首页> 外文期刊>Supportive care in cancer: official journal of the Multinational Association of Supportive Care in Cancer >The use of fentanyl buccal tablets for breakthrough pain by using doses proportional to opioid basal regimen in a home care setting
【24h】

The use of fentanyl buccal tablets for breakthrough pain by using doses proportional to opioid basal regimen in a home care setting

机译:通过在家庭护理环境中使用与阿片类药物基础疗法成正比的剂量来使用芬太尼颊片治疗突破性疼痛

获取原文
获取原文并翻译 | 示例
           

摘要

The dose of rapid onset opioids to be given for breakthrough cancer pain (BTcP) is controversial. Dose proportional to the basal opioid regimen seem to be safe and effective in hospital units. However, data in other less protected settings, like home care, are lacking. The aim of this open-label study was to assess the efficacy and safety in a group of patients with BTcP followed at home, after giving a dose of fentanyl buccal tablets (FBT) proportional to the opioid basal regimen, skipping the steps for dose titration. Consecutive patients admitted to a home care program presenting BTcP episodes and receiving stable doses of opioids for background pain were selected. Data from four consecutive episodes of BTcP were collected. For each episode, patients were instructed to routinely collect changes in pain intensity and severe adverse effects when pain got severe (T0) and to reassess the same items 15 min after FBT, given as a rescue medication in doses proportional to the daily opioid doses used for background pain (T15). One hundred twenty episodes of BTcP were recorded in 30 patients. One hundred eight episodes were defined as successfully treated, while 12 episodes required a further administration of opioids. Pain intensity significantly decreased at T15 (p < 0.001). In 95.5 and 90.8 % of episodes treated, there was a reduction in pain intensity of more than 33 and 50 %, respectively. No relevant adverse effects were recorded, even in older patients. This study suggests that FBT given in doses proportional to the basal opioid regimen for the management of BTcP is very effective and safe in clinical practice in the home care setting.
机译:对于突破性癌症疼痛(BTcP)给予快速发作的阿片类药物的剂量是有争议的。与基础阿片类药物治疗方案成正比的剂量在医院单位中似乎是安全有效的。但是,缺少其他受保护程度较低的设置(例如家庭护理)中的数据。这项开放标签研究的目的是评估在给予BTcP的一组患者中的疗效和安全性,这些患者在给予与阿片类基础疗法剂量成比例的芬太尼颊片剂(FBT)剂量后,跳过了剂量滴定步骤。选择入院治疗的连续患者,这些患者表现出BTcP发作并因背景疼痛而接受稳定剂量的阿片类药物。收集了来自连续四次BTcP的数据。对于每次发作,患者均被指导定期收集疼痛加重(T0)时疼痛强度的变化和严重不良反应,并在FBT后15分钟重新评估相同的项目,以与每日阿片类药物剂量成比例的剂量作为急救药物给予用于背景疼痛(T15)。在30例患者中记录了120次BTcP发作。定义为成功治疗了一百零八次发作,而需要进一步服用阿片类药物的发作为十二次。 T15时疼痛强度明显降低(p <0.001)。在接受治疗的95.5%和90.8%的发作中,疼痛强度分别降低了33%和50%以上。没有记录到相关的不良反应,即使在老年患者中也是如此。这项研究表明,FBT与BTcP的基本阿片类药物治疗剂量成正比,在家庭护理的临床实践中是非常有效和安全的。

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