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首页> 外文期刊>Anesthesia and Analgesia: Journal of the International Anesthesia Research Society >A randomized trial of breakthrough pain during combined spinal-epidural versus epidural labor analgesia in parous women.
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A randomized trial of breakthrough pain during combined spinal-epidural versus epidural labor analgesia in parous women.

机译:产后脊柱硬膜外和硬膜外分娩镇痛联合镇痛的突破性随机试验。

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BACKGROUND: There is controversy regarding the benefits and risks of combined spinal-epidural compared with epidural analgesia (CSE, EPID) for labor analgesia. We hypothesized that CSE would result in fewer patient requests for top-up doses compared to EPID. METHODS: One-hundred ASA physical status I or II parous women at term in early labor (<5 cm cervical dilation) requesting analgesia were randomized in double-blind fashion to the EPID group (epidural bupivacaine 2.5 mg/mL, 3 mL, followed by bupivacaine 1.25 mg/mL, 10 mL with fentanyl 50 microg) or the CSE group (intrathecal bupivacaine 2.5 mg with fentanyl 25 microg). Both groups received identical infusions of bupivacaine 0.625 mg/mL with fentanyl 2 microg/mL at 12 mL/h. The primary outcome variable was the number of top-up doses requested to treat breakthrough pain. RESULTS: There was no significant difference between the two groups in the percentage of patients requesting top-up doses (44% CSE vs 51% EPID; 95% confidence interval of the difference -28% to +14%) nor in the need for multiple top-up doses (14% CSE vs 15% EPID). Visual analog scale scores were lower in the CSE group compared to the EPID group at 10 min after initiation of analgesia [median 0 cm (0, 0) vs 4 cm (1, 6) respectively, P < 0.001] and at 30 min [0 cm (0, 0) vs 0 cm (0, 1), respectively, P = 0.03]. CONCLUSIONS: We did not find a difference in the need for top-up doses in parous patients; however, CSE provided better analgesia in the first 30 min compared to EPID.
机译:背景:对于硬膜外镇痛,硬膜外硬膜外联合硬膜外镇痛(CSE,EPID)的益处和风险存在争议。我们假设,与EPID相比,CSE会导致更少的患者补充剂量要求。方法:将一百例要求分娩镇痛的足月ASA处于I或II级状态的准产妇(<5 cm宫颈扩张期)要求镇痛,以双盲方式随机分为EPID组(硬膜外布比卡因2.5 mg / mL,3 mL,随后通过布比卡因1.25 mg / mL,10毫升芬太尼50微克)或CSE组(鞘内注射布比卡因2.5毫克芬太尼25微克)。两组均以12 mL / h的速度分别接受0.625 mg / mL布比卡因和2 microg / mL芬太尼的输注。主要结果变量是治疗突破性疼痛所需的补充剂量的数量。结果:两组患者在要求补充剂量的患者百分比(44%CSE与51%EPID; 95%置信区间-28%至+ 14%)之间以及所需多次充值(14%CSE与15%EPID)。在开始镇痛后10分钟,CSE组的视觉模拟量表评分低于EPID组[中位数0 cm(0,0)vs 4 cm(1,6),P <0.001]和30 min [ 0厘米(0,0)和0厘米(0,1),P = 0.03]。结论:我们没有发现对产后患者补充剂量的需求有所不同。但是,与EPID相比,CSE在前30分钟内可提供更好的镇痛效果。

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