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喷他佐辛防治瑞芬太尼痛觉过敏的临床效果观察 被引量:3
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作者 王海霞 候梅梅 张熙 《海峡药学》 2015年第5期188-189,共2页
目的观察喷他佐辛防治瑞芬太尼痛觉过敏的临床效果。方法运用随机整群抽样的方法选取我院2014年5月至2014年10月收治的80例接受上腹部择期手术的患者,依据随机数字表法将这些患者分为研究组和对照组两组,各40例。给予研究组患者肌肉注射... 目的观察喷他佐辛防治瑞芬太尼痛觉过敏的临床效果。方法运用随机整群抽样的方法选取我院2014年5月至2014年10月收治的80例接受上腹部择期手术的患者,依据随机数字表法将这些患者分为研究组和对照组两组,各40例。给予研究组患者肌肉注射0.5mg·kg-1喷他佐辛,给予对照组患者肌肉注射5m L生理盐水,然后对两组患者不同时间点VAS评分≥2分的分布情况进行统计分析。结果研究组患者苏醒后即刻、苏醒后5、10、30min VAS评分≥2分的比例均显著低于对照组(P<0.05)。结论喷他佐辛防治瑞芬太尼痛觉过敏的临床效果显著,值得推广。 展开更多
关键词 喷他佐辛 瑞芬太尼痛觉过敏 临床效果
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Effect of parecoxib on remifentanil-induced hyperalgesia after ambulatory surgery
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作者 穆东亮 王东信 +1 位作者 曲元 李春晶 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2013年第4期365-369,共5页
In previous human studies, pretreatment with parecoxib can effectively relieve hyperalgesia after short-term infusion of remifentanil. In this study, we aim to investigate the effect of parecoxib on hyperalgesia after... In previous human studies, pretreatment with parecoxib can effectively relieve hyperalgesia after short-term infusion of remifentanil. In this study, we aim to investigate the effect of parecoxib on hyperalgesia after Short-term infusion of remifentanil in clinical practice. Totally, 120 patients who underwent ambulatory surgery were randomly divided into four groups. All patients received either parecoxib (40 mg) or normal saline (as placebo) 30 min before induction of anesthesia. Group A (placebo + propofol) and Group B (parecoxib + propofol) received only propofol for anesthesia, while Group C (placebo + propofol + remifentanil) and Group D (parecoxib + propofol + remifentanil) received both propofol and remifentanil for anesthesia. Visual analogue score (VAS) was used to evaluate pain score at various time points, including the time of birth date recollection and 30, 60, 90, 120, 180, 240, and 300 min after surgery, respectively. During the phase from discontinuation of anesthesia to 240 min after surgery, there is significant difference in the severity of pain among four groups with the order of: Group B 〈Group A 〈Group D 〈Group C (P〈0.001). Compared with patients in Groups A and B, patients in Group C suffered significantly higher pain score. After admini- stration of parecoxib, patients in Groups B and D experienced similar low pain score with comparison to Groups A and C (P〈0.001). Patients in Groups B and D experienced shorter recovery time to eye opening on verbal command and recollection of birth date among the four groups (P〈0.001). Groups B and D also had significantly improved satisfaction of pain management (P〈0.001). In conclusion, short-term infusion of remifentanil can induce significant hyperalgesia in clinical practice, while pretreatment with parecoxib at 40 mg is effective in relieving such remifentani-induced hyperalgesia. In addition, we also found that pretreatment with parecoxib could significantly improve patients' satisfaction of pain management. 展开更多
关键词 PARECOXIB Short-term infusion REMIFENTANIL HYPERALGESIA
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