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Initial Experience with a Bioresorbable Polymer Anchor

CATEGORY: Ankle; Ankle Arthritis INTRODUCTION/PURPOSE: Anchors are frequently used in reconstructive orthopedic surgery to achieve fixation of soft tissue to bone. Anchors vary with respect to material composition, configuration, and methods of fixation at the site of attachment. The fixation compon...

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Autores principales: Schiff, Adam P., Kumar, Jayanth, Burnham, Robert R., Hamid, Kamran S., Pinzur, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793619/
http://dx.doi.org/10.1177/2473011421S00436
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author Schiff, Adam P.
Kumar, Jayanth
Burnham, Robert R.
Hamid, Kamran S.
Pinzur, Michael S.
author_facet Schiff, Adam P.
Kumar, Jayanth
Burnham, Robert R.
Hamid, Kamran S.
Pinzur, Michael S.
author_sort Schiff, Adam P.
collection PubMed
description CATEGORY: Ankle; Ankle Arthritis INTRODUCTION/PURPOSE: Anchors are frequently used in reconstructive orthopedic surgery to achieve fixation of soft tissue to bone. Anchors vary with respect to material composition, configuration, and methods of fixation at the site of attachment. The fixation component of anchoring devices has generally evolved from metal-fabricated implants to various types of bioresorbable anchors. The SonicAnchor(TM) (Stryker, Kalamazoo, MI USA) polymer implant provides a unique form of anchor fixation using SonicFusion(TM) technology to achieve interdigitation within cancellous bone while being radiolucent and providing a small footprint. METHODS: During a four-year period, 116 patients underwent a reconstructive orthopedic foot and ankle surgical procedure with the use of at least one bioresorbable polymer anchor (SonicAnchor implant). There were 59 males and 57 females, with an average age of 42 years (range: 12-83 years). RESULTS: A total of 233 bioresorbable anchor (SonicAnchor) implants were used in 116 patients. Of the 116 patients, 108 (93.1%) achieved successful clinical healing of their surgery at their most recent follow-up. The average follow-up duration was 309 days (range: 14-1,429 days). Eight (6.9%) patients were lost to follow-up prior to clinical healing. Two (1.7%) patients underwent reoperation. Also, 65 (56%) patients had at least six months of follow-up and 36 (31%) had at least one year of follow-up. CONCLUSION: This preliminary clinical trial of patients undergoing soft tissue repair or reconstruction with a bioresorbable polymer appears to perform comparably to other commercially available devices. The lack of adverse events, mechanical failures, or infections further supports the safety of this device.
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spelling pubmed-87936192022-01-28 Initial Experience with a Bioresorbable Polymer Anchor Schiff, Adam P. Kumar, Jayanth Burnham, Robert R. Hamid, Kamran S. Pinzur, Michael S. Foot Ankle Orthop Article CATEGORY: Ankle; Ankle Arthritis INTRODUCTION/PURPOSE: Anchors are frequently used in reconstructive orthopedic surgery to achieve fixation of soft tissue to bone. Anchors vary with respect to material composition, configuration, and methods of fixation at the site of attachment. The fixation component of anchoring devices has generally evolved from metal-fabricated implants to various types of bioresorbable anchors. The SonicAnchor(TM) (Stryker, Kalamazoo, MI USA) polymer implant provides a unique form of anchor fixation using SonicFusion(TM) technology to achieve interdigitation within cancellous bone while being radiolucent and providing a small footprint. METHODS: During a four-year period, 116 patients underwent a reconstructive orthopedic foot and ankle surgical procedure with the use of at least one bioresorbable polymer anchor (SonicAnchor implant). There were 59 males and 57 females, with an average age of 42 years (range: 12-83 years). RESULTS: A total of 233 bioresorbable anchor (SonicAnchor) implants were used in 116 patients. Of the 116 patients, 108 (93.1%) achieved successful clinical healing of their surgery at their most recent follow-up. The average follow-up duration was 309 days (range: 14-1,429 days). Eight (6.9%) patients were lost to follow-up prior to clinical healing. Two (1.7%) patients underwent reoperation. Also, 65 (56%) patients had at least six months of follow-up and 36 (31%) had at least one year of follow-up. CONCLUSION: This preliminary clinical trial of patients undergoing soft tissue repair or reconstruction with a bioresorbable polymer appears to perform comparably to other commercially available devices. The lack of adverse events, mechanical failures, or infections further supports the safety of this device. SAGE Publications 2022-01-21 /pmc/articles/PMC8793619/ http://dx.doi.org/10.1177/2473011421S00436 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Article
Schiff, Adam P.
Kumar, Jayanth
Burnham, Robert R.
Hamid, Kamran S.
Pinzur, Michael S.
Initial Experience with a Bioresorbable Polymer Anchor
title Initial Experience with a Bioresorbable Polymer Anchor
title_full Initial Experience with a Bioresorbable Polymer Anchor
title_fullStr Initial Experience with a Bioresorbable Polymer Anchor
title_full_unstemmed Initial Experience with a Bioresorbable Polymer Anchor
title_short Initial Experience with a Bioresorbable Polymer Anchor
title_sort initial experience with a bioresorbable polymer anchor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793619/
http://dx.doi.org/10.1177/2473011421S00436
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