Chronic Otitis media definition classification etiology clinical features investigations management

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chronic suppurative otitis media management WHO ear and hearing care

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Chronic otitis media (COM)

Definition

COM is persistent inflammation and structural damage of the middle ear and tympanic membrane, usually following recurrent acute otitis media or otitis media with effusion. It may present with a persistent tympanic membrane perforation, retraction pocket, otorrhoea, ossicular damage, and hearing loss.
Chronic suppurative otitis media (CSOM) specifically denotes chronic middle-ear infection with otorrhoea through a tympanic membrane perforation, often considered chronic after at least 2 weeks to 3 months depending on the definition used. WHO guidance uses persistent discharge for at least 2 weeks as a practical alert threshold.

Classification

1. Modern clinical classification

  1. Active COM
    • Active inflammation with discharge.
  2. Inactive COM
    • Dry ear but residual pathology remains, for example perforation or retraction pocket, with potential to reactivate.
  3. Healed COM
    • Healed tympanic membrane with no active disease or significant potential for reactivation.
Active and inactive disease are further divided into:
TypeMain pathologyTraditional equivalent
Mucosal COMCentral perforation with disease limited largely to middle-ear mucosaTubotympanic or "safe" disease
Squamous COMRetraction pocket, keratin accumulation, or cholesteatomaAtticoantral or "unsafe" disease
Bailey and Love's Short Practice of Surgery, 28th ed., classification of COM.

2. Traditional CSOM classification

  • Tubotympanic disease
    • Central perforation of pars tensa.
    • Usually mucosal disease.
    • Less likely to cause serious complications, but may impair hearing and discharge recurrently.
  • Atticoantral disease
    • Attic or marginal perforation, often with cholesteatoma.
    • Bone-eroding and potentially dangerous.
    • Requires specialist surgical assessment.

3. Cholesteatoma

Cholesteatoma is keratinizing squamous epithelium within the middle ear or mastoid that accumulates keratin debris and can erode ossicles, mastoid, facial canal, labyrinth, and skull base. It may be congenital or acquired. Cummings Otolaryngology Head and Neck Surgery, p. 2683.

Etiology and predisposing factors

Pathogenesis

The central mechanisms are:
  • Recurrent or inadequately resolved acute otitis media
  • Persistent middle-ear effusion
  • Eustachian tube dysfunction, causing negative middle-ear pressure, tympanic membrane retraction, atelectasis, and retraction pockets
  • Persistent perforation allowing repeated contamination of the middle ear
  • Chronic infection and biofilm formation
  • Development of cholesteatoma from a retraction pocket or epithelial migration through a perforation

Risk factors

  • Childhood and recurrent upper respiratory infections
  • Adenoid hypertrophy, chronic rhinitis, sinus disease
  • Cleft palate or craniofacial anomalies
  • Poor socioeconomic conditions, overcrowding, malnutrition
  • Water contamination or repeated water entry into a perforated ear
  • Previous ear trauma or ear surgery
  • Immunodeficiency and poorly controlled diabetes
  • Smoking exposure

Microbiology

Common organisms include:
  • Pseudomonas aeruginosa
  • Staphylococcus aureus
  • Proteus species
  • Klebsiella species
  • Anaerobes, particularly in infected cholesteatoma
Pseudomonas is frequently implicated in chronic otitis media biofilms. K J Lee's Essential Otolaryngology, p. 446.

Clinical features

Symptoms

  • Persistent or recurrent ear discharge, often mucopurulent
  • Conductive hearing loss
  • Ear blockage or tinnitus
  • Usually little pain in uncomplicated disease
  • Foul-smelling scanty discharge suggests cholesteatoma
  • Vertigo, facial weakness, severe headache, fever, or altered sensorium suggest complications

Otoscopic findings

Mucosal COM
  • Central perforation of pars tensa
  • Inflamed, oedematous middle-ear mucosa
  • Mucopus or mucoid discharge
  • Granulations or aural polyp may be present
  • Ossicular erosion can occur in longstanding disease
Squamous COM / cholesteatoma
  • Pars flaccida or posterosuperior retraction pocket
  • White keratin debris
  • Attic or marginal perforation
  • Granulations, aural polyp, scutum erosion
  • Foul-smelling discharge
  • Aural polyp in a chronically discharging ear should be regarded as cholesteatoma until excluded. K J Lee's Essential Otolaryngology, p. 446.

