Feil K, Böttcher N, Kremmyda O, Muth C, Teufel J, Zwergal A, Brandt T, Strupp M
Neurologische Klinik und Deutsches Zentrum für Schwindel- und Gleichgewichtsstörungen, Klinikum der Universität München.
Deutsches Zentrum für Schwindel- und Gleichgewichtsstörungen, Klinikum der Universität München.
Fortschr Neurol Psychiatr. 2015 Sep;83(9):490-8. doi: 10.1055/s-0035-1553667. Epub 2015 Sep 30.
There are currently different groups of drugs for the pharmacotherapy of vertigo, nystagmus and cerebellar disorders: antiemetics; anti-inflammatories, antimenieres, and antimigraineous medications and antidepressants, anticonvulsants, aminopyridines as well as acetyl-DL-leucine. In acute unilateral vestibulopathy, corticosteroids improve the recovery of peripheral vestibular function, but currently there is not sufficient evidence for a general recommendation. There is insufficient evidence to support the view that 16 mg t. i. d. or 48 mg t. i. d. betahistine has an effect in Menière's disease. Therefore, higher dosages are recommended. In animal studies, it was shown that betahistine increases cochlear blood flow. In vestibular paroxysmia, oxcarbazepine was effective (one randomized controlled trial (RCT)). Aminopyridines are recommended for the treatment of downbeat nystagmus (two RCTs) and episodic ataxia type 2 (EA2, one RCT). There has been no RCT on the efficacy of beta-blockers or topiramate but one RCT on flunarizine in vestibular migraine. Based on clinical experience, a treatment analogous to that for migraine without aura can be recommended. Acetyl-DL-leucine improved cerebellar ataxia (two observational studies); it also accelerated central compensation in an animal model of acute unilateral lesion, but RCTs were negative. There are ongoing RCTs on treatment of vestibular paroxysmia with carbamazepine (VESPA), acute unilateral vestibulopathy with betahistine (BETAVEST), vestibular migraine with metoprolol (PROVEMIG), benign paroxysmal positional vertigo with vitamin D (VitD@BPPV), EA2 with 4-aminopyridine versus acetazolamide (EAT-2-TREAT), and cerebellar ataxias with acetyl-DL-leucine (ALCAT).
目前有不同类别的药物用于眩晕、眼球震颤和小脑疾病的药物治疗:止吐药;抗炎药、抗梅尼埃病药、抗偏头痛药以及抗抑郁药、抗惊厥药、氨基吡啶类药物和乙酰 - DL - 亮氨酸。在急性单侧前庭病中,皮质类固醇可改善外周前庭功能的恢复,但目前尚无足够证据支持普遍推荐使用。没有足够证据支持认为每日三次服用16毫克或48毫克倍他司汀对梅尼埃病有疗效的观点。因此,建议使用更高剂量。在动物研究中,已表明倍他司汀可增加耳蜗血流量。在前庭阵发性眩晕中,奥卡西平有效(一项随机对照试验(RCT))。氨基吡啶类药物推荐用于治疗下跳性眼球震颤(两项RCT)和发作性共济失调2型(EA2,一项RCT)。尚无关于β受体阻滞剂或托吡酯疗效的RCT,但有一项关于氟桂利嗪治疗前庭性偏头痛的RCT。基于临床经验,可推荐采用类似于无先兆偏头痛的治疗方法。乙酰 - DL - 亮氨酸改善了小脑共济失调(两项观察性研究);在急性单侧病变的动物模型中,它还加速了中枢代偿,但RCT结果为阴性。目前正在进行关于卡马西平治疗前庭阵发性眩晕(VESPA)、倍他司汀治疗急性单侧前庭病(BETAVEST)、美托洛尔治疗前庭性偏头痛(PROVEMIG)、维生素D治疗良性阵发性位置性眩晕(VitD@BPPV)、4 - 氨基吡啶与乙酰唑胺治疗EA2(EAT - 2 - TREAT)以及乙酰 - DL - 亮氨酸治疗小脑共济失调(ALCAT)的RCT。