- 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、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、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、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
- 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、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、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
地佐辛复合舒芬太尼对结直肠癌患者术后镇痛效果研究
地佐辛复合舒芬太尼对结直肠癌患者术后镇痛效果研究
[摘要] 目的 探讨地佐辛复合舒芬太尼对结直肠癌患者术后镇痛效果。方法 选取2011年1月~2013年6月于本医院治疗的择期行结肠癌、直肠癌根治手术患者68例,随机分为对照组和观察组,每组34例,对照组患者术后给予单纯的舒芬太尼镇痛,观察组患者术后给予地佐辛复合舒芬太尼给患者镇痛,比较两组患者的2h,6h,12h,24h,48 h的VAS和Ramsay镇静评分及镇痛期间的不良反应发生率。结果 两组患者的性别比例、年龄分布、体重、ASA分级、手术时间的差异均无统计学意义(P0.05);两组患者的不同时间点的VAS评分比较的差异均无统计学意义(P0.05);两组患者的不同时间点的Ramsay评分比较的差异均具有统计学意义(P0.05);两组患者镇痛期间的不良反应发生率(嗜睡、恶心呕吐和尿潴留)的差异具有统计学意义(P0.05)。结论 采用地佐辛复合舒芬太尼对结直肠癌患者术后镇痛效果明显,临床不良反应较少,安全性较好,且明显优于单纯舒芬太尼的临床应用效果,值得临床推广。
[关键词] 地佐辛;舒芬太尼;结直肠癌;术后镇痛
[中图分类号] R614[文献标识码] B[文章编号] 1673-9701(2014)18-0071-04
Study on the postoperative analgesic effect of dezocine and sufentanil in patients with colorectal cancer
YU Guocan1 HU Fang1 WANG Li2
1.Department of Anesthesiology,Fuyang People’s Hospital in Zhejiang Province,Fuyang311400, China; 2.Department of Anesthesiology Affiliated Sixth Peoples Hospital to Shanghai Jiaotong University,Shanghai 200240, China
[Abstract] Objective To investigate the postoperative analgesic effect of dezocine and sufentanil in patients with colorectal cancer. Methods Sixty-eight cases with colon cancer, rectal cancer undergoing radical operation in our hospital from January 2011 to June 2013, were randomLy divided into control group and observation group, 34 patients in each group, the patients in control group were given sufentanil analgesia after surgery, and patients in the observation group were given dezocine and sufentanil for analgesia. The VAS and Ramsay sedation score in 2h, 6h, 12h, 24h, 48h and the incidence ratio of adverse reaction during analgesia were compared in two groups. Results There was no statistical significance in the difference of the two groups of sex ratio, age distribution, body weight, ASA classification(P0.05); there was no significnt difference in VAS scores between the two groups at different time points(P0.05); There were statistically significant in differences of Ramsay scores among different time points of two groups(P0.05); There were statistically
文档评论(0)