确定初始罗皮瓦体积的不同度的ED90s,用于长期刺痛的疼痛缓解:随机顺序分配研究
Meijuan Sun1, Yi Chen2, Linsen Sun1
1Department of Anesthesiology, Huai'an Hospital Affiliated to Yangzhou University (The Fifth People's Hospital of Huai'an), Huaian, People's Republic of China.
Drug design, development and therapy
|September 2, 2025
概括
较高的罗皮瓦卡因度 (0. 1% 和 0. 125%) 显著降低了初始有效剂量 (ED90) 通过腹膜刺痛,需要更少的体积. 在所有测试的罗皮瓦卡因度中观察到可比的疼痛缓解和安全性.
科学领域:
- 麻醉学
- 妇产科
- 药理学
背景情况:
- 在分娩过程中对疼痛进行止痛非常重要.
- 腹腔穿刺 (DPE) 是一种有效的产痛疗法.
- 优化局部麻醉剂量是有效和安全的疼痛缓解的关键.
研究的目的:
- 确定不同度的初始ropivacaine剂量的90%有效剂量 (ED90),用于DPE产痛.
- 在DPE中比较不同度的罗皮瓦卡因 (0. 075%, 0. 1%, 0. 125%) 的疗效和安全性.
主要方法:
- 在90名患者中使用了顺序上下分配方法.
- 根据疼痛评分 (VAS) 进行剂量调整.
- 主要结局是最初的罗皮瓦卡因结合剂的ED90;母体和新生儿结局是次要的.
主要成果:
- 罗皮瓦卡因的ED90值分别为0. 075%,0. 1%和0. 125%.
- 较高度 (0. 1% 和 0. 125%) 降低了初始止痛剂体积需求的18. 8% 和 33. 0%,相比之下,0. 075%.
- 在所有度组中,孕产妇和新生儿的结局相似.
结论:
- 增加的罗皮瓦卡因度 (0. 1% 和 0. 125%) 显著降低了有效的DPE分娩止痛所需的初始体积.
- 所有测试度的止痛效果和母亲的满意度都相似.
- 较高度可以更有效地使用局部麻醉剂,而不会影响安全性或有效性.
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