Nervenheilkunde 2020; 39(04): 242-250
DOI: 10.1055/a-1110-9424
Schwerpunkt
© Georg Thieme Verlag KG Stuttgart · New York

Presbyvestibulopathie

Diagnosekriterien Konsensdokument des Klassifikationskomitees der Bárány-GesellschaftPresbyvestibulopathyDiagnostic criteria
Yuri Agrawal
1   Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, USA
,
Raymond Van de Berg
2   Department of Otolaryngology-Head and Neck Surgery, Maastricht University Medical Centre, Maastricht, Niederlande
,
Floris Wuyts
3   Lab for Equilibrium Investigations and Aerospace, University of Antwerp, Antwerpen, Belgien
,
Leif Walther
4   Klinik für Hals-, Nasen-, Ohrenheilkunde, Kopf- und Halschirurgie der Universitätsmedizin Mannheim, Universität Heidelberg
,
Mans Magnusson
5   Department of Otorhinolaryngology, Lund University, Lund, Schweden
,
Esther Oh
6   Department of Geriatric Medicine and Gerontology, Johns Hopkins University, Baltimore, USA
,
Sharpe Margaret
7   Dizziness and Balance Disorders Centre, Adelaide, Australien
,
Michael Strupp
8   Neurologische Klinik und Deutsches Schwindelzentrum, Ludwig-Maximilians-Universität, München
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
02. April 2020 (online)

Zusammenfassung

In dieser Publikation werden die Diagnosekriterien für Presbyvestibulopathie (PVP) durch das Klassifikationskomitee der Bárány-Gesellschaft beschrieben. PVP ist als ein chronisches vestibuläres Syndrom definiert, das durch Gangunsicherheit, Gangstörungen und/oder wiederholte Stürze bei leichten bilateralen vestibulären Defiziten gekennzeichnet ist, mit Labortestbefunden, die zwischen Normalwerten und Schwellenwerten für die bilaterale Vestibulopathie liegen.

Die Diagnose von PVP basiert auf der Anamnese des Patienten, der körperlichen Untersuchung des Patienten und der Auswertung von Untersuchungen des Gleichgewichtssystems. Die Diagnose von PVP setzt eine bilateral verminderte Funktion des vestibulookulären Reflexes (VOR) voraus. Dies kann für den Hochfrequenzbereich des VOR mit dem Video-Kopf-Impuls-Test (vKIT), für den mittleren Frequenzbereich mit dem Drehstuhltest und für den Niederfrequenzbereich mit der kalorischen Prüfung diagnostiziert werden.

Für die Diagnose von PVP sollte der horizontale anguläre VOR-Verstärkungsfaktor (Gain) auf beiden Seiten < 0,8 und > 0,6 betragen, und/oder die Summe der maximalen Spitzengeschwindigkeiten in der langsamen Phase des kalorisch induzierten Nystagmus sollte bei der Stimulation mit warmem und kaltem Wasser auf jeder Seite < 25°/s und > 6°/s betragen, und/oder der horizontale anguläre VOR-Gain sollte bei Drehstuhlpendelung > 0,1 und < 0,3 betragen.

PVP tritt typischerweise zusammen mit anderen altersbedingten Defiziten des Sehvermögens, der Propriozeption und/oder der kortikalen, zerebellären und extrapyramidalen Funktion auf, die ebenfalls zur Manifestation der Symptome von Gangunsicherheit, Gangstörungen und Stürzen beitragen und diese möglicherweise erst auftreten lassen. Die hier beschriebenen Kriterien berücksichtigen lediglich das Vorhandensein dieser Symptome zusammen mit einer dokumentierten Beeinträchtigung der vestibulären Funktion bei älteren Erwachsenen.

Abstract

This paper describes the diagnostic criteria for presbyvestibulopathy (PVP) by the Classification Committee of the Bárány Society. PVP is defined as a chronic vestibular syndrome characterized by unsteadiness, gait disturbance, and/or recurrent falls in the presence of mild bilateral vestibular deficits, with findings on laboratory tests that are between normal values and thresholds established for bilateral vestibulopathy. The diagnosis of PVP is based on the patient history, bedside examination and laboratory evaluation. The diagnosis of PVP requires bilaterally reduced function of the vestibulo-ocular reflex (VOR). This can be diagnosed for the high frequency range of the VOR with the video-HIT (vHIT); for the middle frequency range with rotary chair testing; and for the low frequency range with caloric testing. For the diagnosis of PVP, the horizontal angular VOR gain on both sides should be < 0.8 and > 0.6, and/or the sum of the maximal peak velocities of the slow phase caloric-induced nystagmus for stimulation with warm and cold water on each side should be < 25°/s and > 6°/s, and/or the horizontal angular VOR gain should be > 0.1 and < 0.3 upon sinusoidal stimulation on a rotatory chair.