Complications

Intratemporal
  • Acute mastoiditis
  • Mastoid abscess
  • Facial nerve palsy
  • Labyrinthitis or labyrinthine fistula causing vertigo
  • Petrositis
  • Ossicular destruction and worsening hearing loss
Intracranial
  • Meningitis
  • Extradural or subdural abscess
  • Temporal lobe or cerebellar abscess
  • Lateral sinus thrombosis

Investigations

  1. Otoscopy, otomicroscopy, or otoendoscopy
    • Define perforation, retraction pocket, keratin debris, granulation, and cholesteatoma.
    • Suction clearance of debris may reveal concealed disease.
  2. Pure-tone audiometry
    • Usually shows conductive hearing loss.
    • Mixed loss may occur with longstanding disease or labyrinthine involvement.
    • Speech audiometry as indicated.
  3. Tympanometry
    • Useful when the tympanic membrane is intact or in assessing middle-ear mechanics.
    • Not useful in a large perforation in the usual way.
  4. Ear swab for microscopy, culture, and sensitivity
    • Indicated in persistent, recurrent, severe, or treatment-resistant discharge.
  5. High-resolution CT temporal bone
    • Indicated for suspected cholesteatoma, complications, surgical planning, recurrent disease, facial palsy, or vertigo.
    • Assesses mastoid pneumatization, ossicular erosion, scutum erosion, tegmen, facial canal, and labyrinth.
  6. MRI brain/temporal bone with contrast and diffusion-weighted imaging
    • For suspected intracranial complications.
    • Useful for detecting or following residual/recurrent cholesteatoma.
  7. Biopsy
    • Consider for granulation tissue or aural polyp that does not resolve with appropriate topical treatment, to exclude malignancy.

Management

Principles

The objectives are to create a safe, dry ear, eradicate disease, prevent complications, and restore hearing where feasible.

A. General measures

  • Keep the ear dry: avoid swimming and water entry.
  • Treat associated nasal allergy, rhinosinusitis, or upper respiratory disease.
  • Counsel against inserting cotton buds, oils, or unprescribed ear drops.
  • Assess hearing and its educational, occupational, and communication impact.

B. Active mucosal COM / CSOM

  1. Aural toilet
    • Microsuction or dry mopping to remove pus, debris, and granulation tissue.
    • This improves penetration of topical treatment.
  2. Topical antibiotic ear drops
    • Culture-directed where possible.
    • Non-ototoxic topical fluoroquinolone preparations are commonly preferred when a perforation is present.
    • Add topical corticosteroid only when clinically appropriate for marked inflammation or granulations.
  3. Systemic antibiotics
    • Not routine for uncomplicated chronic discharge.
    • Consider when there is spreading infection, systemic illness, mastoiditis, cellulitis, or an intracranial/intratemporal complication.
    • A 2025 Cochrane review reassessed systemic antibiotics for CSOM, but treatment still needs to be individualized because evidence quality and applicability vary (PMID: 40484405).
  4. Treat granulation tissue
    • Aural toilet and topical therapy first.
    • Persistent polyp requires specialist evaluation and sometimes biopsy.
  5. Tympanoplasty / myringoplasty
    • Indications:
      • Persistent dry central perforation
      • Recurrent discharge despite appropriate medical treatment
      • Conductive hearing loss
      • Need to prevent water-related recurrent infection
    • May be combined with ossiculoplasty if ossicles are damaged.

C. Squamous COM / cholesteatoma

Definitive treatment is surgery. Topical therapy can control infection temporarily but does not remove the keratinizing lesion or stop bone erosion.
  • Tympanomastoidectomy, with cholesteatoma removal
  • Canal-wall-up or canal-wall-down mastoid surgery, depending on disease extent and anatomy
  • Tympanoplasty and ossicular reconstruction when appropriate
  • Long-term postoperative follow-up is essential because residual or recurrent disease can occur
Bailey and Love's Short Practice of Surgery, 28th ed., notes that active squamous COM is acquired cholesteatoma and recommends mastoid surgery for removal.

D. Management of complications

  • Urgent ENT referral or admission
  • IV antibiotics where infection has spread
  • CT temporal bone and MRI brain when indicated
  • Prompt surgical drainage or mastoid surgery for mastoid, labyrinthine, facial nerve, or intracranial complications
  • Neurosurgical input for intracranial abscess or venous sinus thrombosis

Exam summary

  • Central perforation + mucopurulent discharge = mucosal/tubotympanic COM.
  • Attic or marginal perforation, retraction pocket, keratin debris, foul-smelling discharge = suspect cholesteatoma.
  • Investigate with otoscopy/microscopy, audiometry, culture when persistent, HRCT temporal bone for cholesteatoma or surgical planning.
  • Treat uncomplicated active mucosal disease with aural toilet, topical non-ototoxic antibiotic drops, dry-ear precautions, then consider tympanoplasty.
  • Treat cholesteatoma with definitive tympanomastoid surgery.
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