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Review

Prognostic Factors for Hearing Preservation Surgery in Small Vestibular Schwannoma

Section of Otorhinolaryngology-Head and Neck Surgery, Department of Neurosciences, University of Padova, 35128 Padova, Italy
*
Author to whom correspondence should be addressed.
Audiol. Res. 2023, 13(4), 473-483; https://doi.org/10.3390/audiolres13040042
Submission received: 29 January 2023 / Revised: 11 April 2023 / Accepted: 27 June 2023 / Published: 3 July 2023
(This article belongs to the Special Issue Hearing and Balance in Acoustic Neuroma)

Abstract

:
Objective: to evaluate recent contributions to the literature on prognostic factors of hearing preservation in small vestibular schwannoma microsurgery. Methods: review of the most recent studies. Results: factors such as tumor size, preoperative hearing status, tumor growth rate, tumor origin, surgical approach, radiological characteristics, results of preoperative neurophysiological tests, preoperative symptoms and demographic features have been investigated and some of them reported to be significant in the prediction of hearing preservation. Conclusions: tumor size and preoperative hearing status are the most impactful factors and play a key role in patient selection for hearing preservation surgery. Other features such as fundal extension, tumor origin and impaired ABR could have prognostic value on hearing preservation. Tumor growth rate, preoperative impedance, cVEMPs and age have also recently been found to be significant, but more studies are needed. The role of preoperative tinnitus, vertigo and gender is lacking and controversial, whereas the differences between available surgical approaches have been smoothed out in recent years.

1. Introduction

Vestibular schwannoma (VS) is a benign neoplasm, usually arising from the vestibular branch of the eighth cranial nerve, but different origins are possible. It represents the most common lesion of the cerebello-pontine angle (CPA) and 8% of all intracranial tumors [1].
Its real incidence is still debated and can vary from 1 to 20 cases per million, according to different studies [2], but most recent works report 1–2 cases per 100,000 inhabitants, with a possible higher level of diagnosis in the European population [3]. Since the 1970s, there has been a gradual raise in incidence, with a peak in diagnosis in 2003–2005, followed by a progressive decrease to the actual value [3,4,5]. This trend has been explained by increased use of imaging, increased attention to oto-vestibular symptoms, and increased life expectancy, rather than a real increase in tumor incidence [5].
Despite a potentially long asymptomatic phase, one or more of the following symptoms, such as hearing loss, tinnitus, and vestibular dysfunction, are a common finding in VSs patients. Typically, the otological clinical examination is completely negative, while pure tone audiometry may show a unilateral sensorineural hearing loss (SNHL) or an interaural difference in hearing threshold. The vestibular clinical examination may be impaired, but there are no pathognomonic findings. The videonystagmography (VNG) is more sensitive in identifying vestibular nerve disfunction and may also quantify the damaged number of fibers. Neurophysiological tests (e.g., auditory brainstem response—ABR) are used to determine the damage on the cochlear nerve. The facial nerve is often unaffected by small tumors, while larger tumors may present with subclinical or clinical nerve deficit; this can be assessed using the House-Backmann scale and quantified with electromyography.
When a VS is suspected, high-resolution contrast-enhanced MRI is the gold standard to confirm diagnosis. T1 sequences enable identification of a mass in the CPA, iso-hypointense to the cerebral tissue, with intense gadolinium-contrast enhancement; when evaluated in T2, the tumor appears hyperintense. CSF-cisternographies sequences (e.g., CISS/FIESTA seq.) are useful for visualizing cranial nerves and vascular structures at the skull base-sequences and allow accurate for evaluations of tumor relations with them; these sequences are also essential to determining VS extension to the fundus of the internal auditory canal (IAC). High resolution CT scans are useful for evaluating petrosus bone structures in a preoperative setting; they also allow comparisons with the size of the affected IAC, which can be enlarged by the tumor, with the contralateral IAC.
The optimal way to calculate tumor dimension was initially discussed in the first Acoustic Neuroma Conference in 1991 (Copenhagen), but no clear agreement was reached. In 2001, forty specialists met in Tokyo in the Consensus Meeting on Systems for Reporting Results in Acoustic Neuroma [6]; the linear tumor size of the largest available extrameatal diameter was assessed in gadolinium-enhanced axial T1 sequences and “the intracanalicular or intrameatal and extrameatal portion of the tumor should be clearly distinguished”; the length of the intrameatal portion should not be added to the extrameatal tumor diameter. Classification of VSs according to their dimension was defined as reported in Table 1; a small VS is between 1 and 10 mm in diameter [6]. The classification proposed by Koos in 1998 considers tumor relation with the IAC, the CPA and the brainstem and divides VSs in four grades (I–IV) [7].
In the last decades, the increasingly widespread and early use of MRI to assess otological and neurologic symptoms has led to an increased discovery of small tumors in the initial phase of their natural history. These patients usually have no complaints, and their hearing function is often unaffected, making it necessary to implement treatment options that preserve hearing function.
The most widely used scales to report hearing outcomes are Tokyo [6] and AAOHNS [8], both based on PTA2 (Pure Tone Average at 500 Hz, 1000 Hz, 2000 Hz and 3000 Hz in the AAOHNS or 4000 Hz in Tokyo) and SDS values (peak percentage of speech discrimination). The Tokyo scale considers 6 hearing classes (A–F); the second, adopted in 1995, considers only 4 (A–D). The Gardner-Robertson [9] scale is also available.
To date, treatment of small tumors is still a debatable issue and is the object of the present review.
The available therapeutic strategies are: observation with periodic MRI scan, microsurgery, or radiosurgery. Small tumors are traditionally proposed for observation at first, with annual repetition of the MRI scan; active treatments are reserved for growing tumors. However, it has been recently shown that early surgery in small tumors can lead to clear advantages for the patient, in terms of curing disease, hearing function and preservation of the facial nerve, with better outcomes than conservative treatments [10,11]. The role of hearing preservation surgery (HPS) becomes especially evident in the long-term follow up [10,11,12,13]. Among the available surgical procedures, the retrosigmoid approach (RS), with retrolabyrinthine meatotomy (RLM) [11,13] or, in selected cases, endoscopic-assisted, is currently the most used method for removing the tumor from the internal auditory canal in HPS. In our experience [13], this technique allows for the complete removal of the tumor, providing a considerable rate of hearing function preservation (71% A-B classes of Tokyo classification and 85% A-B classes of AAOHNS) [13] and an excellent facial nerve outcome [13]. Other hearing-preservation approaches are the middle cranial fossa approach (MCF), for purely intrameatal tumors, and the retrolabyrinthine-presigmoid approach, for selected small tumors in the CPA, where the combined use of the endoscope helps to remove a limited extension of the tumor in the internal auditory canal. The key issue in HPS is the preoperative selection of patients. Tumor size and hearing play a crucial role, in combination with the patient’s age and adequate counseling about the possible therapeutic alternatives. In our center, HPS is considered a convenient option in <10 mm tumors in the CPA and hearing function with PTA2 < 30 and SDS > 70%, i.e., class AB and class A of Tokyo and AAHONS, respectively [11].
However, the role of the factors influencing and predicting the hearing outcome in the preoperative setting is still debated. This has promoted investigation of possible prognostic factors that would help to select the best candidates for HPS in relation to the inclusion criteria, with the aim of improving the outcome through the identification of reliable prognostic predictors on the likelihood of retaining hearing [14] when using the HPS strategy.
This review focuses on the most recent contributions investigating which prognostic factors can predict successful outcomes, with the aim of selecting the best candidates for HPS.

