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首页> 外文期刊>Anaesthesia: Journal of the Association of Anaesthetists of Great Britain and Ireland >Closed-loop double-vasopressor automated system vs manual bolus vasopressor to treat hypotension during spinal anaesthesia for caesarean section: A randomised controlled trial
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Closed-loop double-vasopressor automated system vs manual bolus vasopressor to treat hypotension during spinal anaesthesia for caesarean section: A randomised controlled trial

机译:闭环双升压自动系统与手动推注升压器在剖腹产脊髓麻醉期间治疗低血压:一项随机对照试验

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Hypotension necessitating vasopressor administration occurs commonly during caesarean section under spinal anaesthesia. We developed a novel vasopressor delivery system that automatically administers phenylephrine or ephedrine based on continuous non-invasive arterial pressure monitoring. A phenylephrine bolus of 50 μg was given at 30-s intervals when systolic blood pressure fell 90% of baseline; an ephedrine bolus of 4 mg was given instead if systolic pressure fell 90% of baseline together with a heart rate 60 beats.min-1. The control group used manual boluses of either phenylephrine 100 μg or ephedrine 8 mg, administered at 1-min intervals based on the same thresholds for systolic pressure and heart rate. This randomised, controlled, double-blinded trial involved 213 healthy women who underwent elective caesarean delivery under spinal anaesthesia using 11 mg hyperbaric bupivacaine with 15 μg fentanyl and 100 μg morphine. The automated vasopressor group had better systolic pressure control, with 37/106 (34.9%) having any beat-to-beat systolic pressure reading 80% of baseline compared with 63/107 (58.9%) in the control group (p 0.001). There was no difference in the incidence of reactive hypertension, defined as systolic pressure 120% of baseline, with 8/106 (7.5%) in the automated vasopressor group vs 14/107 (13.1%) in the control group, or total dose of vasopressors. The automated vasopressor group had lower median absolute performance error of 8.5% vs control of 9.8% (p = 0.013), and reduced incidence of nausea (1/106 (0.9%) vs 11/107 (10.3%), p = 0.005). Neonatal umbilical cord pH, umbilical lactate and Apgar scores were similar. Hence, our system afforded better control of maternal blood pressure and reduced nausea with no increase in reactive hypertension when compared with manual boluses.
机译:低血压导致必须在血管麻醉下进行剖腹产的过程中使用升压药。我们开发了一种新型的血管加压药输送系统,该系统可基于连续的非侵入性动脉压监测自动管理去氧肾上腺素或麻黄碱。当收缩压下降至基线的90%以下时,间隔30秒给予50μg苯肾上腺素推注;如果收缩压下降至基线的90%以下,并且心率<60 beats.min-1,则给予4 mg的麻黄碱推注。对照组使用手动推注100μg苯肾上腺素或8 mg麻黄碱,以相同的收缩压和心率阈值间隔1分钟给药。这项随机,对照,双盲试验包括213名健康妇女,这些妇女在11毫克的高压布比卡因与15μg芬太尼和100μg吗啡在脊髓麻醉下进行了选择性剖腹产。自动升压药组具有更好的收缩压控制,与对照组的63/107(58.9%)相比,37/106(34.9%)的任何逐搏收缩压读数均小于基线的80%(p <0.001 )。反应性高血压的发生率无差异,后者定义为收缩压>基线的120%,自动升压药组为8/106(7.5%),对照组为14/107(13.1%),或总剂量升压药。自动化升压药组的中位绝对性能误差较低,为8.5%,对照组为9.8%(p = 0.013),恶心的发生率也有所降低(1/106(0.9%)vs 11/107(10.3%),p = 0.005) 。新生儿脐带pH,脐带乳酸和Apgar评分相似。因此,与手动推注相比,我们的系统可更好地控制产妇血压并减少恶心,而反应性高血压没有增加。

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