Bone-Conducted oVEMP Latency Delays Assist in the Differential Diagnosis of Large Air-Conducted oVEMP Amplitudes

Background: A sensitive test for Superior Semicircular Canal Dehiscence (SCD) is the air-conducted, ocular vestibular evoked myogenic potential (AC oVEMP). However, not all patients with large AC oVEMPs have SCD. This retrospective study sought to identify alternate diagnoses also producing enlarged...

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Main Authors: Rachael L. Taylor, John S. Magnussen, Belinda Kwok, Allison S. Young, Berina Ihtijarevic, Emma C. Argaet, Nicole Reid, Cheryl Rivas, Jacob M. Pogson, Sally M. Rosengren, G. Michael Halmagyi, Miriam S. Welgampola
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-10-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2020.580184/full
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author Rachael L. Taylor
Rachael L. Taylor
John S. Magnussen
Belinda Kwok
Belinda Kwok
Allison S. Young
Berina Ihtijarevic
Berina Ihtijarevic
Emma C. Argaet
Emma C. Argaet
Nicole Reid
Cheryl Rivas
Jacob M. Pogson
Jacob M. Pogson
Sally M. Rosengren
Sally M. Rosengren
G. Michael Halmagyi
G. Michael Halmagyi
Miriam S. Welgampola
Miriam S. Welgampola
Miriam S. Welgampola
author_facet Rachael L. Taylor
Rachael L. Taylor
John S. Magnussen
Belinda Kwok
Belinda Kwok
Allison S. Young
Berina Ihtijarevic
Berina Ihtijarevic
Emma C. Argaet
Emma C. Argaet
Nicole Reid
Cheryl Rivas
Jacob M. Pogson
Jacob M. Pogson
Sally M. Rosengren
Sally M. Rosengren
G. Michael Halmagyi
G. Michael Halmagyi
Miriam S. Welgampola
Miriam S. Welgampola
Miriam S. Welgampola
author_sort Rachael L. Taylor
collection DOAJ
description Background: A sensitive test for Superior Semicircular Canal Dehiscence (SCD) is the air-conducted, ocular vestibular evoked myogenic potential (AC oVEMP). However, not all patients with large AC oVEMPs have SCD. This retrospective study sought to identify alternate diagnoses also producing enlarged AC oVEMPs and investigated bone-conducted (BC) oVEMP outcome measures that would help differentiate between these, and cases of SCD.Methods: We reviewed the clinical records and BC oVEMP results of 65 patients (86 ears) presenting with dizziness or balance problems who underwent CT imaging to investigate enlarged 105 dB nHL click AC oVEMP amplitudes. All patients were tested with BC oVEMPs using two different stimuli (1 ms square-wave pulse and 8 ms 125 Hz sine wave). Logistic regression and odds ratios were used to determine the efficacy of BC oVEMP amplitudes and latencies in differentiating between enlarged AC oVEMP amplitudes due to dehiscence from those with an alternate diagnosis.Results: Fifty-three ears (61.6%) with enlarged AC oVEMP amplitudes were identified as having frank dehiscence on imaging; 33 (38.4%) had alternate diagnoses that included thinning of the bone covering (near dehiscence, n = 13), vestibular migraine (n = 12 ears of 10 patients), enlarged vestibular aqueduct syndrome (n = 2) and other causes of recurrent episodic vertigo (n = 6). BC oVEMP amplitudes of dehiscent and non-dehiscent ears were not significantly different (p > 0.05); distributions of both groups overlapped with the range of healthy controls. There were significant differences in BC oVEMP latencies between dehiscent and non-dehiscent ears for both stimuli (p < 0.001). A prolonged n1 125 Hz latency (>11.5 ms) was the best predictor of dehiscence (odd ratio = 27.8; 95% CI:7.0-111.4); abnormal n1 latencies were identified in 79.2% of ears with dehiscence compared with 9.1% of ears without dehiscence.Conclusions: A two-step protocol of click AC oVEMP amplitudes and 125 Hz BC oVEMP latency measures optimizes the specificity of VEMP testing in SCD.
