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卡巴拉汀治疗卒中后谵妄的一项初步研究:一种安全的替代方法。

A pilot study of rivastigmine in the treatment of delirium after stroke: a safe alternative.

作者信息

Oldenbeuving Annemarie W, de Kort Paul L M, Jansen Ben P W, Kappelle L Jaap, Roks Gerwin

机构信息

Department of neurology, St Elisabeth Hospital, Tilburg, the Netherlands.

出版信息

BMC Neurol. 2008 Sep 20;8:34. doi: 10.1186/1471-2377-8-34.

Abstract

BACKGROUND

Delirium is a common disorder in the early phase of stroke. Given the presumed cholinergic deficiency in delirium, we tested treatment with the acetylcholinesterase inhibitor rivastigmine.

METHODS

This pilot study was performed within an epidemiological study. In 527 consecutive stroke patients presence of delirium was assessed during the first week with the confusion assessment method. Severity was scored with the delirium rating scale (DRS). Sixty-two patients developed a delirium in the acute phase of stroke. Only patients with a severe and persistent delirium (defined as a DRS of 12 or more for more than 24 hours) were enrolled in the present study. In total 26 fulfilled these criteria of whom 17 were treated with orally administered rivastigmine with a total dose between 3 and 12 mg a day. Eight patients could not be treated because of dysphagia and one because of early discharge.

RESULTS

No major side effects were recorded. In 16 patients there was a considerable decrease in severity of delirium. The mean DRS declined from 14.8 on day one to 8.5 after therapy and 5.6 after tapering. The mean duration of delirium was 6.7 days (range; 2-17).

CONCLUSION

Rivastigmine is safe in stroke patients with delirium even after rapid titration. In the majority of patients the delirium improved after treatment. A randomized controlled trial is needed to establish the usefulness of rivastigmine in delirium after stroke.

TRIAL REGISTRATION

Nederlands Trial Register NTR1395.

摘要

背景

谵妄是卒中早期常见的病症。鉴于谵妄可能存在胆碱能缺乏,我们对乙酰胆碱酯酶抑制剂卡巴拉汀的治疗效果进行了测试。

方法

本初步研究在一项流行病学研究中开展。对527例连续的卒中患者在第一周使用意识模糊评估法评估谵妄的存在情况。用谵妄评定量表(DRS)对严重程度进行评分。62例患者在卒中急性期出现谵妄。本研究仅纳入严重且持续性谵妄(定义为DRS为12分及以上且持续超过24小时)的患者。共有26例符合这些标准,其中17例接受口服卡巴拉汀治疗,总剂量为每日3至12毫克。8例患者因吞咽困难无法接受治疗,1例因过早出院无法接受治疗。

结果

未记录到严重副作用。16例患者谵妄严重程度显著降低。DRS平均分从第1天的14.8降至治疗后的8.5,减药后的5.6。谵妄的平均持续时间为6.7天(范围:2 - 17天)。

结论

卡巴拉汀对伴有谵妄的卒中患者即使在快速滴定后也是安全的。大多数患者治疗后谵妄有所改善。需要进行一项随机对照试验来确定卡巴拉汀在卒中后谵妄中的有效性。

试验注册

荷兰试验注册库NTR1395 。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd76/2556687/2637b8645ada/1471-2377-8-34-1.jpg

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