Abstract
Objective
The purpose of this study was to assess residual dizziness (RD) after successful canalith repositioning maneuvre (CRM) treatment in patients with benign paroxysmal positional vertigo (BPPV) using Dizziness Handicap Inventory (DHI) questionnaire and Visual Analog Scale (VAS).
Methods
One hundred sixty BPPV patients after successful CRM treatment were recruited. All patients were divided into the residual dizziness (RD) group and without RD group. The DHI questionnaire and VAS before CRM and follow-up were asked to complete. For analysis of the improvement in symptom, we defined ∆DHI and ∆VAS as the difference between the baseline score and the follow‐up score.
Results
High incidence of RD was observed in the older patients (p < 0.001). The incidence of hypertension in the RD group was also significantly higher than that of the without RD group (p = 0.022). The ∆DHI-P, ∆DHI-E, ∆DHI-F, ∆DHI-T, and ∆VAS scores in the without RD group were significantly higher than that of the RD group (p < 0.001). When the cutoff point of the ∆DHI total scores was 17, the sensitivity was 64.86% and the specificity was 73.26% for diagnosing RD. When the cutoff point of the ∆VAS scores was 2.5, the sensitivity was 77.03% and the specificity was 81.40% for diagnosing RD.
Conclusions
RD is prone to occur in the older patients and ∆VAS exhibits higher sensitivity and specificity in assessing RD.
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Funding
This study was supported by the Key R&D Program of Shaanxi Province (No. 2022SF-283) and the National Key R&D Program of China (No. 2018YFC2000300).
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WF conception and design of the study, data acquisition and analysis, drafting the article, critical revision, and final approval of the manuscript. FH conception and design of the study, data acquisition and analysis, drafting the article, critical revision, and final approval of the manuscript. YB contribution to the study design, drafting the article, critical revision, and final approval of the manuscript. YW contribution to the study design, critical revision, and final approval of the manuscript. DW contribution to the study design, critical revision, and final approval of the manuscript. YS data acquisition, critical revision, and final approval of the manuscript. XA data acquisition, critical revision, and final approval of the manuscript. JH contribution to the study design, critical revision, and final approval of the manuscript. XW Conception and design of the study, evaluation of patients, critical revision, and final approval of the manuscript.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. The study was approved by institutional Review Board of Xijing Hospital, Air Force Medical University.
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Fu, W., He, F., Bai, Y. et al. Assessment of residual dizziness after successful canalith repositioning maneuvre in benign paroxysmal positional vertigo patients: a questionnaire-based study. Eur Arch Otorhinolaryngol 280, 137–141 (2023). https://doi.org/10.1007/s00405-022-07474-9
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DOI: https://doi.org/10.1007/s00405-022-07474-9