Dexamethasone as an Analgesic Adjunct for Postcesarean Delivery Pain: A Randomized Controlled Trial.

IF 1.6 Q2 ANESTHESIOLOGY
Anesthesiology Research and Practice Pub Date : 2021-09-24 eCollection Date: 2021-01-01 DOI:10.1155/2021/4750149
Jennifer E Mehdiratta, Jennifer E Dominguez, Yi-Ju Li, Remie Saab, Ashraf S Habib, Terrence K Allen
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引用次数: 3

Abstract

Objectives: Dexamethasone has been shown to have analgesic properties in the general surgical population. However, the analgesic effects for women that undergo cesarean deliveries under spinal anesthesia remain unclear and may be related to the timing of dexamethasone administration. We hypothesized that intravenous dexamethasone administered before skin incision would significantly reduce postoperative opioid consumption at 24 h after cesarean delivery under spinal anesthesia with intrathecal morphine.

Methods: Women undergoing elective cesarean deliveries under spinal anesthesia were randomly assigned to receive 8 mg of intravenous dexamethasone or placebo prior to skin incision. Both groups received a standardized spinal anesthetic and multimodal postoperative analgesic regime. The primary outcome was cumulative opioid consumption at 24 h. Secondary outcomes included cumulative opioid consumption at 48 h, time to first analgesic request, and pain scores at rest and on movement at 2, 24, and 48 h.

Results: 47 patients were analyzed-23 subjects that received dexamethasone and 24 subjects that received placebo. There was no difference in the median (Q1, Q3) cumulative opioid consumption in the first 24 hours following cesarean delivery between the dexamethasone group {15 (7.5, 20.0) mg} and the placebo group {13.75 (2.5, 31.25) mg} (P=0.740). There were no differences between the groups in cumulative opioid consumption at 48 h, time to first analgesic request, and pain scores.

Conclusions: Intravenous dexamethasone 8 mg administered prior to skin incision did not reduce the opioid consumption of women that underwent cesarean deliveries under spinal anesthesia with intrathecal morphine and multimodal postoperative analgesic regimen.

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Abstract Image

地塞米松作为剖宫产后疼痛的镇痛辅助剂:一项随机对照试验。
目的:地塞米松已被证明在普通外科人群中具有镇痛特性。然而,脊髓麻醉下剖宫产妇女的镇痛效果尚不清楚,可能与地塞米松给药的时机有关。我们假设在剖宫产术后24 h鞘内吗啡脊髓麻醉下,皮肤切开前静脉给予地塞米松可显著减少术后阿片类药物的消耗。方法:在脊髓麻醉下择期剖宫产的妇女被随机分配在皮肤切开前接受8 mg静脉地塞米松或安慰剂。两组均采用标准化脊髓麻醉和术后多模式镇痛方案。主要终点是24小时阿片类药物的累积消耗。次要结果包括48小时阿片类药物的累积消耗,到首次止痛要求的时间,以及休息和运动时2、24和48小时的疼痛评分。结果:共分析了47例患者,其中地塞米松组23例,安慰剂组24例。剖宫产后24小时内地塞米松组{15 (7.5,20.0)mg}与安慰剂组{13.75 (2.5,31.25)mg}的阿片类药物累积用量中位数(Q1, Q3)无差异(P=0.740)。两组在48小时的阿片类药物累积用量、到第一次止痛要求的时间和疼痛评分方面没有差异。结论:皮肤切开前静脉给予地塞米松8mg并没有减少剖宫产妇女在鞘内吗啡和术后多模式镇痛方案下的阿片类药物消耗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
29
审稿时长
18 weeks
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