2. Materials and Methods

For this narrative review, the most recent studies published on hearing preservation in the surgical management of vestibular schwannoma were considered. The research conducted through the Pubmed library using the proper MeSH term for VS (“Neuroma, Acoustic” [Mesh]), combined with other terms referring to hearing preservation surgery (“hearing preservation surgery”, “HPS”, “hearing preservation”, “retrosigmoid” approach, “middle cranial fossa” approach); both RS and MCF approaches were included. Duplicate records were removed, and the remaining ones were screened for suitable records, i.e., studies investigating prognostic factors for HPS in LV patients. Papers not in English or unavailable for consultation were excluded.
No mandatory time interval has been set a priori in order to obtain as comprehensive a collection of factors as possible; on the other hand, when a large amount of literature was available, only the most updated works were considered; in some cases, older studies were also selected to allow for discussion of the changing role of prognostic aspects over the years.
When the literature investigating the role of a certain factor in the outcomes of HPS in small tumors was available, case series referring to the same predictor in larger VSs were excluded, since the group of small tumors represents the target of the hearing preservation procedures.

3. Results

The reported prognostic factors are tumor size, growth rate, preoperative hearing status, vestibular nerve of origin, surgical approach, presence or absence of the “fundal fluid cap” and other radiologic characteristics (FLAIR signal). Other preoperative neurophysiological tests (ABR, impedance and cVEMPs), symptoms (tinnitus, vertigo) and demographic features (age, gender) were investigated, too.
Articles selected for this review are shown in Table 2. The oldest dates back to 1990, and the most recent to 2022; 65% of the studies were published after 2010.
The considered prognostic factors are summarized in Table 3, which reports whether these factors were found to be significantly prognostic or not, that is, to be statistically associated with better hearing results thanks to appropriate statistical tests and a p-value < 0.05.

4. Discussion

4.1. Tumor Size

Tumor size is the first identified and one of the best-known factors that plays a leading prognostic role and greatly influences patients’ selection.
This aspect was initially investigated by Kemink and colleagues in 1990, who identified a size <1.5 cm as a criterion for predicting good postoperative hearing outcomes [15]. The role of tumor size was subsequently confirmed by various studies, although there are also studies in the literature that have not found statistical significance [16,17]. The paper with the largest number of patients was conducted by Robinette and Mohr, who analyzed, respectively, 104 and 128 cases that had undergone HPS via the RS approach. Both authors agreed in considering an increased tumor size as a factor related to unsuccessful hearing outcomes [18]; additionally, Mohr calculated a cutoff of 15 mm or smaller as independent favorable factors in hearing preservation (OR 37.77) [19]. In 2020, Ren’s study on 151 patients confirmed that smaller tumor size provides better chances for sparing hearing function (OR of tumor diameter: 0.892); best results are achieved in intracanalicular tumors [20].
Gjurik et al. tried to correlate both tumor volume and linear dimension with postoperative audiological outcomes; in their study, only patients with a lesion volume <0.20 cm3 were considered to have significantly better chances for preserving hearing function, while tumor dimension assessed with linear measurement did not reach statistical significance [16].
In 2020, Zanoletti et al., retrospectively analyzed hearing outcomes in a cohort of consecutive patients (100 cases) treated with a HPS procedure. They all were diagnosed with VS and operated on between 2000 and 2012 using the microscopic retrosigmoid approach combined with retrolabyrinthine meatotomy; the multivariate analysis concluded that an extrameatal tumor size of less than 7 mm was an independent predictor of good postoperative hearing function (sensitivity 83.8, specificity 51.8, negative likelihood ratio 1.742, positive likelihood ratio 0.311) [14].
Based on the reported literature and our experience [11,13,21], we propose HPS only to selected patients with a small VS, i.e., <10 mm in the CPA, measured according to Modified Reporting Systems from the Consensus Meeting on Systems for Reporting Results in Vestibular Schwannoma [6].

