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关于H1抗组胺药地氯雷他定的性能与嗜睡情况的研究。

Studies on performance and sleepiness with the H1-antihistamine, desloratadine.

作者信息

Nicholson Anthony N, Handford Alison D F, Turner Claire, Stone Barbara M

机构信息

QinetiQ Ltd., Centre for Human Sciences, Farnborough, Hants., United Kingdom.

出版信息

Aviat Space Environ Med. 2003 Aug;74(8):809-15.

Abstract

INTRODUCTION

The purpose of this study was to establish whether the H1-antihistamine desloratadine (5 mg), the active metabolite of loratadine, is free of effects on performance and sleepiness.

METHOD

Effects of desloratadine (5 mg) on psychomotor performance, daytime sleep latencies, subjective sleepiness, and memory were studied in nine healthy volunteers (four men, five women) between the ages of 20 and 39 yr (mean 28.2). Assessments were made 1.0 h pre-ingestion and from 0.5 to 8.0 h post-ingestion. The study was placebo-controlled and double blind with a crossover design, using promethazine (25 mg) as an active control.

RESULTS

Promethazine impaired tracking (3.5-5.5 h), choice reaction time (3.5-5.5 h), digit symbol substitution (3.5-5.5 h), and attention (2.0-5.5 h). There was increased objective and subjective sleepiness (2.0-5.5 h) and subjective fatigue (3.5-8.0 h). There were no changes in any of these measures with desloratadine (5 mg). With promethazine, memory was impaired from 2.0-5.0 h. Analysis failed to establish a consistent effect on memory with desloratadine, as there was a change in only one (digit memory recall reaction time) of the twelve memory test measures at only one time point (5.5 h). The change was significant with respect to placebo, but not with respect to the pre-ingestion value.

CONCLUSIONS

Desloratadine (5 mg) appears to be free of adverse effects on psychomotor performance, daytime sleep latencies, and subjective sleepiness, and could prove suitable for those involved in skilled activity and transportation.

摘要

引言

本研究旨在确定氯雷他定的活性代谢物H1抗组胺药地氯雷他定(5毫克)是否对行为能力和嗜睡没有影响。

方法

在9名年龄在20至39岁(平均28.2岁)的健康志愿者(4名男性,5名女性)中研究了地氯雷他定(5毫克)对精神运动行为能力、白天入睡潜伏期、主观嗜睡和记忆力的影响。在摄入药物前1.0小时以及摄入后0.5至8.0小时进行评估。该研究采用安慰剂对照、双盲交叉设计,使用异丙嗪(25毫克)作为阳性对照。

结果

异丙嗪损害了跟踪能力(3.5 - 5.5小时)、选择反应时间(3.5 - 5.5小时)、数字符号替换能力(3.5 - 5.5小时)和注意力(2.0 - 5.5小时)。客观和主观嗜睡(2.0 - 5.5小时)以及主观疲劳(3.5 - 8.0小时)均增加。地氯雷他定(5毫克)对这些指标均无影响。使用异丙嗪时,记忆力在2.0 - 5.0小时受到损害。分析未能确定地氯雷他定对记忆力有一致的影响,因为在12项记忆测试指标中,只有一项(数字记忆回忆反应时间)在唯一一个时间点(5.5小时)发生了变化。该变化相对于安慰剂有显著差异,但相对于摄入药物前的值无显著差异。

结论

地氯雷他定(5毫克)似乎对精神运动行为能力、白天入睡潜伏期和主观嗜睡没有不良影响,可能适用于从事需要技能的活动和交通运输的人员。

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