广州医药 ›› 2025, Vol. 56 ›› Issue (7): 988-994.DOI: 10.20223/j.cnki.1000-8535.2025.07.020

• 论著 • 上一篇    下一篇

达格列净联合沙库巴曲缬沙坦治疗射血分数降低的心力衰竭患者的疗效

谭文亮, 吴天源, 刘震   

  1. 华南理工大学附属第二医院(广州市第一人民医院)心血管内科(广东广州 510180)
  • 收稿日期:2024-11-18 出版日期:2025-07-20 发布日期:2025-08-28
  • 通讯作者: 刘震,E-mail:lz71826@163.com
  • 基金资助:
    广州市卫生健康科技重大项目(CZ0102112201)

Efficacy of dapagliflozin combined with sacubitril/valsartan in the treatment of heart failure with reduced ejection fraction

TAN Wenliang, WU Tianyuan, LIU Zhen   

  1. Department of Cardiovascular,The Second Affiliated Hospital of South China Normal University(Guangzhou First People's Hospital),Guangzhou 510180,China
  • Received:2024-11-18 Online:2025-07-20 Published:2025-08-28

摘要: 目的 分析达格列净联合沙库巴曲缬沙坦治疗射血分数降低的心力衰竭(HFrEF)效果。方法 连续抽取2021年1月—2023年6月在广州市第一人民医院心内科住院的射血分数降低的心力衰竭(HFrEF)患者203例,随访至少6个月,按照接受的治疗进行分组。对照组予常规治疗和沙库巴曲缬沙坦治疗;观察组予常规治疗、沙库巴曲缬沙坦和达格列净治疗;对比两组疗效,观察指标包括住院时间,入院及出院后6个月的心功能状态(NYHA纽约心脏病协会心功能分级)、心脏超声指标左室射血分数(LVEF)、左室舒张末内径(LVEDD)、左室收缩末内径(LVSDD)、血液指标-端脑钠肽前体(NT-proBNP N)、糖化血红蛋白(HBA1c)、血肌酐(Cr)、6个月时的再住院率及全因死亡率。结果 观察组心脏监护病房(CCU)停留时间(2.54±1.26)d,短于对照组的(3.73±1.21)d;观察组6个月时观察组心功能NYHA改善≥2级比例为95.05%高于对照组的86.27%,差异有统计学意义(P<0.05);观察组6个月时的LVEDD、LVESD水平分别为(48.22±7.35)(34.61±4.32)mm,低于对照组的(51.47±8.02)(43.07±5.33)mm,LVEF为(51.49±5.40)%,高于对照组的(46.18±4.21)%,差异有统计学意义(P<0.05);6个月时观察组的NT-proBNP为(415.58±31.57)pg/mL,低于对照组的(520.23±385.56)pg/mL,差异有统计学意义(P<0.05);两组的住院时间、血清肌酐(Cr)、HBA1c、6个月时的再住院率、全因病死率对比,差异不显著(P>0.05)。观察组HBA1c值为(6.04±0.66)mmol/L,高于对照组的(5.20±0.56)mmol/L(P<0.05)。结论 HFrEF患者采取达格列净+沙库巴曲缬沙坦治疗,可通过协同作用,缩短CCU停留时间,改善患者6个月时的心功能状态,降低NT-proBNP值,减少心脏扩大趋势,提高LVEF水平。

关键词: HFrEF, 达格列净, 沙库巴曲缬沙坦

Abstract: Objective To analyze the efficacy of dapagliflozin combined with sacubitril/valsartan in the treatment of heart failure with reduced ejection fraction(HFrEF).Methods A total of 203 patients with HFrEF who were hospitalized in the cardiology department of the hospital between January 2021 and June 2023 were enrolled and followed up for at least six months.Patients were divided into groups based on their treatment regimens:the control group received conventional treatment plus sacubitril/valsartan,while the observation group received conventional treatment plus sacubitril/valsartan and dapagliflozin.The two groups were compared for clinical outcomes,including length of hospital stay,cardiac function(NYHA classification)at admission and six months after discharge,echocardiographic indicators(LVEF,LVEDD,LVESD),blood indicators(NT-proBNP,HbA1c,creatinine),six-month rehospitalization rate,and all-cause mortality.Results The observation group had a shorter CCU stay(2.54±1.26 days)compared to the control group(3.73±1.21 days).At sixth month,the proportion of patients in the observation group with an NYHA improvement ≥2 grades(95.05%)was significantly higher than that in the control group(86.27%)(P<0.05).The observation group demonstrated lower LVEDD(48.22±7.35 mm)and LVESD(34.61±4.32 mm)levels and higher LVEF(51.49±5.40%)compared to the control group(LVEDD:[51.47±8.02] mm,LVESD:[43.07±5.33] mm,LVEF:[46.18±4.21]%)(P<0.05).NT-proBNP levels in the observation group([415.58±31.57] pg/mL)were significantly lower than those in the control group([520.23±385.56] pg/ml)(P<0.05).There were no significant differences between the two groups in length of total hospital stay,serum creatinine,HbA1c,six-month rehospitalization rate,or all-cause mortality(P>0.05).However,HbA1c levels in the observation group([6.04±0.66] mmol/L)were higher than those in the control group([5.20±0.56] mmol/L)(P<0.05).Conclusions The combination of dapagliflozin and sacubitril/valsartan in the treatment of HFrEF patients can exert a synergistic effect,shorten CCU stay,improve cardiac function at sixth month,reduce NT-proBNP levels,mitigate cardiac dilation,and increase LVEF.

Key words: HFrEF, dapagliflozin, sacubitril/valsartan