4.2. Tumor Growth Rate

A recent paper by Lovato et al. has retrospectively analyzed 92 patients with a small-medium tumor who underwent an operation using the MCF approach between 1995 and 2015. A tumor growth rate >2.16 mm/year was found to be an independent negative predictor for successful HPS via MCF (OR 8.5) [17]. Further studies are needed to adequately understand the role of this factor in predicting good hearing preservation, and to evaluate if it is reliable in HPS via the RS approach.

4.3. Preoperative Hearing

Pure tone audiometry and speech audiometry in VS patients are the most used tests for assessing preoperative hearing status and estimating tumor damage on the cochlear nerve. The prognostic role of preoperative hearing function in relation to the postoperative hearing preservation rate has been widely debated. Although useful to group results, the use of different classification systems (AAO-HNS [8], Tokyo [6] and Gardner-Robertson [9]) risk greatly reducing our ability to compare hearing outcomes [14].
A recent study by Ochal-Choińska and colleagues analyzed audiological parameters with a prognostic value in predicting good hearing preservation after surgery; a positive correlation was found for ipsilateral hearing thresholds at 125 Hz, 500 Hz and 1000 Hz and for PTA2. A speech discrimination score (SDS) for individual sound intensities from 55 dB to 75 dB in the operated ear and speech detection threshold (SDT) were found to correlate with good hearing outcomes, but no significance was obtained for the SDS value [22]. Di Maio et al. retrospectively analyzed a cohort of 192 large VSs operated using the RS approach and found a positive association between high preoperative hearing class and successful HP [23]. The same results were obtained by Lovato et al. in 92 cases operated via the MCF approach: patients with hearing class A or B according to AAO-HNS achieved better postoperative hearing outcomes (OR 5.89) [17]. The 138 cases operated on by Huo et colleagues (RS and MCF) were more likely to achieve hearing preservation after surgery if they had useful hearing before the operation (Class A or B, according to AAO-HNS; OR 0.204); the considered VSs were small and medium-sized (<20 mm) tumors and never larger than grade 2 according to the Koos Classification system [24].
Our cohort of patients were treated using a RS approach and retrolabyrinthine meatotomy, and the results were recently published; the median tumor size was 10 mm in the CPA. Statistical analysis showed that the optimal preoperative hearing threshold cutoffs for hearing preservation purposes are 21 dB PTA (sensitivity 74.2, specificity 66.7, negative likelihood ratio 2.226, positive likelihood ratio 0.387) and 90% SDS (sensitivity 75.4, specificity 44.4, negative likelihood ratio 1.357, positive likelihood ratio 0.553) and confirmed that better preoperative hearing status allowed for lower rates of post-surgical hearing loss. This can be explained by the greater reserve of functional fibers present in patients with good hearing, which would therefore better support the surgical damage [14]. To date, patients with preoperative hearing class A (AAOHNS) or A-B (Tokyo), i.e., a ≤30 dB PTA2 and ≥70% SDS, were considered good candidates for HPS.

4.4. Tumor Origin

Schwannomas of the pontocerebellar angle usually arise from the vestibular branch of the 8th cranial nerve, but other origins are reported, i.e., the cochlear nerve or facial nerve [25]; at the fundus of the internal auditory canal, the vestibular nerve divides into the superior (SVN) and inferior vestibular nerve (IVN). The most frequent subseat originating the tumor is not clear: it appears to be the upper one in recent studies (57.6–59.2%) [24,26], but an equal distribution or a major percentage of IVN origin are also reported [25,27,28]. Preoperatively, the involved branch may be successfully estimated using a combination of audiological tests, such as VEMPs and the caloric test [26]. In literature, the removal of IVN tumors achieves a significantly higher ratio of impaired hearing compared to SVN tumors (Huo OR 4.570) [24,27,28]. This may be explained by the proximity of the IVN to the cochlear nerve, so that the dissection may damage the auditory nerve itself, or its blood supply [25].

4.5. Surgical Approach

Retrosigmoid (RS) and middle cranial fossa (MCF) are the most used surgical approaches for hearing preservation in VS surgery. The difference between hearing outcomes provided by these techniques has been investigated since the end of the twentieth century; early research seems to show a higher prevalence of hearing preservation in MCF compared to RS [29], respectively 63% vs. 47% [30]; this difference was more evident for tumors <1.5 cm [31]. In the following years, studies showed a progressive improvement in hearing results with the RS approach (even if results vary a lot between different centers due to the heterogeneous nature of surgery itself), and the difference with MCF started to become statistically insignificant [32,33].
Most recent literature seems to provide an inversion in hearing outcomes, with comparable or better ratio of preservation provided by the RS approach (OR 0.744) [24,34], although without reaching statistical significance. This is probably due to the greater confidence among the oto-neurosurgical community in this approach, and to the diffusion of the retrolabyrinthine meatotomy [35]. On the other hand, MCF has been correlated with a high rate of facial nerve impairment [31,33]. In our center, RS with retrolabyrinthine meatotomy is the preferred approach for hearing preservation procedures in small VSs with good preoperative hearing. Auditory and facial nerve outcomes are favorable [13].

