Protocol for semantic segmentation of spinal endoscopic instruments and anatomic structures : how far is robotic endoscopy surgery?

Abstract

Background: Automatic anlysis of endoscopic images will played an important role in the future spine robotic surgery. The study is designed as a translational study to develop AI models of semantic segmentation for spinal endoscopic instruments and anatomic structures. The aim is to provide the visual understanding basis of endoscopic images for future intelligent robotic surgery. Methods: An estimate of 500 cases of endoscopic video will be included in the study. More data may also be included from the internet for external validation. Video clip containing typical spinal endoscopic instruments and distinct anatomic structures will be extracted. Typical spinal endoscopic instruments will include forceps, bipolar electrocoagulation, drill and so on. Endoscopic anatomic structures will include ligament, upper lamina, lower lamina, nerve root, disc, adipofascia, etc. The ratio of training, validation and testing set of included samples is initially set as 8: 1: 1. State-of-art algorithm (namely UNet, Swin-UNet, DeepLab-V3, etc) and self-developed deep learning algorithm will be used to develop the sementic segmentation models. Dice coefficient (DC), Hausdorff distance (HD), and mean surface distance (MSD) will be used to assess the segmentation performance. Discussions: This protocol firstly proposed the research plans to develop deep learning models to achieve multi-task semantic segmentation of spinal endoscopy images. Automatically recognizing and simultaneously contouring the surgical instruments and anatomic structures will teach the robot understand the surgical procedures of human surgeons. The research results and the annotated data will be disclosed and published in the near future.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

The authors did not receive any funding for this work yet.

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:

Ethics committee of Huazhong University of Science and Technology Union Shenzhen Hospital has waived the ethical approval for this work, as the study did not include any identifiable personal data.

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

No data analyzed during the current study. All pertinent data from this study will be disclosed upon study completion.

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