You are in: eMedicine Specialties > Otolaryngology and Facial Plastic Surgery > INNER EAR Inner Ear, Perilymphatic FistulaArticle Last Updated: Apr 10, 2006AUTHOR AND EDITOR INFORMATIONAuthor: Peter S Roland, MD, Professor, Department of Neurological Surgery, Professor and Chairman, Department of Otolaryngology-Head and Neck Surgery, Director of Clinical Center for Auditory, Vestibular and Facial Nerve Disorders, Chief of Pediatric Otology, University of Texas Southwestern Medical Center; Adjunct Professor of Communicative Disorders, School of Human Development, Chief of Medical Services at Callier Center for Communicative Disorders, University of Texas at Dallas Peter S Roland is a member of the following medical societies: Alpha Omega Alpha, American Academy of Otolaryngic Allergy, American Academy of Otolaryngology-Head and Neck Surgery, American Auditory Society, American Laryngological Rhinological and Otological Society, American Neurotology Society, American Otological Society, North American Skull Base Society, and Society of University Otolaryngologists-Head and Neck Surgeons Coauthor(s): William L Meyerhoff, MD, PhD, Former Chair, Former Professor, Department of Otolaryngology, University of Texas Southwestern Medical School Editors: Michael E Hoffer, MD, Co-director of Defense Spatial Orientation Center, Department of Otolaryngology, Naval Medical Center of San Diego; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Gerard J Gianoli, MD, Clinical Associate Professor, Department of Otolaryngology-Head and Neck Surgery, Tulane University School of Medicine; Vice President, The Ear and Balance Institute; Chief Executive Officer, Ponchartrain Surgery Center; Christopher L Slack, MD, Otolaryngology-Facial Plastic Surgery, Private Practice, Associated Coastal ENT; Medical Director, Treasure Coast Sleep Disorders; Arlen D Meyers, MD, MBA, Professor, Department of Otolaryngology-Head and Neck Surgery, University of Colorado School of Medicine Author and Editor Disclosure Synonyms and related keywords: PLF, inner ear membrane rupture, inner ear fluid imbalance, labyrinthine fistula, perilymph fistula, perilymphatic fistula INTRODUCTIONPerilymphatic or labyrinthine fistula is a condition in which an abnormal communication is present between the perilymphatic space of the inner ear and the middle ear or mastoid. The manifestations of this disease vary in severity and complexity, commonly ranging from very mild to incapacitating. Perilymphatic fistulas (PLFs) may induce hearing loss, tinnitus, aural fullness, vertigo, disequilibrium, or a combination of these complaints. The vagueness of symptoms caused by PLF and the overlapping symptoms of other disease processes make the diagnoses elusive. History of the ProcedureSustained interest in PLF began in the mid 1960s. The initial focus was on PLFs that developed following stapedectomy procedures. The recognition that loss of perilymph following stapedectomy could produce hearing loss, disequilibrium, and tinnitus led to the recognition that these same symptoms could arise from perilymph loss caused by other types of trauma. In the early 1970s, Victor Goodhill first distinguished between implosive and explosive forces as potential causes for rupture of the round or oval window membrane leading to PLF. ProblemGeneral agreement exists that PLF occurs and that leakage of perilymph from the inner ear into the middle ear can cause acute hearing loss, paroxysmal vertigo, disequilibrium, and tinnitus. Virtually no consensus exists regarding how frequently PLF occurs, how it should be diagnosed, or how it should be treated when suspected. A high degree of controversy surrounds the appropriate indications for surgical exploration and operative repair of PLF. FrequencyFrequency is unknown and hotly debated. EtiologyPLF occurs when perilymph leaks from the perilymphatic spaces of the bony labyrinth into the middle ear space. The loss of perilymph alters the balance between perilymph and endolymph within the membranous labyrinth. PLF is thus a form of inner ear fluid imbalance. Ménière disease, another form of inner ear fluid imbalance, occurs when endolymph is present in overabundance. Both disease entities alter the endolymph-to-perilymph ratio in the same direction, which may account for the difficulty involved with separating their clinical presentations. PathophysiologyInner ear fluids are almost completely contained within a rigid bony framework. However, the perilymphatic space is connected to the subarachnoid space via the cochlear aqueduct. The size of the cochlear aqueduct varies dramatically between subjects. Even when it is relatively large, the cochlear aqueduct is often completely obstructed with arachnoid tissue. Evidence