首页> 外文期刊>The British Journal of Surgery >Randomized clinical trial of intraoperative superficial cervical plexus block versus incisional local anaesthesia in thyroid and parathyroid surgery
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Randomized clinical trial of intraoperative superficial cervical plexus block versus incisional local anaesthesia in thyroid and parathyroid surgery

机译:甲状腺和甲状旁腺手术中术中颈浅神经丛阻滞与切口局部麻醉的随机临床试验

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Background Moderate wound pain and opiate analgesia requirement is reported following thyroid and parathyroid surgery. A randomized clinical trial was performed to investigate whether intraoperative superficial cervical plexus block (SCPB) would decrease postoperative pain and analgesia use. Methods Patients were randomized to incisional local anaesthesia (control) or incisional local anaesthesia plus intraoperative SCPB. The primary outcome measure was pain, assessed by a visual analogue scale (VAS). Secondary outcome measures were analgesia use (strong opiates defined as having potency at least as strong as that of oral morphine), respiratory rate and sedation score. Primary outcome measures were analysed with non-parametric tests, as well as with receiver operating characteristic (ROC) curves calculated as area under the curve (AUC) to discriminate between trial limbs. Results Twenty-nine patients were randomized to each group. Pain (VAS) scores were lower in patients who received intraoperative SCPB than in controls 30 min after surgery and subsequently (P < 0·020 at all time points), with a median pain score of zero on the day of operation in the SCPB group. Corresponding analysis of ROC curves showed differences between groups at 30 min (AUC = 0·722, P = 0·012), 90 min (AUC = 0·747, P = 0·005), 150 min (AUC = 0·803, P < 0·001) and 210 min (AUC = 0·849, P < 0·001) after surgery, and at 07.00 hours on postoperative day 1 (AUC = 0·710, P = 0·017). Fewer patients in the SCPB group required strong opiates (5 of 29 versus 16 of 29 in the control group; P = 0·003) and rescue opiates (6 of 29 versus 20 of 29; P < 0·001). Conclusion Intraoperative SCPB reduces pain scores following thyroid and parathyroid surgery, and reduces the requirement for strong and rescue opiates. Registration number: 2009-012671-98 (https://www.clinicaltrialsregister.eu). Cervical plexus block reduced postoperative pain
机译:背景技术据报道,甲状腺和甲状旁腺手术后有中等程度的伤口疼痛和阿片类镇痛需要。进行了一项随机临床试验,以调查术中浅表颈丛神经阻滞(SCPB)是否会减少术后疼痛和镇痛药的使用。方法将患者随机分为切开局部麻醉(对照)或切开局部麻醉加术中SCPB。主要结果指标是疼痛,通过视觉模拟量表(VAS)进行评估。次要结果指标是镇痛药的使用(强效阿片类药物的效力至少与口服吗啡一样强),呼吸频率和镇静分数。主要结局指标通过非参数测试进行分析,并通过计算接收者工作特征(ROC)曲线作为曲线下面积(AUC)进行分析,以区分试验肢体。结果29例患者被随机分为两组。术后30分钟及随后(在所有时间点P <0·020)接受术中SCPB的患者的疼痛(VAS)评分均低于对照组,SCPB组在手术当天的中位疼痛评分为零。 ROC曲线的相应分析显示,在30分钟(AUC = 0·722,P = 0·012),90分钟(AUC = 0·747,P = 0·005),150分钟(AUC = 0·803)之间,组之间存在差异,P <0·001)和210分钟(AUC = 0·849,P <0·001),以及术后第一天的07.00小时(AUC = 0·710,P = 0·017)。 SCPB组中需要鸦片制剂的患者较少(对照组为29例中的5例,而29例中为16例; P = 0·003)和抢救鸦片(29例中的6例,相对于29例中的20例; P <0·001)。结论术中SCPB降低了甲状腺和甲状旁腺手术后的疼痛评分,并减少了对阿片类药物的需求。注册号:2009-012671-98(https://www.clinicaltrialsregister.eu)。颈丛神经阻滞减轻术后疼痛

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