4.6. Radiological Characteristics

VSs are preoperatively evaluated with gadolinium enhanced MRI. High resolution T2 sequences (cerebrospinal fluid—cisternography sequences) allows assessment of the presence of the “fundal fluid cap”, i.e., the hyperintense signal corresponding to the presence of cerebrospinal fluid (CSF) at the fundus of the internal auditory channel (IAC). This is typical in VSs not involving the lateral part of the canal. The correlation between this aspect and HP was investigated in literature and results were initially ambiguous. In 2003, Kokaoglu retrospectively studied 22 patients, operated on using either the RS or MCF approach, and confirmed that a tumor involving the fundus or a short distance between the tumor and the fundus are risk factors for unsuccessful HPS [36]. The positive predicting role of the fluid cap was confirmed by the study of Goddard in relation to the MCF approach [27]. Otherwise, Sun et al. recently reviewed their 138 MCF cases and registered the presence of a fundal fluid cap; statistical analysis did not find a significant correlation between increasing fundal fluid size and low postoperative PTA or a high word recognition score (WRS) [37]. Afterwards, large case studies of the RS approach have been described by Tringali et al., in 2010 and Nguyen et al. in 2012, both of which confirmed the lateral extension of the tumor to the fundus as a negative predictive factor for HPS [38,39]. In our experience, a fundus-involving tumor is not necessarily an unfavorable condition for HPS via RS, although the compression of the nerve in this site may severely damage the fibers of the cochlear nerve, and the intraoperative dissection in the fundus may endanger the cochlear nerve preservation; on the other hand, the retrolabyrinthine meatotomy allows complete exposure of the whole internal auditory canal and a safe exposure of the fundus which reduces the at-risk surgical maneuvers of dissection at the fundus, with safe handling of the tumor-nerve. Preoperative MRI findings may also not be predictive of intraoperative conditions [40].
In 2019 a study by Tu et al. evaluated the preoperative and postoperative cochlear signal on FLAIR sequences in VSs cases which had undergone HPS with RS or MCF approaches. Preoperative signal does not change between preserved and unpreserved HPS, but postoperative values are lower in successful cases [41].

4.7. Preoperative Neurophysiological Testing (ABR, Impedance and cVEMPs)

Preoperative assessment of VS patients should also involve neurophysiological tests to better evaluate tumor damage on the nerve. Auditory brainstem response (ABR) is the most used, due to its easy execution and low costs. Many papers have studied the relation between this test and hearing outcomes without finding any correlation [18,42,43]; nevertheless, its role is so important that in our experience an absent preoperative ABR is considered a contraindication to HPS. In 2019, Ochal-Choińska and colleagues analyzed their series of 86 patients (all operated on using the MCF approach) to determinate whether and which ABR findings could be considered a prognostic factor for postoperative hearing function; they found that presence of wave V, lower values of I–V and III–V intervals and higher amplitude value of wave V in the operation correlates with better HPS results [22]. Our recent analysis of 57 patients who had undergone resection via the RS approach confirmed the role of an absent or severely impaired preoperative ABR as a negative prognostic factor for hearing impairment after HPS (OR 13.38 according to AAO-HNS and 8.1 to Tokyo) [14].
Preoperative impedance was also evaluated and successfully correlated with postoperative hearing outcomes: intensity level needed for simulating the stapedial reflex and abnormal reflex are recently reported as prognostic factors [22].
In 2018, Hochet suggested that cVEMPs may be useful for predicting HP outcomes; they calculated the preoperative amplitude asymmetry ratio in their VS patients: it was significatively lower in the group with successful HP compared with the other one. They calculate that an amplitude asymmetry less than 24% has a positive predictive value for assessing postoperative hearing preservation of 91.6% [44].

4.8. Symptoms Other than SNHL

Vestibular schwannoma patients may be asymptomatic or suffer mainly from sensorineural hearing loss, tinnitus and/or vertigo; while the role of the former as an unfavorable predictor of HP has been widely described [14,22,23,24], the others have not been adequately investigated. The literature is lacking studies on the predictive role of vestibular disorders on HP. According to a study conducted in 1995, patients who suffer from vertigo do not differ statistically in HP outcomes compared with those who do not complain of vestibular disorder [45].
Preoperative tinnitus has recently been proposed as an indicator of poor hearing reserve and appears to predict low HP rate [46], but more studies are necessary.

4.9. Demographic Features

Age and gender are demographic features whose role was investigated as prognostic factors for HP. The first one has been reported in the past without reaching statistical significance [42,43], but a recent study by Ren et. colleagues confirmed a higher rate of HP in younger patients [20], confirming the role of age hypothesized by Sughrue et al. in 2010 [30].
Gender has occasionally been evaluated, e.g., by Nadol et colleagues, without finding any difference between male and female patients [47]. Ultimately, a recent study conducted at our institution evaluating these aspects found no role in predicting HP outcomes [14].

4.10. Other Factors

In addition to the varyingly impactful roles of the factors examined in this review, other aspects may influence the audiological outcomes in hearing preservation surgery in VSs and need to be mentioned. As in every surgical procedure, the surgeon’s experience has a certain impact in the outcome; in particular, hearing preservation in VSs needs a very delicate dissection of the cochlear nerve so as to not damage the fibers and or reduce its blood supply. Such complicated procedures should be performed in a tertiary referral center by well-trained surgeons.
Moreover, different techniques have been proposed to monitor the nerve during surgery, i.e., Auditory Brainstem Responses (ABR), Direct Eighth Cranial Nerve Monitoring, Cochlear Compound Nerve Action Potentials (CNAP), Transtympanic Electrocochleography, Distortion Product Otoacoustic Emissions, Postauricular Muscle Responses. All of them may play a role in hearing preservation, but literature is lacking standardized studies, necessary for evaluating their true efficacy, determine the best one for each situation and understand their predictive role for HPS, as a recent review concluded [48]. To date, the choice of the correct method for monitoring the cochlear nerve is left to surgeons and should be based on the characteristics of the tumor, the patient, and the surgery [48].

