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June 11, 2019; 92 (24) Article

Capturing acute vertigo

A vestibular event monitor

View ORCID ProfileAllison S. Young, Corinna Lechner, Andrew P. Bradshaw, Hamish G. MacDougall, Deborah A. Black, G. Michael Halmagyi, Miriam S. Welgampola
First published May 15, 2019, DOI: https://doi.org/10.1212/WNL.0000000000007644
Allison S. Young
From the Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Central Clinical School (A.S.Y., C.L., A.P.B., G.M.H., M.S.W.), Vestibular Research Laboratory, School of Psychology (H.G.M.), and Faculty of Health Sciences (D.A.B.), University of Sydney, Australia.
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  • ORCID record for Allison S. Young
Corinna Lechner
From the Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Central Clinical School (A.S.Y., C.L., A.P.B., G.M.H., M.S.W.), Vestibular Research Laboratory, School of Psychology (H.G.M.), and Faculty of Health Sciences (D.A.B.), University of Sydney, Australia.
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Andrew P. Bradshaw
From the Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Central Clinical School (A.S.Y., C.L., A.P.B., G.M.H., M.S.W.), Vestibular Research Laboratory, School of Psychology (H.G.M.), and Faculty of Health Sciences (D.A.B.), University of Sydney, Australia.
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Hamish G. MacDougall
From the Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Central Clinical School (A.S.Y., C.L., A.P.B., G.M.H., M.S.W.), Vestibular Research Laboratory, School of Psychology (H.G.M.), and Faculty of Health Sciences (D.A.B.), University of Sydney, Australia.
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Deborah A. Black
From the Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Central Clinical School (A.S.Y., C.L., A.P.B., G.M.H., M.S.W.), Vestibular Research Laboratory, School of Psychology (H.G.M.), and Faculty of Health Sciences (D.A.B.), University of Sydney, Australia.
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G. Michael Halmagyi
From the Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Central Clinical School (A.S.Y., C.L., A.P.B., G.M.H., M.S.W.), Vestibular Research Laboratory, School of Psychology (H.G.M.), and Faculty of Health Sciences (D.A.B.), University of Sydney, Australia.
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Miriam S. Welgampola
From the Institute of Clinical Neurosciences, Royal Prince Alfred Hospital, Central Clinical School (A.S.Y., C.L., A.P.B., G.M.H., M.S.W.), Vestibular Research Laboratory, School of Psychology (H.G.M.), and Faculty of Health Sciences (D.A.B.), University of Sydney, Australia.
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Capturing acute vertigo
A vestibular event monitor
Allison S. Young, Corinna Lechner, Andrew P. Bradshaw, Hamish G. MacDougall, Deborah A. Black, G. Michael Halmagyi, Miriam S. Welgampola
Neurology Jun 2019, 92 (24) e2743-e2753; DOI: 10.1212/WNL.0000000000007644

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Abstract

Objective To facilitate the diagnosis of vestibular disorders by patient-initiated capture of ictal nystagmus.

Methods Adults from an Australian neurology outpatient clinic reporting recurrent vertigo were recruited prospectively and taught to self-record spontaneous and positional nystagmus at home while symptomatic, using miniature video-oculography goggles. Consenting patients with ictal videorecordings and a final unblinded clinical diagnosis of Ménière disease (MD), vestibular migraine (VM), or benign paroxysmal positional vertigo (BPPV) were included.

Results Ictal eye videos of 117 patients were analyzed. Of 43 patients with MD, 40 showed high-velocity spontaneous horizontal nystagmus (median slow-phase velocity [SPV] 39.7°/s; 21 showed horizontal nystagmus reversing direction within 12 hours [24 on separate days]). In 44 of 67 patients with VM, spontaneous horizontal (n = 28, 4.9°/s), upbeating (n = 6, 15.5°/s), or downbeating nystagmus (n = 10, 5.1°/s) was observed; 16 showed positional nystagmus only, and 7 had no nystagmus. Spontaneous horizontal nystagmus with SPV >12.05°/s had a sensitivity and specificity of 95.3% and 82.1% for MD (95% confidence interval [CI] 0.84–0.99, 0.71–0.90). Nystagmus direction change within 12 hours was highly specific (95.7%) for MD (95% CI 0.85–0.99). Spontaneous vertical nystagmus was highly specific (93.0%) for VM (95% CI 0.81–0.99). In the 7 patients with BPPV, spontaneous nystagmus was absent or <3°/s. Lying affected-ear down, patients with BPPV demonstrated paroxysmal positional nystagmus. Median time for peak SPV to halve (T50) was 19.0 seconds. Patients with VM and patients with MD demonstrated persistent positional nystagmus (median T50; 93.1 seconds, 213.2 seconds). T50s <47.3 seconds had a sensitivity and specificity of 100% and 77.8% for BPPV (95% CI 0.54–1.00, 0.64–0.88).

Conclusion Patient-initiated vestibular event monitoring is feasible and could facilitate rapid and accurate diagnosis of episodic vestibular disorders.

Glossary

BPPV=
benign paroxysmal positional vertigo;
CI=
confidence interval;
HC=
horizontal canal;
MD=
Ménière disease;
SPV=
slow-phase velocity;
VM=
vestibular migraine

Footnotes

  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Received August 2, 2018.
  • Accepted in final form February 4, 2019.
  • © 2019 American Academy of Neurology
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