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. 2022 Jan 20;17(1):e0262758. doi: 10.1371/journal.pone.0262758

New classification of superior semicircular canal dehiscence in HRCT

Stephan Waldeck 1,2,*, Heinrich Lanfermann 3, Christian von Falck 4, Matthias F Froelich 5, René Chapot 6, Marc Brockmann 2, Daniel Overhoff 1,5
Editor: Jorge Spratley7
PMCID: PMC8775191  PMID: 35051221

Abstract

Background and purpose

The complex anatomy of the temporal bone is difficult to understand and constitutes a challenge in the daily diagnostic routine even for experienced neuroradiologists. In the context of otoneurological (oVEMP) and preoperative diagnostics, the diagnosis of superior semicircular canal dehiscence (SSCD) is of great importance for Ear, Nose, and Throat (ENT) specialists. The gold standard for this diagnosis is a high-resolution CT (HRCT) of the temporal bone. In order to correctly diagnose SSCD, special oblique reconstructions are necessary in addition to standard (axial, coronal, sagittal) reconstructions. We evaluated the frequency of diagnosis and its location in HRCT in correlation with otoneurological examination. From this analysis, we present a new SSCD classification. This classification yields the potential of a differentiated analysis of the patient’s clinical symptoms with correlation to the cross-sectional anatomy and may lead to a differentiated therapy approach.

Study design and setting

We evaluated 1370 temporal bone scans of patients with residual hearing and verified 343 superior semicircular canal dehiscence (SSCD). We conducted a subgroup analysis of these 343 HRCT scans displaying a SSCD and used them as a basis to create a classification.

Results

Three location types of SSCD were identified. These were anterior type 1, superior type 2 and posterior type 3. Type 2 were significantly more frequent in both sexes. SSCD at this location can be overlooked if diagnosis is performed only in the standard axial plane, since it can only be visualized by means of double oblique reconstruction. We present a standardized reconstruction algorithm.

Conclusion

In total, three types of SSCD with differing incidences can be extrapolated from the locations. Superior type 2 is the most frequent one. Both sexes are affected with roughly equal incidence. The use of standardized double oblique reconstruction algorithm ensures that all three types are diagnosed in the HRCT.

Introduction

The clinical picture of superior semicircular canal dehiscence (SSCD) was described for the first time by Minor et al. in 1998 [1]. Patients reported vestibular (vertigo, nystagmus, Tullio phenomenon, Hennebert sign [2]) and acoustic signs and symptoms (conductive or sensorineural hearing loss, autophony, tinnitus).

These problems typically occur in nearly all age groups. The average age for the onset of this illness is during middle age (38–61 years) [25]. In radiological studies the prevalence has been stated to be between 2.1% and 20.4% [69].

Pathophysiologically, the signs and symptoms can be explained by the development of a “third window” caused by an absence of the bone overlying the superior semicircular canal (SSC). This results in a connection between the inner ear and the middle cranial fossa, which is described as a “third window” in addition to the oval and round windows. Pressure changes can trigger endolymph movement in the superior semicircular canal, which can ultimately lead to an excitation of the cupula and cause the described signs and symptoms [10].

The etiology of SSCD is yet to be explained conclusively. Both inflammatory and traumatic causes are being discussed. In the case of trauma, a tearing of the thin superior semicircular canal membrane occurs and the onset of symptoms is instantaneous [1113]. Fig 1 shows the mechanism that can lead to the symptoms.

Fig 1. SSCD symptoms scheme.

Fig 1

The Arrows show the mechanism that can lead to the SSCD symptoms, with both intracranial pressure increases and otoacoustic stimuli acting as possible triggers.

High-resolution computed tomography (HRCT) is an essential part of diagnosing SSCD since it offers a high degree of sensitivity [14]. The positive predictive value is given as 93% for a slice thickness of 0.5 mm [15]. Sensitivity decreases dramatically for thicker slices. It is important to understand that SSCD location can differ. With regard to its location in the superior semicircular canal, dehiscence can be anterior, superior or posterior based on the anatomical location. This new classification is introduced by the authors and is based on the radiological cross-sectional anatomy. In order to make sure that all location types are detected, special reconstructions must be generated from the submillimeter slices.

