首页> 外文期刊>Acute pain: international journal of acute pain management >Motor blockade associated with continuous epidural infusion after abdominal hysterectomy: a randomized controlled trial comparing 0.1% ropivacaine-plus-fentanyl versus 0.2% ropivacaine-alone
【24h】

Motor blockade associated with continuous epidural infusion after abdominal hysterectomy: a randomized controlled trial comparing 0.1% ropivacaine-plus-fentanyl versus 0.2% ropivacaine-alone

机译:子宫子宫切除术后连续硬膜外输注与运动阻滞相关:一项随机对照试验,比较了0.1%罗哌卡因加芬太尼与0.2%罗哌卡因单独治疗

获取原文
获取原文并翻译 | 示例
           

摘要

We compared rates of motor blockade, analgesia, adverse effects and patient satisfaction of 0.1% ropivacaine + fentanyl versus 0.2% ropivacaine-alone in a randomized, controlled trial. Fifty-four women who had undergone abdominal hysterectomy were randomly allocated into two groups to receive an epidural block at L_(1-2) or L_(2-3)- group R received 0.2% ropivacaine-alone and group RF received 0.1% ropivacaine plus 2 mug fentanyl/ml, both at 8ml/h. Rescue analgesia was provided via a morphine-loaded PCA device. Motor blockade (using a modified Bromage scale), pain intensity (visual analogue scale (VAS)), morphine consumption, level of sensory blockade and adverse effects, were measured at 4, 8 and 21 h after infusion. Patient satisfaction with pain management was assessed at the end of the study. The rates of motor blockade were not different at 8 h after infusion but at 21 h, group RF had significantly less motor blockade than group R. There were no differences in VAS, level of sensory blockade, adverse effects and patient satisfaction. Morphine consumption at each measurement was comparable but the total amount used by group RF was less than group R (12 mg versus 20 mg, P = 0.049). Therefore, 0.1% ropivacaine with fentanyl 2 (jig/ml appears to offer advantages over 0.2% ropivacaine-alone.
机译:在一项随机对照试验中,我们比较了0.1%罗哌卡因+芬太尼的运动阻滞,镇痛,不良反应和患者满意度的比率,而单独使用罗哌卡因仅为0.2%。五十四名接受了子宫全子宫切除术的妇女被随机分为两组,分别在L_(1-2)或L_(2-3)接受硬膜外阻滞-R组仅接受0.2%罗哌卡因,RF组接受0.1%罗哌卡因加2杯芬太尼/毫升,均以8ml / h的速度服用。通过装有吗啡的PCA装置提供了急救镇痛作用。在输注后第4、8和21小时测量了运动阻滞(使用改良的Bromage量表),疼痛强度(视觉模拟量表(VAS)),吗啡消耗量,感觉阻滞水平和不良反应。在研究结束时评估患者对疼痛治疗的满意度。输注后8 h,运动阻滞率没有变化,但在21 h,RF组的运动阻滞明显少于R组。VAS,感觉阻滞水平,不良反应和患者满意度无差异。每次测量的吗啡消耗量是可比较的,但RF组的总使用量少于R组(12 mg对20 mg,P = 0.049)。因此,与单独使用0.2%罗哌卡因相比,0.1%罗哌卡因与芬太尼2(jig / ml)似乎具有优势。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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