exists that the arachnoid becomes denser with increasing age. Thus, the patency of the cochlear aqueduct varies among persons. Establishing whether the cochlear aqueduct is patent in any particular individual is impossible. A variety of indirect evidence suggests that pressure changes within the subarachnoid space can be communicated to the inner ear. Such pressure changes may be communicated through the cochlear aqueduct or alternatively through a patent lamina cribrosa, cochlear modiolus, or vestibular aqueduct. At least in some patients, stapes gushers appear to arise from a defective modiolus, allowing free communication between the spinal fluid and perilymphatic space. The length of the cochlear aqueduct and the presence of arachnoid within its lumen tend to dampen the effects of sudden pressure changes in the subarachnoid space, thereby protecting the inner ear from rapid pressure changes. Simultaneous increases in pressure on the endolymphatic sac also protect the intracochlear membranes by equalizing endolymphatic and perilymphatic pressure. Even so, sudden increases in subarachnoid pressure can be transferred from inner ear fluids. At the round window membrane and the annulus of the oval window, the middle ear space is separated from the perilymphatic space by a soft tissue membrane. These areas permit pressure change between the middle ear and perilymphatic space. Excess pressure generated on either side of these membranes can result in tear or rupture leading to the egress of perilymphatic fluid from the membranous labyrinth. In addition to the oval window annulus and round window membrane, which are present in every person with normal hearing, a number of other sites for PLF are possible in some individuals.
Goodhill separated the hydrodynamic forces that could potentially produce PLF into implosive and explosive forces. Everyday activities, such as lifting, straining, coughing, and sneezing, are associated with increases in cerebrospinal fluid (CSF) pressure. Such pressure increases then can be transmitted to the inner ear via a patent cochlear aqueduct or through the lamina cribrosa of the internal auditory canal. A precipitous increase in pressure within inner ear fluids can result in tears of the oval window annulus or round window membrane. Vulnerability to such tears may depend on the inherent strength of these tissues, which may vary among individuals. Goodhill termed tears produced by increased pressure within the inner ear fluid compartment as explosive. Conversely, pressure can increase rapidly within the middle ear space as a result of barometric pressure change, compression trauma of the ear, Valsalva maneuver, and pinched-nose sneezing. Ruptures or tears of the round window membrane, oval window annulus, or membranes protecting a fistula ante fenestram, microfissure, or the Hyrtl fissure that result from increased middle ear pressure also are termed explosive forces by Goodhill. In addition to changes related to hydrodynamic pressure, head injury may produce rupture of the membranes that seal the inner ear and prevent escape of perilymphatic fluid into the middle ear space. The precise mechanism by which perilymph loss produces hearing loss is unclear. Decompression of the perilymphatic space may create secondary endolymphatic hydrops. Consequently, the usual symptoms of endolymphatic hydrops (Ménière disease) arise. Secondary endolymphatic hydrops has been histologically identified in experimental animals with PLF. Compelling indirect evidence exists that hearing loss in this circumstance is the result of loss of perilymphatic pressure. A large number of reports describe hearing loss associated with decreased subarachnoid pressure secondary to spinal anesthesia. Hardy demonstrated that such hearing loss can be reversed by injecting 20 mL of isotonic sodium chloride solution into the subarachnoid space. In 1974, Robertson demonstrated changes in the tuning curves of single spiral ganglion cells from the basal membrane after removal of perilymph from the tympanic scala of the guinea pig. Flint et al showed an increase in auditory brainstem response (ABR) thresholds of 10-15 dB in guinea pigs with artificially created PLF; however, the etiology remains controversial. Bohmer demonstrated no change in auditory thresholds measured in guinea pigs with simple round window membrane perforation, even though a decrease was noted in the normal positive hydrostatic pressure within the cochlea. Evidence of auditory change also has been provided by measuring electrocochleographic changes after the creation of PLF. Ackley demonstrated consistent increase in the ratio of the summating potential (SP) to the action potential (AP) in guinea pigs with obstructed