Pre- and Postoperative Imaging of Cochlear Implantation in Cadaveric Specimens Using Low-Dose Photon-Counting Detector CT.

Bjoern Spahn, Franz-Tassilo Müller-Graff, Kristen Rak, Jonas Engert, Johannes Voelker, Stephan Hackenberg, Rudolf Hagen, Tilmann Neun, Bernhard Petritsch, Thorsten Alexander Bley, Jan-Peter Grunz, Henner Huflage
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Abstract

Background and purpose: Anatomically adapted cochlear implantation and efficient postoperative cochlear implant-fitting strategies benefit from reliable and highly detailed imaging techniques. Since image quality in CT is related to the applied radiation dose, this study aimed to evaluate low-dose cochlear imaging with a photon-counting detector by investigating the accuracy of pre- and postoperative cochlear analysis.

Materials and methods: Photon-counting CT images of 10 temporal bone specimens were acquired with 3 different radiation dose levels (regular dose: 27.1 mGy, low dose: 4.81 mGy, and ultra-low dose: 3.43 mGy) before and after cochlear implant electrode carrier insertion. A clinical scan protocol was used with a tube potential of 120 kV in ultra-high-resolution scan mode (detector collimation 120 × 0.2 mm). The accuracy of cochlear duct length measurements for the organ of Corti and electrode contact determination was investigated for all applied settings by 2 independent otosurgeons.

Results: No substantial differences were ascertained between photon-counting CT scans performed with standard dose and dedicated low-dose imaging regarding the accuracy of neither pre- and postoperative cochlear analysis nor postoperative cochlear implant electrode analysis. Radiation dose reduction of 82.3% (low dose) and 87.3% (ultra-low dose) could be realized compared with the clinical standard protocol.

Conclusions: Ultra-high-resolution cochlear imaging is feasible with very low radiation exposure when using a first-generation photon-counting CT in combination with dedicated low-dose protocols. The accuracy of pre- and postoperative cochlear analysis with the applied dose reduction settings was comparable with a clinical regular-dose protocol.

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