This retrospective multicenter study analyzed 1370 HRCT scans of the temporal bone and verified 343 SSCDs. Their distribution was grouped into three types. The evaluation also included an examination of the incidence of the location types in relation to sex and age.

Materials and methods

Study design

A retrospective multicenter study of high-resolution CT scan from patients with vestibular and/or acoustic symptoms. Local ethics committee (“Ethikkommission Landesärztekammer Rheinland-Pfalz”) approved this retrospective study (Nr: 2018–13750). For this retrospective study only pseudonymized medical records were used.

Ethics committee waived the requirement for informed consent due to the retrospective nature of this study.

Patient cohort

We analyzed 1370 HRCT scans of the temporal bone from Ear, Nose and Throat (ENT) patients who presented with vestibular symptoms (from May 2008 to March 2018) for the presence of SSCDs in this multicenter study. For all diagnosed SSCD we performed a subgroup analysis. These were subdivided by gender and grouped into four age groups (A: 6–24, B:25–49, C:50–74, D:75–95 years).

Data collection

The CT examinations of the temporal bone obtained from the different institutes and departments were conducted based on the following parameters:

Koblenz: Siemens Somatom Force 384-slice scanner; 120 kV; 140 mAs; 0.80 pitch.

Toshiba Vision Edition 320; 120 kV; 200 mAs; 16 cm volume scan

Mainz: Toshiba Aquilon 32-slice scanner; 120 kV; 200 mAs; 0.66 pitch

Hanover: GE LightSpeed 16; 100 kV; 80 mAs; 1.38 pitch

A slice thickness of 0.6 mm was used for multiplanar reconstruction. All data were analyzed with Siemens Syngo Via software (version VB10).

Standardized reconstruction scheme

In order to detect all SSCDs, the image analysis followed a standardized reconstruction scheme on the basis of the MPRs (multiplanar reconstructions). The image reconstruction and the subgroup analysis of the SSCD localization based on it were carried out in 4 steps:

  1. The axial data set is used to generate a reconstruction orthogonal to the superior semi-circular canal with a slice thickness of 0.6 mm (Fig 2A).

  2. This reconstruction is used to generate another oblique reformation parallel to the SSC with a slice thickness of 0.6 mm (Fig 2A).

  3. The result of the 2 reformations is used to create an MIP (maximum intensity projection) image (1mm) to render the entire SSC visible in one image (Fig 2B).

  4. The locations of dehiscence in the superior semicircular canal (SSC) were grouped into three types (Fig 2C).

Fig 2.

Fig 2

A-C: Standardized reconstruction algorithm and SSCD classification: Type 1–3. Fig 2 uses a model to illustrate the reconstruction scheme.

The basis for the classification is the dominant superior type 2 (Fig 2), which is the highest point of circumference the superior semicircular canal (12 o´clock). The borders of this type are defined according to the clock time between 10 am and 2 pm. All superior semicircular dehiscences that lie anteriorly (direction to middle cranial fossa) to this location type 2 are defined as type 1; those that lie posteriorly (direction to posterior cranial fossa) to this location type 2 are definded as type 3.

Statistical analysis

The statistical calculations were performed using SPSS (IBM SPSS Statistics, version 20.0 for Macintosh; SPSS, Inc., Chicago, IL, USA).

All continuous variables are expressed as arithmetic mean ± standard deviation (SD). A significance level of 5% was used. Normal distribution was assumed due to central limit theorem. A multinominal linear regression was performed type-specific SSCD proportions as dependent variable and gender, side of SSCD and age as covariates. For continuous data Student`s t- Test was performed for independent samples to analyze the means. To analyze nominal data Chi- square test was used.

Results

We analyzed 1370 high resolution CT scans of the temporal bone from ENT patients (681 female (49.7%) versus 689 male (50.3%) for the presence of SSCDs and verified 343 diagnoses out of 280 patients (prevalence of 20.4%). Patients with SSCD were on average 6 years older than those without SSCD (mean 46.22 years versus 52.73 years (SSCD) p<0.001).

63 patients had a diagnosis of bilateral SSCD, 116 unilateral left, 101 unilateral right; unilateral/bilateral ratio of 3.44:1. Table 1 summarizes all the results of the gender in relation to the frequency of SSCD types and its locations.

Table 1. Study population.

