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Optimal reassessment time for treatment response in posterior canal benign paroxysmal positional vertigo

Authors
Song, Mee HyunKong, Tae HoonShim, Dae Bo
Issue Date
Feb-2020
Publisher
WILEY
Keywords
Benign paroxysmal positional vertigo; reassessment; treatment; Epley maneuver
Citation
LARYNGOSCOPE, v.130, no.2, pp.496 - 499
Indexed
SCIE
SCOPUS
Journal Title
LARYNGOSCOPE
Volume
130
Number
2
Start Page
496
End Page
499
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/146199
DOI
10.1002/lary.28005
ISSN
0023-852X
Abstract
Objectives/Hypothesis The present study aimed to evaluate the optimal reassessment time for treatment response in posterior canal benign paroxysmal positional vertigo (PC-BPPV) following the initial Epley maneuver. Study Design Prospective, single-blinded, randomized study. Methods One hundred eight patients with PC-BPPV agreed to participate. These patients received a single modified Epley maneuver (recommended by the 2008 American Academy of Otolaryngology–Head and Neck Surgery guidelines) daily until positional nystagmus disappeared during the Dix-Hallpike maneuver 24 hours after the treatment. Repeated Dix-Hallpike testing to reassess the treatment response was performed at 1 hour (post-1 hour), every 24 hours (post-24 hours) until the positional nystagmus resolved, 1 week (post-1 week), and 1 month (post-1 month) following the therapeutic maneuver. The difference in the resolution rates at post-1 hour and post-24 hours reassessment was analyzed, and the recurrence rates at post-1 week and post-1 month were evaluated. Results The resolution rate was 67.6% at post-1 hour, which increased to 79.6% at post-24 hours reassessment. There was a statistically significant difference in the results of the Dix-Hallpike test between post-1 hour and post-24 hours follow-up. After complete resolution, nine out of 108 patients (8.3%) demonstrated recurrence within 1 month. Conclusions Reassessment after 24 hours following the initial Epley maneuver is more advantageous than a 1-hour follow-up in patients with PC-BPPV. This information may be helpful for clinicians in deciding the appropriate follow-up period after treatment for PC-BPPV. Level of Evidence 1b Laryngoscope, 130:496–499, 2020
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