[盐酸氢吗啡酮联合氟比洛芬酯用于鼻内镜手术后患者自控静脉镇痛的效果]

[Efficacy of patient-controlled intravenous analgesia with hydromorphone hydrochloride plus flurbiprofen axetil after endoscopic sinus surgery].

作者信息

Jiang X Y, Shu L W, Pan C X

机构信息

Department of Anesthesiology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2017 Aug 22;97(32):2516-2519. doi: 10.3760/cma.j.issn.0376-2491.2017.32.009.

Abstract

To evaluate the efficacy of patient-controlled intravenous analgesia (PCIA)with hydromorphone hydrochloride plusflurbiprofen axetil after endoscopic sinus surgery(ESS). One hundred patients of American Society of Anesthesiologists physical status Ⅰ or Ⅱ, scheduled for ESS under total intraveous anesthesia with postoperative PCIA in Beijing Tongren Hospital from October 2015 to April 2016 were randomly divided into 3 groups according to the different formula of PCIA pumpin each group: Group A (hydromorphone hydrochloride 1 μg·kg(-1)·h(-1)+ flurbiprofen axetil 200 mg), Group B(hydromorphone hydrochloride 2 μg·kg(-1)·h(-1)), Group C( hydromorphone hydrochloride 1 μg·kg(-1)·h(-1)). The dosage of PCIA in each group was calculated for 50 h, and was diluted in 100 ml normal saline. All the pump was set up background infusion at a rate of 2 ml/h with a 2 ml bolus dose and a 15 min lock-time.Visual analogue scale (VAS) and Ramsay sedation scores at time points of postoperative 1, 4, 8, 12, 24, 48 h, the number of attempts to press bolus and rate of adverse effects within 48 h were recorded. The differences were compared among the groups. VAS at postoperative 1, 4, 8, 12 h in Group A was (1.9±0.6), (1.8±0.6), (1.6±0.6), and (1.2±0.4) respectively, in Group B was (1.8±0.4), (1.7±0.7), (1.6±0.6), and (1.3±0.5) respectively, in Group C was (2.5±0.9), (1.7±0.7), (1.6±0.6), and (1.3±0.5) respectively. The difference among each group were statistically significant (=8.661, 3.105, 4.903, 13.846, <0.05). VAS in Group A was similar to that in Group B(>0.05), but was lower than that in Group C(<0.05). The number of attempts to press bolus within 48 h in group A was 1.4±1.0, which was less than in Group C(2.2±1.8 , <0.05). Ramsay sedation score at postoperative 1, 4, 8 h in Group A was (2.4±0.6), (2.2±0.6), and (2.2±0.4) respectively, in Group B was (2.8±0.7), (2.6±0.7), and (2.4±0.6) respectively, in Group C was (2.3±0.6), (2.1±0.4), and (2.1±0.2) respectively. The difference among each group were statistically significant (=5.660, 6.782, 7.141, <0.05). Ramsay sedation score in group A was similar to that in Group C(>0.05), but was lower than that in Group B(<0.05). The total rate of adverse effects in Group A was 8.8%, which was similar to that in Group C (9.1%, χ(2)=0.001, >0.05), but was significantly lower than that in Group B (42.5%, χ(2)=9.99, <0.05). 1 μg·kg(-1)·h(-1) hydromorphone hydrochloride plus 200 mg flurbiprofen axetil is effective on PCIA for patients after ESS and can reduce the dosage of hydromorphone hydrochloride and the rate of adverse effects as well.

摘要

评估盐酸氢吗啡酮联合氟比洛芬酯用于鼻内镜鼻窦手术(ESS)后患者自控静脉镇痛(PCIA)的效果。选取2015年10月至2016年4月在北京同仁医院择期行ESS、全身静脉麻醉术后行PCIA的美国麻醉医师协会身体状况Ⅰ或Ⅱ级患者100例,根据PCIA泵不同配方随机分为3组:A组(盐酸氢吗啡酮1μg·kg⁻¹·h⁻¹+氟比洛芬酯200mg)、B组(盐酸氢吗啡酮2μg·kg⁻¹·h⁻¹)、C组(盐酸氢吗啡酮1μg·kg⁻¹·h⁻¹)。每组PCIA用量按50小时计算,用100ml生理盐水稀释。所有泵均设置背景输注速度为2ml/h,单次给药剂量为2ml,锁定时间为15分钟。记录术后1、4、8、12、24、48小时的视觉模拟评分(VAS)和Ramsay镇静评分、48小时内按压单次给药按钮的次数及不良反应发生率。比较组间差异。A组术后1、4、8、12小时VAS分别为(1.9±0.6)、(1.8±0.6)、(1.6±0.6)、(1.2±0.4);B组分别为(1.8±0.4)、(1.7±0.7)、(1.6±0.6)、(1.3±0.5);C组分别为(2.5±0.9)、(1.7±0.7)、(1.6±0.6)、(1.3±0.5)。各组间差异有统计学意义(=8.661、3.105、4.903、13.846,<0.05)。A组VAS与B组相似(>0.05),但低于C组(<0.05)。A组48小时内按压单次给药按钮的次数为1.4±1.0,少于C组(2.2±1.8,<0.05)。A组术后1、4、8小时Ramsay镇静评分分别为(2.4±0.6)、(2.2±0.6)、(2.2±0.4);B组分别为(2.8±0.7)、(2.6±0.7)、(2.4±0.6);C组分别为(2.3±0.6)、(2.1±0.4)、(2.1±0.2)。各组间差异有统计学意义(=5.660、6.782、7.141,<0.05)。A组Ramsay镇静评分与C组相似(>0.05),但低于B组(<0.05)。A组不良反应总发生率为8.8%,与C组(9.1%,χ²=0.001,>0.05)相似,但显著低于B组(42.5%,χ²=9.99,<0.05)。1μg·kg⁻¹·h⁻¹盐酸氢吗啡酮联合200mg氟比洛芬酯用于ESS术后患者PCIA效果良好,可减少盐酸氢吗啡酮用量及不良反应发生率。

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