5. Conclusions

The most important factors showing a predictive role in hearing preservation are tumor size and preoperative hearing status; these features play a prominent role in the selection of patients undergoing HPS. Other reported relevant features which might influence the postoperative outcome, although without strong statistical evidence, are fundal extension, tumor origin and, as evidenced in our experience too, impaired ABR. Recently, tumor growth rate, age, preoperative impedance and cVEMPs have also been debated. Studies evaluating the prognostic role of preoperative symptoms (except hearing loss) and gender are lacking. The differences between surgical approaches (the middle cranial fossa and retrosigmoid approach) have smoothed out in recent years and are more greatly influenced by the experience of the surgeon than by objective factors; the combination of the retrolabyrinthine meatotomy with the RS approach to fully expose the whole IAC, on the other hand, has provided safer handling of the tumor-nerve interface at the distal end of the meatus. The role of intraoperative cochlear nerve monitoring techniques has yet to be properly investigated.

Author Contributions

Conceptualization, E.Z.; methodology, E.Z., G.T. and S.C.; software, not applicable; validation, E.Z. and G.T.; investigation, A.D. and S.C.; data curation, S.C. and A.D.; writing—original draft preparation, S.C. and A.D.; writing—review and editing, E.Z., G.T. and S.C.; visualization, S.C.; supervision, E.Z., G.T. and S.C.; project administration, E.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Samii, M.; Gerganov, V.M. Tumors of the cerebellopontine angle. Handb. Clin. Neurol. 2012, 105, 633–639. [Google Scholar] [CrossRef]
  2. Babu, R.; Sharma, R.; Bagley, J.H.; Hatef, J.; Friedman, A.H.; Adamson, C. Vestibular schwannomas in the modern era: Epidemiology, treatment trends, and disparities in management. J. Neurosurg. 2013, 119, 121–130. [Google Scholar] [CrossRef] [Green Version]
  3. Foley, R.W.; Shirazi, S.; Maweni, R.M.; Walsh, K.; Walsh, R.M.; Javadpour, M.; Rawluk, D. Signs and Symptoms of Acoustic Neuroma at Initial Presentation: An Exploratory Analysis. Cureus 2017, 9, e1846. [Google Scholar] [CrossRef] [Green Version]
  4. Tos, M.; Stangerup, S.E.; Cayé-Thomasen, P.; Tos, T.; Thomsen, J. What Is the Real Incidence of Vestibular Schwannoma? Arch. Otolaryngol. Head Neck Surg. 2004, 130, 216–220. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Stangerup, S.-E.E.; Tos, M.; Thomsen, J.; Caye-Thomasen, P. True Incidence of Vestibular Schwannoma? Neurosurgery 2010, 67, 1335–1340. [Google Scholar] [CrossRef] [PubMed]
  6. Kanzaki, J.; Tos, M.; Sanna, M.; Moffat, D.A. New and modified reporting systems from the consensus meeting on systems for reporting results in vestibular schwannoma. Otol. Neurotol. 2003, 24, 642–648; discussion 648–649. [Google Scholar] [CrossRef] [PubMed]
  7. Koos, W.T.; Day, J.D.; Matula, C.; Levy, D.I. Neurotopographic considerations in the microsurgical treatment of small acoustic neurinomas. J. Neurosurg. 1998, 88, 506–512. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Anonymous. Committee on Hearing and Equilibrium guidelines for the evaluation of hearing preservation in acoustic neuroma (vestibular schwannoma). Otolaryngol. Head Neck Surg. 1995, 113, 179–180. [Google Scholar] [CrossRef] [PubMed]
  9. Gardner, G.; Robertson, J.H. Hearing preservation in unilateral acoustic neuroma surgery. Ann. Otol. Rhinol. Laryngol. 1988, 97, 55–66. [Google Scholar] [CrossRef] [PubMed]
  10. Schwartz, M.S.; Lekovic, G.P.; Miller, M.E.; Slattery, W.H.; Wilkinson, E.P. Translabyrinthine microsurgical resection of small vestibular schwannomas. J. Neurosurg. 2018, 129, 128–136. [Google Scholar] [CrossRef] [Green Version]
  11. Zanoletti, E.; Concheri, S.; Tealdo, G.; Cazzador, D.; Denaro, L.; d’Avella, D.; Mazzoni, A. Early surgery and definitive cure in small sporadic vestibular schwannoma. Acta Otorhinolaryngol. Ital. 2022, 42, 481–486. [Google Scholar] [CrossRef] [PubMed]
  12. Kaltoft, M.; Stangerup, S.E.; Caye-Thomasen, P. Facial nerve function after vestibular schwannoma surgery following failed conservative management. Neurosurgery 2012, 70, 278–282. [Google Scholar] [CrossRef]
