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米非司酮和米索前列醇用于≤63 天妊娠药物流产的两种预防性疼痛管理方案:一项多中心、随机、安慰剂对照试验。

Two prophylactic pain management regimens for medical abortion ≤63 days' gestation with mifepristone and misoprostol: A multicenter, randomized, placebo-controlled trial.

机构信息

Gynuity Health Projects, New York, NY, United States.

Advancing New Standards in Reproductive Health (ANSIRH), Bixby Center for Global Reproductive Health, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California San Francisco, Oakland, CA, United States.

出版信息

Contraception. 2021 Mar;103(3):163-170. doi: 10.1016/j.contraception.2020.12.004. Epub 2021 Jan 13.

Abstract

OBJECTIVE

To determine if either prophylactic tramadol 50 mg or ibuprofen 400 mg/metoclopramide 10 mg result in lower maximal pain compared to placebo in women ≤63 days' gestation having a mifepristone-misoprostol medical abortion.

STUDY DESIGN

We conducted a randomized, placebo-controlled trial in Nepal, South Africa, and Vietnam. Participants seeking medical abortion received active treatment or placebo, taken at time of misoprostol and repeated 4 hours later. All had access to additional analgesia. The primary outcome was mean maximum pain score within 8 hours. Participants self-assessed maximum pain using an 11-point numeric rating scale recorded in paper diaries; we analyzed these data using intention-to-treat analysis. Secondary outcomes included use of additional analgesia, side effects, and satisfaction.

RESULTS

We enrolled 563 patients between June 2016 and October 2017; 5 participants failed to follow up. Mean adjusted maximum pain scores within 8 hours in both active arms were lower than placebo (tramadol: n = 188, 6.78 (95% confidence interval [CI] 6.46, 7.11); ibuprofen/metoclopramide: n = 187, 6.43 (95% CI 6.10, 6.75); placebo: n = 188, 7.42 (95% CI 7.10, 7.74); p = 0.0001). Additional analgesia was used by 97 (52.2%) participants in the tramadol group, 80 (43.0%) in the ibuprofen/metoclopramide group, and 103 (55.7%) in the placebo group, p = 0.04. More dizziness (p = 0.004), headache (p = 0.03), and vomiting (p < 0.001) occurred in the tramadol group. More participants reported experienced pain was the same or less than expected in the ibuprofen/metoclopramide group (p = 0.05); overall abortion satisfaction did not differ by group (p = 0.44).

CONCLUSIONS

Compared with placebo, tramadol or ibuprofen/metoclopramide co-administered with misoprostol and repeated 4 h later resulted in lower mean maximum pain scores that failed to achieve clinical significance. Women who received ibuprofen/metoclopramide were least likely to use additional analgesia and reported fewer side effects.

IMPLICATIONS

Given that tramadol, ibuprofen, and metoclopramide are inexpensive, globally available; and, ibuprofen and metoclopramide are included on the World Health Organization Essential Medicines List, these medicines could be considered for prophylactic pain management during medical abortion.

摘要

目的

比较曲马多 50mg 或布洛芬 400mg/甲氧氯普胺 10mg 与安慰剂在≤63 天妊娠的米非司酮-米索前列醇药物流产妇女中预防使用,哪一种可降低最大疼痛程度。

研究设计

我们在尼泊尔、南非和越南进行了一项随机、安慰剂对照试验。参与者在接受米索前列醇时接受活性治疗或安慰剂治疗,并在 4 小时后重复使用。所有参与者都可以获得额外的镇痛剂。主要结局是 8 小时内平均最大疼痛评分。参与者使用 11 点数字评分量表自我评估最大疼痛程度,并记录在纸质日记中;我们使用意向治疗分析来分析这些数据。次要结局包括额外镇痛剂的使用、副作用和满意度。

结果

我们于 2016 年 6 月至 2017 年 10 月期间招募了 563 名患者;5 名参与者未随访。在 8 小时内,两种活性药物组的平均最大疼痛评分均低于安慰剂组(曲马多:n=188,6.78(95%置信区间[CI]6.46,7.11);布洛芬/甲氧氯普胺:n=187,6.43(95%CI 6.10,6.75);安慰剂:n=188,7.42(95%CI 7.10,7.74);p=0.0001)。曲马多组有 97(52.2%)名参与者使用了额外的镇痛剂,布洛芬/甲氧氯普胺组有 80(43.0%)名,安慰剂组有 103(55.7%)名,p=0.04。曲马多组更易出现头晕(p=0.004)、头痛(p=0.03)和呕吐(p<0.001)。布洛芬/甲氧氯普胺组报告经历的疼痛与预期相同或更少的参与者更多(p=0.05);总体流产满意度不因组而异(p=0.44)。

结论

与安慰剂相比,曲马多或布洛芬/甲氧氯普胺与米索前列醇联合使用,并在 4 小时后重复使用,可降低平均最大疼痛评分,但未达到临床意义。接受布洛芬/甲氧氯普胺的女性最不可能使用额外的镇痛剂,且报告的副作用更少。

意义

鉴于曲马多、布洛芬和甲氧氯普胺价格低廉,全球均可获得;并且布洛芬和甲氧氯普胺都被列入世界卫生组织基本药物清单,因此这些药物可以考虑在药物流产期间用于预防疼痛管理。

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