TY - JOUR
T1 - Auricular prostheses attached to osseointegrated implants
T2 - multidisciplinary work-up and clinical evaluation
AU - Vijverberg, Maarten A
AU - Verhamme, Luc
AU - van de Pol, Pascal
AU - Kunst, Henricus P M
AU - Mylanus, Emmanuel A M
AU - Hol, Myrthe K S
PY - 2019/4
Y1 - 2019/4
N2 - PURPOSE: Not long after the introduction of osseointegrated implants outside the oral cavity, auricular prostheses are retrained on osseointegrated implants. New insights have been gained with the next-generation percutaneous osseointegrated titanium implants for bone conduction hearing since its introduction in 2010. As a result, the same technology was introduced in the Vistafix® system (VXI implant) to retain auricular prostheses. The aim of this study is to evaluate the surgical procedure, clinical outcome, and satisfaction of the patient of osseointegration-retained auricular prosthesis using VXI implants.MATERIALS AND METHODS: 11 patients who received an auricular prosthesis using VXI implants between December 2012 and November 2017 were evaluated retrospectively. The patient's medical files were reviewed to assess clinical complications and the necessity for revision surgery. The subjective outcome was measured using the Glasgow benefit inventory (GBI).RESULTS: In total, 31 implants were placed in 11 patients. None of these implants were lost nor revision surgery needed. An adverse skin reaction was observed in 13.0% of the implants and in 27.2% of the patients, adequately treated with an antibiotic ointment. The average follow-up time was 2 years and 7 months. The GBI displayed a positive score in every patient.CONCLUSIONS: The VXI implants used are a safe and reliable treatment option for retaining auricular prostheses in patients with an absent auricle. Patients were satisfied with their auricular prosthesis and showed benefit in quality of life. Studies with larger numbers and preferably a prospective character are needed to draw statistically significant conclusions.
AB - PURPOSE: Not long after the introduction of osseointegrated implants outside the oral cavity, auricular prostheses are retrained on osseointegrated implants. New insights have been gained with the next-generation percutaneous osseointegrated titanium implants for bone conduction hearing since its introduction in 2010. As a result, the same technology was introduced in the Vistafix® system (VXI implant) to retain auricular prostheses. The aim of this study is to evaluate the surgical procedure, clinical outcome, and satisfaction of the patient of osseointegration-retained auricular prosthesis using VXI implants.MATERIALS AND METHODS: 11 patients who received an auricular prosthesis using VXI implants between December 2012 and November 2017 were evaluated retrospectively. The patient's medical files were reviewed to assess clinical complications and the necessity for revision surgery. The subjective outcome was measured using the Glasgow benefit inventory (GBI).RESULTS: In total, 31 implants were placed in 11 patients. None of these implants were lost nor revision surgery needed. An adverse skin reaction was observed in 13.0% of the implants and in 27.2% of the patients, adequately treated with an antibiotic ointment. The average follow-up time was 2 years and 7 months. The GBI displayed a positive score in every patient.CONCLUSIONS: The VXI implants used are a safe and reliable treatment option for retaining auricular prostheses in patients with an absent auricle. Patients were satisfied with their auricular prosthesis and showed benefit in quality of life. Studies with larger numbers and preferably a prospective character are needed to draw statistically significant conclusions.
KW - Adult
KW - Aged
KW - Bone Conduction
KW - Bone-Anchored Prosthesis
KW - Congenital Microtia/epidemiology
KW - Ear Auricle/pathology
KW - Ear Deformities, Acquired/epidemiology
KW - Female
KW - Humans
KW - Male
KW - Middle Aged
KW - Netherlands
KW - Osseointegration
KW - Outcome and Process Assessment, Health Care
KW - Postoperative Complications/epidemiology
KW - Prospective Studies
KW - Prostheses and Implants
KW - Prosthesis Design
KW - Prosthesis Implantation/adverse effects
KW - Quality of Life
KW - Reoperation/methods
KW - Retrospective Studies
KW - Titanium
U2 - 10.1007/s00405-019-05311-0
DO - 10.1007/s00405-019-05311-0
M3 - Article
C2 - 30847547
SN - 0937-4477
VL - 276
SP - 1017
EP - 1027
JO - European Archives of Oto-Rhino-Laryngology
JF - European Archives of Oto-Rhino-Laryngology
IS - 4
ER -