Peer-reviewed veterinary case report
Complications after Phasix mesh hernia repair in pets over time
By van den Berg R et al.·2025·Department of Surgery, Netherlands·View original on Europe PMC →
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Original publication title: Short- and long-term complications after slowly resorbable biosynthetic P4HB mesh (Phasix) implantation in European centres: a protocol paper for a multiregistry study.
Plain-English summary
This study is looking into the use of a special type of mesh called Phasix, which is used to repair hernias (a condition where an organ pushes through a weak spot in the muscle) in pets. The researchers want to find out about any long-term problems that might happen after using this mesh, especially after it has completely dissolved in the body. They will be collecting data from several veterinary centers across Europe over a period of 2 to 5 years to see how well the mesh works and if any complications arise. The study is based on information that has already been collected with the consent of pet owners, and the findings will be shared in veterinary journals and at conferences. The outcome of the study will help determine how safe and effective this mesh is for hernia repairs in pets.
Abstract
<h4>Background</h4>Phasix mesh is a fully resorbable synthetic mesh for use in clean and contaminated ventral incisional hernia repairs. Long-term absorbable Phasix mesh appears to be a safe and promising device in incisional hernia repair, with low recurrence rates; however, data on long-term complications after surgery, particularly after the resorption period of the mesh, are scarce.<h4>Methods and analysis</h4>This protocol describes a study of several European registries on the use of a Phasix mesh in incisional hernia repair. The primary endpoint of the study is long-term complications at 2-5 year follow-up after mesh implantation, with secondary endpoints including hernia recurrence and complications during short-term follow-up.<h4>Ethics and dissemination</h4>Ethical approval was not required for this protocol as the study is based on anonymised registry data collected with prior patient consent in each registry. Each participating registry has its own ethical approval process, and this study will adhere to those regulations. The results will be disseminated through peer-reviewed publications and conference presentations.
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Search related cases →Original publication on Europe PMC: https://europepmc.org/article/MED/41298268