Population n = 1370 SSCD
sex male female
157 (11.5%) 123 (9.0%)
side right left both
101 (7.4%) 116 (8.5%) 63 (4.6%)
type n = 2740 1 2 3
99 (3.6%) 133 (4.9%) 111 (4.1%)
male/ female male/ female male/ female
56(2.0%)/43(1.6%) 78(2.8%)/55(2.0%) 57(2.1%)/54(2.0%)

In brackets the relative values compared to the total study population; Superior semicircular canal type with n = 2740 resulting from both temporal bones of each patient (n = 1370).

We were able to visualize all SSCD types with the standardized reconstruction scheme (Fig 3).

Fig 3. HR CT reconstruction.

Fig 3

Fig 3 illustrates the practical implementation with a temporal bone preparation.

The total of 280 patients with SSCD (123 female and 157 male; p = 0.030) were grouped into four age groups (A:6–24, B:25–49, C:50–74, D:75–95 years).

Of a total of 343 SSCD, 99 (28.9%) displayed dehiscence of an anterior location type (type 1), 133 (38.8%) displayed the dominant superior location type (type 2) and 111 (32.4%) displayed the posterior location type (type 3). The different Types are shown in Fig 4.

Fig 4. SSCD location types.

Fig 4

Fig 4 shows the three different SSCD Types in high resolution CT. Type 2 SSCDs are defined as the highest point of the circumference the superior semicircular canal. All SSCDs that lie anteriorly in direction to the middle cranial fossa are defined as type 1; those that lie posteriorly in direction to the posterior cranial fossa are definded as type 3.

SSCD type 2 is significantly more common in males (p = 0.048) and significantly more common in age group C (p = 0.012) and D (p = 0.004), whereas the multinominal linear regression showed just a tendency with p = 0.064 for sex without significancy.

The multinominal linear regression was significant for age and not for side of the SSCD location.

SSCD type 1 and SSCD type 3 are not significantly more common in all age groups.

Overall, no significant difference was evident between the sexes in terms of incidence, as shown by the multinominal linear regression model.

The age-correlated increase of SSCDs lead to a significant change in the location of dehiscence. There was a dominance of the superior location of dehiscence corresponding to type 2 in 3 of the 4 age groups (group 2: 25–49 y; group 3: 50–74 y; group 4: 75–95 y). Across all age groups, SSCD type 2 is significantly more common than type 3 and than type 1 (type 2 > type3 > type1).

Table 2 summarizes all the results of the different age groups in relation to the frequency of SSCD types.

Table 2. Differentiation of SSCD types by age cohorts.

0–24 yo 25–49 yo 50–74 yo >75 yo all ages
SSCD Type 1 19 (2.7%) 26 (3.5%) 27(3.3%) 27(5.0%) 99(7.2%)
SSCD Type 2 26 (3.7%) 32 (4.3%) 39(5.2%) 36(6.7%) 133(9.7%)
SSCD Type 3 20(2.8%) 25(3.4%) 36(5.0%) 30(5.6%) 111(8.1%)
SSCD Type1-3 65(9.2%) 83(11.2%) 102(13.5%) 93(17.2%) 343(25.0%)

Relative values in percent in parentheses. The relative values of the age cohort columns refer to the respective age cohort. The relative values of the "all ages" columns refer to the total study population.

Discussion

Superior Semicircular Canal Dehiscence (SSCD) is still a relatively new pathologic condition that requires a high suspicion for its correct diagnosis and high quality CT scan imaging. While different surgical approaches and techniques have been published in the literature, the exact location of the SSCD is of high importance. To the best of our knowledge the presented analysis includes a considerably larger number of cases than other published radiological studies before [8]. We are the first to analyze the location of superior semicircular canal dehiscence based on a fixed reconstruction scheme. CT is still said to result in an overdiagnosis of SSCD, especially for slice thicknesses of ≥ 1 mm [7]. In our experience, significant misdiagnosis occurs when attempting to diagnose SSCD with CT slice thicknesses greater than 1 mm. Furthermore, we consider it imperative to verify the SSCD diagnosis multiplanar, otherwise overdiagnosis or misdiagnosis may occur. Nevertheless the high resolution CT, it is an integral part of equipment-based diagnostics of SSCD in case of clinical suspicion. In the future, newer ultra high resolution cross-sectional imaging techniques, such as using photon counting CT (UHR PCD-CT), have the potential to provide even better visualizations of SSCD at low radiation dose [16].