PVP typically occurs along with other age-related deficits of vision, proprioception, and/or cortical, cerebellar and extrapyramidal function which also contribute and might even be required for the manifestation of the symptoms of unsteadiness, gait disturbance, and falls. These criteria simply consider the presence of these symptoms, along with documented impairment of vestibular function, in older adults.

 
  • Literatur

  • 1 Agrawal Y, Carey J, Della Santina C. et al Minor, Disorders of balance and vestibular function in US adults: Data from the National Health and Nutrition Examination Survey, 2001–2004. Arch Intern Med 2009; 169 (10) 938-944
  • 2 Agrawal Y, Davalos-Bichara M, Zuniga M. et al Head impulse test abnormalities and influence on gait speed and falls in older individuals. Otology & Neurotology 2013; 34 (09) 1729-1735
  • 3 Agrawal Y, Pineault K, Semenov Y. Health-related quality of life and economic burden of vestibular loss in older adults. Laryngoscope Investigative Otolaryngology 2017; 3 (01) 8-15
  • 4 Agrawal Y, Zuniga M, Davalos-Bichara M. et al Decline in semicircular canal and otolith function with age. Otol Neurotol 2012; 33 (05) 832-839
  • 5 Anson E, Bigelow R, Carey J. et al VOR Gain Is Related to Compensatory Saccades in Healthy Older Adults. Front Aging Neurosci 2016; 8: 150
  • 6 Baloh R, Jacobson K, Socotch T. The effect of aging on visual-vestibuloocular responses. Experimental Brain Research 1993; 95 (03) 509-516
  • 7 Baloh R, Enrietto J, Jacobson K. et al Agerelated changes in vestibular function: A longitudinal study. Ann N Y Acad Sci 2001; 942: 210-219
  • 8 Baloh R, Ying S, Jacobson K. A longitudinal study of gait and balance dysfunction in normal older people. Arch Neurol 2003; 60 (06) 835-839
  • 9 Baltes P, Lindenberger U. Emergence of a powerful connection between sensory and cognitive functions across the adult life span: A new window to the study of cognitive aging?. Psychol Aging 1997; 12 (01) 12
  • 10 Bartl K, Lehnen N, Kohlbecher S. et al Head impulse testing using video-oculography. Ann N Y Acad Sci 2009; 1164: 331-333
  • 11 Bergstrom B. Morphology of the vestibular nerve: II. The number of myelinated vestibular nerve fibers in man at various ages. Acta Otolaryngol 1973; 76 1–6 173-179
  • 12 Bigelow R, Agrawal Y. Vestibular involvement in cognition: Visuospatial ability, attention, executive function, and memory. Journal of Vestibular Research 2015; 25 (02) 73-89
  • 13 Bigelow R, Semenov Y, du Lac S. et al Vestibular vertigo and comorbid cognitive and psychiatric impairment: The 2008 National Health Interview Survey. J Neurol Neurosurg Psychiatr 2015; 86 (03) 302-8
  • 14 Bigelow R, Semenov Y, Trevino C. et al Association between visuospatial ability and vestibular function in the Baltimore Longitudinal Study of Aging. J Am Geriatr Soc 2015; 63 (09) 1837-1844
  • 15 Bisdorff A, Von Brevern M, Lempert T. et al Classification of vestibular symptoms: Towards an international classification of vestibular disorders. Journal of Vestibular Research 2009; 19 (01) 1-13
  • 16 Brantberg K, Granath K, Schart N. Age-related changes in vestibular evoked myogenic potentials. Audiol Neurootol 2007; 12 (04) 247-253
  • 17 Brody B, Gamst A, Williams R. et al Depression, visual acuity, comorbidity, and disability associated with age-related macular degeneration. Ophthalmology 2001; 108 (10) 1893-1900
  • 18 Campos A, Canizares F, Sanchez-Quevedo M. et al Otoconial Degeneration in the Aged Utricle and Saccule1. New York: Karger Publishers; 1990: 143-153
  • 19 Chan F, Galatioto J, Amato M. et al Normative data for rotational chair stratified by age. Laryngoscope 2016; 126 (02) 460-463
  • 20 Cumming R, Ivers R, Clemson L. et al Improving vision to prevent falls in frail older people: A randomized trial. J Am Geriatr Soc 2007; 55 (02) 175-181
