期刊文献+

曲美他嗪与尼可地尔对经皮冠状动脉介入治疗相关心肌损伤干预作用的比较 被引量:69

Comparative Study for Trimetazidine and Nicorandil in Patients With PCI Related Myocardial Injure
下载PDF
导出
摘要 目的:比较口服常规剂量曲美他嗪或尼可地尔对经皮冠状动脉介入治疗(PCI)相关心肌损伤的干预作用。方法:147例行择期PCI的急性心肌梗死或不稳定型心绞痛患者于术前72 h,随机分为四组,即曲美他嗪+尼可地尔组(41例)、曲美他嗪组(n=34例)、尼可地尔组(n=40例)和对照组(n=32例)。对照组接受阿司匹林、β受体阻滞剂、他汀类药物等冠心病常规药物治疗,前三组在上述治疗基础上于术前72 h开始口服常规剂量的曲美他嗪和(或)尼可地尔。四组分别于术前、术后12 h、18 h、24 h抽血检测心肌酶、肌钙蛋白I(cTnI)、血小板平均体积(MPV)水平。结果:对照组术后各时间点的肌酸激酶MB同工酶(CK-MB)与cTnI水平均较术前增高,其中CK-MB水平在术后18 h增高最明显(P=0.049),差异具有统计学意义。而曲美他嗪+尼可地尔组、曲美他嗪组和尼可地尔组术后CKMB、cTnI水平较各组术前相比差异均无统计学意义(P>0.05),且低于对照组同时间点数值。曲美他嗪组各时间点的CK-MB及cTnI水平与尼可地尔组相应时间的数值相比均无统计学差异(P>0.05)。曲美他嗪+尼可地尔组、曲美他嗪组与尼可地尔组术后各时间点的MPV水平较各组术前均有下降,其中曲美他嗪+尼可地尔组与尼可地尔组术后12 h、24 h的MPV水平明显下降(P<0.001),差异具有统计学意义。结论:口服常规剂量曲美他嗪或尼可地尔均可减少PCI引起的心肌损伤,发挥心肌保护作用,两药对PCI心肌损伤的干预作用无显著性差异,且尚未发现两药联用对PCI心肌损伤有更强大的保护作用。本研究还发现,曲美他嗪和尼可地尔均可以减少炎症反应,其中又以尼可地尔作用更明显,这可能是曲美他嗪和尼可地尔能够减少PCI心肌损伤的原因之一。 Objective: To compare the effect of trimetazidine and nicorandil in patients with percutaneous coronary intervention (PCI) related myocardial injure. Methods: A total of 147 patients of acute myocardial infarction (AMI) or unstable angina pectoris with elective PCI were randomly divided into 4 groups. Trimetazidine plus nicorandil group, n=41, Trimetazidine group, n=34, Nicorandil group, n=40 and Control group, n=32 patients received the conventional treatment including aspirin, [3 receptor blocker, statin, etc. In addition to conventional treatment, the first 3 groups received their medication at 72 hours prior to PCI. The levels of myocardial enzymes, cTnl and mean platelet volume (MPV) were examined and compared at before and 12,18 and 24 hours after PCI among different groups. Results: In control group, the post-operative levels of CK-MB and cTnI were increased at each time point, especially for CK-MB, it reached the highest level at 18 h after the operation, P=0.049. In the other 3 groups, the levels of CK-MBand cTnI were similar at before and post-operation, P〉0.05, and they were all lower than that in Control group at the same time point. CK-MB and cTnI were similar between Trimetazidine group and Nicorandil group at each time point, P〉0.05. In those 3 groups, the post-operative MPV level decreased at each time point, in Trimetazidine plus nicorandil group and Nicorandil group, MPV significantly decreased at 12 and 24 h after the operation, P〈0.001. Conclusion: The conventional dose of trimetazidine or nicorandil may reduce myocardial injury after PCI and the combined medication had no special effect. Furthermore, either trimetazidine or nicorandil may reduce the inflammatory response, and nicorandil was stronger, which might be one of the mechanisms for reducing the PCI related myocardial injure.
出处 《中国循环杂志》 CSCD 北大核心 2014年第4期256-260,共5页 Chinese Circulation Journal
关键词 曲美他嗪 尼可地尔 经皮冠状动脉介入治疗 心肌损伤 Trimetazidine Nicorandil Percutaneous coronary intervention Myocardial injury
  • 相关文献

