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首页> 外文期刊>European journal of anaesthesiology >Dose-dependency of dexamethasone on the analgesic effect of interscalene block for arthroscopic shoulder surgery using ropivacaine 0.5% A randomised controlled trial
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Dose-dependency of dexamethasone on the analgesic effect of interscalene block for arthroscopic shoulder surgery using ropivacaine 0.5% A randomised controlled trial

机译:地塞米松对0.5%罗哌卡因关节镜肩关节手术中斜角肌间阻滞镇痛作用的剂量依赖性一项随机对照试验

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BACKGROUNDDexamethasone prolongs the duration of single-shot interscalene brachial plexus block (SISB). However, dose-dependency of dexamethasone as an adjuvant for SISB remains insufficiently understood.OBJECTIVEThe objective of this study is to evaluate the effect of different doses of dexamethasone on the duration of SISB using ropivacaine 0.5%.DESIGNA randomised, double-blind controlled trial.SETTINGSingle university tertiary care centre.PATIENTSOne hundred and forty-four patients scheduled for elective arthroscopic shoulder surgery were allocated randomly to one of four groups.INTERVENTIONSPatients received 12ml of ropivacaine 0.5% in 0.9% saline (control group), or containing dexamethasone 2.5, 5.0 or 7.5mg for SISB.MAIN OUTCOME MEASURESThe primary endpoint was the time to the first analgesic request. Pain scores and adverse effects were also assessed up to 48h postoperatively.RESULTSInclusion of dexamethasone 2.5, 5.0 and 7.5mg resulted in significant (P<0.001) increases in time to the first analgesic request by factors of 1.6, 2.2 and 1.8, respectively. The percentages of patients not requiring analgesics in the first 48h postoperatively with dexamethasone 0.0, 2.5, 5.0 and 7.5mg were 3, 22, 39 and 33%, respectively (P<0.001). There were no significant effects on pain scores or incidences of adverse effects.CONCLUSIONDexamethasone demonstrated significant beneficial dose-dependent effects on duration to the first analgesic request, the number of patients not requiring analgesics and analgesic use in the first 48h after SISB for arthroscopic shoulder surgery. There were no significant effects on pain scores or incidences of adverse effects.TRIAL REGISTRATIONthe trial was registered with the Clinical Trial Registry of Korea: https://cris.nih.go.kr/cris/index.jsp. Identifier: KCT0001078
机译:背景地塞米松延长了单次肌间沟臂丛神经阻滞(SISB)的持续时间。然而,地塞米松作为SISB佐剂的剂量依赖性尚不十分清楚。目的本研究的目的是使用0.5%罗哌卡因评估不同剂量地塞米松对SISB持续时间的影响。DESIGNA一项随机,双盲对照试验。设置单一大学三级护理中心的患者144例行选择性关节镜肩部手术的患者被随机分配到四组中的一组中。干预患者接受12ml 0.5%的罗哌卡因,0.9%生理盐水(对照组)或含地塞米松2.5、5.0主要观察指标主要观察指标是首次使用镇痛药的时间。术后48h还评估疼痛评分和不良反应。结果包括地塞米松2.5、5.0和7.5mg可使首次镇痛的时间显着增加(P <0.001),分别为1.6、2.2和1.8倍。术后第一个48小时使用地塞米松0.0、2.5、5.0和7.5mg的患者不需要镇痛药的百分比分别为3%,22%,39%和33%(P <0.001)。结论:地塞米松对首次镇痛的持续时间,在SISB关节镜下肩关节手术后48h内不需要镇痛和使用镇痛剂的患者数量有显着的剂量依赖性效应,对疼痛评分或不良反应的发生率没有显着影响。 。对疼痛评分或不良反应的发生率没有显着影响。试验注册该试验已在韩国临床试验注册中心进行了注册:https://cris.nih.go.kr/cris/index.jsp。识别码:KCT0001078

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