首页> 外文期刊>Therapeutic Drug Monitoring >High plasma concentrations of paroxetine impede clinical response in patients with panic disorder.
【24h】

High plasma concentrations of paroxetine impede clinical response in patients with panic disorder.

机译:血浆高浓度的帕罗西汀会阻碍恐慌症患者的临床反应。

获取原文
获取原文并翻译 | 示例
       

摘要

Selective serotonin reuptake inhibitors are thought to interact with serotonergic neurons and be effective for treatment of panic disorder. In the present study, the authors investigated an association between plasma concentrations of paroxetine in patients with panic disorder and clinical response to initial treatment with paroxetine. Subjects were 21 unrelated Japanese patients who fulfilled DSM-IV-TR criteria for a diagnosis of panic disorder (6 males, 15 females, mean age 35.9 +/- 11.3 years). Subjects were administered 10 mg/day of paroxetine for 2 weeks as initial treatment. Improvement of the symptoms of the disorder was assessed with the Panic and Agoraphobia Scale (PAS). In the range of plasma levels >20 ng/mL, none of the subjects showed the reduction ratio in PAS score >0.2. The subjects whose plasma concentrations of paroxetine were less than 20 ng/mL had a significantly higher mean reduction ratio in PAS score than the subjects whose plasma concentrations of paroxetine were >20 ng/mL. Multiple regression analysis showed that the plasma concentration of paroxetine was the only significant factor and accounted for 28.0% of the variability in the reduction ratio of PAS score of the subjects. The final model of correlation was: reduction ratio in PAS score = 0.423 - 0.009 x (plasma concentrations of paroxetine) (R = 0.529, P = 0.014, coefficient of determination (R2) = 0.280). Assuming that the reduction ratio in PAS score was 0.2 in the equation above, plasma concentration of paroxetine is calculated to be about 25 ng/mL, which is suggested to be the upper end of the therapeutic window for the initial phase of the treatment with paroxetine for panic disorder.
机译:选择性5-羟色胺再摄取抑制剂被认为与5-羟色胺能神经元相互作用,并有效治疗恐慌症。在本研究中,作者研究了恐慌症患者血浆帕罗西汀的浓度与对帕罗西汀初始治疗的临床反应之间的关系。受试者为21例不相关的日本患者,这些患者符合DSM-IV-TR诊断恐慌症的标准(男性6例,女性15例,平均年龄35.9 +/- 11.3岁)。作为初始治疗,受试者接受10 mg /天的帕罗西汀治疗2周。使用恐慌和恐惧症量表(PAS)评估疾病症状的改善。在血浆水平> 20 ng / mL的范围内,没有受试者显示出PAS得分的降低率> 0.2。帕罗西汀血浆浓度低于20 ng / mL的受试者的PAS评分平均降低率明显高于帕罗西汀血浆浓度> 20 ng / mL的受试者。多元回归分析表明,帕罗西汀的血浆浓度是唯一的重要因素,占受试者PAS得分降低率变异性的28.0%。最终的相关模型为:PAS分数降低比= 0.423-0.009 x(帕罗西汀的血浆浓度)(R = 0.529,P = 0.014,测定系数(R2)= 0.280)。假设上式中PAS分数的降低率为0.2,则帕罗西汀的血浆浓度经计算约为25 ng / mL,这被认为是帕罗西汀治疗初始阶段治疗窗的上限对于惊恐症。

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