首页> 外文期刊>Anaesthesia: Journal of the Association of Anaesthetists of Great Britain and Ireland >A randomised, controlled, double blind, non-inferiority trial of ultrasound-guided fascia iliaca block vs. spinal morphine for analgesia after primary hip arthroplasty
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A randomised, controlled, double blind, non-inferiority trial of ultrasound-guided fascia iliaca block vs. spinal morphine for analgesia after primary hip arthroplasty

机译:超声引导骨筋膜阻滞与脊髓吗啡镇静用于原发性髋关节置换术后的镇痛效果的随机对照双盲非劣效性试验

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摘要

We performed a single centre, double blind, randomised, controlled, non-inferiority study comparing ultrasound-guided fascia iliaca block with spinal morphine for the primary outcome of 24-h postoperative morphine consumption in patients undergoing primary total hip arthroplasty under spinal anaesthesia with levobupivacaine. One hundred and eight patients were randomly allocated to receive either ultrasound-guided fascia iliaca block with 2 mg. kg(-1) levobupivacaine (fascia iliaca group) or spinal morphine 100 mu g plus a sham ultrasound-guided fascia iliaca block using saline (spinal morphine group). The pre-defined non-inferiority margin was a median difference between the groups of 10 mg in cumulative intravenous morphine use in the first 24 h postoperatively. Patients in the fascia iliaca group received 25 mg more intravenous morphine than patients in the spinal morphine group (95% CI 9.0-30.5 mg, p < 0.001). Ultrasound-guided fascia iliaca block was significantly worse than spinal morphine in the provision of analgesia in the first 24 h after total hip arthroplasty. No increase in side-effects was noted in the spinal morphine group but the study was not powered to investigate all secondary outcomes.
机译:我们进行了一项单中心,双盲,随机,对照,非劣效性研究,比较了超声引导下fa肌筋膜阻滞与脊髓吗啡在接受左旋布比卡因脊柱麻醉下接受全髋关节置换术的患者术后24小时吗啡消耗的主要结果。 108名患者被随机分配接受2 mg超声引导的ilia筋膜阻滞。 kg(-1)左旋布比卡因(fa肌筋膜组)或脊髓吗啡100μg,再加生理盐水假超声引导的fa肌筋膜阻滞剂(脊髓吗啡组)。预先定义的非劣效性差是术后开始的24小时内静脉注射吗啡累积使用量10 mg组之间的中位数差异。 ilia筋膜组的患者接受的吗啡静脉注射剂量比脊髓吗啡组的患者多25毫克(95%CI 9.0-30.5 mg,p <0.001)。在全髋关节置换术后24小时内,在提供镇痛作用时,超声引导的block肌筋膜阻滞明显比脊髓吗啡差。脊髓吗啡组未观察到副作用增加,但该研究无权调查所有次要结局。

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