In our study all multiplanar reconstructions were evaluated based on sub-millimeter slices and complemented by standardized double-oblique reconstruction [17]. Our patient group displayed a relative dominance of the type 2 location regardless of sex and age. This SSCD type 2 can be overlooked in standard axial reconstructions because it is in the superior semicircular canal apex. We were able to reliably visualize SSCD location type 2 in all cases using the reconstruction algorithm presented here.

343 SSCD data sets from 280 patients were analyzed for our subgroup analysis. The data originated from an analysis of 1370 petrous temporal bone HRCTs. At a prevalence of up to 20.42%, SSCD is a new but not rare diagnosis in patients with residual hearing. The results largely correspond to those of other radiological studies (Nadgir et al.: 7.9% (n = 304) [18]; Stimmer et al.: 12.6% (n = 350) [8]; Williamson et al.: 13.5% (n = 223) [7]; Ceylan et al.: 17.5% (n = 108) [9]).

It is important to know about and correctly diagnose SSCD. Our reconstruction scheme notably reduces the risk of overdiagnosis when using CT. The risk of overdiagnosis is especially large if slice thicknesses of ≥ 1 mm are used. Belden et al. demonstrated the importance of selecting a slice thickness of < 1 mm in diagnosing SSCD when they disproved in all 36 cases an initial suspicion of SSCD formed after acquisition based on 1 mm slice thickness by re-examining the cases with 0.5 mm slices [15]. We therefore recommend the use of a scan protocol with a slice thickness of ≤ 0.6 mm.

The present retrospective analysis showed overall age groups no significant difference in the relative incidence of SSCD for women and men. In the subgroup analysis SSCD type 2 is significantly more common in males and significantly more common in age group C and D. These results are in line with the observations made by Crovetto et al. [19], da Cunha Ferreira et al. [20] and Martin et al. [21].

Study limitations

Our retrospective study focused on the incidental findings of SSCD in the HRCT imaging as primary outcome. A multiparametric analysis with respect to clinical parameters such as vestibular symptoms or in the correlation of new high frequency ocular vestibular evoked myogenic potential (oVEMP n10 response) for the study cohort were not the primary target of this study. Clinical parameters should be analyzed in another prospective study approach to demonstrate the clinical added value of the classification of SSCD. Statistically reliable investigations about the different SSCD types in comparison with the clinical parameters remain to be conducted in a prospective study.

Conclusions

From the neuroradiological point of view, the relatively new SSCD diagnosis with its prevalence of up to 20.42% among individuals with residual hearing is not a rare one. This makes it even more important for the radiologist to obtain certainty by confirming the diagnosis by means of HRCT with slice thickness under 0.6 mm. Our reconstruction scheme makes a reliable visualization and clear classification of SSCD possible. This standardization yields the potential of a correlation of the patient’s clinical symptoms with cross-sectional anatomy and may lead to a differentiated therapy approach.

Abbreviations

HRCT

high resolution computed tomography

SSC

superior semicircular canal

SSCD

superior semicircular canal dehiscence

oVEMP

ocular vestibular evoked myogenic potential

Data Availability

Data will not be held in a public repository due to the restrictions of the ethics committee. Due to the multicenter data, general publication to protect patient data is not possible and not covered by the ethical vote. Data can be requested from the corresponding author or from BwZKrhsKoblenzKlinikVIIIRadiologie@bundeswehr.org.

Funding Statement

The author(s) received no specific funding for this work.

