4.6 Article

Effects of Traditional Chinese Medicine Shensong Yangxin Capsules on Heart Rhythm and Function in Congestive Heart Failure Patients with Frequent Ventricular Premature Complexes: A Randomized, Double-blind, Multicenter Clinical Trial

Journal

CHINESE MEDICAL JOURNAL
Volume 130, Issue 14, Pages 1639-1647

Publisher

WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/0366-6999.209906

Keywords

Congestive Heart Failure; Randomized Controlled Trial; Shensong Yangxin Capsules; Ventricular Premature Complexes

Funding

  1. 973 Program of China [2012CN518606]

Ask authors/readers for more resources

Background: Pharmacological therapy for congestive heart failure (CHF) with ventricular arrhythmia is limited. In the study, our aim was to evaluate the effects of Chinese traditional medicine Shensong Yangxin capsules (SSYX) on heart rhythm and function in CHF patients with frequent ventricular premature complexes (VPCs). Methods: This double-blind, placebo-controlled, multicenter study randomized 465 CHF patients with frequent VPCs to the SSYX (n = 232) and placebo groups (n = 233) for 12(th) weeks of treatment. The primary endpoint was the VPCs monitored by a 24-h ambulatory electrocardiogram. The secondary endpoints included the left ventricular ejection fraction (LVEF), left ventricular end-diastolic diameter, N-terminal pro-brain natriuretic peptide (NT-proBNP), New York Heart Association (NYHA) classification, 6-min walking distance (6MWD), Minnesota Living with Heart Failure Questionnaire (MLHFQ) scores, and composite cardiac events (CCEs). Results: The clinical characteristics were similar at baseline. SSYX caused a significantly greater decline in the total number of VPCs than the placebo did (-2145 +/- 2848 vs. -841 +/- 3411, P < 0.05). The secondary endpoints of the LVEF, NYHA classification, NT-proBNP, 6MWD, and MLHFQ scores showed a greater improvements in the SSYX group than in the placebo group (Delta LVEF at 12(th) week: 4.75 +/- 7.13 vs. 3.30 +/- 6.53; NYHA improvement rate at the 8(th) and 12(th) week: 32.6% vs. 21.8%, 40.5% vs. 25.7%; mean level of NT-proBNP in patients with NT-proBNP = 125 pg/ml at 12(th) week: -122 [Q1, Q3: -524, 0] vs. -75 [Q1, Q3: -245, 0];.6MWD at 12(th) week: 35.1 +/- 38.6 vs. 17.2 +/- 45.6; Delta MLHFQ at the 4(th), 8(th), and 12(th) week: -4.24 +/- 6.15 vs. -2.31 +/- 6.96, -8.19 +/- 8.41 vs. -3.25 +/- 9.40, -10.60 +/- 9.41 vs. -4.83 +/- 11.23, all P < 0.05). CCEs were not different between the groups during the study period. Conclusions: In this 12(th) week pilot study, SSYX was demonstrated to have the benefits of VPCs suppression and cardiac function improvement with good compliance on a background of standard treatment for CHF.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available