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:邢文阁[1] 郭志[1] 刘方[1] 于海鹏[1] 李保国[1] 王海涛[1] 邹强[1] 郭秀英[1]
机构地区:[1]天津医科大学附属肿瘤医院介入治疗科,天津300060
出 处:《中国新药杂志》2009年第12期1116-1118,1140,共4页Chinese Journal of New Drugs
基 金:国家十一五科技支撑计划项目(2007BAI05B06)
摘 要:目的:观察肝癌选择性肝动脉栓塞化疗(Transarterial chemoembolization,TACE)术后口服氨酚羟考酮(泰勒宁)和盐酸曲马多(奇曼丁)进行治疗栓塞后综合征的有效性和安全性。方法:60例NRS评分>3分的肝癌TACE术后男性患者,随机分两组,分别口服泰勒宁和奇曼丁。观察并记录术后即刻、术后0.5,0,1,2,6,12,24,48,72 h的NRS评分、疼痛强度与缓解度变化、EORTC QLQ-C30评分以及不良反应。结果:氨酚羟考酮组、曲马多组均能在术后1 h达到较为满意止痛效果,但氨酚羟考酮组起效时间较曲马多组为短,在术后0.5 h可达到满意效果。与治疗前比较,两组生活质量均有提高。曲马多组发热高于氨酚羟考酮组,两组恶心、呕吐、头晕发生率相仿,但氨酚羟考酮组的消化道反应及嗜睡较曲马多组为多。结论:氨酚羟考酮较曲马多更适于肝癌TACE栓塞后综合征的对症治疗,值得临床推广使用。Objective: To compare the efficacy and safety of oxycodone-acetaminophen versus tramadol in the treatment of post embolization syndrome after transarterial chemoembolization (TACE) in patients with primary hepatic carcinoma. Methods: In 60 male patients with primary hepatic carcinoma, whose numerical rating scales (NRS) 〉 3 after TACE procedure, were randomly divided into two groups. They were treated with either oxycodone-acetaminophen (n = 30) or tramadol (n = 30). NRS scores, odynolysis, EORTC QLQ-C30 and untoward reactions were observed and recorded 0.5, 1 , 2, 6, 12, 24, 48 and 72 h after the operation. Results: Patients in both groups showed satisfaction effects in 1 h after the operation. The pain-relieving effect of oxycodone-acetaminophen at 0.5 h was better than that of tramadol. The quality of life of patients was higher in oxycodone-acetaminophen group than in tramadol group. However, the digestive tract reactions and drowsiness were more frequent in oxycodone-acetaminophen group. Conclusion: Oxycodone-acetaminophen is more suitable than tramadol for the treatment of HCC paitents with post embolization syndrome after TACE.
关 键 词:肝癌 选择性肝动脉栓塞化疗 氨酚羟考酮 曲马多 栓塞后综合征
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:18.223.33.204