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Pre- and post-operative
imaging of cochlear implants:
a pictorial review
Intan Kartika Nursyahbani, MD
Otorhinolaryngology Head and Neck Surgery Department
Introduction
1.A cochlear implant (CI) is a surgically implanted
device consisting of external and internal components
1.An external microphone and speech processor are
worn behind the ear and convert sound into an electric
signal.
Introduction
1.A magnet held external transmitter sends the signal via
electromagnetic induction through the skin to an internal
receiver–stimulator.
1.The receiver–stimulator converts the signal into rapid electrical
impulses which are distributed to multiple electrodes on an
electrode array implanted within the cochlea.
Indication
Children (12– 24 months)
with profound SNHL (> 90
dB) and limited benefit
from binaural amplification
Children (2– 17 years) with
severe to profound SNHL
(> 70 dB) with limited
benefit from binaural
amplification
Adults with moderate to
profound SNHL in both
ears (> 40 dB) with limited
benefit from binaural
amplification
Patients with single-sided
deafness and ipsilateral
vestibular schwannoma
Contraindications
Complete labyrinthine aplasia
Cochlear aplasia
Complete cochlear ossification
Cochlear nerve aplasia or
hypoplasia
Imaging Evaluation
Preoperative imaging is essential
to diagnose any type of inner ear
malformations and to identify other
abnormalties in the temporal bone
that may be encountered
Post-operative imaging is
important to confirm and document
the intended electrode position and
to demonstrate any scalar
dislocation, cochlear dislocation,
electrode fold, or malposition
Pre-operative
Imaging
HRCT
detailed visualization of the
bony structures of the
middle and inner ear
MRI
visualization of the fluid
content of the
membraneous labyrinth
Normal HRCT axial cochlear
Normal MRI 3D-CISS axial cochlear
Key Features Impacting Surgery
Common cavity
malformation
Cochlear
hypoplasia
Incomplete
partition
Large vestibular
aqueduct
syndrome
Abnormal
position of facial
nerve
Hypoplastic
round or oval
window
Cochlear
aperture
abnormalities
Cochlear fibrosis
Otosclerosis
Chronic otitis
media and
cholesteatoma
Common Cavity
Cochlear
Hypoplasia
Type I : bud-like cochlea
Type II : cystic hypoplastic
cochlea
Type III : cochlea with less
than 2 turns
Type IV : normal basal turn,
but severely hypoplastic
middle and apical turns
Incomplete
Partition
Incomplete
Partition
Incomplete
Partition
Large Vestibular
Aqueduct Syndrome
Abnormal Position
of facial nerve
Hypoplastic round
or oval window
Cochlear aperture abnormalities
Cochlear
fibrosis
Otosclerosis
Chronic otitis media and cholesteatoma
Post-operative
Imaging
HRCT or Cone-Beam CT
Required when malfunction of
device is suspected
CBCT has a higher spatial resolution
but the performance of different models
of CBCT may vary
Normal Post Surgery HRCT
Regular
electrode
Split
electrode
Retrograde
electrode
Regular electrode
Split electrode
Retrograde electrode
Immediate Complication
Lifting of the
basilar
membrane
Scala vestibuli
Scalar
translocation
Overinsertion
Underinsertion
Electrode
pinching
Tip fold-over Basal fold-over
Malposition in
tympanic cavity
Malposition in
internal auditory
canal
Malposition in
vestibulum and
semi-circular
canals
Lifting of Basilar
Membrane
Scala vestibuli
Scalar
Translocation
Over & Underinsertion
Electrode Pinching
Tip & Basal Fold Over
Malposition Electrode
Late Complication
Electrode
migration
Flap
complications
Bacterial
labyrinthitis,
OM,
cholesteatoma
Fibrosis and
delayed neural
injury
Electrode
Migration
Conclusion
CI candidates need a
thorough pre-operative
imaging for diagnosis and
classification of inner ear
malformations and to identify
any other abnormality in the
temporal bone.
HRCT and MRI are
complementary and both
image modalities are useful in
patients
Important contraindications
such as aplasia and labyrinth
sclerosis need to be ruled out.
After surgery, the position of
the electrode can be
evaluated using CBCT or
HRCT.
Thank You
Pre post operative imaging of cochlear implant.pptx

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Pre post operative imaging of cochlear implant.pptx

Editor's Notes

  1. Eight different types of cochlear malformations can be differentiated by HRCT: (1) complete labyrinthine apla- sia—Michel deformity (complete absence of cochlea, vestibule, vestibular aqueduct, and cochlear aqueduct), (2) cochlear aplasia (absence of the cochlea), (3) rudi- mentary otocyst (incomplete millimetric otic capsule remnant), (4) common cavity (cochlea and vestibule are represented by a single chamber), (5) incomplete parti- tion of the cochlea (defect in the modiolus and the inter- scalar septa with three subtypes), (6) cochlear hypoplasia (cochlea with dimensions less than normal with four subtypes), (7) large vestibular aqueduct syndrome (en- larged vestibular aqueduct in the presence of normal cochlea, vestibule, and semicircular canals), and (8) cochlear aperture abnormalities (narrow cochlear nerve canal or internal auditory canal, possibility of an absent, or hypoplastic cochlear nerve) Visualization of the vestibulocochlear nerve in the fluid- filled internal auditory canal and cerebellopontine angle is only possible by the MRI