  • 21 Dillon C, Gu Q, Hoffman H. et al Vision, hearing, balance, and sensory impairment in Americans aged 70 years and over: United States, 1999–2006. NCHS data Brief 2010; (31) 1-8
  • 22 Ekwall A, Lindberg A, Magnusson M. Dizzy – why not take a walk? Low level physical activity improves quality of life among elderly with dizziness. Gerontology 2009; 55 (06) 652-659
  • 23 Ekvall Hansson E, Magnusson M. Vestibular asymmetry predicts falls among elderly patients with multisensory dizziness. BMC Geriatr 2013; 13 (01) 77
  • 24 Fife T, Colebatch J, Kerber K. et al Practice guideline: Cervical and ocular vestibular evoked myogenic potential testing Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology. Neurology 2017 10.1212/WNL.0000000000004690
  • 25 Gadkaree S, Sun D, Li C. et al Does sensory function decline independently or concomitantly with age? Data from the Baltimore Longitudinal Study of Aging. Journal of Aging Research 2016; 2016: 1865038
  • 26 Genther D, Betz J, Pratt S. et al Association of hearing impairment and mortality in older adults. Journals of Gerontology Series A 2014; 70 (01) 85-90
  • 27 Gittings N, Fozard J. Age related changes in visual acuity. Exp Gerontol 1986; 21 4–5 423-433
  • 28 Gopinath B, McMahon C, Rochtchina E. et al Dizziness and vertigo in an older population: The Blue Mountains prospective cross-sectional study. Clinical Otolaryngology 2009; 34 (06) 552-556
  • 29 Grimby A, Rosenhall U. Health-related quality of life and dizziness in old age. Gerontology 1995; 41 (05) 286-298
  • 30 Guralnik J, Ferrucci L, Simonsick E. et al Lower-extremity function in persons over the age of 70 years as a predictor of subsequent disability. N Engl J Med 1995; 332 (09) 556-561
  • 31 Harun A, Semenov Y, Agrawal Y. Vestibular function and activities of daily living: Analysis of the 1999 to 2004 National Health and Nutrition Examination Surveys. Gerontology and Geriatric Medicine 2015; 1: 2333721415607124
  • 32 Harwood R. Visual problems and falls. Age Ageing 2001; 30 (04) 13-18
  • 33 He W, Goodkind D, Kowal P. An aging world: 2015. International population reports 2016. 31
  • 34 Hicks G, Shardell M, Alley D. et al Absolute strength and loss of strength as predictors of mobility decline in older adults: The InCHIANTI study. J Gerontol A Biol Sci Med Sci 2012; 67 (01) 66-73
  • 35 Ishiyama G. Imbalance and vertigo: The aging human vestibular periphery. Semin Neurol 2009; 29 (05) 491-499
  • 36 Jacobson G, McCaslin D, Grantham S. et al Significant vestibular system impairment is common in a cohort of elderly patients referred for assessment of falls risk. J Am Acad Audiol 2008; 19 (10) 799-807
  • 37 Jacobson G, Newman C. The development of the Dizziness Handicap Inventory. Arch Otolaryngol Head Neck 1990; 116 (04) 424-427
  • 38 Kao A, Nanda A, Williams C. et al Validation of dizziness as a possible geriatric syndrome. J Am Geriatr Soc 2001; 49 (01) 72-75
  • 39 Katsarkas A. Dizziness in aging: A retrospective study of 1194 cases. Otolaryngol Head Neck Surg 1994; 110 (03) 296-301
  • 40 Keshner E. Head-trunk coordination in elderly subjects during linear anterior-posterior translations. Exp Brain Res 2004; 158 (02) 213-222
  • 41 Kristinsdottir E, Jarnlo G, Magnusson M. Asymmetric vestibular function in the elderly might be a significant contributor to hip fractures. Scand J Rehabil Med 2000; 32 (02) 56-60
  • 42 Kristinsdottir E, Nordell E, Jarnlo G. et al Observation of vestibular asymmetry in a majority of patients over 50 years with fall-related wrist fractures. Acta Otolaryngol 2001; 121 (04) 481-485
  • 43 Li C, Layman A, Geary R. et al Epidemiology of vestibulo-ocular reflex function: Data from the Baltimore Longitudinal Study of Aging. Otology & neurotology 2015; 36 (02) 267
  • 44 Lin H, Bhattacharyya N. Balance disorders in the elderly: Epidemiology and functional impact. Laryngo-scope 2012; 122 (08) 1858-1861