cochlear aqueducts after the creation of PLF. Others have subsequently confirmed these results. ClinicalSeltzer and McCabe gathered clinical data from 91 patients with surgically confirmed PLF. Most patients (90%) had auditory symptoms, generally hearing loss. The character of the loss varied from sudden and profound to mild and fluctuating. Tinnitus was noted in 63% of patients, and aural fullness was noted in 25%. Glasscock et al reported that 83% of their patients with traumatic PLF had complaints of sudden or fluctuating sensorineural loss. Vestibular symptoms occur in most patients. Balance disturbance can be described as true rotational vertigo, lightheadedness, disequilibrium, intolerance to motion, or any combination of these symptoms. Seltzer and McCabe reported such symptoms in 80% of patients with PLF, and Glasscock et al reported 77% incidence of true vertigo or disequilibrium. In obvious cases, membrane rupture is accompanied (or followed within a few minutes) by rapid severe hearing loss, loud roaring tinnitus, and severe rotational vertigo. Vertigo often is incapacitating and accompanied by visceral symptoms (eg, sweating, pallor, nausea, vomiting). Even cursory examination demonstrates marked instability and nystagmus. Audiometric evaluation reveals sensorineural hearing loss. Platform posturography confirms disequilibrium with a vestibular pattern, and platform fistula test results are positive. Vertigo and, to a lesser degree, tinnitus and hearing loss are sometimes exacerbated by straining (the Valsalva maneuver). Unfortunately, many PLFs do not manifest in a straightforward fashion. A combination of otologic symptoms may result, and symptoms may fluctuate in complex ways that are difficult for the patient to explain. Onset of symptoms may be delayed by several days, or the acute phase may be masked by more serious injuries in other areas. Rotational vertigo may be entirely absent, and disequilibrium may be mild, vague, and episodic. Hearing loss, tinnitus, and aural fullness may come and go unpredictably. Such elusive symptomatology is partially responsible for the controversy surrounding this disorder. The diagnosis of PLF often depends on the antecedent history of otologic surgery, trauma, diving, or congenital ear malformation. Fluctuating or sudden hearing loss with or without vestibular symptoms in a patient with a previous stapedectomy, for example, is highly suggestive of PLF. Trauma frequently is cited as the cause of a PLF. Changes in the middle ear pressure sufficient enough to implode the round window membrane can occur during descent while flying, forced Valsalva maneuver, or suppressed sneezing. Pullen reported that 48 of 62 patients with suggested PLF following scuba diving had round window membrane rupture. Pressure sufficient to rupture the round window membrane can develop at a depth of water as shallow as 4 ft. Explosive PLFs can arise from CSF pressure increases caused by physical exertion, coughing, and straining. Klokker and Vesterhauge have reported on 4 cases of perilymph fistula that occurred in flight attendants who flew with upper respiratory infections during a 6-month period. All 4 flight attendants work for a major Scandinavian airline that employs approximately 3,000 flight attendants. PLF may be the ultimate etiology of progressive neurosensory hearing loss in some children. Its frequency remains unknown and is contested. Grundfast and Bluestone reported that 66% of 33 children with progressive neurosensory hearing loss had PLF at exploratory tympanotomy. Reilly and Kenna prospectively evaluated 244 children with sensorineural hearing loss of unknown etiology; of the 54 ears that were surgically explored, 42% demonstrated active PLF. Weber et al, in a follow-up article, confirmed that surgical repair of perilymph fistula does not result in a significant risk of postoperative hearing loss and that fistula repair may prevent further hearing loss, even in patients in whom a perilymph fistula was not identified at the time of surgery. INDICATIONSThe indications for exploratory tympanotomy are controversial. Accurate diagnosis is difficult. If the patient's history is suggestive of PLF, objective testing should be used to reinforce or reject the initial assessment. The signs and symptoms of PLF are relatively nonspecific and overlap greatly with those seen in other otolaryngologic and neurologic diseases. PLF can be particularly difficult to differentiate from Ménière disease. Histologically, the 2 diseases are similar. However, the final diagnosis of PLF requires integration of all available information. Because PLFs can be difficult to diagnose, some surgeons believe that patients should be given the opportunity to choose