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老年人良性阵发性位置性眩晕的临床特征

Clinical features of benign paroxysmal positional vertigo in the elderly.

作者信息

Zhou Ran, Wang Huan, Shan Jiachen, Li Chengcheng, Han Lin

机构信息

Department of Anesthesiology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

Department of Neurology, West China School of Public Health and West China Forth Hospital, Sichuan University, Chengdu, China.

出版信息

Front Neurol. 2025 Jun 16;16:1623914. doi: 10.3389/fneur.2025.1623914. eCollection 2025.

DOI:10.3389/fneur.2025.1623914
PMID:40589989
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12206830/
Abstract

OBJECTIVES

The typical age of benign paroxysmal positional vertigo (BPPV) is between 50 and 60 years. With the development of diagnostic techniques and the growth of the elderly, the number of elderly patients has been on the rise gradually. This study compared the clinical characteristics, treatments, and prognoses with patients.

METHODS

Patients were divided into two age groups based on age at onset of the disease: middle-aged BPPV (50-59 years) and elderly BPPV (60-80 years old). We compared clinical characteristics, treatment, prognosis, BPPV location, questionnaires between the two groups.

RESULTS

Female patients constituted a high proportion in both the middle-aged BPPV group (21, 75.0%) and the elderly BPPV group (39, 67.2%). The elderly group had significantly higher median scores in the DHI impact than the middle-aged group (24 vs. 16,  = 0.008). In contrast, the BBS score decreased (44 vs. 49,  = 0.019), and the elderly group exhibited higher fall rates (6.9% vs. 0%,  = 0.381) at the last follow-up. However, the elderly BPPV group had lower rates of maneuver (82.8% vs. 89.3%,  = 0.638). Age at onset was positively correlated with the DHI score (r = 0.316,  = 0.005) and negatively correlated with the BBS score (r = -0.330,  = 0.002).

CONCLUSION

Compared to the middle-aged BPPV group, elderly patients with BPPV exhibited a higher DHI score, increased fall rates, lower BBS scores, and lower rate maneuver, which had a more significant negative impact on daily life.

摘要

目的

良性阵发性位置性眩晕(BPPV)的典型发病年龄在50至60岁之间。随着诊断技术的发展和老年人口的增加,老年患者数量逐渐上升。本研究对患者的临床特征、治疗方法和预后进行了比较。

方法

根据疾病发病年龄将患者分为两个年龄组:中年BPPV组(50 - 59岁)和老年BPPV组(60 - 80岁)。我们比较了两组之间的临床特征、治疗、预后、BPPV定位及问卷调查情况。

结果

中年BPPV组(21例,75.0%)和老年BPPV组(39例,67.2%)中女性患者占比均较高。老年组DHI影响评分中位数显著高于中年组(24对16,P = 0.008)。相比之下,在最后一次随访时,BBS评分降低(44对49,P = 0.019),且老年组跌倒率更高(6.9%对0%,P = 0.381)。然而,老年BPPV组手法复位成功率较低(82.8%对89.3%,P = 0.638)。发病年龄与DHI评分呈正相关(r = 0.316,P = 0.005),与BBS评分呈负相关(r = -0.330,P = 0.002)。

结论

与中年BPPV组相比,老年BPPV患者DHI评分更高、跌倒率增加、BBS评分更低且手法复位成功率更低,对日常生活的负面影响更大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a5a/12206830/6f718d795861/fneur-16-1623914-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a5a/12206830/4e4771663930/fneur-16-1623914-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a5a/12206830/6f718d795861/fneur-16-1623914-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a5a/12206830/4e4771663930/fneur-16-1623914-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a5a/12206830/6f718d795861/fneur-16-1623914-g002.jpg

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本文引用的文献

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Corrigendum: Residual dizziness after BPPV management: exploring pathophysiology and treatment beyond canalith repositioning maneuvers.勘误:良性阵发性位置性眩晕(BPPV)治疗后的残余头晕:探索除耳石复位手法之外的病理生理学及治疗方法
Front Neurol. 2024 Jul 29;15:1461600. doi: 10.3389/fneur.2024.1461600. eCollection 2024.
2
Association between vitamin D deficiency and benign paroxysmal positional vertigo (BPPV) incidence and recurrence: a systematic review and meta-analysis.维生素D缺乏与良性阵发性位置性眩晕(BPPV)的发病率及复发之间的关联:一项系统评价和荟萃分析
BMJ Open. 2024 Apr 22;14(4):e077986. doi: 10.1136/bmjopen-2023-077986.
3
We should be screening for benign paroxysmal positional vertigo (BPPV) in all older adults at risk of falling: a commentary on the World Falls Guidelines.
我们应该对所有有跌倒风险的老年患者进行良性阵发性位置性眩晕(BPPV)筛查:对世界跌倒指南的评论。
Age Ageing. 2023 Nov 2;52(11). doi: 10.1093/ageing/afad206.
4
Geriatric benign paroxysmal positional vertigo: a single-center study.老年良性阵发性位置性眩晕:单中心研究。
Braz J Otorhinolaryngol. 2023 Jul-Aug;89(4):101277. doi: 10.1016/j.bjorl.2023.101277. Epub 2023 Jun 3.
5
Effect of age on treatment outcomes in benign paroxysmal positional vertigo: A systematic review.年龄对良性阵发性位置性眩晕治疗效果的影响:系统评价。
J Am Geriatr Soc. 2022 Jan;70(1):281-293. doi: 10.1111/jgs.17485. Epub 2021 Oct 26.
6
Measuring Vestibular Contributions to Age-Related Balance Impairment: A Review.测量前庭对年龄相关性平衡障碍的影响:综述
Front Neurol. 2021 Feb 9;12:635305. doi: 10.3389/fneur.2021.635305. eCollection 2021.
7
A novel maneuver for diagnosis and treatment of torsional-vertical down beating positioning nystagmus: anterior canal and apogeotropic posterior canal BPPV.一种用于诊断和治疗扭转-垂直向下摆动定位性眼球震颤的新手法:前半规管及向地性后半规管良性阵发性位置性眩晕。
Braz J Otorhinolaryngol. 2022 Sep-Oct;88(5):708-716. doi: 10.1016/j.bjorl.2020.09.009. Epub 2020 Oct 28.
8
Review of the pathology underlying benign paroxysmal positional vertigo.良性阵发性位置性眩晕的病理回顾。
J Int Med Res. 2020 Apr;48(4):300060519892370. doi: 10.1177/0300060519892370. Epub 2019 Dec 29.
9
The Component Structure of the Dizziness Handicap Inventory (DHI): A Reappraisal.眩晕残障程度评定量表(DHI)的构成要素:再评价。
Otol Neurotol. 2019 Oct;40(9):1217-1223. doi: 10.1097/MAO.0000000000002365.
10
Increased risk of benign paroxysmal positional vertigo in osteoporosis: a nationwide population-based cohort study.骨质疏松症患者良性阵发性位置性眩晕风险增加:一项全国基于人群的队列研究。
Sci Rep. 2019 Mar 5;9(1):3469. doi: 10.1038/s41598-019-39830-x.