Assessment of the performance of Lyoplant(R) Onlay for duraplasty. An observational, multi-center Post Market Clinical Follow-up study.

Abstract

Objective: Duraplasty with a dura mater substitute can become necessary after cranial or spinal surgery. Several dura grafts from different materials are available. The goal of this study was to assess the clinical performance of a suturable onlay dura substitute composed of bovine collagen. Methods: A prospective, observational, multicenter, single-arm clinical study with the dura substitute Lyoplant® Onlay was performed. Different performance parameters for safety and performance were assessed. Additionally, postoperative MRI / CT images were evaluated. Results: Data of 61 patients recruited by three study centers were included. Lyoplant® Onlay was used by a variety of surgeons with different levels of experience. Cranial and spinal cases with a wide range of dura defect sizes were included. No reoperation due to a cerebrospinal fluid leakage occurred until discharge (primary endpoint), as well as to the follow-up (about four months postoperatively). The incidence rate of cerebrospinal fluid leakages was 6.6%. All of these adverse events were reported as non-serious complications without the need of a surgical intervention and were resolved without sequelae. The handling properties of Lyoplant® Onlay were positively rated. In external radiologic analysis of postoperative MRI / CT images at discharge and follow-up, additional fluid collection, edema, and swelling were observed. However, they were clinically inapparent and considered normal postsurgical findings. Conclusions: The incidence rate of cerebrospinal fluid leakages was 6.6% and ranged in the values reported in the literature. These results show that Lyoplant® Onlay is a safe and efficient dura substitute.

Competing Interest Statement

Franziska Greifzu is an employee of Aesculap AG. Axel Stadie has prepared a second clinical study with Aesculap AG. Therefore, he has received expense allowances personally. He is also advising Aesculap AG during the processes of certification of medical products and is therefore receiving expense allowances. Moreover, Axel Stadie has received expense allowances and the traveling costs for presentations and workshops by Aesculap AG. The other authors have no financial conflict of interest.

Clinical Trial

NCT02678156

Funding Statement

This study was funded by Aesculap AG.

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/IRB of Aerztekammer des Saarlandes, ethics Committee/IRB of Landesaerztekammer Rheinland-Pfalz and ethics Committee of Landesaerztekammer Hessen gave ethical approval for this work.

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Yes

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

Yes

Data Availability

All data produced in the present work are contained in the manuscript

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