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中国医药导刊 ›› 2023, Vol. 25 ›› Issue (7): 756-761.

• 临床医药 • 上一篇    下一篇

沙库巴曲缬沙坦钠联合呋塞米治疗高血压伴慢性心力衰竭的临床疗效

  陆燕1, 刘凯1, 周航1, 陈启稚2   

  1. 1.上海市黄浦区老年护理医院内科, 上海 200010;
    2.上海交通大学医学院附属第九人民医院心血管内科, 上海 200011
  • 收稿日期:2023-06-30 修回日期:2023-07-04 出版日期:2023-07-28 发布日期:2023-07-28

The Clinical Efficacy of Combination Therapy with Sacubitril Valsartan Sodium and Furosemide in the Treatment of Hypertension Patients with Chronic Heart Failure

  1. 1.Internal Medicine Department, Shanghai Huangpu District Elderly Care Hospital, Shanghai 200010, China;
    2.Cardiovascular Medicine Department, the Ninth People′s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine,Shanghai 200011, China
  • Received:2023-06-30 Revised:2023-07-04 Online:2023-07-28 Published:2023-07-28

摘要: 目的:探讨沙库巴曲缬沙坦钠联合呋塞米治疗高血压伴慢性心力衰竭(CHF)的疗效及对心功能、炎症因子水平的影响。方法:选择2021年3月至2022年3月我院收治的100例高血压伴CHF患者展开研究,用简单随机数字表法将其分为观察组和对照组,每组各50例。对照组患者给予呋塞米治疗,观察组患者给予沙库巴曲缬沙坦钠+呋塞米联合治疗。治疗3个月后,比较两组患者临床疗效。记录患者治疗前后心功能[左心室舒张末期内径(LVEDD)、左心室收缩末期内径(LVESD)、左心室射血分数(LVEF)]、血压(舒张压、收缩压、心率)、血清炎症因子[N末端脑钠肽前体(NT-proBNP)、C反应蛋白(CRP)、血清肿瘤坏死因子-α(TNF-α)、心肌肌钙蛋白I(cTnI)]水平变化,记录两组患者不良反应。结果:观察组患者治疗总有效率为96.00%,高于对照组的80.00%(P<0.05)。治疗后,两组患者的LVEDD、LVESD水平均降低,观察组患者降低幅度大于对照组;两组患者LVEF水平均升高,观察组患者升高幅度大于对照组(P<0.05)。治疗后,两组患者的舒张压、收缩压、心率均降低,且观察组患者的降低幅度大于对照组(P<0.05)。治疗后,两组患者血清NT-proBNP、CRP、cTnI、TNF-α指标水平均降低,且观察组患者的降低幅度大于对照组(P<0.05)。两组患者不良反应发生率差异无统计学意义(P>0.05)。结论:沙库巴曲缬沙坦钠联合呋塞米治疗高血压伴CHF效果理想,可有效改善患者心功能,有效降低血清炎症因子水平,且不会增加不良反应。

关键词: font-size:medium, ">高血压;慢性心力衰竭;沙库巴曲缬沙坦钠;呋塞米;疗效;不良反应

Abstract: Objective: To investigate the efficacy of combination therapy with sacubitril valsartan sodium and furosemide in the treatment of hypertension patients with chronic heart failure (CHF) and its effects on cardiac function and inflammatory factors levels. Methods:A total of 100 hypertension patients with CHF admitted in our hospital from March 2021 to March 2022 were selected, and were divided into the observation group and the control group according to random number table method, with 50 cases in each group. The control group was treated with furosemide, and the observation group was treated with sacubitril valsartan sodium and furosemide. After 3 months of treatment, the clinical efficacy of the two groups was compared. The levels of cardiac function indicators [left ventricular end diastolic diameter (LVEDD), left ventricular end systolic diameter (LVESD), left ventricular ejection fraction (LVEF)], blood pressure (diastolic pressure, systolic pressure, heart rate), serum inflammatory factors [NT-proBNP, C-reactive protein (CRP), serum tumor necrosis factor-α(TNF-α), cardiac troponin I (cTnI))] were recorded before and after the treatment, and the adverse reactions were recorded for both groups. Results: The total effective rate of the observation group was 96.00%, which was higher than that of the control group (80.00%, P<0.05). After the treatment, the levels of LVEDD and LVESD of patients in both groups decreased, and the observation group was lower than the control group, while the level of LVEF of both groups increased, and the observation group was higher than the control group (P<0.05). After treatment, the diastolic blood pressure, systolic blood pressure, and heart rate of patients in both groups decreased, and the observation group was lower than the control group (P<0.05). After treatment, the serum NT-proBNP, CRP, cTnI, and TNF-α levels of patients in both groups decreased, and the observation group was lower than the control group (P<0.05).There was no statistical difference in the incidence of adverse reactions between the observation group and the control group (P>0.05). Conclusion:The combination therapy of sacubitril valsartan sodium and furosemide has an ideal effect on the treatment of hypertension patients with CHF, which can effectively improve the patient′s heart function, reduce serum inflammatory factor levels, and do not increase adverse reactions.

Key words: font-size:medium, ">Hypertension; Chronic heart failure; Sacubitril valsartan sodium; Furosemide; Efficacy; Adverse reactions

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