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首页> 外文期刊>Journal of Pain Research >Effect of oxycodone patient-controlled intravenous analgesia after cesarean section: a randomized controlled study
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Effect of oxycodone patient-controlled intravenous analgesia after cesarean section: a randomized controlled study

机译:羟考酮剖宫产后患者自控静脉镇痛的效果:一项随机对照研究

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Background: Oxycodone is a semisynthetic μ-opioid receptor agonist with a potentially good analgesic efficacy in visceral pain. This study aims to compare the efficacy of oxycodone with sufentanil patient-controlled intravenous analgesia (PCIA). Methods: One hundred and twenty primiparas undergoing elective cesarean section were randomized into four groups by different drugs of PCIA: group S (sufentanil 100 μg), group OS1 (sufentanil 70 μg, oxycodone 30 mg), group OS2 (sufentanil 50 μg, oxycodone 50 mg), and group O (oxycodone 100 mg). Ramosetron 0.3 mg was added to each group. In all groups, drugs were diluted to 100 mL and managed with a continuous infusion of 1 mL·h?1, a bolus dose of 2 mL, and a lockout interval of 15 min. The maximum dose of PCIA per hour was 10?mL. After surgery, pain scores, PCIA doses, and side effects were compared among groups. Results: At all time points (6, 12, and 24 h after surgery), Numerical Rating Scale (NRS) of uterine cramping pain (NRS-U) scores in group O were lower than those in groups OS1 and S ( P <0.008) and NRS-U scores in groups OS2 and OS1 were lower than that in group S ( P <0.008). NRS of moving into the sitting position (NRS-S) scores in group O were lower than those in the other groups ( P <0.008). NRS-S scores in group OS2 were lower than those in groups OS1 and S ( P <0.008). At 12 and 24 h after surgery, NRS of incision pain at rest (NRS-R) scores in group O were lower than those in the other groups ( P <0.008). At all time points, NRS-R scores in group OS2 were lower than those in groups OS1 and S ( P <0.008). The number of PCIA boluses and amount of opioid consumption in group O were lower than those in groups OS1 and S at all time points ( P <0.008). Conclusion: Oxycodone PCIA may be more effective than sufentanil PCIA for pain relief after cesarean section but the incidence of side effects needs further investigation.
机译:背景:羟考酮是一种半合成的μ阿片受体激动剂,对内脏痛具有潜在的良好止痛作用。本研究旨在比较羟考酮与舒芬太尼患者自控静脉镇痛(PCIA)的疗效。方法:将120例行选择性剖宫产的初产妇通过不同的PCIA药物随机分为四组:S组(舒芬太尼100μg),OS1组(舒芬太尼70μg,羟考酮30 mg),OS2组(舒芬太尼50μg,羟考酮) 50毫克)和O组(羟考酮100毫克)。将雷莫司琼0.3 mg添加到每组中。在所有组中,将药物稀释至100 mL,并以1 mL·h ?1 的连续输注,2 mL的推注剂量和15分钟的锁定间隔进行管理。每小时PCIA的最大剂量为10?mL。手术后,比较各组的疼痛评分,PCIA剂量和副作用。结果:在所有时间点(手术后6、12和24小时),O组子宫痉挛性疼痛(NRS-U)评分的数字量表(NRS)均低于OS1和S组(P <0.008 ),OS2和OS1组的NRS-U得分低于S组(P <0.008)。 O组的入座NRS评分低于其他组(P <0.008)。 OS2组的NRS-S得分低于OS1和S组的NRS-S得分(P <0.008)。手术后12和24 h,O组的静息切口疼痛NRS(NRS-R)得分低于其他组(P <0.008)。在所有时间点上,OS2组的NRS-R得分均低于OS1和S组的NRS-R得分(P <0.008)。在所有时间点,O组的PCIA推注次数和阿片类药物消耗量均低于OS1和S组(P <0.008)。结论:剖宫产术后羟考酮PCIA可能比舒芬太尼PCIA更有效,但副作用的发生率有待进一步研究。

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