检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:王贵齐[1] 于桂香[1] 鞠凤环[1] 马跃华[1] 郝长清[1] 魏文强[1]
机构地区:[1]中国医学科学院肿瘤医院内镜科,北京100021
出 处:《中国内镜杂志》2003年第1期9-11,共3页China Journal of Endoscopy
基 金:卫生部部属 (管 )医院 2 0 0 1- 2 0 0 3临床学科重点项目"食管癌早期诊断及早期治疗的临床规范化研究"
摘 要:目的 :探讨咪唑安定在早期食管癌及其癌前病变内镜治疗过程中的镇静作用。方法 :在对 99例早期食管癌及其癌前病变行内镜下黏膜切除及氩气等离子凝固治疗过程中 ,静脉应用咪唑安定进行镇静。进镜前2min静脉给予咪唑安定 ,首次剂量为 2mg ,治疗前常规静脉追加 1mg ,根据情况间隔 2min以上可追加 1mg ,但总剂量不超过 5mg。术中观察镇静分级及术中症状。术后评价病人对治疗过程的配合程度、感受、耐受程度及记忆缺失情况。治疗过程中给予病人持续吸氧 ,持续心电、血氧、血压、脉搏监测。结果 :本组患者咪唑安定剂量均≤ 5mg ,其中 97例 (98% )在患者治疗过程中无焦虑且能配合治疗。 7例 (8% )患者治疗时略有不适 ,无 1例患者不能耐受内镜治疗。 74例 (75 % )患者对内镜治疗过程记忆缺失 ,2 5例 (2 5 % )患者记忆或部分记忆。治疗成功率 1 0 0 % ,无 1例并发症及意外发生。除 1例由于病人肝功能欠佳出现嗜睡外 ,余无不良反应及副作用。结论 :咪唑安定在一定剂量 (≤ 5mg)范围内作为早期食管癌及其癌前病变内镜治疗的镇静用药是安全有效的。Objective:To study the effect of Midazolam in endoscopic therapy to severe dysplasia and early esophageal cancer on sedation.Method:Ninty nine patients undergoing esophageal mucosal resection(EMR) and Argon Plasma Coagulation(APC) under sedation with intravenously given midazolam. The first dose of midazolam is two milligramme, then it can be added another one milligarmme at two minutes interval, but total dose of midazolam is not more than five milligramme, the sedation scores,symptom, HR and SPO 2 were observed.Result:Whole patients were not more than five milligramme, ninty seven patients were cooperation and without anxiety during therapy, seven patients had slightly uncomfortable, seventy four patients lost their memory to endoscopic therapy, all therapy are successful. No one could not endure endoscopic therapy, except one patient with liver dysfunction is sleepy, no one case have accident and side effect. Conclusion:Midazolam (5mg)can produce safe and effective sedation for endoscopic therapy during endoscopic Mucosal Resection and Argon Plasma Coagulation.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.117