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大剂量皮质类固醇疗法治疗面神经麻痹:一项回顾性研究。

High-Dose Corticosteroid Therapy in Facial Nerve Palsy: A Retrospective Study.

作者信息

Hyakusoku Hiroshi, Katsumata Noriyuki, Nakayama Meijin

机构信息

Otorhinolaryngology, Yokosuka Kyosai Hospital, Yokosuka, JPN.

出版信息

Cureus. 2025 Apr 9;17(4):e81949. doi: 10.7759/cureus.81949. eCollection 2025 Apr.

DOI:10.7759/cureus.81949
PMID:40352019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12063513/
Abstract

Objectives The difference in therapeutic efficacy between an initial dosage of 200 mg and 100 mg prednisolone (PSL) with a taper for Bell's palsy and Ramsay Hunt syndrome was retrospectively investigated. Methods A total of 259 patients (172 with Bell's palsy and 87 with Ramsay Hunt syndrome) were treated with high-dose corticosteroid therapy (HDCT) with PSL (the standard HDCT: 200 mg/day for three days with a seven-day taper, or the reduced HDCT: 100 mg/day for three days with a seven-day taper) and evaluated once a month by the Yanagihara facial nerve grading system until facial nerve paralysis was cured or six months after the onset. Results The therapeutic efficacy of the standard HDCT was not significantly improved, compared to the reduced HDCT, in Bell's palsy and Ramsay Hunt syndrome, and even in less than 20.0% of electroneuronography in Bell's palsy and Ramsay Hunt syndrome. Conclusion HDCT with more than an initial dosage of 100 mg/day PSL with a taper for Bell's palsy and Ramsay Hunt syndrome does not increase the therapeutic efficacy.

摘要

目的 回顾性研究泼尼松龙(PSL)初始剂量200 mg与100 mg减量治疗贝尔面瘫和拉姆齐·亨特综合征的疗效差异。方法 共有259例患者(172例贝尔面瘫患者和87例拉姆齐·亨特综合征患者)接受了PSL大剂量皮质类固醇治疗(HDCT)(标准HDCT:200 mg/天,连用3天,然后7天减量;或减量HDCT:100 mg/天,连用3天,然后7天减量),并每月通过柳原面神经分级系统进行评估,直至面神经麻痹治愈或发病后6个月。结果 在贝尔面瘫和拉姆齐·亨特综合征中,标准HDCT与减量HDCT相比,疗效并未显著提高,在贝尔面瘫和拉姆齐·亨特综合征中,即使在不到20.0%的神经电图检查中也是如此。结论 对于贝尔面瘫和拉姆齐·亨特综合征,初始剂量超过100 mg/天PSL减量的HDCT不会提高治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94d/12063513/1240be808888/cureus-0017-00000081949-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94d/12063513/d43abde83518/cureus-0017-00000081949-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94d/12063513/fec41e241f4b/cureus-0017-00000081949-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94d/12063513/1240be808888/cureus-0017-00000081949-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94d/12063513/d43abde83518/cureus-0017-00000081949-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94d/12063513/fec41e241f4b/cureus-0017-00000081949-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94d/12063513/1240be808888/cureus-0017-00000081949-i03.jpg

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A Retrospective Study on the Gender Differences in Clinical Manifestations of Bell's Palsy.贝尔面瘫临床表现性别差异的回顾性研究
Clin Otolaryngol. 2025 Mar;50(2):307-315. doi: 10.1111/coa.14259. Epub 2024 Nov 21.
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Biomaterial-Based bFGF Delivery for Nerve Repair.基于生物材料的 bFGF 递送来修复神经。
Oxid Med Cell Longev. 2023 Apr 10;2023:8003821. doi: 10.1155/2023/8003821. eCollection 2023.
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Lack of Evidence to Support the Beneficial Role of Intratympanic Dexamethasone Injection in Acute Peripheral Facial Palsy.
缺乏证据支持鼓室内注射地塞米松在急性周围性面瘫中的有益作用。
Otol Neurotol. 2019 Dec;40(10):e1024-e1029. doi: 10.1097/MAO.0000000000001266.
4
Concurrent Treatment With Intratympanic Dexamethasone for Moderate-Severe Through Severe Bell's Palsy.鼓室内地塞米松注射治疗中重度至重度贝尔氏面瘫
Otol Neurotol. 2019 Dec;40(10):e1018-e1023. doi: 10.1097/MAO.0000000000002377.
5
High-dose Corticosteroids for Adult Bell's Palsy: Systematic Review and Meta-analysis.大剂量皮质类固醇治疗成人贝尔氏面瘫:系统评价和荟萃分析。
Otol Neurotol. 2019 Sep;40(8):1101-1108. doi: 10.1097/MAO.0000000000002317.
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The etiology of Bell's palsy: a review.贝尔面瘫的病因:综述
J Neurol. 2020 Jul;267(7):1896-1905. doi: 10.1007/s00415-019-09282-4. Epub 2019 Mar 28.
7
High-dose corticosteroids improve the prognosis of Bell's palsy compared with low-dose corticosteroids: A propensity score analysis.与低剂量皮质类固醇相比,高剂量皮质类固醇可改善贝尔面瘫的预后:一项倾向评分分析。
Auris Nasus Larynx. 2018 Jun;45(3):465-470. doi: 10.1016/j.anl.2017.09.008. Epub 2017 Sep 22.
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Benefits of High-dose Steroid + Hespander + Mannitol Administration in the Treatment of Bell's Palsy.大剂量类固醇+贺斯+甘露醇联合应用治疗贝尔面瘫的益处。
Otol Neurotol. 2017 Feb;38(2):272-277. doi: 10.1097/MAO.0000000000001307.
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Cochrane Database Syst Rev. 2016 Jul 18;7(7):CD001942. doi: 10.1002/14651858.CD001942.pub5.
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