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四苯嗪成功用于一名中风后顽固性呃逆患者。

Successful use of tetrabenazine in a patient with intractable hiccups after stroke.

作者信息

Naro Antonino, Bramanti Placido, Calabrò Rocco Salvatore

机构信息

IRCCS Centro Neurolesi "Bonino-Pulejo", Messina, Italy.

出版信息

Pharmacotherapy. 2014 Dec;34(12):e345-8. doi: 10.1002/phar.1523. Epub 2014 Dec 4.

Abstract

A hiccup is a myoclonic jerk of the diaphragm, and cases of hiccups may last for more than 48 hours (persistent hiccups) or even more than 2 months (intractable hiccups). Current pharmacologic treatment of persistent or intractable hiccups mainly includes antidopaminergic drugs. We describe the case of a 60-year-old man with a recent diagnosis of right insular ischemic stroke who presented with frequent, intense, and disabling hiccups for more than 1 month. As diagnosis of poststroke hiccups was assumed, the patient was treated over the next 6 months with adequate doses of various antipsychotic drugs commonly used for the treatment of hiccups; however, all were discontinued because of adverse effects. Indeed, dyskinesia after chlorpromazine (up to 75 mg/day for 4 wks), as well as somnolence and dyskinesia after haloperidol (up to 6 mg/day for 6 wks), somnolence after gabapentin (up to 1800 mg/day for 8 wks), and severe somnolence and hypotension after baclofen (up to 50 mg/day for 6 wks) were reported. The patient was then prescribed tetrabenazine at a starting dose of 12.5 mg twice/day (25 mg/day), with a nearly complete remission of the hiccup symptomatology after ~6 weeks, when a daily dose of 150 mg was reached. We therefore hypothesize that a supratentorial lesion may disrupt the modulation of dopaminergic pathways involved in the regulation of medullar centers responsible for the hiccup reflex. To our knowledge, this is the first case report of poststroke hiccups responding to tetrabenazine. The dramatic response of our patient to tetrabenazine monotherapy suggests that this drug may be a valuable pharmacologic alternative for patients with hiccups after stroke who are intolerant or unresponsive to classic antipsychotic agents.

摘要

呃逆是膈肌的肌阵挛性抽搐,呃逆病例可能持续超过48小时(持续性呃逆),甚至超过2个月(顽固性呃逆)。目前,持续性或顽固性呃逆的药物治疗主要包括抗多巴胺能药物。我们报告一例60岁男性患者,近期诊断为右侧岛叶缺血性卒中,出现频繁、剧烈且致残的呃逆超过1个月。由于假定为卒中后呃逆,该患者在接下来的6个月中接受了常用的各种抗精神病药物的足量治疗;然而,由于不良反应,所有药物均停药。事实上,有报告称,服用氯丙嗪(最高75mg/天,持续4周)后出现运动障碍,服用氟哌啶醇(最高6mg/天,持续6周)后出现嗜睡和运动障碍,服用加巴喷丁(最高1800mg/天,持续8周)后出现嗜睡,服用巴氯芬(最高50mg/天,持续6周)后出现严重嗜睡和低血压。随后该患者开始服用丁苯那嗪,起始剂量为12.5mg,每日两次(25mg/天),当每日剂量达到150mg时约6周后,呃逆症状几乎完全缓解。因此,我们推测幕上病变可能会破坏参与调节负责呃逆反射的延髓中枢的多巴胺能通路的调节。据我们所知,这是首例对丁苯那嗪有反应的卒中后呃逆病例报告。我们的患者对丁苯那嗪单一疗法的显著反应表明,对于对经典抗精神病药物不耐受或无反应性的卒中后呃逆患者而言, 这种药物可能是一种有价值的药物选择。

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