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优化新生脉散方对慢性心力衰竭气虚血瘀水饮证患者运动耐量的影响OA

Effect of Optimized New Shengmai Powder(优化新生脉散方)on Exercise Tolerance in Patients with Chronic Heart Failure of Qi Deficiency,Blood Stasis and Fluid Retention Syndrome:A Randomized,Double-Blind,Placebo-Controlled Trial

中文摘要英文摘要

目的 评价优化新生脉散方对慢性心力衰竭气虚血瘀水饮证患者运动耐量的影响和安全性.方法 采用随机、双盲、安慰剂对照试验设计,将78例慢性心力衰竭气虚血瘀水饮证患者随机分为治疗组和对照组各39例.治疗组在原西医常规治疗基础上加用优化新生脉散方颗粒剂,对照组同时给予优化新生脉散方安慰剂口服,两组患者均每次服用30.6 g、每日2次,水冲服,共用药4周.主要疗效指标为6分钟步行距离(6MWD)和心肺运动试验峰值摄氧量(Peak VO2).次要疗效指标为纽约心脏病协会(NYHA)心功能分级、血清B型利钠肽(BNP)水平、心功能指标[包括左室射血分数(LVEF)、左室收缩末期内径(LVESD)、左室舒张末期内径(LVEDD)]、明尼苏达心力衰竭生活质量量表(MLHFQ)评分及中医四诊信息计分,分别于治疗前后各评价1次.进行安全性指标评价,记录试验期间不良事件发生情况.结果 治疗组和对照组各39例患者符合全分析集(FAS)和安全性数据集(SS).与本组治疗前比较,治疗组患者治疗后6MWD、心肺运动试验Peak VO2均升高,MLHFQ评分、血清BNP水平、中医四诊信息计分均降低,NYHA心功能分级改善(P<0.01).治疗组治疗后6MWD、心肺运动试验Peak VO2及其与治疗前差值均高于对照组,MLHFQ评分、血清BNP水平、中医四诊信息计分均低于对照组,NYHA心功能分级改善程度优于对照组(P<0.01).对照组治疗前后各指标比较差异均无统计学意义(P>0.05).治疗组不良事件发生率为5.1%(2/39),对照组为2.6%(1/39),两组间不良事件发生率比较差异无统计学意义(P>0.05).结论 在西医常规治疗基础上加用优化新生脉散方,可进一步提高慢性心力衰竭气虚血瘀水饮证患者运动耐量,改善心功能及生活质量,且安全性良好.

Objective To evaluate the effects and safety of the optimized new Shengmai Powder(优化新生脉散方)on exercise tolerance in patients with chronic heart failure(CHF)of qi deficiency,blood stasis,and fluid reten-tion syndrome.Methods A randomized,double-blind,placebo-controlled trial was conducted.A total of 78 CHF patients with qi deficiency,blood stasis,and fluid retention syndrome were recruited and randomly assigned to a treat-ment group(39 cases)and a control group(39 cases).On the basis of conventional western medical therapy,patients in the treatment group additionally received the optimized new Shengmai Powder granules,while the control group was given an oral placebo of optimized new Shengmai Powder granules.Patients in both groups took 30.6 g each time,twice a day,mixed with water for administration,with a total treatment course of 4 weeks.The primary outcomes were 6-minute walk distance(6MWD)and peak oxygen uptake(Peak VO2)measured by cardiopulmonary exercise testing.Secondary outcomes included New York Heart Association(NYHA)functional classification,B-type natri-uretic peptide(BNP)levels,cardiac function indexes including left ventricular ejection fraction(LVEF),left ventri-cular end-systolic diameter(LVESD)and left ventricular end-diastolic diameter(LVEDD),Minnesota Living with Heart Failure Questionnaire(MLHFQ)scores,and scores of four diagnostic information of traditional Chinese medicine(TCM).All indicators were assessed once before and after treatment respectively.Safety indicators were evaluated,and adverse events during the trial were recorded.Results All patients in both groups were included in the full ana-lysis set(FAS)and safety set(SS).Compared with baseline,the 6MWD and Peak VO2 of cardiopulmonary exercise test in the treatment group significantly increased after treatment,while the MLHFQ scores,serum BNP levels and scores of TCM four diagnostic information significantly decreased,and the NYHA cardiac function grade significantly improved(P<0.01).After treatment,the 6MWD and Peak VO2 of cardiopulmonary exercise test,as well as their changes from baseline in the treatment group were higher than those in the control group;the MLHFQ scores,serum BNP levels and scores of TCM four diagnostic information in the treatment group were lower than those in the control group;and the improvement of NYHA cardiac function grade in the treatment group was superior to that in the control group(P<0.01).There was no statistically significant differences in all indicators after treatment in the control group(P>0.05).The incidence of adverse events was 5.1%(2/39)in the treatment group and 2.6%(1/39)in the control group,with no statistically significant difference between groups(P>0.05).Conclusion On the basis of con-ventional western medicine treatment,the addition of the optimized new Shengmai Powder can further improve exer-cise tolerance,cardiac function and quality of life in patients with CHF of qi deficiency,blood stasis and fluid reten-tion syndrome,and show good safety.

王贤良;郑颖;毛静远;张静宜;葛昭;刘桐作;张茂泽;王帅;赵志强;毕颖斐;周瑞娟

天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381天津中医药大学天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381||天津中医药大学天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381天津中医药大学第一附属医院/中医国家临床医学研究中心,天津市西青区昌凌路88号,300381

慢性心力衰竭运动耐量生活质量心功能随机对照试验气虚血瘀水饮证优化新生脉散方

chronic heart failureexercise tolerancequality of lifecardiac functionrandomized controlled trialqi deficiency,blood stasis,and fluid retention syndromeoptimized new Shengmai Powder(优化新生脉散方)

《中医杂志》 2026 (4)

425-431,7

国家中医药管理局中医药创新团队项目(ZYYCXTD-C-202203)中华中医药学会青年求实项目(2022-QNQSDEP-11)

10.13288/j.11-2166/r.2026.04.014

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