呋塞米注射液联合rhBNP治疗AHF疗效及对心功能、NT-proBNP、cTnI水平的影响
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兴国县第二医院急诊科

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Efficacy of furosemide injection combined with rhBNP in the treatment of AHF and its influence on cardiac function, NT-proBNP and cTnI levels
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    摘要:

    目的:观察呋塞米注射液联合重组人B型利钠肽(Recombinant Human B-type Natriuretic Peptide, rhBNP)治疗急性心力衰竭(Acute Heart Failure, AHF)疗效及对心功能、N末端B型利钠肽原(N-terminal pro-B-type Natriuretic Peptide, NT-proBNP)、心肌肌钙蛋白I(Cardiac Troponin I, cTnI)水平的影响。方法:本研究共纳入62例2021.01~2025.01收治的AHF患者,并按随机数字表法将其均分为两组,常规组和联合组,每组31例。常规组给予常规对症治疗+呋塞米注射液(20 mg.次-1,1次.d-1,静脉推注,治疗14 d),联合组在常规组基础上加用rhBNP(1.5 μg.kg-1,作为负荷量静脉推注,后以0.0075-0.010 μg.kg-1.min-1的速度静脉泵连续泵注,治疗14 d)。在治疗14 d后观察两组临床疗效,在治疗前和治疗14 d后,通过心脏彩色多普勒超声评估两组心功能[左心室射血分数(Left Ventricular Ejection Fraction, LVEF)、左心室舒张末期内径(Left Ventricular End-Diastolic Diameter, LVEDD)、左心室收缩末期内径(Left Ventricular End-Systolic Diameter, LVESD)和心排血量(Cardiac Output, CO)],并采用酶联免疫法检测血清中NT-proBNP和cTnI,记录两组治疗期间不良反应及随访90 d内主要心血管不良事件(Major Adverse Cardiac Events, MACE)。结果:联合组的治疗总有效率显著高于常规组(P < 0.05);治疗14 d后,两组LVEF和CO均显著提升(P < 0.05),LVEDD和LVESD均显著下降(P < 0.05),且常规组的心功能指标均优于联合组(P < 0.05);治疗14 d后,两组NT-proBNP和cTnI水平显著下降(P < 0.05),且联合组的血清生物学标志物水平低于常规组(P < 0.05);两组治疗期间(14 d)的药物不良反应及随访90 d内的MACE发生率无显著差异(P > 0.05)。结论:呋塞米注射液联合rhBNP可有效治疗AHF患者,改善其心功能和心肌损伤,同时安全性良好,具有较高临床应用价值。

    Abstract:

    Objective: To observe the efficacy of furosemide injection combined with recombinant human B-type natriuretic peptide (rhBNP) in the treatment of acute heart failure (AHF) and its influence on cardiac function, N-terminal pro-B-type natriuretic peptide (NT-proBNP) and cardiac troponin I (cTnI) levels. Methods: This study included 62 patients with AHF from January 2021 to January 2025. The above patients were evenly divided into two groups by random number table method, including conventional group and combined group, with 31 cases in each group. The conventional group was given conventional symptomatic treatment and furosemide injection (20 mg.time-1, once.d-1, intravenous bolus, treatment for 14 days), and the combined group was added with rhBNP (1.5 μg.kg-1 as a loading dose for intravenous bolus, followed by continuous intravenous pump at a rate of 0.0075-0.010 μg.kg-1.min-1, treatment for 14 days) on the basis of the conventional group. After 14 days of treatment, the clinical efficacy in the two groups was observed. Before treatment and after 14 days of treatment, cardiac color Doppler ultrasound was used to evaluate the cardiac function [left ventricular ejection fraction (LVEF), left ventricular end-diastolic diameter (LVEDD), left ventricular end-systolic diameter (LVESD) and cardiac output (CO)] in the two groups. Serum NT-proBNP and cTnI were detected by enzyme-linked immunosorbent assay. Adverse reactions during treatment and major adverse cardiac events (MACE) within 90 days of follow-up were recorded in the two groups. Results: The total effective rate of treatment in combined group was significantly higher than that in conventional group (P<0.05). After 14 days of treatment, LVEF and CO in the two groups were significantly increased (P<0.05) while LVEDD and LVESD were significantly decreased (P<0.05), and the left ventricular function indexes in conventional group were better than those in combined group (P<0.05). After 14 days of treatment, the levels of NT-proBNP and cTnI in the two groups were decreased significantly (P<0.05), and the levels of serum biomarkers in combined group were lower than those in conventional group (P<0.05). There were no significant differences in the incidence rates of adverse drug reactions during treatment (14 days) and incidence rate of MACE within 90 days of follow-up between the two groups (P>0.05). Conclusion: Furosemide injection combined with rhBNP can effectively treat patients with AHF, and improve the cardiac function and myocardial injury, with good safety and high clinical application value.

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  • 收稿日期:2025-10-21
  • 最后修改日期:2025-11-12
  • 录用日期:2025-11-14
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