吴林栩, 王卿语, 叶张章, 郭琰. 常规治疗加用左西孟旦治疗慢性进展性心力衰竭的疗效[J]. 心脏杂志, 2018, 30(6): 713-715. DOI: 10.13191/j.chj.2018.0169
    引用本文: 吴林栩, 王卿语, 叶张章, 郭琰. 常规治疗加用左西孟旦治疗慢性进展性心力衰竭的疗效[J]. 心脏杂志, 2018, 30(6): 713-715. DOI: 10.13191/j.chj.2018.0169
    WU Lin-xu, WANG Qing-yu, YE Zhang-zhang, GUO Yan. Efficacy of routine therapy combined levosimendan in the treatment of chronic progressive heart failure[J]. Chinese Heart Journal, 2018, 30(6): 713-715. DOI: 10.13191/j.chj.2018.0169
    Citation: WU Lin-xu, WANG Qing-yu, YE Zhang-zhang, GUO Yan. Efficacy of routine therapy combined levosimendan in the treatment of chronic progressive heart failure[J]. Chinese Heart Journal, 2018, 30(6): 713-715. DOI: 10.13191/j.chj.2018.0169

    常规治疗加用左西孟旦治疗慢性进展性心力衰竭的疗效

    Efficacy of routine therapy combined levosimendan in the treatment of chronic progressive heart failure

    • 摘要: 目的 观察常规治疗加用左西孟旦对慢性进展性心力衰竭的疗效。 方法 由广州总医院及琼海市人民医院收治的150例慢性进展性心衰患者在对症及常规抗心衰药物的基础上给予左西孟旦治疗,疗程28 d。观察治疗前后心功能指标的变化,并注意药物副作用的发生情况。 结果 左西孟旦治疗后,77.3%患者左室舒张末期内径(LVEDD)较给药前显著缩小由(57±6)mm降至(49±5)mm (P<0.01);左房内径(LAD)由(40±4)mm降至(34±5)mm (P<0.01);左室射血分数(LVEF)由(32±5)%增加至(40±8)%(P<0.01),血清N末端脑钠尿肽原(NT-proBNP)水平由(3.3±1.6)ng/ml降至(1.9±1.2)ng/ml (P<0.01)。其中11例患者出现不良反应,不良反应发生率为0.73%。 结论 常规治疗加用左西孟旦治疗慢性进展性心力衰竭有显著疗效,安全性好。

       

      Abstract: AIM To observe the efficacy of routine therapy combined with levosimendan in the treatment of chronic progressive heart failure. METHODS 150 chronic progressive heart failure patients selected by General Hospital of Guangzhou Military Command of PLA and Qionghai people hospital were treated with levosimendan for 28 days with symptomatic and conventional anti-heart failure drugs. Changes in cardiac function index before and after the treatment were observed, and side effects of the drugs were documented. RESULTS After levosimendan treatment, the left ventricular end-diastolic dimension (LVEDD) in 77.3% patients significantly decreased when compared with cardiac state before administration, LVEDD decreased from (57±6) mm to (49±5) mm (P <0.01); Left atrial diameter diminished from (40±4) mm to (34±5) mm. The left ventricular ejection fraction increased from (32±5)% to (40±8)% (P<0.01), and serum NT-proBNP levels decreased from (3.3±1.6) ng/ml to (1.9±1.2) ng/ml (P<0.01). Eleven patients showed adverse reactions, the incidence of adverse reactions was 0.73%. CONCLUSION Therapy combined with levosimendan has a significant therapeutic effect on chronic progressive heart failure, which can effectively relieve ventricular remodeling and has a good safety profile.

       

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