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Congenital Aural Atresia PowerPoint Presentation

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Description : Check out this medical PowerPoint presentation titled "CONGENITAL AURAL ATRESIA" by Dennis R. Maceri, M.D., F.A.C.S.

This medical PowerPoint presentation is about congenital aural atresia, a medical condition in which an individual is born with an underdeveloped or absent ear canal. This can cause hearing loss or deafness in one ear or both ears.

The condition is usually caused by a failure of the external ear canal to develop properly during fetal development. It can occur as an isolated anomaly or as part of a syndrome involving other facial or cranial abnormalities.

Symptoms of congenital aural atresia can include hearing loss or deafness, ear infections, and discharge or drainage from the affected ear. Treatment options for the condition include hearing aids, bone conduction devices, or surgical interventions such as aural atresia repair or bone-anchored hearing aid surgery.

Individuals with congenital aural atresia may also benefit from speech therapy, auditory rehabilitation, and other supportive measures to improve their communication and quality of life.

Tags : congenital aural atresia, absent ear canal, hearing loss, deafness

Published on : Jun 23, 2023 | Views : 563 | Downloads : 0

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Slide 1-

CONGENITAL AURAL ATRESIA Dennis R. Maceri, M.D., F.A.C.S. Associate Professor Otolaryngology- Head and Neck Surgery Keck School of Medicine
Slide 2-

“ The better developed the auricle the better the middle ear”Kountakis, 1995
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Atresia Epidemiology 1 in 10,000 to 15,000 births Up to 50% of the time associated with some craniofacial syndrome Unilateral : Bilateral, about 3:1 30% are bilateral Atresia : Microtia, 7:1 Slightly more common on the right Male : Female, 2:1
Slide 4-

Atresia Aural atresia associated with 22/71 known craniofacial syndromes Treacher Collins (Mandibulofacial Dysostosis) Nager Syndrome (Acrofacial Dysostosis) Cruzoun’s Craniofacial Dysostosis Goldenhar’s Syndrome Hemifacial Microsomia
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Aresia Surgery First attempt to surgically correct aural atresia was by Thomson in 1843 Shambaugh, 1967, recommended unilateral surgery only if the cochlear reserve allowed hearing to improve by 25dB Jahrsdoerfer, 1978, first large series using the anterior approach
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Embryology 8 Week Stage
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Embryology 8 Week Stage
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Embryology The external ear forms earlier than the middle ear Microtia and Atresia imply an arrest in development at any stage The earlier the arrest, the less developed the middle ear
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Embryology Inner ear and labyrinth develop at 3 weeks from an invagination of ectoderm called the ottic placode Middle ear space, mastoid, eustachian tube and part of the drum develop from the first pharyngeal pouch at 30 weeks Mastoid air cells continue to develop up to age 5
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Embryology First Branchial Arch-(Meckel’s) Malleus head, body, tensor tympani (V3) Short process of the Incus Second Arch (Hyoid) (Reicherts) Manubrium of the malleus Stapes superstructure VIIth nerve Foot plate from the otic capsule and 2nd arch
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Embryology External ear (ectoderm) is derived from the 1st branchial cleft. A solid core of epithelium migrates inward toward the 1st branchial pouch (endoderm)
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Embryology Solid core of tissue migrates inward External canal re-canalizes by the 6th month
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Embryology The external canal starts to hollow out (recanalize) during the 6th month and progresses from medial to lateral Arrest of recanalization process leads to the various deformities seen in atresia Formed tympanic membrane and bony canal with a stenotic membranous canal leads to canal cholesteatoma
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Embryology Arrested growth of the ossicles leaves them in various stages of formation Stapes often malformed but mobile The incus and malleus are fused Altered course of facial nerve
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Atresia Embryology – 7th Month Canalization complete Mastoid separation from mandible Normal posterior-inferior growth No mastoid growth Normal Atresia
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Atresia Embryology Mastoid growth affects the facial nerve position Normal 120o Curve Acute Curve in Atresia
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Atresia
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Classification of Deformities After Colman-3 types Minor Aplasia-incomplete recanalization Moderate Aplasia- the tympanic bone has developed but has failed to recanalize Severe Aplasia-complete absence of the external canal
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Atresia Classification-Severe Aplasia, no tympanic bone
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Atresia Complete Atresia
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Atresia Complete Atresia
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Atresia Moderate Aplasia The most common, solid mass of compact bone that has failed to recanalize
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Atresia Minor Aplasia-partial recanalization Middle space constricted, often with severe ossicular abnormalities
Slide 24-

