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Comparison of remifentanil: Entonox with Entonox alone in labor analgesia

机译:瑞芬太尼:Entonox与单独使用Entonox在分娩镇痛中的比较

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Background: We designed a study to evaluate the effectiveness of continuous low dose infusion of remifentanil adding to self-administration of entonox administered for pain relief during the active phase of first stage of labor. Materials and Methods: Thirty healthy term pregnant women recruited in our randomized double-blind, cross over study. They received the study medicines during two 30-min periods with a 15-min wash-out sequence after each period. Fifteen parturient used remifentanil as a single bolus dose followed by constant low dose infusion and self-administration of entonox (group R) during the first period and entonox and saline (group P) during the second period, while the remainder of the parturient used the drugs in a reverse order. Pain and Ramsay score, maternal and fetal hemodynamic, and ventilation were assessed during each intervention. Results: In this study, mean pain severity scores were 8 ± 0.9 before and 5.4 ± 1.7 after intervention in group P, and 7.8 ± 0.1, 3.5 ± 1.3 in group R, respectively. Mean pain severity difference was 2.6 ± 1.5 in group P, while 4.3 ± 1.5 in group R; so, use of entonox and remifentanil can decrease labor pain two times more in comparison with entonox/placebo (normal saline). However, hemodynamic and ventilation parameter in remifentanil/entonox period were same as in entonox/placebo period. No statistical differences were seen in mean Ramsay score between group R and P. There was no episode of maternal bradycardia, hypotension, or hypoxemia. Conclusion: Not only adding low dose infusion of remifentanil to self-administration of entonox was notable in labor pain reduction, it did n't make more parturient and neonatal side-effects.
机译:背景:我们设计了一项研究,以评估连续小剂量瑞芬太尼输注的效果,以及在分娩第一阶段活动期自我缓解疼痛时所用依托诺克斯的自我给药。材料和方法:在我们的随机双盲,交叉研究中招募了30名健康足月孕妇。他们在两个30分钟的时间内接受了研究药物,每个时期后的冲洗时间为15分钟。十五名分娩者使用瑞芬太尼作为单次推注剂量,随后在第一期中持续低剂量输注Entonox(R组),第二期进行Entonox和生理盐水(P组),而其余的分娩者则使用药物顺序相反。在每次干预过程中评估疼痛和拉姆齐评分,母婴血液动力学和通气量。结果:在这项研究中,P组的平均疼痛严重度评分在干预前分别为8±0.9和5.4±1.7,在R组中分别为7.8±0.1、3.5±1.3。 P组的平均疼痛严重程度差异为2.6±1.5,R组为4.3±1.5。因此,与依托诺克/安慰剂(生理盐水)相比,使用依托诺克和瑞芬太尼可减轻分娩疼痛两倍。然而,瑞芬太尼/恩托诺期的血液动力学和通气参数与恩托昔/安慰剂期相同。 R组和P组之间在Ramsay平均得分上没有统计学差异。没有发生母亲心动过缓,低血压或低氧血症。结论:不仅在自我给药中添加低剂量的瑞芬太尼输注在减轻分娩痛方面是显着的,而且没有产生更多的产程和新生儿副作用。

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