  13. Mazzoni, A.; Zanoletti, E.; Denaro, L.; Martini, A.; d’Avella, D. Retrolabyrinthine meatotomy as part of retrosigmoid approach to expose the whole internal auditory canal: Rationale, technique, and outcome in hearing preservation surgery for vestibular schwannoma. Oper. Neurosurg. 2018, 14, 36–44. [Google Scholar] [CrossRef]
  14. Zanoletti, E.; Mazzoni, A.; Frigo, A.C.; Borsetto, D.; Cazzador, D. Hearing Preservation Outcomes and Prognostic Factors in Acoustic Neuroma Surgery: Predicting Cutoffs. Otol. Neurotol. 2020, 41, 686–693. [Google Scholar] [CrossRef] [PubMed]
  15. Kemink, J.L.; LaRouere, M.J.; Kileny, P.R.; Telian, S.A.; Hoff, J.T. Hearing Preservation Following Suboccipital Removal of Acoustic Neuromas. Laryngoscope 1990, 100, 597–602. [Google Scholar] [CrossRef] [PubMed]
  16. Gjuric, M.; Mitrecic, M.Z.; Greess, H.; Berg, M. Vestibular schwannoma volume as a predictor of hearing outcome after surgery. Otol. Neurotol. 2007, 28, 822–827. [Google Scholar] [CrossRef]
  17. Lovato, A.; García Ibañez, E.; García Ibañez, L.; de Filippis, C. Tumor growth rate: A new prognostic indicator of hearing preservation in vestibular schwannoma surgery. Laryngoscope 2019, 129, 2378–2383. [Google Scholar] [CrossRef]
  18. Robinette, M.S.; Bauch, C.D.; Olsen, W.O.; Harner, S.G.; Beatty, C.W. Nonsurgical factors predictive of postoperative hearing for patients with vestibular schwannoma. Am. J. Otol. 1997, 18, 738–745. Available online: http://www.ncbi.nlm.nih.gov/pubmed/9391670 (accessed on 10 October 2022).
  19. Mohr, G.; Sade, B.; Dufour, J.J.; Rappaport, J.M. Preservation of hearing in patients undergoing microsurgery for vestibular schwannoma: Degree of meatal filling. J. Neurosurg. 2005, 102, 1–5. [Google Scholar] [CrossRef]
  20. Ren, Y.; Tawfik, K.O.; Mastrodimos, B.J.; Cueva, R.A. Preoperative Radiographic Predictors of Hearing Preservation after Retrosigmoid Resection of Vestibular Schwannomas. Otolaryngol. Head Neck Surg. 2021, 165, 344–353. [Google Scholar] [CrossRef]
  21. Mazzoni, A.; Biroli, F.; Foresti, C.; Signorelli, A.; Sortino, C.; Zanoletti, E. Hearing preservation surgery in acoustic neuroma. Slow progress and new strategies. Acta Otorhinolaryngol. Ital. 2011, 31, 76–84. [Google Scholar]
  22. Ochal-choińska, A.; Lachowska, M.; Kurczak, K.; Niemczyk, K. Audiologic prognostic factors for hearing preservation following vestibular schwannoma surgery. Adv. Clin. Exp. Med. 2019, 28, 747–757. [Google Scholar] [CrossRef]
  23. Di Maio, S.; Malebranche, A.D.; Westerberg, B.; Akagami, R. Hearing preservation after microsurgical resection of large vestibular schwannomas. Neurosurgery 2011, 68, 632–640. [Google Scholar] [CrossRef]
  24. Huo, Z.; Chen, J.; Wang, Z.; Zhang, Z.; Wu, H. Prognostic Factors of Long-Term Hearing Preservation in Small and Medium-Sized Vestibular Schwannomas after Microsurgery. Otol. Neurotol. 2019, 40, 957–964. [Google Scholar] [CrossRef] [PubMed]
  25. Jacob, A.; Robinson, L.L.; Bortman, J.S.; Yu, L.; Dodson, E.E.; Welling, D.B. Nerve of origin, tumor size, hearing preservation, and facial nerve outcomes in 359 vestibular schwannoma resections at a tertiary care academic center. Laryngoscope 2007, 117, 2087–2092. [Google Scholar] [CrossRef]
  26. Cianfrone, F.; Cantore, I.; Roperto, R.; Tauro, F.; Bianco, F.; Mastronardi, L.; Ruscito, P. Preoperative vestibular evoked myogenic potentials (VEMPs), caloric test, and pure tone audiometry to identify the vestibular nerve branch of schwannoma origin: Preliminary results in a series of 26 cases. Neurosurg. Rev. 2022, 45, 3231–3236. [Google Scholar] [CrossRef] [PubMed]
  27. Goddard, J.C.; Schwartz, M.S.; Friedman, R.A. Fundal fluid as a predictor of hearing preservation in the middle cranial fossa approach for vestibular schwannoma. Otol. Neurotol. 2010, 31, 1128–1134. [Google Scholar] [CrossRef]
  28. Rachinger, J.; Rampp, S.; Prell, J.; Scheller, C.; Alfieri, A.; Strauss, C. Tumor origin and hearing preservation in vestibular schwannoma surgery. J. Neurosurg. 2011, 115, 900–905. [Google Scholar] [CrossRef] [Green Version]
  29. Bennett, M.; Haynes, D.S. Surgical Approaches and Complications in the Removal of Vestibular Schwannomas. Otolaryngol. Clin. N. Am. 2007, 40, 589–609. [Google Scholar] [CrossRef]
  30. Sughrue, M.E.; Yang, I.; Aranda, D.; Kane, A.J.; Parsa, A.T. Hearing preservation rates after microsurgical resection of vestibular schwannoma. J. Clin. Neurosci. 2010, 17, 1126–1129. [Google Scholar] [CrossRef] [PubMed]