  • 45 Lin F, Metter E, O’Brien R. et al Hearing loss and incident Dementia. Arch Neurol 2011; 68 (02) 214-220
  • 46 Liston M, Bamiou D, Martin F. et al Peripheral vestibular dysfunction is prevalent in older adults experiencing multiple non-syncopal falls versus age-matched non-fallers: A pilot study. Age Ageing 2014; 43 (01) 38-43
  • 47 Lopez I, Honrubia V, Baloh R. Aging and the human vestibular nucleus. Journal of Vestibular Research 1997; 7 (01) 77-85
  • 48 MacDougall H, Weber K, McGarvie L. et al The video head impulse test: Diagnostic accuracy in peripheral vestibulopathy. Neurology 2009; 73 (14) 1134-1141
  • 49 Maes L, Dhooge I, D’haenens W. et al The effect of age on the sinusoidal harmonic acceleration test, pseudorandom rotation test, velocity step test, caloric test, and vestibular-evoked myogenic potential test. Ear Hear 2010; 31 (01) 84-94
  • 50 Marchetti G, Whitney S. Older adults and balance dysfunction. Neurol Clin 2005; 23 (03) 785-805
  • 51 Matheson A, Darlington C, Smith P. Dizziness in the elderly and age-related degeneration of the vestibular system. New Zealand Journal of Psychology 1999; 28 (01) 10
  • 52 Matiño-Soler E, Esteller-More E, Martin-Sanchez J. et al Normative data on angular vestibulo-ocular responses in the yaw axis measured using the video head impulse test. Otology & Neurotology 2015; 36 (03) 466-471
  • 53 McGarvie L, MacDougall H, Halmagyi G. et al The video head impulse test (vHIT) of semicircular canal function–age-dependent normative values of VOR gain in healthy subjects. Frontiers in Neurology 2015: 6
  • 54 Mener D, Betz J, Genther D. et al Hearing loss and depression in older adults. J Am Geriatr Soc 2013; 61 (09) 1627
  • 55 Merchant S, Velazquez-Villasenor L, Tsuji K. et al Temporal bone studies of the human peripheral vestibular system. Normative vestibular hair cell data. Ann Otol Rhinol Laryngol Suppl 2000; 181: 3-13
  • 56 Mossman B, Mossman S, Purdie G. et al Age dependent normal horizontal VOR gain of head impulse test as measured with video-oculography. Journal of Otolaryngology-Head & Neck Surgery 2015; 44 (01) 29
  • 57 Neuhauser H, Radtke A, von Brevern M. et al Burden of dizziness and vertigo in the community. Arch Intern Med 2008; 168 (19) 2118-2124
  • 58 Neuhauser H, von Brevern M, Radtke A. et al Epidemiology of vestibular vertigo: A neurotologic survey of the general population. Neurology 2005; 65 (06) 898-904
  • 59 Nordell E, Kristinsdottir E, Jarnlo G. et al Older patients with distal forearm fracture. A challenge to future fall and fracture prevention. Aging Clin Exp Res 2005; 17 (02) 90-95
  • 60 Oghalai J, Manolidis S, Barth J. et al Unrecognized benign paroxysmal positional vertigo in elderly patients. Otolaryngol Head Neck Surg 2000; 122 (05) 630-634
  • 61 Paige G. Senescence of human visual-vestibular interactions. 1. Vestibulo-ocular reflex and adaptive plasticity with aging. J Vestib Res 1992; 2 (02) 133-151
  • 62 Peterka R, Black F, Schoenhoff M. Age-related changes in human vestibulo-ocular and optokinetic reflexes: Pseudorandom rotation tests. J Vestib Res 1990; 1 (01) 61-71
  • 63 Rauch S, Velazquez-Villasenor L, Dimitri P. et al Decreasing hair cell counts in aging humans. Ann N Y Acad Sci 2001; 942: 220-227
  • 64 Rey M, Clark T, Wang W. et al Vestibular perceptual thresholds increase above the age of 40. Front Neurol 2016: 7
  • 65 Richter E. Quantitative study of human Scarpa’s ganglion and vestibular sensory epithelia. Acta Otolaryngol 1980; 90 1–6 199-208
  • 66 Robbins S, Waked E, McClaran J. Proprioception and stability: Foot position awareness as a function of age and footware. Age Ageing 1995; 24 (01) 67-72
  • 67 Roditi R, Crane B. Directional asymmetries and age effects in human self-motion perception. J Assoc Res Otolaryngol 2012; 13 (03) 381-401
