首页> 外文期刊>Pharmacological research: The official journal of The Italian Pharmacological Society >Trazodone addition for insomnia in venlafaxine-treated, depressed inpatients: a semi-naturalistic study.
【24h】

Trazodone addition for insomnia in venlafaxine-treated, depressed inpatients: a semi-naturalistic study.

机译:服用曲唑酮治疗文拉法辛的抑郁症患者的失眠:一项半自然研究。

获取原文
获取原文并翻译 | 示例
           

摘要

In this paper, we present the results of a prospective semi-naturalistic study of the addition of trazodone for insomnia to a 4 week, 300mg/day venlafaxine treatment in 50 depressed inpatients. The Montgomery and Asberg depression rating scale was used as a rating instrument. The study is designated as semi-naturalistic due to the fact that, although the venlafaxine treatment regimen was strictly defined, the timing of the trazodone introduction and the dosage were determined by the clinicians. The indication was based on the persistency of insomnia despite the use of authorized sedative co-medication (zopiclone as a hypnotic, clorazepate as an anxiolytic). Among the 42 patients who completed the study, 27 did not receive trazodone (G1) while 15 did (G2). Although the two groups were not clinically different at study entry, G2 patients showed less improvement than G1 patients during venlafaxine treatment alone, both in terms of insomnia (MADRS item 4) and inner tension (MADRS item 3). After trazodone introduction, insomnia improved and the median (interquartile range) of this item in G1 and G2 patients showed no statistically significant difference on Day 28 (G1:0 (0-1); G2:0 (0-2)). However, inner tension did not improve and the median (interquartile range) was higher on Day 28 in G2 patients (G1: 1 (0-2); G2: 2(1-4); P < 0.05). Thus, trazodone is probably used for patients who develop not only insomnia, but also inner tension/anxiety during venlafaxine treatment. However, it alleviates only the first symptom, not the second.
机译:在本文中,我们提供了一项前瞻性半自然研究的结果,该研究在50名抑郁症患者中于4周内以300mg /天的文拉法辛治疗失眠,加入曲唑酮治疗失眠。蒙哥马利和阿斯伯格抑郁量表用作评分工具。由于严格定义了文拉法辛治疗方案,但曲唑酮的导入时间和剂量由临床医生决定,因此该研究被指定为半自然疗法。尽管使用了授权的镇静性联合用药(佐匹克隆作为催眠药,氯硝西ate作为抗焦虑药),但适应症仍基于失眠的持续性。在完成研究的42位患者中,有27位没有接受曲唑酮(G1),有15位没有接受(G2)。尽管两组在入学时临床上均无差异,但就失眠(MADRS第4项)和内在张力(MADRS第3项)而言,仅在文拉法辛治疗期间,G2组患者的症状改善不及G1组。引入曲唑酮后,失眠得到改善,G1和G2患者中该项目的中位数(四分位间距)在第28天显示无统计学显着差异(G1:0(0-1); G2:0(0-2))。然而,G2患者在第28天的内在紧张并没有改善,中位值(四分位间距)更高(G1:1(0-2); G2:2(1-4); P <0.05)。因此,曲唑酮可能不仅用于在文拉法辛治疗期间出现失眠而且还会产生内在紧张/焦虑的患者。但是,它只能缓解第一种症状,而不能缓解第二种症状。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号