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用5-羟色胺2拮抗剂利坦色林治疗抗精神病药所致静坐不能。

Treatment of neuroleptic induced akathisia with the 5-HT2 antagonist ritanserin.

作者信息

Miller C H, Fleischhacker W W, Ehrmann H, Kane J M

机构信息

Department of Psychiatry, Innsbruck University Hospital, Austria.

出版信息

Psychopharmacol Bull. 1990;26(3):373-6.

PMID:1980375
Abstract

Akathisia is a frequent and distressing side effect of antipsychotic medication. Little is known about its pathophysiology. Treatment trials of serotonin antagonists in Parkinson's disease and neuroleptic-induced Parkinsonism have been disappointing, with the possible exception of akathisia which has been reported to respond favorably to ritanserin. We report first results of a single-blind trial of ritanserin in the treatment of neuroleptic-induced akathisia. Ten patients received a mean dose of 13.5 mg/day (SD +/- 5.8) ritanserin for 2 to 4 days. Treatment response was assessed by the Hillside Akathisia Scale (HAS). HAS baseline ratings were 16.4 (+/- 6). After 3 days of treatment, these values dropped to 7.4 (+/- 5.2). This amelioration was statistically significant (p = .0069 matched-pairs signed rank test). Two patients did not respond. These results, although preliminary in nature, are encouraging and warrant further studies.

摘要

静坐不能是抗精神病药物常见且令人苦恼的副作用。关于其病理生理学知之甚少。血清素拮抗剂在帕金森病和抗精神病药物所致帕金森综合征中的治疗试验令人失望,但静坐不能可能是个例外,有报道称ritanserin对其治疗有效。我们报告了ritanserin治疗抗精神病药物所致静坐不能单盲试验的初步结果。10名患者接受了平均剂量为13.5毫克/天(标准差±5.8)的ritanserin治疗2至4天。通过山坡静坐不能量表(HAS)评估治疗反应。HAS基线评分为16.4(±6)。治疗3天后,这些值降至7.4(±5.2)。这种改善具有统计学意义(p = 0.0069,配对符号秩检验)。两名患者无反应。这些结果虽然本质上是初步的,但令人鼓舞,值得进一步研究。

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