Article Summary
余 玲,包春燕,宁 苗,王晓玲,刘婷婷.麦角新碱联合米索前列醇治疗前置胎盘的临床疗效及对血清ROS、SOD、GSH-px水平的影响[J].现代生物医学进展英文版,2019,19(14):2712-2715.
麦角新碱联合米索前列醇治疗前置胎盘的临床疗效及对血清ROS、SOD、GSH-px水平的影响
Curative Efficacy of Ergosine Plus Misoprostolin in the Treatment of Placenta Previa and Its Effects on the Serum ROS, SOD and GSH-px Levels
Received:February 06, 2019  Revised:February 28, 2019
DOI:10.13241/j.cnki.pmb.2019.14.023
中文关键词: 麦角新碱  米索前列醇  前置胎盘  活性氧  超氧化物歧化酶  谷胱甘肽过氧化物酶
英文关键词: Ergosine  Misoprostol  Placenta previa  Reactive oxygen species  Superoxide dismutase  Glutathione peroxidase
基金项目:陕西省自然科学基金项目(20141209)
Author NameAffiliationE-mail
YU Ling Department of obstetrics, Hanzhong 3201 hospital, Hanzhong, Shaanxi, 723000, China jiankanghappy@tom.com 
BAO Chun-yan Department of obstetrics, Hanzhong 3201 hospital, Hanzhong, Shaanxi, 723000, China  
NING Miao Department of obstetrics, Hanzhong 3201 hospital, Hanzhong, Shaanxi, 723000, China  
WANG Xiao-ling Department of obstetrics, Hanzhong 3201 hospital, Hanzhong, Shaanxi, 723000, China  
LIU Ting-ting Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, 710000, China  
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中文摘要:
      摘要 目的:分析麦角新碱联合米索前列醇治疗前置胎盘的临床疗效及对血清活性氧(ROS)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-px)水平的影响。方法:选择2016年5月-2017年5月我院收治的前置胎盘患者100例纳入本次研究,根据随机分组法分为观察组(n=52)和对照组(n=48)。对照组使用米索前列醇治疗,观察组采用麦角新碱联合米索前列醇进行治疗。比较两组患者的临床疗效、治疗前后血清ROS、SOD、GSH-px水平的变化、术中、术后出血量、止血时间及不良反应的发生情况。结果:治疗后,两组患者的总有效率分别为96.15%、81.25%,观察组显著高于对照组(P<0.05);两组患者血清ROS、SOD、GSH-px水平均较治疗前显著改善,且观察组患者血清ROS低于对照组,血清SOD、GSH-px水平显著高于对照组(P<0.05);观察组患者术中、术后出血量及止血时间均显著低于对照组(P<0.05);两组患者不良反应总发生率分别为7.69%、22.92%,观察组显著低于对照组(P>0.05)。结论:麦角新碱联合米索前列醇治疗前置胎盘的疗效和安全性均显著优于单用米索前列醇治疗,可能与其有效改善血清ROS、SOD、GSH-px水平有关。
英文摘要:
      ABSTRACT Objective: To study the curative efficacy of Ergosine plus misoprostol in the treatment of Placenta previa and its effects on the serum Reactive oxygen species (ROS), superoxide dismutase (SOD), glutathione peroxidase (gsh-px) levels. Methods: 100 cases of placenta previa patients admitted to our hospital from May 2016 to May 2017 were selected and divided into the observation group (n=52) and the control group (n=48) according to the random grouping method. The control group was treated with misoprostol, while the observation group was treated with ergoxin combined with misoprostol. The clinical efficacy, changes of serum ROS, SOD and GSH-px levels before and after treatment, intraoperative and postoperative blood loss, hemostasis time and incidence of adverse reactions were compared between the two groups. Results: After treatment, the total effective rates of observation group and control group were 96.15% and 81.25%, respectively, which was significantly higher in the observation group than that of the control group(P<0.05). The levels of serum ROS, SOD and GSH-px in the two groups were significantly improved compared with those before treatment, and the levels of serum ROS in the observation group were lower than those in the control group, the levels of serum SOD and gsh-px were significantly higher than those in the control group(P<0.05). The intraoperative and postoperative blood loss and hemostasis time in the observation group were significantly lower than those in the control group(P<0.05). The total incidence of adverse reactions in the two groups was 7.69% and 22.92%, respectively, which was significantly lower in the observation group than that of the control group(P>0.05). Conclusion: The efficacy and safety of ergoxin combined with misoprostol in the treatment of placenta previa are significantly better than those of misoprostol alone, which may be related to the effective improvement of serum ROS, SOD and GSH-px levels.
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