JIA Jun-bing, FAN Rui-hong. Clinical Efficacy of Tongbu Xinbao Capsule on Qi Deficiency Blood Stasis and Water Flux Type Chronic Heart Failure[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(8): 171-175.
JIA Jun-bing, FAN Rui-hong. Clinical Efficacy of Tongbu Xinbao Capsule on Qi Deficiency Blood Stasis and Water Flux Type Chronic Heart Failure[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(8): 171-175. DOI: 10.13422/j.cnki.syfjx.20180818.
Objective: To observe the clinical efficacy of Tongbu Xinbao capsule on chronic heart failure (Qi deficiency blood stasis and water flux type)
in order to investigate the mechanism of Tongbu Xinbao capsule on chronic heart failure. Method: A total of 120 patients with chronic heart failure outpatients or inpatient patients were randomly divided into treatment group and control group
with 60 cases in each group. The control group got western medicine for basic treatment; in addition to the therapy of the control group
the treatment group was also given Tongbu Xinbao capsule
4 capsule
tid
for 4 weeks. After the treatment
the clinical efficacy of the two groups were observed; and before and after treatment
symptom score
N-terminal-proBNP (NT-proBNP)
plasma renin aetivity (PRA)
aldosterone (ALD)
angiotensin Ⅱ (AngⅡ) and homocysteic acid (HCY) levels were observed
and the blood
urine
stool routine
liver and kidney function and other laboratory parameters were detected to determine the toxic and side effects of Tongbu Xinbao capsule. Result: Efficacy of traditional Chinese medicine(TCM) syndrome of treatment group was 91.67%
which was significantly higher than 81.67% of control group. After treatment
PRA
AngⅡ
ALD
HCY
NT-proBNP were significantly decreased than before treatment
and those in the treatment group were superior to those of the control group (P<0.05). Conclusion: Conventional western medicine combined with Tongbu Xinbao capsule showed a significant therapeutic effect
suggesting that the combined administration can better inhibit RASS activity and reduced HCYof patients with heart failure
which may be related to the inhibition of PRA
Ang11
ALD
HCY
with no toxic or side effect and a reliable efficacy.