Microtia Types of Microtia (Based on Marx 1926) Class I Mild deformity, auricle smaller, all parts of ear identifiable Class II ½ to 2/3 normal size with partially retained structures Class III Severely malformed, peanut shaped
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Radiological Evaluation High resolution CT in coronal and axial planes Axial to delineate malleus, incus and I-S joint and round window Coronal to delineate stapes, oval window and vestibule 3-D CT of little help Timing indicated by timing of surgery
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Grading System Based on high resolution CT scan A score of 5 or less denotes a poor candidate Microtia indicates an arrest in development and abnormalities of the middle ear Kountakis, Helidonis and Jahrsdoerfer Arch. Oto 1995
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Atresia Grade of Microtia as an Indicator of ME Development Microtia Grade Radiological Score I 8.5 II 7.2 III 5.9 Kountakis Arch Otolaryngol 1995
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Radiological Evaluation Good middle ear and mastoid aeration Prominent ossicular mass with incus and malleus fused Open oval window Score of 8
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Radiological Evaluation Score of 8 2-stapes & OW 2-I-S joint, Incus 1-Aerated ME space 1-Bony cover on VII 1-Aerated mastoid 1-Pinna
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Radiological Evaluation Poor middle ear and mastoid development No definable ossicular mass Closed oval window Not a good candidate A score of 3
Slide 31-

Microtia
Slide 32-

Microtia Repair
Slide 33-

Audiological Evaluation 50-60 dB conductive loss Usually normal sensorineural function Unilateral- behavioral audiometry ABR for infants Bilateral atresia presents a masking dilemma Bone conduction ABR can help resolve the masking problem (Wave I on stimulated ear)
Slide 34-

Surgical Considerations Most consider repair in bilateral atresia Many are reluctant to operate on unilateral cases Not simply the hearing loss Expectations of hearing recovery Lifetime care of mastoid cavity Potential risks to facial nerve and labyrinth 55-65% achieve 25 dB speech-hearing level
Slide 35-

Surgical Considerations Most surgeons choose the anterior approach to avoid the mastoid cavity 40% of patients with unilateral atresia are not surgical candidates such as those with severe aplasia as in Treacher Collins syndrome Bilateral atresia- best ear by CT done as child approaches school age
Slide 36-

Surgical Considerations Timing of surgery Usually performed after age 6 or 7 years This allows for microtia repair to be done first (If Medpor used,canalplasty done first) Canal cholesteatoma in the stenotic ear usually develops in canals less than 2mm in diameter. If ear unfavorable, canalplasty alone is offered
Slide 37-

Canal Cholesteatoma Usually in ears with minor aplasia Canal <4mm, 50% incidence
Slide 38-

Surgical Technique Minor aplasia- canal widening and middle ear ossicular work with tympanoplasty Moderate Aplasia Mastoid or posterior approach Anterior approach
Slide 39-

Surgical Technique Anterior Approach Middle ear approached through the atretic bone with a limited mastoid opening
Slide 40-

Surgical Technique The posterior wall of the glenoid fossa becomes the anterior wall of the new ear canal The epitympanum is the first part of the middle ear encountered Fused ossicles identified
Slide 41-

Surgical Technique Atretic bone removed at times with a curette Globular mass separated from the stapes to avoid cochlear trauma Course of facial nerve determined Ossiculoplasty performed Tympanic membrane grafted Meatoplasty Split thickness skin graft (.008-.010 inches) lines the canal
Slide 42-

Surgical Technique The Meatoplasty must be aligned with the newly created bony canal
Slide 43-

Surgical Technique 4cm X 6cm split thickness skin graft The graft is positioned in the canal and sewn to the meatal margin Graft stabilized with Merocel wicks and hydrated with ear drops
Slide 44-

Hearing Results Post-op hearing level of 30 dB or better In 50-75% of patients with moderate or severe aplasia 20 dB or better in 15-20% Bellucci 20 dB in 50% @ 2 years Schuknect similar results at 1.3 years De La Cruz 56 patients 53% @ 20 dB at 6 mo. Lambert early 60% @25 dB, 46% >1 yr.
Slide 45-

Alternatives to Surgery Bone anchored hearing aid (BAHA)
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BAHA Hearing results better than with BC aids
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Surgical Complications Persistent or recurrent conductive hearing loss Lateralization of graft Scar tissue SNHL VIIth Nerve injury 30 % revision rate Re-stenosis Graft migration Inadequate hearing Chronic cavity infection
Slide 48-

Summary Choose your patients carefully Realize your potential v. patient expectations Appropriate radiographic studies Accurate audiological analysis Facial nerve monitoring Know when NOT to operate