References

  • 1.Minor LB, Solomon D, Zinreich JS, Zee DS. Sound- and/or pressure-induced vertigo due to bone dehiscence of the superior semicircular canal. Archives of otolaryngology—head & neck surgery. 1998;124(3):249–58. [DOI] [PubMed] [Google Scholar]
  • 2.Chi FL, Ren DD, Dai CF. Variety of audiologic manifestations in patients with superior semicircular canal dehiscence. Otology & neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 2010;31(1):2–10. doi: 10.1097/mao.0b013e3181bc35ce [DOI] [PubMed] [Google Scholar]
  • 3.Strupp M, Eggert T, Straube A, Jager L, Querner V, Brandt T. ["Inner perilymph fistula" of the anterior semicircular canal. A new disease picture with recurrent attacks of vertigo]. Der Nervenarzt. 2000;71(2):138–42. doi: 10.1007/s001150050021 [DOI] [PubMed] [Google Scholar]
  • 4.Minor LB, Carey JP, Cremer PD, Lustig LR, Streubel S-O. Dehiscence of bone overlying the superior canal as a cause of apparent conductive hearing loss. Otology & Neurotology. 2003;24(2):270–8. [DOI] [PubMed] [Google Scholar]
  • 5.Minor LB. Clinical manifestations of superior semicircular canal dehiscence. The Laryngoscope. 2005;115(10):1717–27. doi: 10.1097/01.mlg.0000178324.55729.b7 [DOI] [PubMed] [Google Scholar]
  • 6.Loke SC, Goh JP. Incidence of semicircular canal dehiscence in Singapore. The British journal of radiology. 2009;82(977):371–3. doi: 10.1259/bjr/32471003 [DOI] [PubMed] [Google Scholar]
  • 7.Williamson RA, Vrabec JT, Coker NJ, Sandlin M. Coronal computed tomography prevalence of superior semicircular canal dehiscence. Otolaryngology—head and neck surgery: official journal of American Academy of Otolaryngology-Head and Neck Surgery. 2003;129(5):481–9. doi: 10.1016/s0194-5998(03)01391-3 [DOI] [PubMed] [Google Scholar]
  • 8.Stimmer H, Hamann KF, Zeiter S, Naumann A, Rummeny EJ. Semicircular canal dehiscence in HR multislice computed tomography: distribution, frequency, and clinical relevance. European archives of oto-rhino-laryngology: official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS): affiliated with the German Society for Oto-Rhino-Laryngology—Head and Neck Surgery. 2012;269(2):475–80. [DOI] [PubMed] [Google Scholar]
  • 9.Ceylan N, Bayraktaroglu S, Alper H, Savas R, Bilgen C, Kirazli T, et al. CT imaging of superior semicircular canal dehiscence: added value of reformatted images. Acta oto-laryngologica. 2010;130(9):996–1001. doi: 10.3109/00016481003602108 [DOI] [PubMed] [Google Scholar]
  • 10.Banerjee A, Whyte A, Atlas MD. Superior canal dehiscence: review of a new condition. Clin Otolaryngol. 2005;30(1):9–15. doi: 10.1111/j.1365-2273.2004.00940.x [DOI] [PubMed] [Google Scholar]
  • 11.Mehlenbacher A, Capehart B, Bass D, Burke JR. Sound induced vertigo: superior canal dehiscence resulting from blast exposure. Archives of physical medicine and rehabilitation. 2012;93(4):723–4. doi: 10.1016/j.apmr.2011.09.020 [DOI] [PubMed] [Google Scholar]
  • 12.Adams ME, Levine SC. The first new otologic disorder in a century: superior canal dehiscence syndrome. Minnesota medicine. 2011;94(11):29–32. [PubMed] [Google Scholar]
  • 13.Ogutha J, Page NC, Hullar TE. Postpartum vertigo and superior semicircular canal dehiscence syndrome. Obstetrics and gynecology. 2009;114(2 Pt 2):434–6. doi: 10.1097/AOG.0b013e3181ae8da0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Phillips DJ, Souter MA, Vitkovic J, Briggs RJ. Diagnosis and outcomes of middle cranial fossa repair for patients with superior semicircular canal dehiscence syndrome. Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia. 2010;17(3):339–41. doi: 10.1016/j.jocn.2009.06.021 [DOI] [PubMed] [Google Scholar]
  • 15.Belden CJ, Weg N, Minor LB, Zinreich SJ. CT evaluation of bone dehiscence of the superior semicircular canal as a cause of sound- and/or pressure-induced vertigo. Radiology. 2003;226(2):337–43. doi: 10.1148/radiol.2262010897 [DOI] [PubMed] [Google Scholar]
  • 16.Zhou W, Lane JI, Carlson ML, Bruesewitz MR, Witte RJ, Koeller KK, et al. Comparison of a Photon-Counting-Detector CT with an Energy-Integrating-Detector CT for Temporal Bone Imaging: A Cadaveric Study. AJNR American journal of neuroradiology. 2018;39(9):1733–8. doi: 10.3174/ajnr.A5768 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Crane BT, Minor LB, Carey JP. Three-dimensional computed tomography of superior canal dehiscence syndrome. Otology & neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 2008;29(5):699–705. doi: 10.1097/MAO.0b013e3181776726 [DOI] [PubMed] [Google Scholar]
  • 18.Nadgir RN, Ozonoff A, Devaiah AK, Halderman AA, Sakai O. Superior semicircular canal dehiscence: congenital or acquired condition? AJNR American journal of neuroradiology. 2011;32(5):947–9. doi: 10.3174/ajnr.A2437 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Crovetto M, Whyte J, Rodriguez OM, Lecumberri I, Martinez C, Elexpuru J. Anatomo-radiological study of the Superior Semicircular Canal Dehiscence Radiological considerations of Superior and Posterior Semicircular Canals. European journal of radiology. 2010;76(2):167–72. doi: 10.1016/j.ejrad.2009.05.038 [DOI] [PubMed] [Google Scholar]
  • 20.da Cunha Ferreira S, de Melo Tavares de Lima MA. Superior Canal Dehiscence Syndrome. Brazilian journal of otorhinolaryngology. 2006;72(3):414–8. doi: 10.1016/s1808-8694(15)30978-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Martin C, Chahine P, Veyret C, Richard C, Prades JM, Pouget JF. Prospective radiological study concerning a series of patients suffering from conductive or mixed hearing loss due to superior semicircular canal dehiscence. European archives of oto-rhino-laryngology: official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS): affiliated with the German Society for Oto-Rhino-Laryngology—Head and Neck Surgery. 2009;266(8):1175–81. doi: 10.1007/s00405-008-0862-y [DOI] [PubMed] [Google Scholar]

