中华麻醉学杂志2024,Vol.44Issue(12) :1437-1440.DOI:10.3760/cma.j.cn131073.20240919.01207

复合丙泊酚时奥赛利定用于不同分娩史患者人工流产术镇痛的半数有效剂量

Median effective dose of oliceridine combined with propofol for analgesia during induced abortion in patients with different labor histories

张贝贝 张伟 贾佳 王振丽 李帼双 张加强
中华麻醉学杂志2024,Vol.44Issue(12) :1437-1440.DOI:10.3760/cma.j.cn131073.20240919.01207

复合丙泊酚时奥赛利定用于不同分娩史患者人工流产术镇痛的半数有效剂量

Median effective dose of oliceridine combined with propofol for analgesia during induced abortion in patients with different labor histories

张贝贝 1张伟 1贾佳 1王振丽 1李帼双 1张加强1
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作者信息

  • 1. 河南省人民医院(郑州大学人民医院)麻醉与围术期医学科,郑州 450003
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摘要

目的 确定复合丙泊酚时奥赛利定用于不同分娩史患者人工流产术镇痛的半数有效剂量(ED50).方法 本研究为前瞻性研究.选择河南省人民医院(郑州大学人民医院)2024年7月1日至2024年8月20日拟行人工流产术患者,ASA分级Ⅰ或Ⅱ级,年龄20~45岁,BMI 18~28 kg/m2.根据有无经阴道分娩史将患者分为有分娩史组(D组)和无分娩史组(N组).采用改良Dixon序贯法进行试验,每组首例患者静脉注射奥赛利定剂量为0.015 mg/kg,根据患者术中体动反应确定下一例奥赛利定给药剂量.若体动反应为阳性则下一例升高1个阶梯剂量,否则降低1个阶梯剂量,相邻阶梯剂量比值为1.2,直至出现7个转折点试验结束.采用Dixon序贯法公式计算ED50及其95%置信区间.记录不良反应发生情况.结果 本研究共纳入患者54例,D组25例,N组29例.D组和N组复合丙泊酚时奥赛利定用于人工流产术镇痛的ED50及其95%置信区间分别为0.019(0.014~0.031)mg/kg和0.026(0.020~0.044)mg/kg.与D组比较,N组复合丙泊酚时奥赛利定用于人工流产术镇痛的ED50升高(P<0.05).2组患者静脉注射奥赛利定后均出现头晕症状,未见丙泊酚注射痛等其他不良反应发生.结论 复合丙泊酚时,奥赛利定用于有经阴道分娩史和无经阴道分娩史患者人工流产术镇痛的ED5o分别为0.019 mg/kg和0.026 mg/kg;相比有经阴道分娩史患者,奥赛利定对无阴道分娩史患者的镇痛效力降低.

Abstract

Objective To determine the median effective dose(ED50)of oliceridine combined with propofol for analgesia during induced abortion in patients with different labor histories.Methods This was a prospective study.American Society of Anesthesiologists Physical Status classification Ⅰ or Ⅱ patients,aged 18-45 yr,with a body mass index of 20-28 kg/m2,scheduled for elective induced abortion at Henan Provincial People's Hospital(Zhengzhou University People's Hospital)from July 1,2024 to August 20,2024,were selected.Patients were divided into a delivery group(group D)and a non-delivery group(group N)based on their histories of vaginal delivery.The modified Dixon's up and down method was used to conduct the trial.Oliceridine was intravenously injected at a dose of 0.015 mg/kg in the first patient in each group,and the dose was determined based on the intraoperative body movement.The positive response was defined as the body movement of grade 2 or higher during induced abortion.If the response was positive,the next patient received a higher dose of oliceridine,or conversely,a lower dose was given.The ratio be-tween the two successive concentrations was 1.2,and the trial was terminated until 7 turning points were a-chieved.The ED50 and 95%confidence interval were calculated using the Dixon sequential method formula.The occurrence of adverse reactions was recorded.Results A total of 54 patients were included in this study,with 25 in group D and 29 in group N.The ED50 and 95%confidence interval of oliceridine for pain-less abortion were 0.019(0.014-0.031)mg/kg and 0.026(0.020-0.044)mg/kg in group D and group N,respectively.Compared with group D,the ED50 of oliceridine for analgesia during induced abortion was sig-nificantly increased when combined with propofol in group N(P<0.05).Patients in both groups experienced dizziness after intravenous oliceridine injection,and no other adverse reactions such as injection pain were observed.Conclusions When combined with propofol,the ED50 of oliceridine for analgesia is 0.019 mg/kg and 0.026 mg/kg during induced abortion in patients with and without vaginal delivery history,respectively.The analgesic potency of oliceridine is decreased in patients without a history of vaginal delivery compared to patients with a history of vaginal delivery.

关键词

镇痛药,阿片类/二异丙酚/流产,人工/剂量效应关系,药物

Key words

Analgesics,opioid/Propofol/Abortion,induced/Dose-response relationship,drug

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出版年

2024
中华麻醉学杂志
中华医学会

中华麻醉学杂志

CSTPCDCSCD北大核心
影响因子:1.235
ISSN:0254-1416
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