首页|螺内酯对射血分数轻度降低心力衰竭合并2型糖尿病患者的临床疗效观察及预后研究

螺内酯对射血分数轻度降低心力衰竭合并2型糖尿病患者的临床疗效观察及预后研究

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目的 探究螺内酯对射血分数轻度降低的心力衰竭合并2型糖尿病患者的临床疗效及预后观察。方法 纳入2019年2月至2022年12月于北京朝阳医院治疗的射血分数轻度降低的心力衰竭合并2型糖尿病患者共409例。所有患者在试验前均未服用过螺内酯,已接受其他心衰标准药物治疗及降糖药物治疗至少半年。通过随机分组将纳入患者分为试验组及对照组,试验组在对照组治疗基础上加用螺内酯10~20 mg/d。比较两组患者治疗前后的糖化血红蛋白(glycated hemoglobin,HbA1c)、体质量指数、血浆N末端B型利钠肽原(NT-proBNP)、左室射血分数(LVEF)、左室舒张末期内径(LVEDD)、舒张期二尖瓣峰值流速与二尖瓣环舒张早期运动峰速度的比值(E/e')、血清肌酐(Scr)、血清尿酸(SUA)、肌酐清除率(Ccr)、血钾水平等指标的变化,观察治疗相关不良反应、心血管死亡或心衰恶化再住院复合终点事件发生率,评估临床治疗效果。结果 两组患者于治疗前的一般资料比较差异无统计学意义(P>0。05);治疗后试验组患者的HbA1c水平较对照组下降[(7。2±0。5)vs。(7。9±0。7),P<0。05],NT-proBNP水平较对照组降低[(423±155)vs。(640±157),P<0。05];试验组治疗后的心功能及肾功能多项指标的改善情况优于对照组(均P<0。05),心功能Ⅱ~Ⅳ级的试验组患者于治疗期间血钾水平相对稳定(均P>0。05)。治疗后试验组的临床显效率及总有效率高于对照组(均P<0。05),复合终点事件发生率及药物治疗相关不良反应在两组中差异无统计学意义(均P>0。05)。结论 螺内酯有助于射血分数轻度降低的心力衰竭合并2型糖尿病患者的血糖管理,并能进一步改善心脏功能及肾功能,同时具有良好的药物使用安全性。
Clinical Efficacy and Prognosis of Spironolactone in Patients with Heart Failure with Mildly Reduced Ejection Fraction and Type 2 Diatetes Mellitus
Objective To explore the clinical efficacy and prognosis of spironolactone in patients with heart failure and type 2 diabetes with slightly reduced ejection fraction.Methods A total of 409 patients with heart failure and type 2 diabetes with slightly reduced ejection fraction who were treated in Beijing Chaoyang Hospital from February 2019 to December 2022 were in-cluded.All patients had not taken spironolactone before the trial and had received treatment with other standard heart failure drugs and hypoglycemic drugs for at least six months.Patients will be randomly divided into an experimental group and a con-trol group.The experimental group will receive 10-20 mg/d of spironolactone in addition to the treatment in the control group.The changes in glycated hemoglobin(HbA1c),body mass index,plasma N-terminal B-type natriuretic peptide(NT proB-NP),left ventricular ejection fraction(LVEF),left ventricular end diastolic diameter(LVEDD),ratio of diastolic peak mitral valve velocity to early mitral annulary(E/e'),serum creatinine(Scr),serum uric acid(SUA),creatinine clearance rate(Ccr),and blood potassium levels between two groups of patients before and after treatment were compared.The incidence of treatment-re-lated adverse reactions,cardiovascular death,or worsening heart failure readmission composite endpoint events were ob-served.Evaluate Clinical treatment efficacy were evaluated.Results There was no statistically significant difference in general information between the two groups of patients before treatment(P>).05).After treatment,the HbA1c level in the experimen-tal group decreased when compared to the control group[(7.2±0.5)vs.(7.9±0.7),P<0.05],and the NT proBNP level de-creased when compared to the control group[(423±155)vs.(640±157),P<0.05].The improvement of various indicators of cardiac and renal function in the experimental group after treatment was better than that in the control group(all P>0.05).Pa-tients in the experimental group with heart function grades Ⅱ-Ⅳ had relatively stable blood potassium levels during treatment(all P>0.05).The clinical efficacy and total effective rate of the experimental group after treatment were higher than those of the control group(both P>0.05),and there was no statistically significant difference in the incidence of composite endpoint e-vents and drug-related adverse reactions between the two groups(P>0.05).Conclusion Spironolactone is helpful to the blood sugar management of heart failure patients with type 2 diabetes and slightly reduced ejection fraction,and can further improve the heart function and renal function,with satisfying drug safety.

spironolactoneejection fractionheart failuretype 2 diabetesrenal function

乐音、吴小朋、刘文婷、张建军

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首都医科大学附属北京朝阳医院心内科,北京 100043

螺内酯 射血分数 心力衰竭 2型糖尿病 肾功能

国家自然科学基金资助项目

82001815

2024

华中科技大学学报(医学版)
华中科技大学

华中科技大学学报(医学版)

CSTPCD北大核心
影响因子:1.443
ISSN:1672-0741
年,卷(期):2024.53(3)