Decision Letter 0

Jorge Spratley

10 Dec 2021

PONE-D-21-25618

New classification of superior semicircular canal dehisence in HRCT

PLOS ONE

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2. The limitations of CT scan in diagnosing SSCC dehiscence should be discussed in a more comprehensive fashion, in particular on the risk of imaging overdiagnosis.

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Reviewer #1: General Comments

The study submitted to PLOSONE presents the results of an original research study of superior semicircular canal dehiscence (SCCD), after an extensive review of 1370 temporal bones. Altogether, It tries to overcome one of the major problems on SSCD diagnosis which is its common over diagnostic rate.

The tests, statistics, and other analyses performed are described in detail.

Conclusions are presented in an appropriate fashion and are supported by the data.

The article is presented in an intelligible fashion and is written in standard English, however with some minor errors.

The research meets all applicable standards for the ethics of experimentation and research integrity.

The article adheres to appropriate reporting guidelines and community standards for data availability.

The paper globally shows how a standardized reconstruction scheme on CT can improve the diagnosis and help a more accurate clinical approach on the involved pathology.

Specific comments

It would have been interesting and very much clinically valuable to have compared the CT results with the vestibular myogenic potentials results. A simple exam that apports decisive information of SSCD. If available, that information and analysis should be added to the evaluation.

Minor errors in the text:

und (page 4)

Initials MPR and MIP are not presented previously (page 5)

Legend Table 1. sex relative values to the sex; side, type relative values to total population

Reviewer #2: PONE-D-21-25618: statistical review

SUMMARY. This study relies on a large sample (n=1370) of high-resolution scans of the temporal bone in ENT patients. The principal outcome is the proportion of cases of superior semicircular canal dehiscence (SSCD), clustered according to three location types. The statistical analysis compares these proportions between genders and across age groups. Although the relationship between SSCD proportions and relevant clinical parameters of the patients would have been much more interesting, the authors explicitly declare that this was not the target of the study. With this limitation, the study reduces to an epidemiological study of SSCD incidence across demographic groups. I list below two major issues that should be addressed and three specific points that should be clarified.

MAJOR ISSUES

1) Little information is provided about the sample. Do the subjects share specific characteristics? Is it a multi-center study? What were the reasons for visiting these patients? Without these information, we are unable to evaluate whether the results of the study can be extended to a target population.

2) The statistical tools are below the level required by the Journal. As the purpose of the study is the comparison of proportions across age and gender groups, the natural approach is a multinomial regression where type-specific SSCD proportions is the outcome and age and gender are the two regressors. Multinomial regression is also able to test a possible interaction effect between age and gender. The model is available in SPSS, which is the software used by the authors.

