首页> 美国卫生研究院文献>Anesthesiology Research and Practice >Prediction of Optimal Reversal Dose of Sugammadex after Rocuronium Administration in Adult Surgical Patients
【2h】

Prediction of Optimal Reversal Dose of Sugammadex after Rocuronium Administration in Adult Surgical Patients

机译:成人手术患者服用罗库溴铵后Sugammadex最佳逆转剂量的预测

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

The objective of this study was to determine the point after sugammadex administration at which sufficient or insufficient dose could be determined, using first twitch height of train-of-four (T1 height) or train-of-four ratio (TOFR) as indicators. Groups A and B received 1 mg/kg and 0.5 mg/kg of sugammadex, respectively, as a first dose when the second twitch reappeared in train-of-four stimulation, and Groups C and D received 1 mg/kg and 0.5 mg/kg of sugammadex, respectively, as the first dose at posttetanic counts 1–3. Five minutes after the first dose, an additional 1 mg/kg of sugammadex was administered and changes in T1 height and TOFR were observed. Patients were divided into a recovered group and a partly recovered group, based on percentage changes in T1 height after additional dosing. T1 height and TOFR during the 5 min after first dose were then compared. In the recovered group, TOFR exceeded 90% in all patients at 3 min after sugammadex administration. In the partly recovered group, none of the patients had a TOFR above 90% at 3 min after sugammadex administration. An additional dose of sugammadex can be considered unnecessary if the train-of-four ratio is ≥90% at 3 min after sugammadex administration. This trial is registered with UMIN000007245.
机译:这项研究的目的是确定在使用舒马葡糖后的点,可以使用四列训练的第一抽动高度(T1高度)或四列训练比的第一抽动高度(TOFR)作为指标,确定可以确定足够或不足的剂量。当第二次抽搐在四次刺激中再次出现时,A组和B组分别以1μmg/ kg和0.5μmg/ kg的sugammadex作为第一剂,而C组和D组分别以1μmg/ kg和0.5μmg/ kg的剂量接受第一剂量。 sugammadex公斤,分别是在强直后的第一剂1-3。第一次给药后五分钟,每人再加1μmg/ kg的Sugammadex,观察到T1高度和TOFR的变化。根据额外服药后T1高度的百分比变化,将患者分为恢复组和部分恢复组。然后比较第一次给药后5分钟内的T1高度和TOFR。在康复组中,给予舒马葡糖后3分钟,所有患者的TOFR均超过90%。在部分康复组中,给予舒马葡糖后3分钟,所有患者的TOFR均未超过90%。如果在服用Sugammadex后3分钟时四分之四的比率≥90%,则可以认为无需额外剂量的Sugammadex。该试用版已在UMIN000007245中注册。

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