Literature DB >> 15880943

Effect of click duration on vestibular-evoked myogenic potentials.

Tsung-Wei Huang1, Hsuan-Chao Su, Po-Wen Cheng.   

Abstract

CONCLUSIONS: The 0.5-VEMP demonstrated a more prominent waveform morphology than either the 0.1- or 0.2-VEMPs. In addition, the 0.5-VEMP had smaller interaural latency differences than the 1.0-VEMP. These findings suggest that 0.5 ms is superior to other click durations in terms of yielding VEMP responses for clinical use.
OBJECTIVE: In order to establish the ideal stimulus condition for vestibular-evoked myogenic potentials (VEMPs), we studied the use of various click durations to generate different response patterns in normal subjects. The influence of click durations on VEMPs is described and the optimal stimulation duration for clinical use is suggested.
MATERIAL AND METHODS: This was a prospective study. Eighteen healthy volunteers (36 ears) underwent VEMP tests. Four click durations (0.1, 0.2, 0.5 and 1.0 ms) were used in a random order to elicit VEMP responses (0.1-, 0.2-, 0.5- and 1.0-VEMP, respectively). The latency of each peak (p13, n23), the peak-to-peak interval and amplitude (p 13-n23) and the relative amplitude (defined as the amplitude divided by that of the 0.5-VEMP) were measured and compared.
RESULTS: Click stimulation of 34 ears (94%) produced 0.1-VEMP responses, whereas positive 0.2-, 0.5- and 1.0-VEMP responses were observed in 36 (100%). The latencies of peaks p13 and n23 were significantly prolonged between successive stimulus durations from 0.1 to 1.0 ms (p <0.05), in contrast to the p13-n23 intervals (p >0.05). The 1.0-VEMP displayed the largest SDs of latencies and interval among the four different VEMPs. The relative amplitude was significantly increased between successive durations from 0.1 to 0.5 ms (alphaT <0.05), but there was no significant difference between 0.5 and 1.0 ms (alphaT >0.05).

Entities:  

Mesh:

Year:  2005        PMID: 15880943     DOI: 10.1080/00016480410016900

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  8 in total

1.  Band limited chirp stimulation in vestibular evoked myogenic potentials.

Authors:  Leif Erik Walther; Mario Cebulla
Journal:  Eur Arch Otorhinolaryngol       Date:  2016-01-12       Impact factor: 2.503

2.  Big Stimulus, Little Ears: Safety in Administering Vestibular-Evoked Myogenic Potentials in Children.

Authors:  Megan L A Thomas; Denis Fitzpatrick; Ryan McCreery; Kristen L Janky
Journal:  J Am Acad Audiol       Date:  2017-05       Impact factor: 1.664

3.  Input-output functions of vestibular afferent responses to air-conducted clicks in rats.

Authors:  Hong Zhu; Xuehui Tang; Wei Wei; Adel Maklad; William Mustain; Richard Rabbitt; Steve Highstein; Jerome Allison; Wu Zhou
Journal:  J Assoc Res Otolaryngol       Date:  2013-12-03

4.  Vestibular evoked myogenic potential (VEMP) testing: normative threshold response curves and effects of age.

Authors:  Kristen L Janky; Neil Shepard
Journal:  J Am Acad Audiol       Date:  2009-09       Impact factor: 1.664

5.  The impact of stimulation rates in vestibular evoked myogenic potential testing.

Authors:  Aline Tenório Lins Carnaúba; Otávio Gomes Lins; Ilka do Amaral Soares; Kelly Cristina Lira de Andrade; Pedro de Lemos Menezes
Journal:  Braz J Otorhinolaryngol       Date:  2013 Sep-Oct

6.  Vestibular evoked myogenic potentials using low frequency stimuli.

Authors:  Aline Cabral de Oliveira; José Fernando Colafêmina; Pedro de Lemos Menezes
Journal:  Braz J Otorhinolaryngol       Date:  2011 Nov-Dec

7.  Reproducibility (test-retest) of vestibular evoked myogenic potential.

Authors:  Aline Cabral de Oliveira; Pedro de Lemos Menezes; Liliane Desgualdo Pereira
Journal:  Braz J Otorhinolaryngol       Date:  2014-08-28

Review 8.  Vestibular evoked myogenic potential: recording methods in humans and guinea pigs.

Authors:  Aline Cabral de Oliveira; Ricardo David; José Fernando Colafêmina
Journal:  Braz J Otorhinolaryngol       Date:  2008 Sep-Oct
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.