首页> 美国卫生研究院文献>Journal of the Canadian Association of Gastroenterology >A157 THE THRESHOLD FOR INFLIXIMAB TROUGH LEVELS LEADING TO DOSE ESCALATION DIFFERS BETWEEN CROHN’S DISEASE AND ULCERATIVE COLITIS
【2h】

A157 THE THRESHOLD FOR INFLIXIMAB TROUGH LEVELS LEADING TO DOSE ESCALATION DIFFERS BETWEEN CROHN’S DISEASE AND ULCERATIVE COLITIS

机译:A157克罗恩昔单抗水平上升的阈值导致克罗恩病和溃疡性结肠炎的剂量增加

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BackgroundTherapeutic drug monitoring (TDM) of infliximab (IFX) provides an objective measure that allows physicians to optimize the dose for patients on biologic therapies and potentially reduce loss of response (LOR). The currently accepted therapeutic range is 3 – 7 μg/mL. With the potential for LOR with low drug levels and the high cost of IFX, it is important to manage medications efficiently. To better understand how physicians at the University of Alberta Hospital are using TDM, we conducted a retrospective chart review to see the clinical decisions made in response to TDM. Major clinical decisions include: no change, dose escalate (increase in dose or shorten interval), reload (2 extra doses 2 weeks apart), or dose de-escalate (decrease in dose or lengthen interval).
机译:背景英夫利昔单抗(IFX)的治疗性药物监测(TDM)提供了一种客观的措施,使医生可以优化采用生物疗法治疗的患者的剂量,并有可能减少反应丧失(LOR)。目前公认的治疗范围是3 – 7μg/ mL。由于低药物水平和IFX成本高的LOR潜力,有效管理药物非常重要。为了更好地了解艾伯塔大学医院的医生如何使用TDM,我们进行了回顾性图表审查,以查看针对TDM做出的临床决策。主要的临床决策包括:无变化,剂量递增(增加剂量或缩短间隔),重载(2个额外的剂量,间隔2周)或剂量降低(剂量减少或延长间隔)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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