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Vestibular suppressants after canalith repositioning in benign paroxysmal positional vertigo

机译:良性阵发性位置性眩晕中小管复位后的前庭抑制剂

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Objectives/Hypothesis: To investigate the characteristics of residual symptoms and to evaluate the effects of adjuvant vestibular suppressants on residual symptoms after successful canalith repositioning procedures (CRPs). Study Design: Individual randomized controlled trial. Methods: One hundred fifty patients with idiopathic benign paroxysmal positional vertigo who achieved successful CRPs on initial visit participated in this study. Dizziness Handicap Inventory (DHI) questionnaires were completed before CRPs. All study populations were divided into three groups after successful CRPs on the initial visit day: the medication (V) group (treated with a vestibular suppressant [dimenhydrinate 50 mg per day]), the placebo (P) group, and the no medication (N) group. One week after successful CRPs, residual symptoms were checked and repeated DHI questionnaires were completed to compare residual symptoms. Results: Among the 138 patients who did not show positional nystagmus at follow-up, 67 (48.5%) complained of residual symptoms. The presence of residual symptoms was more prevalent in the P and N group compared with the V group (P = .035, P = .017, respectively). The most frequent residual symptom was lightheadedness (n = 42). Moreover, in the V group, lightheadedness was significantly reduced compared with the P group (P = .029). However, in the analysis of DHI, total and subscale scores did not differ across the three groups before or after successful CRP. Conclusions: Vestibular suppressants significantly reduced residual symptoms compared to both placebo and no medication after CRP. However, there was no significant reduction in DHI score compared with the control group, suggesting that the residual symptoms could not be evaluated by DHI score alone.
机译:目的/假设:为了研究残留症状的特征,并评估成功的小管再定位手术(CRP)后,前庭抑制剂对残留症状的影响。研究设计:个体随机对照试验。方法:150名特发性良性阵发性位置性眩晕患者在初次就诊时获得了成功的CRP,参加了这项研究。在进行CRP之前已完成了头晕障碍清单(DHI)问卷。在首次就诊当天成功进行CRP后,将所有研究人群分为三组:药物治疗(V)组(用前庭抑制剂[苯海莫明50毫克/天]治疗),安慰剂(P)组和无药物治疗( N)组。成功的CRP后一周,检查残留症状并完成重复的DHI问卷以比较残留症状。结果:138例随访中未显示位置性眼球震颤的患者中,有67例(48.5%)抱怨残留症状。与V组相比,P组和N组中残留症状的存在更为普遍(分别为P = .035,P = .017)。最常见的残留症状是头晕(n = 42)。此外,与P组相比,V组的头晕明显减少(P = .029)。然而,在DHI的分析中,成功进行CRP前后,三组的总分和分量表得分没有差异。结论:与安慰剂相比,CRP后无药物治疗,前庭抑制剂可显着减少残留症状。然而,与对照组相比,DHI评分没有显着降低,这表明不能仅通过DHI评分来评估残留症状。

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