Cochlear Implant Atlas
CI Atlas · Devices & Electrode Arrays · Module 17

17Special Arrays for the Difficult Cochlea

Not every cochlea is patent or normally formed. Ossification after meningitis can wall off the lumen; malformations can erase the modiolus entirely. This module follows the surgeon's tiered escalation through ossified cochleae and the Sennaroglu malformation spectrum to the auditory brainstem implant, where the array leaves the cochlea behind altogether.

TThe ossified basal turn

Cochlear ossification (labyrinthitis ossificans), most often after pneumococcal meningitis or otosclerosis, usually confines new bone to the basal turn near the round window, so a 1 mm bur can extend the basal-turn opening anteriorly until a patent lumen is found. The drill-out must NOT exceed ~8 mm: beyond that the dissection risks the internal carotid artery, and bleeding from the vasa vasorum signals the surgeon to stop (cross-ref Ch.15 Surgery).[2002]

CEscalating the drill-out

When scala tympani is obliterated, the strategy escalates: extend superiorly to insert into scala vestibuli, then a circummodiolar drill-out (working between the anterior carotid, superior tympanic facial nerve and labyrinthine facial segment), and finally split/double arrays — two short bundles in separate cochleostomies into the basal and middle/upper turns — or compressed arrays for a short patent segment.[2012]

The ossified cochlea — finding → array strategy

Ascending-turn obstructionsplit / scala vestibuli
Next stepScala-vestibuli insertion, a 'double-array' or a compressed/split array to reach surviving apical neurons.

Ossification (most often post-meningitic, cross-ref Ch.12) forces special arrays. The strategy follows the intra-operative finding: a basal drill-out for limited disease, a scala-vestibuli route or a split/double array for ascending obstruction, and an extensive drill-out — or an auditory brainstem implant — for total obliteration with no usable lumen or nerve. Because ossification progresses, these cases are implanted early. Schematic.

TThe Sennaroglu spectrum

Inner-ear malformations are classified by the Sennaroglu & Saatci (2002) system: Michel deformity, cochlear aplasia (~3–7%), common cavity, cochlear hypoplasia (~7–15%), incomplete partition I (absent modiolus, cystic), IP-II (classic Mondini, 1.5 turns, dilated vestibule, enlarged vestibular aqueduct) and IP-III (X-linked). Deformities are bilateral in ~65% of cases and similar in ~93% of those.[2014]

The Sennaroglu spectrum — earlier developmental arrest, more severe malformation

more severenormalarrest week →Michel~3Otocyst~3–4Aplasia~3 (late)Cavity~4IP-I~5Hypo~6IP-II~7Normalterm
MalformationIncomplete partition type II (Mondini)ModiolusPartial (apex deficient)

Normal basal turn, cystic apical 1.5 turns, dilated vestibule + EVA. Implant: Standard array inserts well; watch for a gusher.

Sennaroglu & Saatci classify cochleovestibular malformations by when inner-ear development arrested: the earlier the arrest, the less the cochlea has differentiated. Reading left to right, the spiral fills in — from no inner ear (Michel), through a single undifferentiated common cavity and the cystic incomplete partitions, to the normal 2.5-turn cochlea around an intact modiolus. The practical consequence tracks the same axis: severe early arrests have no modiolus (or no cochlea at all), pushing array choice toward straight wall-hugging electrodes or an ABI, while the milder right-hand forms accept a near-standard insertion. Schematic, not to scale.

CArray choice without a modiolus

Array choice follows the anatomy: when no modiolus exists (IP-I, common cavity), perimodiolar arrays are contraindicated and a straight lateral-wall or custom cavity/ring electrode is used, positioned against the OUTER wall of the cavity where surviving neuroepithelium lies; a transmastoid labyrinthotomy or transcanal approach helps avoid the aberrant facial nerve (cross-ref Ch.12 Imaging).[2009]

TThe auditory brainstem implant

The auditory brainstem implant (ABI) bypasses cochlea and cochlear nerve entirely, laying a flat silicone surface paddle (typically ~12–21 contacts) on the cochlear nucleus in the lateral recess of the fourth ventricle via a translabyrinthine or retrosigmoid approach — for NF2 after schwannoma resection and increasingly children with cochlear-nerve aplasia or complete labyrinthine aplasia.

CABI outcomes

ABI place-coding is crude, so outcomes generally fall below cochlear-implant performance — often sound awareness and lip-reading support rather than open-set speech — and non-tumour/pediatric recipients generally do better than NF2 patients. Penetrating-microelectrode ABI variants were trialled for finer selectivity but showed no clear benefit.

Malformation → which array?

Straight, full-banded arrayfor Common cavity
WhyNeural tissue lines the cavity wall, so a straight array placed against the wall reaches it — NOT a modiolus-hugging design.

Malformations (Sennaroglu spectrum, cross-ref Ch.12) reshape array choice. The key insight is the common cavity: with neural tissue lining the cavity wall, a straight, full-banded array laid against the wall reaches it — a modiolus-hugging design has no modiolus to hug. Hypoplasia takes a short array; high-gusher forms (IP-I/II) need sealing and packing; and true cochlear or cochlear-nerve aplasia has no target for a cochlear implant at all, redirecting to an ABI. Schematic.

Case 13.17 · No modiolus
Imaging shows a common-cavity malformation with no modiolus.

Which array is appropriate?

Self-assessment — Module 172 questions
Question 1

In basal-turn ossification, the drill-out should not exceed about…

Question 2

When no modiolus exists (common cavity, IP-I)…

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