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Otosclerosis: Detailed Surgical Management

Stapedectomy and stapedotomy techniques: indications, prosthesis selection, and outcomes

Written by: Saygı Hospital Health Guide Editorial Board
Last updated:

This content has been compiled by the Saygı Hospital Health Guide Editorial Board and is periodically reviewed by a specialist physician.

References (5)

This content is for informational purposes only and does not constitute medical advice. You can book an appointment at our KBB (Kulak Burun Boğaz) department. Book Appointment →

What is Otosclerosis: Detailed Surgical Management?

Otosclerosis is a primary disease of the otic capsule (bony labyrinth) characterized by abnormal bone remodeling — replacement of normal endochondral bone with spongy vascular bone (otospongiosis), then sclerotic bone. The fissula ante fenestram (anterior to the oval window) is the most common focus, leading to stapes footplate fixation and conductive hearing loss.

Surgical options: stapedotomy (small fenestra in footplate, prosthesis through hole) is preferred today over stapedectomy (footplate removal). Prosthesis types: piston prosthesis (fluoroplastic, titanium, platinum-band), lengths 4.0-4.5 mm, diameter 0.4-0.6 mm. Laser-assisted stapedotomy (CO2, KTP, argon) reduces footplate trauma and improves outcomes.

Outcomes: air-bone gap closure to <10 dB in 90-95%, sensorineural hearing loss <1%, dead ear <1%. Indications: conductive/mixed loss with air-bone gap >25 dB, normal tympanic membrane, present Carhart notch (2 kHz), good speech discrimination. Contraindications: only-hearing ear, active Ménière's, far-advanced otosclerosis (consider cochlear implant).

Symptoms

Progressive bilateral conductive hearing loss (often asymmetric)
Tinnitus (low-pitched, often improves post-op)
Paracusis Willisii (better hearing in noisy environments)
Schwartze sign (reddish promontory through tympanic membrane - active otospongiosis)
Vertigo (rare, post-op transient)
Speech discrimination preserved early, declines in mixed phase

Risk Factors

Family history of otosclerosis (autosomal dominant, 25-50% penetrance)
Female gender (2:1 ratio)
Pregnancy (accelerates progression)
Caucasian ethnicity (highest prevalence)
Age 20-40 at onset
Measles virus exposure (controversial association)

When to See a Doctor?

If you experience any of the following symptoms, seek medical attention promptly:

  • Progressive hearing loss in young-middle-aged adult without ear infection
  • Family history with developing hearing problems
  • Hearing loss accelerating during pregnancy
  • Tinnitus accompanying hearing loss
  • Audiometry showing Carhart notch (2 kHz dip in bone conduction)
  • Air-bone gap >25 dB on audiogram (surgical candidacy)

Treatment Methods

01
Stapedotomy (small fenestra technique) - gold standard surgical option
02
Stapedectomy (footplate removal) - alternative for select cases
03
Laser-assisted stapedotomy (CO2/KTP) - reduces footplate trauma
04
Prosthesis selection (titanium/fluoroplastic piston, 4.0-4.5 mm × 0.4-0.6 mm)
05
Hearing aids (alternative for non-surgical candidates)
06
Sodium fluoride therapy (50 mg/day - controversial, slows progression)
07
Cochlear implantation (far-advanced otosclerosis with profound SNHL)
08
Bisphosphonates (experimental - active otospongiosis)
09
Annual audiometry follow-up post-surgery

Which Department to Visit?

You can visit our KBB (Kulak Burun Boğaz) department for these complaints. Our specialist physicians will create the most suitable treatment plan for you.

Learn About KBB (Kulak Burun Boğaz) Department

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Health Disclaimer: The information on this page is prepared for general informational purposes only. It does not replace medical diagnosis and treatment. Please consult your physician for your complaints. Saygı Hospital does not accept responsibility for actions taken based on the information on this page.