  • 68 Rosengren S, Welgampola M, Colebatch J. Vestibular evoked myogenic potentials: Past, present and future. Clinical Neurophysiology 2010; 121 (05) 636-651
  • 69 Rosenhall U. Degenerative patterns in the aging human vestibular neuro-epithelia. Acta Otolaryngol 1973; 76 (02) 208-220
  • 70 Semenov Y, Bigelow R, Xue Q. et al Association between vestibular and cognitive function in US adults: Data from the National Health and Nutrition Examination Survey. The Journals of Gerontology Series A: 2016; 71 (02) 243-250
  • 71 Serrador J, Lipsitz L, Gopalakrishnan G. et al Wood, Loss of otolith function with age is associated with increased postural sway measures. Neurosci Lett 2009; 465 (01) 10-15
  • 72 Skinner H, Barrack R, Cook R. Age-related decline in proprioception. Clin Orthop 1984; 184: 208-211
  • 73 Stevens K, Lang I, Guralnik J. et al Epidemiology of balance and dizziness in a national population: Findings from the English Longitudinal Study of Ageing. Age Ageing 2008; 37 (03) 300-305
  • 74 Strupp M, Kim J, Murofushi T. et al Bilateral vestibulopathy: Diagnostic criteria Consensus document of the Classification Committee of the Bárány Society. Journal of Vestibular Research 2017; 27 (04) 177-189
  • 75 Swenor B, Ramulu P, Willis J. et al The prevalence of concurrent hearing and vision impairment in the United States. JAMA Internal Medicine 2013; 173 (04) 312-313
  • 76 Tian J, Shubayev I, Baloh R. et al Impairments in the initial horizontal vestibulo-ocular reflex of older humans. Exp Brain Res 2001; 137 3–4 309-322
  • 77 Tinetti M, Richman D, Powell L. Falls efficacy as a measure of fear of falling. J Gerontol 1990; 45 (06) 239
  • 78 Tuunainen E, Poe D, Jantti P. et al Presbyequilibrium in the oldest old, a combination of vestibular, oculomotor and postural deficits. Aging Clin Exp Res 2011; 23 5–6 364-371
  • 79 United Nations, Department of Economic and, Social Affairs World Population Ageing 2015. 2015 ST/ESA/SER.A/390
  • 80 Van Der Stappen A, Wuyts F, Van De Heyning P. Computerized electronystagmography: Normative data revisited. Acta Otolaryngol 2000; 120 (06) 724-730
  • 81 von Brevern M, Radtke A, Lezius F. et al Epidemiology of benign paroxysmal positional vertigo: A population based study. J Neurol Neurosurg Psychiatr 2007; 78 (07) 710-715
  • 82 Walther L, Westhofen M. Presbyvertigo-aging of otoconia and vestibular sensory cells. Journal of Vestibular Research 2007; 17 (02) 89-92
  • 83 Warren D, Thurtell M, Carroll J. et al Perimetric Evaluation of Saccadic Latency, Saccadic Accuracy, and Visual Threshold for Peripheral Visual Stimuli in Young Compared With Older Adults Perimetric Evaluation Using Saccadic Eye Movements. Invest Ophthalmol Vis Sci 2013; 54 (08) 5778-5787
  • 84 Welgampola M, Colebatch J. Vestibulocollic reflexes: Normal values and the effect of age. Clin Neurophysiol 2001; 112 (11) 1971-1979
  • 85 Whitney S, Wrisley D, Marchetti G. et al The effect of age on vestibular rehabilitation outcomes. Laryngoscope 2001; 112 (10) 1785-1790
  • 86 Wrisley D, Kumar N. Functional gait assessment: Concurrent, discriminative, and predictive validity in community-dwelling older adults. Phys Ther 2010; 90 (05) 761-773
  • 87 Xie Y, Bigelow R, Frankenthaler S. et al Vestibular Loss in Older Adults is Associated with Impaired Spatial Navigation: Data from the Triangle Completion Task. Front Neurol 2017; 8: 173
  • 88 Xie J, Liu E, Anson E. et al Age-Related Imbalance Is Associated With Slower Walking Speed: An Analysis From the National Health and Nutrition Examination Survey. J Geriatr Phys Ther 2016 Jun 23; epub
  • 89 Yardley L, Donovan-Hall M, Smith H. et al Effectiveness of primary carebased vestibular rehabilitation for chronic dizziness. Ann Intern Med 2004; 141 (08) 598-605
  • 90 You S. Joint position sense in elderly fallers: A preliminary investigation of the validity and reliability of the SENSERite measure. Arch Phys Med Rehabil 2005; 86 (02) 346-352