  31. Ansari, S.F.; Terry, C.; Cohen-Gadol, A.A. Surgery for vestibular schwannomas: A systematic review of complications by approach. Neurosurg. Focus 2012, 33, E14. [Google Scholar] [CrossRef] [Green Version]
  32. Noudel, R.; Gomis, P.; Duntze, J.; Marnet, D.; Bazin, A.; Roche, P.H. Hearing preservation and facial nerve function after microsurgery for intracanalicular vestibular schwannomas: Comparison of middle fossa and restrosigmoid approaches. Acta Neurochir. 2009, 151, 935–945. [Google Scholar] [CrossRef]
  33. De Freitas, M.R.; Russo, A.; Sequino, G.; Piccirillo, E.; Sanna, M. Analysis of hearing preservation and facial nerve function for patients undergoing vestibular schwannoma surgery: The middle cranial fossa approach versus the retrosigmoid approach-personal experience and literature review. Audiol. Neurotol. 2012, 17, 71–81. [Google Scholar] [CrossRef] [PubMed]
  34. Sameshima, T.; Fukushima, T.; McElveen, J.T.; Friedman, A.H. Critical assessment of operative approaches for hearing preservation in small acoustic neuroma surgery: Retrosigmoid vs middle fossa approach. Neurosurgery 2010, 67, 640–644. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Mazzoni, A.; Calabrese, V.; Danesi, G. A modified retrosigmoid approach for direct exposure of the fundus of the internal auditory canal for hearing preservation in acoustic neuroma surgery. Am. J. Otol. 2000, 21, 98–109. [Google Scholar] [CrossRef]
  36. Kocaoglu, M.; Bulakbasi, N.; Ucoz, T.; Ustunsoz, B.; Pabuscu, Y.; Tayfun, C.; Somuncu, I. Comparison of contrast-enhanced T1-weighted and 3D constructive interference in steady state images for predicting outcome after hearing-preservation surgery for vestibular schwannoma. Neuroradiology 2003, 45, 476–481. [Google Scholar] [CrossRef]
  37. Sun, D.Q.; Kung, R.W.; Hansen, M.R.; Gantz, B.J. Does a “fundal Fluid Cap” Predict Successful Hearing Preservation in Vestibular Schwannoma Resections Via the Middle Cranial Fossa Approach? Otol. Neurotol. 2018, 39, 772–777. [Google Scholar] [CrossRef]
  38. Tringali, S.; Ferber-Viart, C.; Fuchsmann, C.; Buiret, G.; Zaouche, S.; Dubreuil, C. Hearing preservation in retrosigmoid approach of small vestibular schwannomas: Prognostic value of the degree of internal auditory canal filling. Otol. Neurotol. 2010, 31, 1469–1472. [Google Scholar] [CrossRef]
  39. Nguyen, Q.T.; Wu, A.P.; Mastrodimos, B.J.; Cueva, R.A. Impact of fundal extension on hearing after surgery for vestibular schwannomas. Otol. Neurotol. 2012, 33, 455–458. [Google Scholar] [CrossRef] [PubMed]
  40. Selesnick, S.H.; Rebol, J.; Heier, L.A.; Wise, J.B.; Gutin, P.H.; Lavyne, M.H. Internal auditory canal involvement of acoustic neuromas: Surgical correlates to magnetic resonance imaging findings. Otol. Neurotol. 2001, 22, 912–916. [Google Scholar] [CrossRef] [PubMed]
  41. Tu NC, Y.; Dogaru, G.B.; Huang, P.; Kim, J.; Diegnan, B.; Go, J.L.; Friedman, R.A. Cochlear FLAIR Signal Changes in Hearing Preservation Vestibular Schwannoma Surgery. Otol. Neurotol. 2019, 40, 375–383. [Google Scholar] [CrossRef]
  42. Fischer, G.; Fischer, C.; Rémond, J. Hearing preservation in acoustic neurinoma surgery. J. Neurosurg. 1992, 76, 910–917. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Cohen, N.L.; Lewis, W.S.; Ransohoff, J. Hearing preservation in cerebellopontine angle tumor surgery: The NYU experience 1974–1991. Otol. Neurotol. 1993, 14, 423–433. [Google Scholar] [CrossRef] [PubMed]
  44. Hochet, B.; Achard, S.; Lorenz, M.B.; Baroncini, M.; Berama, A.; Gabanou, F.; Devambez, M.; Lejeune, J.-P.; Vincent, C.; Bonne, N.-X. Preoperative assessment of cervical vestibular evoked myogenic potentials (cVEMPs) help in predicting hearing preservation after removal of vestibular schwannomas through a middle fossa craniotomy. Otol. Neurotol. 2018, 39, e1143–e1149. [Google Scholar] [CrossRef]
  45. Dornhoffer, J.L.; Helms, J.; Hoehmann, D.H. Hearing preservation in acoustic tumor surgery: Results and prognostic factors. Laryngoscope 1995, 105, 184–187. [Google Scholar] [CrossRef]
  46. Mastronardi, L.; Cacciotti, G.; Roperto, R.; Di Scipio, E. Negative influence of preoperative tinnitus on hearing preservation in vestibular schwannoma surgery. J. Neurosurg. Sci. 2021, 64, 537–543. [Google Scholar] [CrossRef] [PubMed]
