitivity and 3D spatial resolution, offering the opportunities to imply specific deficits in personalized PFM functions and customized interventions accordingly. Significantly, various subclinical PFM abnormalities can be identified by the 3D accurate PFM-strength distributions, which is not possible using traditional PFM-evaluating methods, providing a visual biomechanical foundation for clinical early diagnosis and physiotherapy precise treatment of PFD. Combined with the additional advance in physical comfortability, patients-friendliness universality, and stability without motion artifact achieved by the novel designed vaginal probe, this proof of concept research holds the promise for paradigm revolution in PFM pathological research, and promotes the transformation of clinical pelvic-floor medicine from empirical medicine to data-driven precision medicine.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This work was funded by the National Key Research and Development Program of China (2021YFC2009100), the Science and Technology Department of Sichuan Province Project (2023YFS0024), and the Sichuan Provincial Health Commission Project (21ZD002).

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 Research Medical Ethics Committee of the West China Second University Hospital in Sichuan University gave ethical approval for this work.

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).

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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

All data produced in the present study are available upon reasonable request to the authors.

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