首页> 外文期刊>BMC Pulmonary Medicine >Rhomboid intercostal block combined with sub-serratus plane block versus rhomboid intercostal block for postoperative analgesia after video-assisted thoracoscopic surgery: a prospective randomized-controlled trial
【24h】

Rhomboid intercostal block combined with sub-serratus plane block versus rhomboid intercostal block for postoperative analgesia after video-assisted thoracoscopic surgery: a prospective randomized-controlled trial

机译:rhomboid肋间嵌段联合潜水胸腔嵌段嵌入式镇痛与术后镇痛障碍嵌段,术后术后镇痛:一项前瞻性随机对照试验

获取原文
           

摘要

Rhomboid intercostal block (RIB) and Rhomboid intercostal block with sub-serratus plane block (RISS) are the two types of plane blocks used for postoperative analgesia after video-assisted thoracoscopic surgery (VATS). This prospective randomized controlled trial was performed to analyze the postoperative analgesic effects of ultrasound-guided RIB block and RISS block after video-assisted thoracoscopic surgery. Ninety patients aged between 18 and 80?years, with American Society of Anesthesiologists physical status Classes I–II and scheduled for elective unilateral VATS were randomly allocated into three groups. In group C, no block intervention was performed. Patients in group RIB received ultrasound-guided RIB with 20-mL 0.375% ropivacaine and those in group RISS received ultrasound-guided RIB and serratus plane block using a total of 40-mL 0.375% ropivacaine. All patients received intravenous sufentanil patient-controlled analgesia upon arrival in the recovery room. Postoperative sufentanil consumption and pain scores were compared among the groups. The dosages of sufentanil consumption at 24?h after the surgery in the RIB and RISS groups were significantly lower than that in group C (p??0.001 and p??0.001 for all comparisons, respectively), the postoperative Numerical Rating Scale (NRS) scores in the RIB and RISS groups at 0.5, 1, 3, 6, 12, 18, and 24?h after surgery when patients were at rest or active were significantly lower than that in group C (p??0.05 for all comparisons). The required dosage of sufentanil and time to first postoperative analgesic request in groupRISS were less than those in the group RIB at 24?h after the surgery (p??0.001 and p??0.001 for all comparisons, respectively). Similarly, the Numerical Rating Scale scores for group RISS at 12, 18, and 24?h after the surgery when the patients were active were significantly lower than those for group RIB (p??0.05 for all comparisons). Both ultrasound-guided RIB block and RISS block can effectively reduce the demand for sufentanil within 24?h after VATS, and less sufentanil dosage is needed in patient with RISS block. Ultrasound-guided RIB block and RISS block can effectively relieve pain within 24?h after VATS, and RISS block is more effective.
机译:菱形肋间嵌段(肋骨)和带有亚塞拉图平面块(RISS)的菱形肋间嵌段是视频辅助胸腔镜手术(VATS)后用于术后镇痛的两种平面嵌段。该预期随机对照试验进行了分析了视频辅助胸腔镜手术后超声引导肋骨块和RIS块的术后镇痛作用。年龄在18至80岁之间的九十名患者,随机地区,与美国麻醉学家的身体状况课程I-II,并定于选修单边VATS被随机分配成三组。在C组中,没有进行块干预。组肋骨患者接收超声引导肋,20-mL 0.375%Ropivacaine,riss中的那些,使用总共40-mL 0.375%Ropivacaine获得超声引导的肋骨和Serratus平面块。抵达恢复室后,所有患者均接受静脉内苏芬太尼患者控制的镇痛。在群体中比较了术后苏芬太尼消费和疼痛评分。在肋骨和riss基团手术后24μm的素丹尼尔消耗量的剂量显着低于C组(P 1〜0.001和p≤0.001,分别为所有比较),术后数值当患者处于静止或活性时,肋骨和riss组在肋骨和riss组中分数在0.5,1,3,6,12,18和24μm(pβ&lt所有比较0.05)。在手术后,Groupriss在Groupriss中所需剂量和第一次术后镇痛请求的时间少于组肋骨(P 1 0.0.001和P≤0.001,分别用于所有比较。同样,当患者有效的手术后,在手术后,在手术后,群体的数值评定尺度分数在手术后的术后显着低于基团肋(p≤0.β.<0.05)。在VATS之后,超声引导的肋骨和RIS块可以有效地减少对24℃的24℃内对Sufentanil的需求,并且在患者中患者需要较少的Sufentanil剂量。超声引导肋骨块和RISS块可以在大桶后24℃的24°内有效缓解疼痛,而Riss块更有效。

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