surgical exploration even when PLF is unlikely. Such an approach leads to many explorations with negative findings and many patients who do not benefit from the procedure. Conversely, a few patients benefit who would otherwise have had undiagnosed PLF. Other surgeons prefer to use fairly rigid criteria for the diagnosis of PLF. These surgeons explore fewer individuals and have a much higher rate of positive intraoperative findings. A high percentage of their operative cases improve following surgery; however, some cases of PLF are missed. These patients may have lost an opportunity for clinical improvement or cure. Objective testing becomes especially important when the history of antecedent trauma is vague or remote. A PLF test or elevated SP/AP ratio on electrocochleography (ECoG) significantly raises the likelihood of PLF. CONTRAINDICATIONSNo absolute contraindications exist to exploratory tympanotomy with round and oval window grafting in patients who can tolerate either a local or general anesthetic. A physician must exercise the usual cautions in an only-hearing ear, even though the incidence of significant hearing loss associated with this operation is low. To justify operative intervention, one must feel convinced that the likelihood of additional hearing loss is greater without surgery than with surgery. WORKUPLab Studies
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Other Tests
Diagnostic Procedures
TREATMENTMedical therapySome tears of the inner ear membranes probably heal without surgical intervention. Medical management includes bed rest, elevation of the head of the bed, use of stool softeners, avoidance of Valsalva maneuver, and sedation. Repeated audiometric evaluations should be performed, and medical management should be reconsidered if hearing deteriorates or balance disturbance fails to improve. Preoperative detailsThe definitive treatment of PLF is surgical exploration with grafting of the fistula. Early repair of PLF offers the potential for resolution of vestibular symptoms and preservation of residual auditory function. Many authors recommend immediate surgical exploration when the likelihood of PLF is high. The timing of surgical exploration in the less-defined case is controversial. Depending on strict diagnostic criteria risks underdiagnosis of the disease, whereas overzealous exploration of all patients with auditory and vestibular complaints risks performing many procedures that, in retrospect, are unnecessary. Meyerhoff and Pollock have recommended that the patient become intimately involved in the decision-making process. Intraoperative detailsThe procedure can be performed with the patient under local or general anesthesia. A standard tympanomeatal flap is designed, incised, and elevated. Generally, curetting away the posterior bony overhang (scutum) is necessary to permit adequate visualization of the round and oval window niche. These areas are then very carefully observed for the accumulation of clear fluid. However, even intraoperative observation can be inconclusive. Transudates from middle ear mucosa, irrigation, or injected anesthetic materials can collect within the dependent areas of the round window or oval window niche. The absence of detectable fluid in these areas does not exclude an intermittent or recurrent PLF. Use of intravenous fluorescein is not helpful because it can accumulate in the round window niches as a transudate from middle ear tissues. Beta2-transferrin is specific for human aqueous humor, CSF, and perilymph. Western blot analysis for beta2-transferrin allows identification with very small amounts of dilute fluid. Unfortunately, the time required to perform the test prevents its use in surgical decision making. Preoperative irrigation of the middle ear via myringotomy has been suggested as a method of obtaining dilute perilymph that could be tested by Western blot analysis for the presence of beta2-transferrin, thus providing preoperative evidence of PLF. Intermittent or inactive PLF is overlooked by this test, and its risk to the patient approaches the risk of exploratory tympanotomy. Additionally, sensitivity of Western blot analysis for beta2-transferrin has been demonstrated to be very low (29%) in one study testing specimens of known perilymph. Provocative testing to confirm PLF is advocated by some and includes intraoperative Valsalva maneuver, Trendelenburg positioning, increase in intrathoracic pressure, and compression of the internal jugular vein. Black et al observed postoperative hearing loss after intraoperative performance of provocative maneuvers in several patients; they since have discontinued this practice. Grafting is performed by removing mucosa of the round and oval window area. Autogenous