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Effects of Xuefu Zhuyu Granules on Patients with Stable Coronary Heart Disease: A Double-Blind, Randomized, and Placebo-Controlled Study

机译:Xuefu zuuyu颗粒对稳定冠心病患者的影响:双盲,随机和安慰剂对照研究

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Despite advances in the drug treatment strategy for stable coronary heart disease (CHD), the mortality of CHD continues to rise. New or adjuvant treatments would be desirable for CHD. Xuefu Zhuyu granules are derived from the formula of traditional Chinese medicine. To determine whether Xuefu Zhuyu granules might have adjuvant effects on stable CHD, we conducted a controlled clinical trial. Patients with stable CHD were enrolled and randomly assigned to receive Xuefu Zhuyu granules or placebo for 12 weeks in addition to their standard medications for the treatment of CHD. The primary endpoints comprise the Canadian Cardiovascular Society Angina Grading Scale (CCS class), echocardiographic measures, Seattle Angina Questionnaire (SAQ), and coronary artery CT. The secondary endpoints included the parameters of nailfold capillary measurement and cutaneous blood perfusion (CBP). After 12 weeks of follow-up, there was a great improvement of the Canadian Cardiovascular Society Angina Grading Scale (CCS class) in the Xuefu Zhuyu group compared with the placebo group ( ). Also, a decrease was found in the percentage of patients with CCS class II in the Xuefu Zhuyu group between follow-up at 12 weeks and baseline ( ). We observed a significant increase in SAQ scores of physical limitation ( ) and treatment satisfaction ( ) in patients receiving Xuefu Zhuyu treatment at 12 weeks in comparison with those at baseline, but not in placebo treatment ( ). Amelioration in coronary artery stenosis in the Xuefu Zhuyu group was noted ( ). Xuefu Zhuyu granule treatment led to great improvements in cutaneous blood perfusion at follow-up of 12 weeks compared with placebo ( ). These findings suggest that on a background of standard medications, Xuefu Zhuyu granules have the ability to further improve the prognosis of patients with stable CHD.
机译:尽管对稳定冠心病(CHD)的药物治疗策略进行了进展,但CHD的死亡率仍在继续上升。对于CHD来说,新的或佐剂治疗是可取的。薛府朱裕颗粒源自中药式。为了确定血府逐瘀颗粒是否可能对稳定型冠心病的辅助效果,我们进行了对照临床试验。除了用于治疗CHD的标准药物外,患有稳定CHD的患者均已注册并随机分配给接受Xuefu Buuyu颗粒或安慰剂12周。主要终点包括加拿大心血管学会心绞痛分级量表(CCS级),超声心动图的措施,西雅图心绞痛问卷(SAQ)和冠状动脉CT。辅助端点包括钉子毛细管测量和皮肤血液灌注(CBP)的参数。随访12周后,与安慰剂集团()相比,加拿大心血管社会Angina Zuyu集团的加拿大心血管社会(CCS类)巨大改善。此外,在12周和基线()的后续行动之间的Xuefu Zhuyu集团中CCS二级患者的百分比中发现了减少。与基线的12周接受Xuefu zhuyu治疗的患者,观察到Xuefu zuuyu治疗的患者的患者的SAQ分数和治疗满意度()显着增加,但不适用于安慰剂治疗()。注意到薛福朱云集团冠状动脉狭窄的改善()。薛福朱裕颗粒治疗导致皮肤血液灌注的巨大改善与安慰剂()相比随后的12周随访。这些研究结果表明,在标准药物的背景下,薛福朱裕颗粒具有进一步改善稳定CHD患者预后的能力。

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