TY - JOUR
T1 - Vestibular evoked myogenic potentials and motion sickness medications
AU - Tal, Dror
AU - Shemy, Shir
AU - Kaminski-Graif, Gil
AU - Wiener, Guy
AU - Hershkovitz, Dov
N1 - Publisher Copyright:
© 2016 International Federation of Clinical Neurophysiology.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Objective: Seasickness is a widespread problem among naval crew, and has a major impact on their performance at sea. The three pharmacological agents most commonly employed in the treatment of seasickness are dimenhydrinate, cinnarizine, and scopolamine. At present, the effectiveness of anti-seasickness drugs is tested by a process of "trial and error", while sailing and exposed to sea conditions. A physiological test to evaluate the action of a drug might save crew members long periods of suffering, as well as simplifying the procedure of selecting the appropriate treatment for each individual. The cervical vestibular evoked myogenic potentials (cVEMP) test has come to be recognized as a reliable procedure for the objective evaluation of saccular function. It was the hypothesis of the present study that cVEMP otolith responses may be affected by anti-motion sickness drugs, which might thus make cVEMP a useful clinical neurophysiological tool for the assessment of drug absorption and efficacy. Methods: Thirty male sailors who regularly took medication for the treatment of seasickness participated in the study. Participants underwent the cVEMP test pre- and 1 h post-drug administration. Results: A statistically significant decrease in p13 latency was found after administration of scopolamine compared with baseline (14.46 ms vs. 15.09 ms, p = 0.0049), with significant prolongation of the binaural average inter-latency in this group. No differences were found in the dimenhydrinate and cinnarizine study groups. Conclusions: This study demonstrated that scopolamine absorption can be verified by changes in cVEMP latencies. Significance: The potential of the cVEMP test for predicting action of scopolamine on the vestibular system.
AB - Objective: Seasickness is a widespread problem among naval crew, and has a major impact on their performance at sea. The three pharmacological agents most commonly employed in the treatment of seasickness are dimenhydrinate, cinnarizine, and scopolamine. At present, the effectiveness of anti-seasickness drugs is tested by a process of "trial and error", while sailing and exposed to sea conditions. A physiological test to evaluate the action of a drug might save crew members long periods of suffering, as well as simplifying the procedure of selecting the appropriate treatment for each individual. The cervical vestibular evoked myogenic potentials (cVEMP) test has come to be recognized as a reliable procedure for the objective evaluation of saccular function. It was the hypothesis of the present study that cVEMP otolith responses may be affected by anti-motion sickness drugs, which might thus make cVEMP a useful clinical neurophysiological tool for the assessment of drug absorption and efficacy. Methods: Thirty male sailors who regularly took medication for the treatment of seasickness participated in the study. Participants underwent the cVEMP test pre- and 1 h post-drug administration. Results: A statistically significant decrease in p13 latency was found after administration of scopolamine compared with baseline (14.46 ms vs. 15.09 ms, p = 0.0049), with significant prolongation of the binaural average inter-latency in this group. No differences were found in the dimenhydrinate and cinnarizine study groups. Conclusions: This study demonstrated that scopolamine absorption can be verified by changes in cVEMP latencies. Significance: The potential of the cVEMP test for predicting action of scopolamine on the vestibular system.
KW - Cinnarizine
KW - Dimenhydrinate
KW - Motion sickness
KW - Scopolamine
KW - Seasickness
KW - Vestibular evoked myogenic potentials
UR - http://www.scopus.com/inward/record.url?scp=84963700693&partnerID=8YFLogxK
U2 - 10.1016/j.clinph.2016.03.010
DO - 10.1016/j.clinph.2016.03.010
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C2 - 27178852
AN - SCOPUS:84963700693
SN - 1388-2457
VL - 127
SP - 2350
EP - 2354
JO - Clinical Neurophysiology
JF - Clinical Neurophysiology
IS - 6
ER -