tissue grafts are placed directly over the leak. If no actual leak is identified, the footplate and round window are grafted prophylactically. Adipose tissue originally was used, but its use resulted in an unacceptably high rate of recurrent fistula. Fascia or perichondrium now is used; this is reported to have decreased the incidence of recurrent fistula. Surgeons at the University of Texas Southwestern Medical Center make a small incision beneath the lobule from which parotid masseteric fascia is harvested for use as a graft. Some authors use fibrin glue; others do not. Some surgeons do not graft unless an active leak is visualized. Other surgeons graft routinely, even if no leak can be detected by visual inspection. A poll of 167 members of the American Otologic and Neurotologic Society revealed that 78% placed grafts in all patients undergoing exploratory tympanotomy for PLF, regardless of whether a fistula could be demonstrated at operation. Postoperative detailsPostoperative care is directed at maintaining the integrity of the graft. Patients are instructed to avoid heavy lifting, straining, and activities that place the head in a dependent position, all of which could lead to increasing intracranial pressure. Stool softeners are given for the first 10 postoperative days. Antinausea medications are used as necessary. Air flight is well tolerated in the immediate postoperative period because the middle ear space is filled with transudated blood, therefore providing no air-filled space upon which pressure can act. Follow-upThe patient should be seen again 1-3 weeks postoperatively. A follow-up audiogram should be obtained at 6 weeks, and another follow-up audiogram should be obtained at 6 months. Beyond 6 months, follow-up care is determined by the patient's condition. COMPLICATIONSFew complications result from PLF repair. Tympanic membrane perforations occur in 1-2% of patients. Postoperative conductive hearing loss may persist longer after round and oval window grafting than with simple exploratory tympanotomy. Approximately 5% of patients still have persistent mild (5-10 dB) postoperative hearing loss 2-3 months following surgery; however, in most patients, the loss resolves within 6 months. Some risk exists of severe-to-profound hearing loss. This is especially likely in individuals with Mondini dysplasia or other morphologic defects. These ears are unstable, and surgical manipulation can result in hearing deterioration. Conversely, additional hearing loss is almost certain in such cases, and surgical intervention with round and oval window grafting frequently is the least risky alternative. Alteration of taste as a result of chorda tympani injury occurs with some frequency. It generally resolves within a few weeks to a couple of months. OUTCOME AND PROGNOSISRizer and House examined the outcome of 86 patients who underwent exploratory tympanotomy for suggested PLF. Active PLF was found in 35 of the patients, and all patients had placement of oval and round window grafts. Improvement was seen in 68% of patients with surgically confirmed PLFs, as opposed to 29% who did not demonstrate active PLF. Hearing improvement or restoration is less likely than elimination of balance disturbance after surgical repair of PLF. Seltzer and McCabe reported that 49% of treated ears improved in terms of auditory function, but only 23% improved to serviceable hearing levels, and 11% had continued hearing deterioration. Rizer and House noted 13.3% of their patients had hearing improvement. Black et al demonstrated hearing improvement in 17% of patients, stabilization of hearing in 67%, and continued progression in 17%. The same authors report improvement of vestibular systems in 83-94% of patients. Surgical exploration is highly effective for vestibular symptomatology, but its effect on hearing loss is less predictable. FUTURE AND CONTROVERSIESThe entire area of PLF is fraught with disagreement. Investigations in this area are severely constrained by the absence of any reliable tests to determine the presence of PLF. Since the presence or absence of the condition cannot be determined with certainty, its incidence remains unclear. Frequently, a physician cannot know whether an individual patient had a PLF; therefore, definitively constructing a typical clinical picture for the disorder is impossible. A method of determining with certainty whether perilymph is within the middle ear space is needed. Perhaps a rapid assay for beta2-transferrin that could be performed intraoperatively can be developed. Until a technique is developed for unequivocal diagnosis, PLF will remain mired in controversy. REFERENCES
Inner Ear, Perilymphatic Fistula excerpt Article Last Updated: Apr 10, 2006 |