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spelling doaj.art-5967d28fd071414290c2cb384ca2ebb02022-12-21T19:18:30ZengFrontiers Media S.A.Frontiers in Neurology1664-22952020-10-011110.3389/fneur.2020.580184580184Bone-Conducted oVEMP Latency Delays Assist in the Differential Diagnosis of Large Air-Conducted oVEMP AmplitudesRachael L. Taylor0Rachael L. Taylor1John S. Magnussen2Belinda Kwok3Belinda Kwok4Allison S. Young5Berina Ihtijarevic6Berina Ihtijarevic7Emma C. Argaet8Emma C. Argaet9Nicole Reid10Cheryl Rivas11Jacob M. Pogson12Jacob M. Pogson13Sally M. Rosengren14Sally M. Rosengren15G. Michael Halmagyi16G. Michael Halmagyi17Miriam S. Welgampola18Miriam S. Welgampola19Miriam S. Welgampola20Department of Physiology and Center for Brain Research, The University of Auckland, Auckland, New ZealandCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaMacquarie Medical Imaging, Macquarie University Hospital, Sydney, NSW, AustraliaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaThe Balance Clinic and Laboratory, Sydney, NSW, AustraliaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaThe Balance Clinic and Laboratory, Sydney, NSW, AustraliaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaThe Balance Clinic and Laboratory, Sydney, NSW, AustraliaNeurology Department and Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Sydney, NSW, AustraliaThe Balance Clinic and Laboratory, Sydney, NSW, AustraliaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaNeurology Department and Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Sydney, NSW, AustraliaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaNeurology Department and Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Sydney, NSW, AustraliaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaNeurology Department and Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Sydney, NSW, AustraliaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, AustraliaThe Balance Clinic and Laboratory, Sydney, NSW, AustraliaNeurology Department and Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Sydney, NSW, AustraliaBackground: A sensitive test for Superior Semicircular Canal Dehiscence (SCD) is the air-conducted, ocular vestibular evoked myogenic potential (AC oVEMP). However, not all patients with large AC oVEMPs have SCD. This retrospective study sought to identify alternate diagnoses also producing enlarged AC oVEMPs and investigated bone-conducted (BC) oVEMP outcome measures that would help differentiate between these, and cases of SCD.Methods: We reviewed the clinical records and BC oVEMP results of 65 patients (86 ears) presenting with dizziness or balance problems who underwent CT imaging to investigate enlarged 105 dB nHL click AC oVEMP amplitudes. All patients were tested with BC oVEMPs using two different stimuli (1 ms square-wave pulse and 8 ms 125 Hz sine wave). Logistic regression and odds ratios were used to determine the efficacy of BC oVEMP amplitudes and latencies in differentiating between enlarged AC oVEMP amplitudes due to dehiscence from those with an alternate diagnosis.Results: Fifty-three ears (61.6%) with enlarged AC oVEMP amplitudes were identified as having frank dehiscence on imaging; 33 (38.4%) had alternate diagnoses that included thinning of the bone covering (near dehiscence, n = 13), vestibular migraine (n = 12 ears of 10 patients), enlarged vestibular aqueduct syndrome (n = 2) and other causes of recurrent episodic vertigo (n = 6). BC oVEMP amplitudes of dehiscent and non-dehiscent ears were not significantly different (p > 0.05); distributions of both groups overlapped with the range of healthy controls. There were significant differences in BC oVEMP latencies between dehiscent and non-dehiscent ears for both stimuli (p < 0.001). A prolonged n1 125 Hz latency (>11.5 ms) was the best predictor of dehiscence (odd ratio = 27.8; 95% CI:7.0-111.4); abnormal n1 latencies were identified in 79.2% of ears with dehiscence compared with 9.1% of ears without dehiscence.Conclusions: A two-step protocol of click AC oVEMP amplitudes and 125 Hz BC oVEMP latency measures optimizes the specificity of VEMP testing in SCD.https://www.frontiersin.org/articles/10.3389/fneur.2020.580184/fullvestibular-evoked myogenic potentialssuperior semicircular canal dehiscencetullio phenomenonvertigohyperacusisbone-conduction
spellingShingle Rachael L. Taylor
Rachael L. Taylor
John S. Magnussen
Belinda Kwok
Belinda Kwok
Allison S. Young
Berina Ihtijarevic
Berina Ihtijarevic
Emma C. Argaet
Emma C. Argaet
Nicole Reid
Cheryl Rivas
Jacob M. Pogson
Jacob M. Pogson
Sally M. Rosengren
Sally M. Rosengren
G. Michael Halmagyi
G. Michael Halmagyi
Miriam S. Welgampola
Miriam S. Welgampola
Miriam S. Welgampola
Bone-Conducted oVEMP Latency Delays Assist in the Differential Diagnosis of Large Air-Conducted oVEMP Amplitudes
Frontiers in Neurology
vestibular-evoked myogenic potentials
superior semicircular canal dehiscence
tullio phenomenon
vertigo
hyperacusis
bone-conduction
title Bone-Conducted oVEMP Latency Delays Assist in the Differential Diagnosis of Large Air-Conducted oVEMP Amplitudes
title_full Bone-Conducted oVEMP Latency Delays Assist in the Differential Diagnosis of Large Air-Conducted oVEMP Amplitudes
title_fullStr Bone-Conducted oVEMP Latency Delays Assist in the Differential Diagnosis of Large Air-Conducted oVEMP Amplitudes
title_full_unstemmed Bone-Conducted oVEMP Latency Delays Assist in the Differential Diagnosis of Large Air-Conducted oVEMP Amplitudes
title_short Bone-Conducted oVEMP Latency Delays Assist in the Differential Diagnosis of Large Air-Conducted oVEMP Amplitudes
title_sort bone conducted ovemp latency delays assist in the differential diagnosis of large air conducted ovemp amplitudes
topic vestibular-evoked myogenic potentials
superior semicircular canal dehiscence
tullio phenomenon
vertigo
hyperacusis
bone-conduction
url https://www.frontiersin.org/articles/10.3389/fneur.2020.580184/full
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