期刊文献+

倍他洛克加钾镁极化液预防阿霉素所致心脏毒性疗效分析 被引量:1

Efficacy of combination of polarized solution of Ka and Mg with Betaloc for treatment of cardiac muscle toxicity caused by Adriamycin
下载PDF
导出
摘要 目的分析倍他洛克加钾镁极化液预防阿霉素的心脏毒性的效果。方法120例肿瘤患者,随机分为2组,对照组60例常规预处理后用含阿霉素方案化疗。治疗组60例,给予倍他洛克加钾镁极化液加常规预处理后用含阿霉素的方案化疗,比较2组心脏毒性的发生情况。结果治疗组心脏毒性发生率8.33%,心电图改变发生率13.33%;对照组心脏毒性发生率33.33%,心电图改变发生率35.00%;治疗组心脏毒性发生率、心电图改变发生率明显低于对照组(P<0.01)。结论倍他洛克加钾镁极化液治疗肿瘤患者能够降低阿霉素的心脏毒性。 Objective To analyze of efficacy of combination of polarized solution of Ka and Mg with Betaloc for treatment of cardiac muscle toxicity caused by Adriamycin. Methods One hundred and twenty patients with tumors were divided into two groups. The patients in control group were treated with chemotherapy including Adriamycin,the patients in treatment group were performed with protocol of pretreatment with polarized solution of Ka and Mg with Betaloc followed by Adriamycin. Occurrence of cardiac muscle toxicity in two groups was compared. Results The incidence of cardiac muscle toxicity of the treatment group was 8.33% ,The incidence of arrhythmia of the treatment group was 13.33% ,and the incidence of cardiac muscle toxicity of the control team was 33.33% ,the incidence of arrhythmia of the control group was 35.00%. Incidence of cardiac muscle toxicity and arrhythmia in treatment group was obviously lower than that in control group(P 〈 0.05 ). Conclusion Combination of polarized solution of Ka and Mg with Betaloc can decrease cardiac muscle toxicity caused by Adriamycin.
作者 翟中武 袁宇
出处 《新乡医学院学报》 CAS 2007年第2期152-153,共2页 Journal of Xinxiang Medical University
关键词 阿霉素 倍他洛克 极化液 心脏毒性 adriamycin Betaloc polarization liquid cardiac muscle toxicity
  • 相关文献

参考文献6

二级参考文献30

  • 1李拥军,周秀娟,程蕴琳.卡维地洛与充血性心力衰竭[J].医学综述,2004,10(10):608-611. 被引量:12
  • 2李学文,华琦.卡维地洛药理作用机制研究进展[J].实用医学杂志,2005,21(11):1233-1235. 被引量:21
  • 3徐淑云.临床用药指南[M].合肥:安徽科学技术出版社,1989.1047.
  • 4黄焕莉.临床治疗手册[M].广州:广州教育出版社,1997.691.
  • 5Michelle A, Grenier, Steven EL. Epidemiology of Anthracycline Cardiotoxicity in Children and Adults[J]. Semi Oncol. 1998, 25(4suppl 10):72-85.
  • 6Yoav M, Fatih MU. A critical risk-benefit assessment argues against the use of anthracyclines in induction regimens for newly diagnosed childhood acute lymphoblastic leukemia[J ]. Leukemia and lymphoma, 1999, 34(5-6) :415-432.
  • 7Nousiainen T, Vanninen E, Jantunen E, et al. Anthracycline-induced cardiomyopathy:long term of effects on myocardial cell indegrity, cardiac asrenergic innervation and fatty axid uptake [J].Clin Physiol, 2001,21(1) : 123-128.
  • 8Kremer LC, Van-Dalen EC, Offringa M, et al. Anthracycline-induced clinical heart filure in a cohort of 607 child: long-term follow-up study[J]. J Clin Oncol, 2001,19(1): 191-196.
  • 9James S, Carolyn W. Strategies for reduction of anthracycline cardiac toxicity[J]. Semi Oncol, 1998, 25(5): 525-537.
  • 10Krischer JP, Cuthvertson DD, Epster S, et al. Risk factors for early anthracycline clinical cardiotoxicity in the children: the Pediatric Oncology group experience[J]. Progress in pediatric cardiology, 1998, 8:83-90.

共引文献19

同被引文献9

引证文献1

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部