SPECIFIC ISSUES

1) Page 5. “Normal distribution was assumed due to central limit theorem”. This sentence is a bit obscure. Do you want to explain why proportions are being compared by a t-test?

2) Page 5. “For continuous data Student`s t- Test was performed for independent samples to analyze the means”. I don’t see continuous data in your study: you have proportions, age groups (taken as factors) and gender. Please clarify.

3) Page 5. “To analyze ordinal data Chi- square test was used.” Similar to above: where are the ordinal data in this paper? In addition: I'm not aware of a Chi Square test for ordinal data: could you please specify the test that has bneen used?

Reviewer #3: the subject in the article is an interesting approach to SSCD and may contribute to better diagnosis and understanting of the disease. about the classification in type 1, 2 or 3 a better explanation about the imaging criteria is needed.

the authors need to review also one of the tables.

The article may be accepted with minor review

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Reviewer #1: No

Reviewer #2: No

Reviewer #3: No

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Attachment

Submitted filename: PONE-D-21-25618 reviewed.pdf

Attachment

Submitted filename: Review of the manuscript PONE-D-21-25618.docx

PLoS One. 2022 Jan 20;17(1):e0262758. doi: 10.1371/journal.pone.0262758.r002

Author response to Decision Letter 0


27 Dec 2021

Additional Editor Comments (if provided):

Dear Authors,

Thank you for having submitted your original manuscript to PlosOne and for patiening for the decision.

Please carefully address and reply to all reviewers comments and questions, as appropriate.

Also please take into consideration the following remarks:

1. Your citations on the text do not match the References list (see last paragraph of discussion). Please correct.

We thank the editor for this comment and corrected the passage accordingly. In this case there was no citation in-tended at this passage.

2. The limitations of CT scan in diagnosing SSCC dehiscence should be discussed in a more comprehensive fash-ion, in particular on the risk of imaging overdiagnosis.

Thank you very much for this suggestion, which we have gladly implemented. In the discussion, we more clearly highlighted the risk of overdiagnosis by monoplanar CT with 1 mm thick slices and made a recommendation for high-resolution imaging.

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We made the changes according to the journal style requirements.

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Reviewers' comments:

Reviewer #1: General Comments

The study submitted to PLOSONE presents the results of an original research study of superior semicircular canal dehiscence (SCCD), after an extensive review of 1370 temporal bones. Altogether, It tries to overcome one of the major problems on SSCD diagnosis which is its common over diagnostic rate.

The tests, statistics, and other analyses performed are described in detail.

Conclusions are presented in an appropriate fashion and are supported by the data.

The article is presented in an intelligible fashion and is written in standard English, however with some minor errors.

The research meets all applicable standards for the ethics of experimentation and research integrity.

The article adheres to appropriate reporting guidelines and community standards for data availability.

The paper globally shows how a standardized reconstruction scheme on CT can improve the diagnosis and help a more accurate clinical approach on the involved pathology.

Specific comments

It would have been interesting and very much clinically valuable to have compared the CT results with the vestibular myogenic potentials results. A simple exam that apports decisive information of SSCD. If available, that information and analysis should be added to the evaluation.

Thank you very much for this recommendation. Due to the retrospective multicenter analysis, these clinical data were not available and could not be provided. We will be happy to include this recommendation in a prospective approach. We have added this information to the text under study limitations.

Minor errors in the text:

und (page 4)

We thank the reviewer for this hint. We corrected that mistake.

Initials MPR and MIP are not presented previously (page 5)

We added this information to the manuscript.

Legend Table 1. sex relative values to the sex; side, type relative values to total population

We have restructured the table legend and hope that the table is now easier to interpret.

Reviewer #2: PONE-D-21-25618: statistical review

SUMMARY. This study relies on a large sample (n=1370) of high-resolution scans of the temporal bone in ENT pa-tients. The principal outcome is the proportion of cases of superior semicircular canal dehiscence (SSCD), clustered according to three location types. The statistical analysis compares these proportions between genders and across age groups. Although the relationship between SSCD proportions and relevant clinical parameters of the patients would have been much more interesting, the authors explicitly declare that this was not the target of the study. With this limitation, the study reduces to an epidemiological study of SSCD incidence across demographic groups. I list below two major issues that should be addressed and three specific points that should be clarified.

