吴利杰, 董发. 左卡尼汀治疗慢性心力衰竭患者的疗效及安全性[J]. 实用临床医药杂志, 2020, 24(2): 104-107. DOI: 10.7619/jcmp.202002030
引用本文: 吴利杰, 董发. 左卡尼汀治疗慢性心力衰竭患者的疗效及安全性[J]. 实用临床医药杂志, 2020, 24(2): 104-107. DOI: 10.7619/jcmp.202002030
WU Lijie, DONG Fa. Effect and safety of L-carnitine in the treatment of chronic heart failure[J]. Journal of Clinical Medicine in Practice, 2020, 24(2): 104-107. DOI: 10.7619/jcmp.202002030
Citation: WU Lijie, DONG Fa. Effect and safety of L-carnitine in the treatment of chronic heart failure[J]. Journal of Clinical Medicine in Practice, 2020, 24(2): 104-107. DOI: 10.7619/jcmp.202002030

左卡尼汀治疗慢性心力衰竭患者的疗效及安全性

Effect and safety of L-carnitine in the treatment of chronic heart failure

  • 摘要: 目的 探讨左卡尼汀(左旋肉毒碱)治疗慢性心力衰竭(CHF)的疗效及安全性。 方法 将120例CHF患者随机分为对照组(n=60)与观察组(n=60), 对照组予以常规抗CHF药物治疗,观察组在对照组基础上加用左卡尼丁注射液治疗, 2组均连续治疗14 d。比较2组临床疗效、血清N末端脑钠肽前体(NT-proBNP)、半乳糖凝集素-3(Gal-3)、糖类抗原125(CA125)水平及左心室射血分数(LVEF)、左心室内径(LVID)、6 min步行试验最大距离(6MWT)。记录2组不良反应发生情况。 结果 观察组总有效率为91.67%, 显著高于对照组的71.67%(P<0.05)。治疗后,观察组血清NT-pro BNP、Gal-3、CA125水平及LVID水平低于对照组, LVEF、6MWT高于对照组,差异均有统计学意义(P<0.05)。观察组不良反应发生率为21.67%, 与对照组的16.67%相比无显著差异(P>0.05)。 结论 左卡尼汀治疗CHF疗效显著,能够有效降低血清NT-proBNP、Gal-3、CA125表达水平,改善心功能,且安全性良好。

     

    Abstract: Objective To explore efficacy and safety of L-carnitine in the treatment of chronic heart failure(CHF). Methods Totally 120 patients with CHF were randomly divided into control group(n=60)and observation group(n=60). The control group was treated with conventional anti-CHF drugs, while the observation group was treated with L-carnitine injection on the basis of the control group. Both groups were continuously treated for 14 days. The clinical efficacy, serum N-terminal pro-brain natriuretic peptide(NT-proBNP), galectin-3(Gal-3)and carbohydrate antigen 125(CA125)levels, left ventricular ejection fraction(LVEF), left ventricular internal diameter(LVID)and the maximum distance of 6-min walking test(6MWT)were compared between the two groups. Adverse reactions were recorded. Results The total effective rate of the observation group was significantly higher than that of the control group(91.67% vs. 71.67%, P<0.05). After treatment, levels of serum NT-proBNP, Gal-3 and CA125 and LVID in the observation group were significantly lower than those in the control group, while LVEF and 6MWT were significantly higher than the control group(P<0.05). There was no significant difference in the incidence of adverse reactions between the two groups during treatment(21.67% in the observation group vs. 16.67% in the control group, P>0.05). Conclusion L-carnitine is effective in the treatment of CHF, which can effectively reduce the expression levels of serum NT-proBNP, Gal-3 and CA125, improve cardiac function, and it is safe in clinical use.

     

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