Median effective volume

有效容积中位数
  • 文章类型: Journal Article
    确定1-6岁儿童超声引导锁骨上臂丛神经阻滞(SC-BPB)的0.2%罗哌卡因的中位有效量(EV50)。
    招募在重庆医科大学儿童医院进行单侧上肢手术的美国麻醉医师协会(ASA)1至6岁的儿童。所有患者均在全麻联合臂丛神经阻滞下进行手术。麻醉诱导后超声引导SC-BPB,定位后给予0.2%罗哌卡因。在研究中,我们使用Dixon的上下方法,初始剂量为0.50ml/kg。考虑到上一块的效果,成功或失败的块可以产生0.05ml/kg的体积减少或增加,相应地。实验在有7个拐点时停止。使用等渗回归和自举算法,计算EV50,95%有效体积(EV95)和95%置信区间(CI)。患者的一般信息,术后疼痛评分,并记录不良事件.
    27名患者参与了这项研究。0.2%罗哌卡因的EV50为0.150ml/kg(95%CI,0.131-0.169ml/kg),EV95(次要指标)为0.195ml/kg(95%CI,0.188-0.197ml/kg)。研究期间未发生不良事件。
    对于1-6岁接受单侧上肢手术的儿童的超声引导SC-BPB,0.2%罗哌卡因的EV50为0.150ml/kg(95%CI,0.131~0.169ml/kg).
    UNASSIGNED: To determine the median effective volume (EV50) of 0.2% ropivacaine for ultrasound-guided supraclavicular brachial plexus block (SC-BPB) in children aged 1-6 years.
    UNASSIGNED: Children aged from 1 to 6 years with an American Society of Anaesthesiologists (ASA) physical status I-II who were scheduled for unilateral upper extremity surgery at the Children\'s Hospital of Chongqing Medical University were recruited. All patients underwent surgery under general anaesthesia combined with brachial plexus block. SC-BPB was guided by ultrasound after anaesthesia induction, and 0.2% ropivacaine was given after localization. In the study, we used Dixon\'s up-and-down approach with an initial dose of 0.50 ml/kg. Considering the effect of the previous block, a successful or failed block could produce a 0.05 ml/kg decrement or increment in volume, correspondingly. The experiment was stopped when there were 7 inflection points. Using isotonic regression and bootstrapping algorithms, the EV50, the 95% effective volume (EV95) and the 95% confidence interval (CI) were calculated. The patients\' general information, postoperative pain scores, and adverse events were also recorded.
    UNASSIGNED: Twenty-seven patients were involved in this study. The EV50 of 0.2% ropivacaine was 0.150 ml/kg (95% CI, 0.131-0.169 ml/kg) and the EV95 (secondary metric) was 0.195 ml/kg (95% CI, 0.188-0.197 ml/kg). No adverse events occurred during the research study.
    UNASSIGNED: For ultrasound-guided SC-BPB in children aged 1-6 years undergoing unilateral upper extremity surgery, the EV50 of 0.2% ropivacaine was 0.150 ml/kg (95% CI, 0.131-0.169 ml/kg).
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  • 文章类型: Journal Article
    背景:超声引导下的针头放置彻底改变了胸椎旁阻滞技术,可应用于胸腔镜手术。
    目的:本研究调查了超声引导单次注射0.3%罗哌卡因作为胸椎旁神经阻滞用于肺癌胸腔镜根治术的中位有效体积(EV50)。
    方法:2018年2月10日至8月13日,共纳入27例接受超声引导下胸椎旁神经单次阻滞并接受胸腔镜肺癌根治术的患者。所有患者均被评为ASA等级I或II。使用超声波作为指导,通过平面内技术,将阻滞针逐渐穿过肋横断韧带到达胸椎旁间隙。在确认没有血液或脑脊液后,注射0.3%盐酸罗哌卡因1-2毫升,以确认针头位置合适,然后给患者服用预定体积的0.3%盐酸罗哌卡因。胸椎旁阻滞注射后每5分钟进行一次针刺的感觉测试,持续30分钟,以确定发生针刺感觉丧失及其阻滞作用的时间段。
    结果:所有患者均完成研究,14例(51.8%)阻断成功。
    结论:0.3%罗哌卡因的EV50为18.46ml(95%CI17.09-19.95ml),EV95为20.89ml。
    BACKGROUND: Ultrasound-guided needle placement has revolutionized the thoracic paravertebral block technique and can be applied in thoracoscopic surgery.
    OBJECTIVE: This study investigated the median effective volume (EV50) of an ultrasound-guided single shot of 0.3% ropivacaine used as a thoracic paravertebral nerve block for the radical thoracoscopic resection of lung cancer.
    METHODS: A total of 27 patients who received a single shot of ultrasound-guided thoracic paravertebral nerve block and underwent radical thoracoscopic resection of lung cancer were enrolled in this study between February 10 and August 13, 2018. All patients were rated as ASA grades I or II. Using ultrasound as a guide, the block needle was gradually pushed through the lateral costotransverse ligaments to the thoracic paravertebral space by the in-plane technique. After confirming the absence of blood or cerebrospinal fluid, 1-2 ml of 0.3% ropivacaine hydrochloride was injected to confirm that the position of the needle was appropriate, and a pre-determined volume of 0.3% ropivacaine hydrochloride was then administered to the patients. Sensory testing by pinprick was performed every 5 minutes for 30 minutes following the thoracic paravertebral block injection to identify the time segments during which the loss of sensation to the pinprick and its blocking effect occurred.
    RESULTS: All patients completed the study and 14 (51.8%) had a successful block.
    CONCLUSIONS: The EV50 of 0.3% ropivacaine was 18.46 ml (95% CI 17.09-19.95 ml) and the EV95 was 20.89 ml.
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