伊伐布雷定治疗中重度慢性心力衰竭伴窦性心动过速的临床研究

黄琨, 马威, 郑川燕, 等. 伊伐布雷定治疗中重度慢性心力衰竭伴窦性心动过速的临床研究[J]. 临床心血管病杂志, 2017, 33(9): 841-845. doi: 10.13201/j.issn.1001-1439.2017.09.007
引用本文: 黄琨, 马威, 郑川燕, 等. 伊伐布雷定治疗中重度慢性心力衰竭伴窦性心动过速的临床研究[J]. 临床心血管病杂志, 2017, 33(9): 841-845. doi: 10.13201/j.issn.1001-1439.2017.09.007
HUANG Kun, MA Wei, ZHENG Chuanyan, et al. Clinical study of ivabradine in the treatment of moderate and severe chronic heart failure complicated with sinus tachycardia[J]. J Clin Cardiol, 2017, 33(9): 841-845. doi: 10.13201/j.issn.1001-1439.2017.09.007
Citation: HUANG Kun, MA Wei, ZHENG Chuanyan, et al. Clinical study of ivabradine in the treatment of moderate and severe chronic heart failure complicated with sinus tachycardia[J]. J Clin Cardiol, 2017, 33(9): 841-845. doi: 10.13201/j.issn.1001-1439.2017.09.007

伊伐布雷定治疗中重度慢性心力衰竭伴窦性心动过速的临床研究

  • 基金项目:

    国家自然科学基金 (No:81070227)

    北京市自然科学基金 (No:7142048)

    唐山市科技指令科学技术研究与发展项目 (No:12150222B-15)

详细信息
    通讯作者: 张春来, E-mail:huangkun_hk@sina.com
  • 中图分类号: R541.6

Clinical study of ivabradine in the treatment of moderate and severe chronic heart failure complicated with sinus tachycardia

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  • 目的:观察并探讨伊伐布雷定(IVB)治疗Ⅲ~Ⅳ级老年慢性心力衰竭(CHF)伴窦性心动过速的临床疗效与安全性。方法:将2015-07-2016-10收治的95例患者按照随机数字表分为观察组(42例)和对照组(44例),在常规抗心力衰竭(心衰)的治疗基础上,对照组加服富马酸比索洛尔,观察组加服盐酸IVB,疗程2个月,治疗前后测定超声心动图参数[左心室舒张末期内径(LVEDD)、左室收缩末期内径(LVESD、左室射血分数(LVEF)]、血清生物标志物[B型脑钠肽(BNP)、半乳糖凝集素-3(Gal-3)]、心率(HR)及6 min步行距离(6MWD),记录治疗期间药物相关不良反应。结果:治疗后,2组超声心动图参数、生物标志物水平、HR、6MWD均较治疗前改善。2组治疗后LVEDD、LVESD、LVEF差异均无统计学意义(P>0.05);观察组治疗后BNP、Gal-3下降数值均显著高于对照组[(482.6±53.5) pg/ml∶(457.6±48.7) pg/ml、(13.9±4.1) ng/ml∶(12.5±3.6) ng/ml](P<0.05);观察组治疗后HR下降数值[(56.6±4.9)次/min∶(54.4±4.2)次/min]与6MWD提高数值[(212.8±41.5) m∶(193.7±35.2) m]均显著高于对照组(P<0.05);对照组4例比索洛尔达最大推荐剂量但HR仍未达标者,改服IVB后达到目标HR;观察组光幻视发生率23.8%,对照组低血压或心动过缓发生率11.4%,组间差异均有统计学意义(P<0.05),其余不良反应无显著性差异(P>0.05)。结论:IVB较β受体阻滞剂治疗中重度心衰伴窦性心动过速短期内在减缓HR、提高运动耐力及临床安全性方面具有比较优势,为β受体阻滞剂反应性不佳患者提供了另一种选择。
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出版历程
收稿日期:  2017-03-27

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