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Post-cesarean section analgesia.剖宫产术后镇痛。
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2
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3
PROSPECT guideline for elective caesarean section: updated systematic review and procedure-specific postoperative pain management recommendations.择期剖宫产 PROSPECT 指南:更新的系统评价和特定手术术后疼痛管理建议。
Anaesthesia. 2021 May;76(5):665-680. doi: 10.1111/anae.15339. Epub 2020 Dec 28.
4
Pentazocine Alone Versus Pentazocine Plus Diclofenac for Pain Relief in the First 24 Hours after Caesarean Section: A Randomized Controlled Study.喷他佐辛单药与喷他佐辛联合双氯芬酸用于剖宫产术后24小时内镇痛的随机对照研究。
J Clin Diagn Res. 2017 Apr;11(4):QC01-QC05. doi: 10.7860/JCDR/2017/25294.9519. Epub 2017 Apr 1.
5
Post-caesarean analgesia: What is new?剖宫产术后镇痛:有哪些新进展?
Indian J Anaesth. 2017 Mar;61(3):200-214. doi: 10.4103/ija.IJA_313_16.
6
Optimal Pain Management After Cesarean Delivery.剖宫产术后的最佳疼痛管理
Anesthesiol Clin. 2017 Mar;35(1):107-124. doi: 10.1016/j.anclin.2016.09.010. Epub 2016 Dec 12.
7
Clinical effectiveness of transversus abdominis plane (TAP) blocks for pain relief after caesarean section: a meta-analysis.腹横肌平面(TAP)阻滞用于剖宫产术后镇痛的临床效果:一项荟萃分析。
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8
PENTAZOCINE VERSUS PENTAZOCINE WITH RECTAL DICLOFENAC FOR POSTOPERATIVE PAIN RELIEF AFTER CESAREAN SECTION- A DOUBLE BLIND RANDOMIZED PLACEBO CONTROLLED TRIAL IN A LOW RESOURCE AREA.喷他佐辛与喷他佐辛联合直肠用双氯芬酸用于剖宫产术后疼痛缓解——在资源匮乏地区进行的双盲随机安慰剂对照试验
Middle East J Anaesthesiol. 2016 Feb;23(4):443-8.
9
The Increasing Trend in Caesarean Section Rates: Global, Regional and National Estimates: 1990-2014.剖宫产率的上升趋势:全球、区域和国家估计:1990 - 2014年
PLoS One. 2016 Feb 5;11(2):e0148343. doi: 10.1371/journal.pone.0148343. eCollection 2016.
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WHO Statement on Caesarean Section Rates.世界卫生组织关于剖宫产率的声明。
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塞来昔布直肠给药联合喷他佐辛用于尼日利亚埃努古剖宫产术后镇痛:一项随机对照试验。

Pentazocine with rectal diclofenac versus pentazocine alone for pain relief following caesarean delivery in Enugu, Nigeria: A randomized controlled trial.

机构信息

Department of Obstetrics and Gynaecology, Enugu State University of Science and Technology - Teaching Hospital, Parklane, Enugu, Nigeria.

Department of Obstetrics and Gynaecology, Enugu State University of Science and Technology, College of Medicine, Government Residential Area, Parklane, Enugu, Nigeria.

出版信息

J Int Med Res. 2022 May;50(5):3000605221102092. doi: 10.1177/03000605221102092.

DOI:10.1177/03000605221102092
PMID:35638533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9160910/
Abstract

OBJECTIVE

To measure postoperative pain relief following the use of rectal diclofenac combined with intramuscular pentazocine compared with intramuscular pentazocine alone in patients undergoing a caesarean delivery.

METHODS

This single-blind randomized controlled trial enrolled pregnant women that had a caesarean section at the Enugu State University of Science and Technology Teaching Hospital, Enugu, Nigeria. Study participants were randomized to receive either 100 mg of rectal diclofenac given every 12 h plus 30 mg of intramuscular pentazocine given every 6 h (group A) or 60 mg of intramuscular pentazocine given every 6 h (group B). The primary outcome was the level of pain as measured using a visual analogue scale. The secondary outcomes were the level of satisfaction with pain relief and need for rescue analgesia.

RESULTS

A total of 200 participants were randomized equally into the two groups. Participants in group A had significantly better pain control and satisfaction over the 48 h after surgery compared with group B. Significantly more of group B required rescue analgesia for breakthrough pain compared with group A.

CONCLUSION

Rectal diclofenac combined with intramuscular pentazocine was significantly better at controlling pain compared with pentazocine alone in the first 48 h following caesarean section. PACTR202107706925314 at www.pactr.org on 28 July 2021.

摘要

目的

比较剖宫产术后直肠使用双氯芬酸与单独肌内注射戊乙奎醚的术后止痛效果。

方法

本单盲随机对照试验纳入了在尼日利亚埃努古州科技大学教学医院行剖宫产术的孕妇。研究参与者被随机分为两组,分别接受每 12 小时直肠给予 100mg 双氯芬酸加每 6 小时肌内给予 30mg 戊乙奎醚(A 组)或每 6 小时肌内给予 60mg 戊乙奎醚(B 组)。主要结局指标为视觉模拟评分法测量的疼痛程度。次要结局指标为疼痛缓解满意度和需要解救性镇痛的程度。

结果

共有 200 名参与者被平均随机分配到两组。与 B 组相比,A 组在手术后 48 小时内疼痛控制和满意度明显更好。与 A 组相比,B 组有更多的患者需要解救性镇痛来缓解突破性疼痛。

结论

与单独使用戊乙奎醚相比,剖宫产术后前 48 小时直肠使用双氯芬酸加肌内注射戊乙奎醚能更有效地控制疼痛。试验注册号:PACTR202107706925314,于 2021 年 7 月 28 日在 pactr.org 上注册。