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Yiqi Fumai injection improved BNP reduction and heart function in acute heart failure patients compared to standard therapy alone

Yiqi Fumai injection improved BNP reduction and heart function in acute heart failure patients…
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Key Takeaway
Adding Yiqi Fumai lyophilized injection to standard therapy significantly improved BNP reduction and heart function markers in acute heart failure patients without increasing safety risks.

This randomized controlled trial evaluated the efficacy of Yiqi Fumai lyophilized injection in patients with acute decompensated ischemic heart failure. The study involved 666 patients across 37 hospitals in China, comparing the injection plus guideline-directed medical therapy against medical therapy alone.

The primary outcome measured the proportion of patients achieving a decrease in B-type natriuretic peptide of at least 30% by day eight. Results showed a significantly higher proportion of patients met this target in the treatment group compared to the control group.

Secondary analyses revealed statistically significant improvements in left ventricular ejection fraction, New York Heart Association functional class, and quality of life scores for those receiving the injection. No significant differences were observed for composite endpoint events or adverse events between the two groups.

Safety data indicated that the addition of Yiqi Fumai lyophilized injection did not increase safety risks or lead to discontinuations. The findings suggest a favorable benefit-risk profile for this intervention in the acute setting.

Study Details

Study typeRct
Sample sizen = 666
EvidenceLevel 2
PublishedJun 2026
View Original Abstract ↓
BACKGROUND: Patients with acute decompensated ischemic heart failure (ADIHF) often present with severe clinical symptoms and poor quality of life. In China, Yiqi Fumai lyophilized injection (YQFM) is widely used in the treatment of ADIHF. However, high-quality evidence is still needed to support its efficacy and safety. PURPOSE: This study aims to assess the therapeutic efficacy and safety of YQFM in patients with ADIHF. STUDY DESIGN AND METHODS: By conducting a multicenter, open-label, blinded-outcome, randomized controlled trial, we recruited patients with ADIHF from 37 hospitals in 20 regions of China from October 2015 to October 2018. Patients were allocated in a 1:1 ratio to either the YQFM group or the control group. Both groups received guideline-directed medical therapy (GDMT), with the YQFM group additionally receiving YQFM for 7 days. The primary outcome included the proportion of patients with a decrease from baseline B-type natriuretic peptide (BNP) value ≥ 30% on day 8 post-randomization. We evaluated the left ventricular ejection fraction (LVEF), New York Heart Association (NYHA) functional class, Minnesota Living with Heart Failure Questionnaire (MLHFQ) score, and composite endpoints. RESULTS: A total of 666 patients with ADIHF (332 in the YQFM group and 334 in the control group) were enrolled. The full analysis set (FAS) analysis revealed that the proportion of patients in the YQFM group with a reduction of at least 30% in BNP value on day 8 was higher than that in the control group (175 [55.21%] vs. 135 [41.93%], one-sided p < 0.001, two-sided p < 0.001; RR, 1.32 [95% CI, 1.12-1.56]). The YQFM group showed statistically significant improvements in LVEF, NYHA functional class, and MLHFQ scores compared to controls. There was no statistically significant difference between the two groups regarding composite endpoint events and adverse events during the follow-up period. CONCLUSIONS: Based on GDMT, the combined use of YQFM was associated with further reductions in BNP levels, improve quality of life and cardiac function in patients with ADIHF, without increasing safety risks. However, no significant differences were observed in clinical events, such as mortality or hospitalization, during the follow-up period.
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