  47. Nadol, J.B.; Chiong, C.M.; Ojemann, R.G.; Mckenna, M.J.; Martuza, R.L.; Montgomery, W.W.; Levine, R.A.; Ronner, S.F.; Glynn, R.J. Preservation of hearing and facial nerve function in resection of acoustic neuroma. Laryngoscope 1992, 102, 1153–1158. [Google Scholar] [CrossRef] [PubMed]
  48. Ariano, M.; Franchella, S.; Tealdo, G.; Zanoletti, E. Intra-Operative Cochlear Nerve Function Monitoring in Hearing Preservation Surgery: A Systematic Review of the Literature. Audiol. Res. 2022, 12, 696–708. [Google Scholar] [CrossRef]
Table 1. Tumor classification based on extrameatal dimension, according to the Consensus Meeting on Systems for Reporting Results in Acoustic Neuroma (Tokyo, 2001).
Table 1. Tumor classification based on extrameatal dimension, according to the Consensus Meeting on Systems for Reporting Results in Acoustic Neuroma (Tokyo, 2001).
1–10 mmSmallGrade 1
11–20 mmMediumGrade 2
21–30 mmModerately largeGrade 3
31–40 mmLargeGrade 4
>40 mmGiantGrade 5
Table 2. Studies considered for this review.
Table 2. Studies considered for this review.
First AuthorYearDesignPatients (n)
Kemink1990RCS20
Fischer1992RCS99
Nadol1992RCS144
Cohen1993RCS161
Robinette1997RCS104
Selesnick2001RCS6
Kocaoglu2003PCS22
Moh2005RCS386
Gjuric2007RCS29
Jacob2007RCS356
Noudel2009NRn.a.
Tringali2010RCS278
Goddard2010RCS101
Sughrue2010NR998
Sameshima2010RCS504
Rachinger2011RCS90
Mazzoni2011RCS115
Di Maio2011RCS192
Nguyen2012RCS53
Ansari2012NRn.a.
De Freitas2012RCS175
Mazzoni2018RCS100
Sun2018RCS138
Hochet2018RCS18
Lovato2019RCS92
Tu2019RCS18
Ochal-choińska2019RCS86
Huo2019RCS138
Zanoletti2020RCS100
Ren2021RCS151
Cianfrone2022RCS26
Abbreviations: n.a. not available; RCS retrospective cohort study; PCS prospective cohort study; NR narrative review.
Table 3. Prognostic factors available and their role in predicting hearing outcome in HPS. SNHL: sensorineural hearing loss.
Table 3. Prognostic factors available and their role in predicting hearing outcome in HPS. SNHL: sensorineural hearing loss.
Prognostic FactorsStudies Describing a Significative
Prognostic Role
Studies Not Finding a Significative Prognostic Role
Tumor sizeKemink 1990, Fischer 1992, Nadol 1992, Cohen 1993, Robinette 1997, Mohr 2005, Gjuric 2007, Jacob 2007, Tringali 2010, Sughrue 2010, Mazzoni 2011, Ansari 2012, Sun 2018, Zanoletti 2020, Ren 2021Goddard 2010, Rachinger 2011, De Freitas 2012, Lovato 2019, Huo 2019
Tumor growth rateLovato 2019Gjuric 2007
Preoperative HearingKemink 1990, Fischer 1992, Nadol 1992, Cohen 1993, Robinette 1997, Tringali 2010, Rachinger 2011, Mazzoni 2011, Di Maio 2011, Lovato 2019, Ochal-choińska 2019, Huo 2019, Zanoletti 2020Mohr 2005, Gjuric 2007, Jacob 2007, Goddard 2010, Sun 2018
Tumor originCohen 1993, Jacob 2007, Goddard 2010, Rachinger 2011, Huo 2019Gjuric 2007, Lovato 2019
Surgical approachKemink 1990, Sughrue 2010, Nguyen 2012, Ansari 2012, Mazzoni 2018, Ren 2021,Noudel 2009, Sameshima 2010, Rachinger 2011, De Freitas 2012
Radiological characteristicsKocaoglu 2003, Tringali 2010, Goddard 2010, Nguyen 2012, Tu 2019Selesnick 2001, Gjuric 2007, Sun 2018, Huo 2019
Preoperative neurophysio-logical testsRobinette 1997, Di Maio 2011, Sun 2018, Hochet 2018, Ochal-choińska 2019, Zanoletti 2020, Cianfrone 2022Kemink 1990, Fischer 1992, Nadol 1992, Cohen 1993 Gjuric 2007, Jacob 2007
Symptoms
(other than SNHL)
Huo 2019, Zanoletti 2020, Ren 2021Lovato 2019
Demographics featuresRen 2021Fischer 1992, Nadol 1992, Cohen 1993, Robinette 1997 Sughrue 2010, Rachinger 2011, Sun 2018, Lovato 2019, Zanoletti 2020
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Concheri, S.; Deretti, A.; Tealdo, G.; Zanoletti, E. Prognostic Factors for Hearing Preservation Surgery in Small Vestibular Schwannoma. Audiol. Res. 2023, 13, 473-483. https://doi.org/10.3390/audiolres13040042

AMA Style

Concheri S, Deretti A, Tealdo G, Zanoletti E. Prognostic Factors for Hearing Preservation Surgery in Small Vestibular Schwannoma. Audiology Research. 2023; 13(4):473-483. https://doi.org/10.3390/audiolres13040042

Chicago/Turabian Style

Concheri, Stefano, Alessandra Deretti, Giulia Tealdo, and Elisabetta Zanoletti. 2023. "Prognostic Factors for Hearing Preservation Surgery in Small Vestibular Schwannoma" Audiology Research 13, no. 4: 473-483. https://doi.org/10.3390/audiolres13040042

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