欧维婷软膏联合米索前列醇用于绝经后妇女取环临床分析.docVIP

欧维婷软膏联合米索前列醇用于绝经后妇女取环临床分析.doc

  1. 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
  2. 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  3. 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
  4. 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
  5. 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们
  6. 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
  7. 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
欧维婷软膏联合米索前列醇用于绝经后妇女取环临床分析

欧维婷软膏联合米索前列醇用于绝经后妇女取环临床分析   [摘要] 目的 探析?W维婷软膏联合米索前列醇用于绝经后妇女取环的临床效果。方法 方便选取该院2014年3月―2016年12月期间收治的116例绝经后妇女取环患者,将其随机分为研究组和对照组,各为58例,对照组仅术前4 h米索前列醇600 μg置于阴道后穹窿,研究组在对照组的基础上取环前5 d开始每晚阴道用欧维婷软膏0.5 g,比较两组患者宫颈软化程度、取环成功率、取出时间、出血量等。结果 研究组软化率84.48%与对照组12.07%比较差异有统计学意义(P0.05);研究组取环时间(5.3±1.2)min、出血量(4.2±1.1)mL与对照组比较差异有统计学意义(P0.05);研究组取环成功率100.00%与对照组82.76%比较差异有统计学意义(P0.05);研究组轻度疼痛86.21%、中度疼痛13.79%与对照组比较差异有统计学意义(P0.05);两组均未出现严重不良反应。 结论 欧维婷软膏联合米索前列醇用于绝经后妇女取环比单一运用米索前列醇效果显著,能够减轻患者痛苦,减少出血量,缩短手术时间,提高取环成功率。   [关键词] 欧维婷软膏;米索前列醇;绝经后取环;临床效果   [中图分类号] R969 [文献标识码] A [文章编号] 1674-0742(2017)10(c)-0129-03   Clinical Analysis of Ovestin Ointment Combined with Misoprostol for Postmenopausal Women of Taking the Ring   ZHANG Chun-ling, SONG Li   Department of Obstetrics and Gynecology, Siyang County People’s Hospital, Suqian, Jiangsu Province, 223700 China   [Abstract] Objective This paper tries to study the clinical effect of Ovestin ointment combined with misoprostol in postmenopausal women of taking the ring. Methods A total of 116 postmenopausal women admitted in this hospital from March 2014 to December 2016 were convenient selected and randomly divided into the study group and the control group, with 58 cases in each group. The control group was treated with only 4 h misoprostol 600 μg in the vaginal fornix, the study group on the basis of the control group adopted ovestin ointment for the first 5 d before the vagina every night of 0.5 g, the cervical softening, success rate of taking the ring, removal time, bleeding amount of the two groups were compared. Results The softening rate was 84.48% in the study group and 12.07% in the control group, the difference was significant(P0.05). The removal time in the study group was (5.3±1.2)min and bleeding amount was (4.2±1.1)mL, significantly different from that in the control group(P0.05). The success rate of taking the ring was 100.00%, significantly different from that in the control group of 82.76%(P0.05). The mild pain degree in the st

文档评论(0)

3471161553 + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档