Porous High-Density Polyethylene Implants in Auricular Reconstruction
James D. Williams, MD;
Thomas Romo, Ill, MD;
Anthony P. Sclafani, MD;
Hyun Cho, MD
Arch Otolaryngol Head Neck Surg. 1997;123(6):578-583.
Abstract
| |
Objective
To evaluate the ability of porous high-density polyethylene (Medpor) implants to tolerate exposure and support skin grafts when used to reconstruct defects in auricular cartilage in an animal model.
Design
Polyethylene implants placed in surgically created defects in auricular cartilage and covered with a skin flap were then exposed at either 4, 7, or 21 days after implantation. The exposed implants were then allowed to heal secondarily or received a skin graft 1 week later. The ability of polyethylene implants to tolerate exposure and support skin grafts was observed clinically and via histological study of the implantation sites.
Subjects
Nine adult New Zealand rabbits.
Results
Polyethylene implants demonstrated excellent ability to tolerate wound exposure as early as 4 days after implantation, with extrusion of 1 of the 36 implants placed. The degree of secondary wound healing increased as the interval from implantation to exposure increased from 4 to 21 days. Exposed polyethylene implants in all groups also supported all 18 skin grafts placed 1 week after exposure of the implant surface.
Conclusions
Polyethylene implants are well tolerated as replacements for native cartilage in auricular reconstruction. Polyethylene implants tolerated wound exposure as early as 4 days after implantation and demonstrated the ability to heal by secondary intention and support skin grafts. This is likely because of the extent of fibrovascular ingrowth from surrounding tissue, which allows the material to behave more like native tissue and less like a foreign body in this setting.
Arch Otolaryngol Head Neck Surg. 1997;123:578-583
Author Affiliations
From the Department of Otolaryngology—Head and Neck Surgery (Drs Williams and Sclafani) and the Division of Facial Plastic and Reconstructive Surgery (Dr Romo), The New York Eye and Ear Infirmary, New York, NY; the Department of Otolaryngology—Head and Neck Surgery, New York Medical College, Valhalla (Dr Romo); and the Division of Otolaryngology—Head and Neck Surgery, Beth Israel Medical Center, New York (Dr Cho). None of the authors holds any financial interests in Porex Surgical Inc or any of its affiliates.
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
Cleft Lip Nasal Reconstruction Using Porous High-Density Polyethylene
Romo et al.
Arch Facial Plast Surg 2003;5:175-179.
ABSTRACT
| FULL TEXT
|
