Myringoplasty and Tympanostomy Tube Placement

Abstract

Myringoplasty with tympanostomy tube placement may be performed for patients with a variety of middle ear conditions. Often, eustachian tube dysfunction causes otitis media, tympanic membrane perforation, or conductive hearing loss. In the present case, myringoplasty was performed using the CO₂ laser, providing reorganization of collagen fibers and improved compliance of the tympanic membrane. Given the ongoing eustachian tube dysfunction, a pressure equalization tube was placed to prevent recurrent retraction and atelectasis of the eardrum.

Case Overview

Background

Patients with middle ear disease may present in a variety of ways. At the root of many middle ear disorders is the eustachian tube. When functioning properly, the eustachian tube allows for pressure equalization between the middle ear and the surrounding atmosphere.¹ However, dysfunction of the eustachian tube can lead to the development of negative pressure in the middle ear, leading to effusion and tympanic membrane retraction. Patients may present to primary care providers or specialists with complaints of hearing loss, fullness/pressure in the ear, otorrhea, or pain. Over time, retraction of the tympanic membrane can lead to structural changes, resulting in hearing loss even in the absence of effusion.² Treatments for this condition are aimed at establishing an equal pressure gradient across the tympanic membrane. This can be accomplished with procedures such as myringotomy, tympanostomy tube placement, and eustachian balloon tuboplasty. Myringoplasty can help restore a more normal structural anatomy to the eardrum, promoting greater sound transduction to the middle and inner ear.

Focused History of the Patient

In this case, the patient presented with a history of recurrent otitis media with effusion. This resulted in discomfort and conductive hearing loss. She had several sets of tympanostomy tubes placed in the clinic with drainage of the effusion and resolution of hearing loss. Over time, however, these tubes remained in place for only 2–3 months. Chronic eustachian tube dysfunction led to tympanic membrane retraction and atelectasis.

Physical Exam

The patient’s external ear was normal in appearance, as was the external auditory canal. The tympanic membrane was globally retracted and atelectatic with adherence to the promontory. There was no evidence of a deep retraction pocket or keratinaceous debris to suggest cholesteatoma. Tuning fork testing with a 512-Hz fork was notable for a negative Rinne test on the affected ear as well as Weber lateralization to the affected ear. The nasal exam was normal without evidence of turbinate hypertrophy or chronic rhinitis/sinusitis.

Adjunctive Studies

The patient’s audiometric testing demonstrated a mild conductive hearing loss in the affected ear in addition to a type C tympanogram (negative pressure).

Natural History

With chronic negative pressure in the middle ear, there is a risk of the development of retraction pockets and cholesteatoma. This could lead to additional associated complications such as severe or permanent hearing loss, meningitis, or labyrinthine fistulas.

Options for Treatment

There are several treatment options for eustachian tube dysfunction and middle ear effusion. Because the patient had received many sets of tympanostomy tubes in the clinic with the relief of effusion, this remained an option. However, atelectasis of the tympanic membrane and adherence to the promontory made doing so more difficult. Balloon eustachian tuboplasty is a relatively new treatment modality for eustachian tube dysfunction. Despite the fact that this patient had negative middle ear pressure, nasal endoscopy did not confirm the presence of dilatory eustachian tube dysfunction, and she was able to insufflate her middle ear space with a Valsalva maneuver.

Rationale for Treatment

For patients who have undergone multiple treatments or have had long-standing negative pressure of the middle ear, the collagen fibers of the tympanic membrane can become disorganized.

The objectives of treatment, in this case, were to release the fluid in the middle ear, improve the tensile strength of the tympanic membrane, and reduce future episodes of retraction and effusion.

Special Considerations

There are no specific contraindications for this procedure from a patient-selection standpoint.

Step-by-Step Technique

Anesthesia

General anesthesia is used. An endotracheal tube or laryngeal mask airway can be used given the short duration of the procedure. One advantage of using endotracheal intubation is that administration of nitrous oxide can promote middle ear inflation, aiding in the release of an atelectatic tympanic membrane from the promontory.

Patient Positioning

The patient should be placed supine on the operating table and secured with straps. The bed can either be rotated or just brought away from the anesthesia machine in its standard orientation. The head is turned away from the surgeon, and the arm on the operative side is tucked. Although less important in a short case, the blood pressure cuff should ideally be placed on the contralateral arm.

Prepping the Patient

No specific prep (e.g. Betadine) or draping was required in this case.

Procedure Details

Laser safety is paramount in all cases. The OmniGuide (Lexington, MA, USA) carbon dioxide laser is used, and all participants in the operating room should be provided with appropriate eye protection. This is not required for the primary surgeon using the microscope.

The laser should be tested on a moistened tongue depressor. It should be placed in “stand-by” mode unless in active use by the surgeon, who should instruct the circulating nurse or laser operator by confirming “laser-on” and “laser-standby.”

The settings for this laser are 2 W for a 100-ms pulse duration, single pulse. It is important to position the laser at a distance that allows for accurate localization of the target but that is also far enough back that it does not penetrate the membrane. The key is to start back further and work inwards. Each area of the tympanic membrane that appears flaccid or hyperinflated can be treated with the laser to achieve the desired effect.

The myringotomy is made with a radial incision along the tympanic membrane. Standard teaching instructs surgeons to place the incision in the anterior-inferior quadrant. If this area is not well-visualized due to patient anatomy (e.g. anterior canal hump), it can be placed in the posterior-inferior quadrant. The superior aspect should be avoided due to the risk of injuring underlying anatomical structures (e.g. ossicular chain).

The tympanostomy tube can be trimmed to size and should be placed with the flanges in the middle ear. Once placed, the tube itself should be directed laterally to ensure patency, allow for monitoring, and facilitate the administration of topical medications if they are required.

Dressing

A cotton ball can be placed in the external meatus if there is drainage, otherwise no dressing is required.

Postoperative Restrictions

While patients may feel relatively normal or improved immediately after surgery, they should not drive or make any important decisions for 24 hours after surgery. If there is significant effusion, a prescription for otic drops should be provided (ofloxacin or ciprofloxacin/dexamethasone). Patients should be instructed to administer 3–5 drops once daily for 5 days. Patients may shower immediately after surgery but should avoid getting water directly in the ear or submerging in soapy water.

Discussion

While myringotomy is one of the most commonly performed otolaryngological procedures, this case is unique for its use of the CO₂ laser and myringoplasty. The operative time for the case is typically 10–15 minutes, and the patient goes home on the same day. Patients may experience some transient otorrhea; however, the pain is minimal and is controlled with over-the-counter analgesics. If an effusion is present, the patient can be treated with ofloxacin (0.3% otic solution) drops for 3–5 days, 1–2 times daily. Tubes typically extrude between 6–9 months, and recurrence of symptoms with ongoing eustachian tube dysfunction is common. Nevertheless, the performance of myringoplasty can reduce the incidence of recurrent retractions. The patient should have a follow-up hearing test 4–6 weeks after the surgery and should be monitored every 3–6 months thereafter.

Equipment

• Standard otolaryngology ear tray (alligator, Rosen needle, straight pick, 3- and 5-suction)
• OmniGuide CO₂ Laser with Oto-M fiber
• Tympanostomy tube (brand and type at the discretion of the operating surgeon)

Disclosure

C. Scott Brown also works as editor of the Otolaryngology section of the Journal of Medical Insight.

Statement of Consent

The patient referred to in this video article has given their informed consent to be filmed and is aware that information and images will be published online.