慢性疼痛的门诊交叉定位到布普伦诺芬:一个回顾性分析
Satoru Ito1, Mackenzie Welsh1, Christina Bockman1
1Department of Pharmacy Services, University of Washington Medicine, Seattle, Washington.
Journal of opioid management
|January 8, 2024
概括
华盛顿大学 华盛顿大学
科学领域:
- 疼痛管理 疼痛管理
- 药理学 药理学是指药理学的学科.
- 临床医学 临床医学
背景情况:
- 慢性疼痛管理通常涉及完全的μ-阿片类药物激动剂.
- 将患者转换为布普伦诺芬的患者提供了具有不同安全性配置的替代方案.
- 为了安全有效的布普伦诺芬交叉定位,需要标准化的协议.
研究的目的:
- 评估华盛顿大学布普伦诺啡交叉定位协议的有效性和安全性.
- 评估患者在从完整的μ-阿片类药物激动剂过渡到布普伦诺芬治疗慢性疼痛期间在门诊环境中获得的结果.
主要方法:
- 对150名从全μ-阿片类药物激动剂转换为布普伦诺芬的患者的回顾性图表审查.
- 使用了华盛顿大学医学中心疼痛诊所的交叉标配协议.
- 评估了4周成功转换的初级结果和包括不良事件和剂量要求在内的二次结果.
主要成果:
- 大约48.4%的患者成功完成了对布普伦诺芬的交叉定位.
- 交叉定位的平均持续时间为29天,最终的布普伦诺芬剂量可变.
- 失败的常见原因包括不充分的疼痛控制和不良反应.
结论:
- 布普伦诺芬交叉定位方案在约一半的患者中是成功的,并且通常耐受良好.
- 临床反应和所需的布普伦诺芬剂量差异很大,需要个性化治疗.
- 密切监测和协议调整对于在慢性疼痛管理中成功进行布普伦诺芬交叉定位至关重要.
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