Hubert T. Faber

Learn More
OBJECTIVE This study assesses soft tissue reactions and implant stability of 1,132 percutaneous titanium implants (970 patients) for bone conduction devices (BCDs). In addition, it examines BCD usage and comparisons between different patient groups. STUDY DESIGN Retrospective survey. Mean follow-up time of 4.6 years. SETTING Tertiary care referral(More)
OBJECTIVE To evaluate the effect of implant location and skin thickness on the frequency and degree of adverse skin reactions around the abutment. DESIGN Retrospective multivariate analysis of implant position related to skin thickness and clinical variables. SETTING Tertiary referral center. PATIENTS Random sample of 248 patients with bone-anchored(More)
OBJECTIVE To clinically evaluate the performance of a titanium percutaneous bone-anchored hearing implant (BAHI) using a 3-week healing period. Short-term implant survival, stability changes, and skin reactions are evaluated from the initial implantation to 6 months postimplantation. METHODS Thirty patients eligible for a BAHI were included in an open,(More)
The objective of this study was to ascertain the long-term safety of loading osseointegrated implants for bone conduction hearing 3 weeks post-surgery. Thirty consecutive adult patients were implanted with the Baha BI300 (Cochlear Bone Anchored Solutions) in our tertiary referral center. Implants were loaded with the sound processor 3 weeks post-surgery.(More)
OBJECTIVE To determine factors predicting whether patients with single-sided deafness (SSD) opt for a bone conduction device (BCD) for the contralateral routing of sound (CROS) after a regular trial with a BCD on a headband. DESIGN Retrospective case-control study. SETTING Nijmegen, the Netherlands. PATIENTS Thirty consecutive patients with SSD. (More)
The objective of this study is to determine the benefits of bone-anchored hearing aid (Baha) contralateral routing of signal (CROS) in the older adult population with single-sided deafness. Five questionnaires [general usage questionnaire, Glasgow benefit inventory (GBI), Abbreviated profile of hearing aid benefit (APHAB), Nijmegen cochlear implant(More)
OBJECTIVE To identify risk factors for complications after bone-anchored hearing implant (BAHI) surgery. STUDY DESIGN Retrospective cohort study. SETTING Tertiary referral center. PATIENTS All adult patients who received titanium bone-anchored hearing implants at our clinic between September 1, 1988 and December 31, 2007 were approached to fill out a(More)
OBJECTIVES/HYPOTHESIS To examine the long-term satisfaction and possible effects of gender in patients with single-sided deafness (SSD) who underwent bone-anchored hearing implant (BAHI) surgery. STUDY DESIGN Retrospective case-control study. METHODS All (n = 145) consecutive SSD patients fitted with a BAHI between January 2001 and October 2011 were(More)
OBJECTIVE To describe the clinical characteristics of a 70-year-old female with occipital neuropathy following bone conduction device surgery. DESCRIPTION A 65-year-old woman underwent bone conduction device placement surgery on the left temporal bone. Postoperatively she progressively developed chronic pain at the implantation site. The pain led to(More)
In the past 30 years, a large amount of clinical and audiological research on bone conduction hearing devices has been performed. In this review, we give a brief history of the developments in indications, surgical techniques and sound processors with respect to implantable bone conduction devices like the bone-anchored hearing aid or Baha. Starting with(More)