MAJOR ISSUES

1) Little information is provided about the sample. Do the subjects share specific characteristics? Is it a multi-center study? What were the reasons for visiting these patients? Without these information, we are unable to evaluate whether the results of the study can be extended to a target population.

Thank you very much for these excellent questions. We have incorporated all the requested information in various places in the text. Here is a brief summary again. This is a multicenter study. All patients presented you with different vestibular symptoms (like vertigo, nystagmus, Tullio phenomenon) in the three participating clinics and received high resolution CT imaging of the petrous bone for clarification in the context of these symptoms.

2) The statistical tools are below the level required by the Journal. As the purpose of the study is the comparison of proportions across age and gender groups, the natural approach is a multinomial regression where type-specific SSCD proportions is the outcome and age and gender are the two regressors. Multinomial regression is also able to test a possible interaction effect between age and gender. The model is available in SPSS, which is the software used by the authors.

We are grateful for the reviewer's comment. We have accordingly calculated a

multinomial linear regression with type-specific SSCD proportions as dependent variable and gender, side of SSCD and age as covariates. We added the fact to the manuscript accordingly.

SPECIFIC ISSUES

1) Page 5. “Normal distribution was assumed due to central limit theorem”. This sentence is a bit obscure. Do you want to explain why proportions are being compared by a t-test?

The central limit theorem states that above a certain size, specified in the literature as 30, the distribution of a popula-tion can be assumed to be bell-shaped and the normal distribution can therefore be taken as given. It would certainly have been possible to test for a normal distribution for the t-test, but we considered this unnecessary for the very large study population.

2) Page 5. “For continuous data Student`s t- Test was performed for independent samples to analyze the means”. I don’t see continuous data in your study: you have proportions, age groups (taken as factors) and gender. Please clari-fy.

We thank the reviewer for this remark. Age was examined as an independent category from the subsequent classifica-tion into age groups. This was also stated in the results:

“Patients with SSCD were on average 6 years older than those without SSCD (mean 46.22 years versus 52.73 years (SSCD) p<0.001).”

Although there is some discourse in the literature as to whether age should be considered continuous or discrete, we believe it is acceptable to refer to it as continuous data. We think that this will also be approved by the reviewer.

3) Page 5. “To analyze ordinal data Chi- square test was used.” Similar to above: where are the ordinal data in this paper? In addition: I'm not aware of a Chi Square test for ordinal data: could you please specify the test that has bneen used?

We thank the reviewer for the excellent comment. This is an error on our part. What was meant here, of course, was nominal data (age, gender, side). This also explains the answer to the question about the choice of the statistical test "Chi-square test", which is permissible for nominal data. We have corrected this fact

Reviewer #3: the subject in the article is an interesting approach to SSCD and may contribute to better diagnosis and understanding of the disease. about the classification in type 1, 2 or 3 a better explanation about the imaging criteria is needed.

Thank you very much for this recommendation which we have implemented very gladly in the text. We have added the comprehensive explanation under Figure 2.

The authors need to review also one of the tables.

We corrected table 1 and the legend of table 1.

Decision Letter 1

Jorge Spratley

5 Jan 2022

New Classification of superior semicircular canal dehiscence in HRCT

PONE-D-21-25618R1

Dear Dr. Waldeck,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

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Kind regards,

Jorge Spratley, MD, PhD

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Thank you for the sound revision and improvement of the manuscript.

Again, I would like to express our appreciation for having patiented for the referees' revisions.

The paper has now reached the level to be published at PlosOne. Congratulations!

Reviewers' comments:

Acceptance letter

Jorge Spratley

7 Jan 2022

PONE-D-21-25618R1

New Classification of superior semicircular canal dehiscence in HRCT

Dear Dr. Waldeck:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Professor Jorge Spratley

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    Attachment

    Submitted filename: PONE-D-21-25618 reviewed.pdf

    Attachment

    Submitted filename: Review of the manuscript PONE-D-21-25618.docx

    Data Availability Statement

    Data will not be held in a public repository due to the restrictions of the ethics committee. Due to the multicenter data, general publication to protect patient data is not possible and not covered by the ethical vote. Data can be requested from the corresponding author or from BwZKrhsKoblenzKlinikVIIIRadiologie@bundeswehr.org.


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