参考文献12

  • 1陈韵岱,赵立坤,田峰,杜志民,江洪,魏盟.曲美他嗪对冠状动脉介入治疗患者的心脏保护作用[J].中华内科杂志,2010,49(6):473-476. 被引量:30
  • 2Bonello L, Sbragia P, Amabile N, et al. Protective effect of an acute oral loading dose of trimetazidine on myocardial injury followingpercutaneous coronary intervention. Heart, 2007, 93: 703-707.
  • 3Ito N, Nanto S, Doi Y, et al. High index of microcirculatory resistance level after successful primary percutaneous coronary intervention can be improved by intraeoronary administration of nicorandil. (]ire J, 2010, 74: 909-915.
  • 4Isono T, Kamihata H, Sutani Y, et al. Nicorandil suppressed myocardial injury after percutaneous coronary intervention. Int J Cardiol, 2008, 123: 123-128.
  • 5张燕,任艺虹,周超飞,张庆考,刘国树,刘陪沛.经皮冠状动脉介入治疗术后急性、亚急性支架内血栓形成的危险因素分析[J].中国循环杂志,2013,28(1):17-20. 被引量:33
  • 6Babu GG, Walker JM, Yellnn DM, et al. Peri-procedural myocardial injury during percutaneous coronary intervention: animportant target for cardioprotection. Eur Heart J, 2011.32: 23-31.
  • 7Kawai Y, Hisamatsu K, Matsllbara H, et al. Intravenous administration of nicorandil immediately before percutaneous coronaryintervention can prevent slow coronary flow phenomenon. Eur Heart J, 2009, 30: 765-772.
  • 8陈韵岱,王长华.急性心肌梗死经皮冠状动脉介入治疗术后无复流的防治进展[J].中国循环杂志,2010,25(3):165-166. 被引量:42
  • 9Ono H, Osanai T, lshizaka H, et al. Nicorandil improves cardiac function and clinical outcome in patients with acute myoeardial infarction undergoing primary percutaneous coronary intervention: role of inhibitory effect on reactive oxygen species formation. Am Heart J, 2004, 148: El5.
  • 10Krolikowski JG, Bienengraeber M, Weihrauch D, et al. Inhibition of mitochondrial permeability transition enhances isoflurane-induced eardioprotectiun during early reperfusion: the role of mitoehondrial KATPcbannels. Anesth Analg, 2005, 101: 1590-1596.

二级参考文献33

  • 1杜润,张瑞岩.晚期支架贴壁不良研究进展[J].国际心血管病杂志,2008,35(6):353-356. 被引量:4
  • 2Schiano P,Gabriel Steg P.Measurement and prevention of myocardial injury during percutaneous coronary intervention.Heart,2007,93:656-657.
  • 3Kantor PF,Lucien A,Kozak R,et al.The antianginal drug trimetazidine shifts cardiac energy metabolism from fatty acid oxidation to glucose oxidation by inhibiting mitochondrial long-chain 3-ketoacyl coenzyme A thiolase.Circ Res,2000,86:580-588.
  • 4Lavanchy N,Martin J,Rossi A.Anti-ischemic effects of trimetazidine:31P-NMR spectroscopy in the isolated rat heart.Arch Int Pharmacodyn Ther,1987,286:97-110.
  • 5Renaud JF.Internal pH,Na +,and Ca2 + regulation by trimetazidine during cardiac cell acidosis.Cardiovasc Drugs Ther,1988,1:677-686.
  • 6Cuamieri C,Muscari C.Effect of trimetazidine on mitochondrial function and oxidative damage during reperfusion of ischemic hypertrophied rat myocardium.Pharmacology,1993,46:324-331.
  • 7Boucher FR,Hearse DJ,Opie LH.Effects of trimetazidine on ischemic contracture in isolated perfused rat hearts.J Cardiovasc Pharmacol,1994,24:45-49.
  • 8Belcher PR,Drake-Holland AJ,Hynd JW,et al.Effects of trimetazidine on in vivo coronary arterial platelet thrombosis.Cardiovasc Drugs Ther,1993,7:149-157.
  • 9Williams FM,Tanda K,Kus M,et al.Trimetazidine inhibits neutrophil accumulation after myocardial ischaemia and reperfusion in rabbits.J Cardiovasc Pharmacol,1993,22:828-833.
  • 10Kantor PF,Lucien A,Kozak R,et al.The antianginal drug trimetazidine shifts cardiac energy metabolism from fatty acid oxidation to glucose oxidation by inhibiting mitochondrial longchain 3-ketoacyl coenzyme A thiolase.Circ Res,2000,86:580-588.

共引文献100

同被引文献585

引证文献69

二级引证文献431

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