罗哌卡因复合舒芬太尼在硬膜外麻醉无痛分娩中的临床观察.docVIP

罗哌卡因复合舒芬太尼在硬膜外麻醉无痛分娩中的临床观察.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
罗哌卡因复合舒芬太尼在硬膜外麻醉无痛分娩中的临床观察.doc

罗哌卡因复合舒芬太尼在硬膜外麻醉无痛分 娩中的临床观察 [ ]H的研究罗哌卡因复合舒芬太尼在硬膜外麻醉分娩镇痛的 安全性及有效性。方法随机选择96例初产临产妇,以入产房的单双 例分为两组:A组注入0.2%罗哌卡因与5 ug舒芬太尼混合液6mL,后 接硬膜外?子止痛泵维持剂量7mL/h (n=48例);B组为普通分娩对照 组(n=48例)。观察两组分娩过程的疼痛分级和胎儿评分,产妇的血 压心率变化,产妇的VAS评分,产程时间,顺产率,产后尿潴留等情 况。结果疼痛分级效果镇痛组显著优于对照组(P〈0. 01),产程时间 长于镇痛组,差异有显著性意义(P〈0.05); B组产妇在产程中MAP、 IIR明显升高,变化有明显差异(P〈0.05); A组剖腹产率比普通组低 (P0. 05);缩宫素使用率、围生期出血、Apgar评分、产后尿潴留等 比较两组无明显差异(P〉0. 05)。结论罗哌卡因复合舒芬太尼在硬膜 外用于分娩镇痛可以降低分娩时期的疼痛,提高舒适度和安全性。 ,供学习和研宄 使用, 和著作权归原 所有, 如果需耍分享, 请保留本段说明 [关键词]无痛分娩;罗哌卡因;舒芬太尼;硬膜外麻醉 [ ]R614 [ ]A [ ]2095-0616 (2017) 07-134-04 Clinical observation of ropivacainc combined with sufentanil in painless delivor epidural anesthesia CHEN Changliang CHEN Yuansheng Department of Anesthesiology , Qingyuan Hospital of Ttraditional Chinese Medicine, Guangdong, Qingyuan 511500, China [Abstract] Objective To explore the safety and effectiveness of ropivacaine combined with sufentanil in painless delivor epidural anesthesia. Methods 96 cases of primipara were randomly selected and divided into two groups according to single and double cases in delivery room. Patients in group A were treated with injection of 0.2% ropivacaine and 5 u g sufentanil mixture 6mL, and then maintenance dose of epidural analgesia pump 7mL/h (n=48) . Patients in group B were treated with general delivery (n=48) . Pain classification and fetal outcome during delivery, maternal blood pressure and heart rate changes, maternal VAS score, labor time, labor rate, postpartum urinary retention and so on of the two group were observed. Results The analgesic effect of pain grade group was significantly better than that of control group (P0. 01) . The labor time was longer than that in the analgesia group, and the difference was significant (P0. 05) . The MAP and HR were significantly higher in the group B, and the changes were significantly different (P0. 05) . The caesarean section rate of group A was l ower than that of normal group (P0. 05) . There was no significant difference between the two gr

文档评论(0)

ggkkppp + 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