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Naoxintong Supplementation Reduces Heart Failure Risk Following Acute Myocardial InfarctionNew treatment may lower heart failure risk after heart attack

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Key Takeaway
Naoxintong significantly reduces heart failure incidence and MACE in post-reperfusion myocardial infarction patients.

This randomized, double-blind, placebo-controlled trial evaluated the efficacy of Naoxintong in 379 patients with acute myocardial infarction following reperfusion. Participants received either Naoxintong or a matching placebo in addition to standard guideline-directed medical therapy (GDMT) over a 12-month period.

The primary endpoint was the incidence of new-onset heart failure. Patients receiving Naoxintong demonstrated a significantly lower rate of heart failure compared to the placebo group (5.98% vs. 14.06%; HR 0.41, p = 0.01). This suggests a substantial reduction in the risk of developing heart failure in the early post-infarction period.

Secondary outcomes also favored the intervention group. There was a significant reduction in major adverse cardiovascular events (7.97% vs. 14.84%; p = 0.04) and serious adverse events (p = 0.042). Furthermore, the overall rate of adverse events was significantly lower in the group receiving the polyherbal formulation.

Safety data indicated that Naoxintong was well-tolerated by patients. The study suggests that this polyherbal formulation may serve as a viable complementary strategy for secondary prevention in patients following acute myocardial infarction, potentially improving long-term outcomes and safety profiles compared to standard care alone.

How this fits prior evidence

How this fits prior evidence: This finding addresses a gap in secondary prevention strategies for patients following myocardial infarction. While previous coverage noted that heart failure doubles mortality risk in ischemic stroke patients undergoing mechanical thrombectomy, this study focuses on the prevention of new-onset heart failure following myocardial infarction. The results provide a new data point for adjunctive therapies to heart failure prevention in the post-reperfusion phase.

Living with a heart condition after a heart attack is a constant worry for many patients. One of the biggest fears is the development of heart failure, a condition where the heart cannot pump enough blood to meet the body's needs. Researchers recently looked for ways to better protect patients during this critical recovery window.

A trial involving 379 patients in China tested a herbal formula called Naoxintong. Patients who received this formula along with their standard medical treatment showed a much lower rate of new heart failure within one year compared to those who received a placebo. The study also found that those taking the herbal formula had fewer major heart problems and fewer overall side effects.

While the results are promising, it is important to remember that Naoxintong is a polyherbal formulation. The study suggests it could be a helpful extra step in preventing heart issues after a heart attack, but it is meant to be used alongside standard medical care, not instead of it.

What this means for you:
Adding a specific herbal formula to standard care may lower heart failure and major heart risks after a heart attack.

Common questions

What is Naoxintong?

Naoxintong is a polyherbal formulation. In this study, it was given to patients as 4 capsules, three times daily, in addition to their standard medical treatment. It was tested to see if it could help prevent heart failure and other major heart problems after a heart attack.

How did the treatment affect heart failure rates?

The study found that the group taking Naoxintong had a heart failure rate of 5.98% over 12 months. In contrast, the group taking a placebo had a much higher heart failure rate of 14.06%.

Was the treatment safe for the patients?

The study reported a favorable safety profile. Patients taking Naoxintong had fewer overall adverse events (7.97% vs. 21.09%) and fewer serious adverse events (7.97% vs. 14.84%) compared to those who took the placebo.

Study Details

Study typeRct
Sample sizen = 379
EvidenceLevel 2
Follow-up3.0 mo
PublishedOct 2026
View Original Abstract ↓
BACKGROUND: . Despite advances in reperfusion therapy, the incidence and mortality risk of heart failure (HF) remain high among patients with acute myocardial infarction (AMI). Naoxintong (NXT), a well-characterized polyherbal formulation derived from traditional Chinese medicine, has shown potential benefits in preclinical and small-scale clinical studies, but its efficacy has not been tested in a large-scale randomized controlled trial. AIM: . To rigorously evaluate the efficacy and safety of NXT in reducing HF and major adverse cardiovascular events (MACEs) among AMI patients after reperfusion therapy. STUDY DESIGN: . A prospective, multicenter, randomized, double-blind, placebo-controlled, superiority trial. METHODS: . Eligible post-reperfusion AMI patients from 21 hospitals in China were randomly assigned to receive either NXT (4 capsules, three times daily) or a matching placebo for 3 months, in addition to guideline-directed medical therapy (GDMT), with follow-up through 12 months. The primary endpoint was the incidence of new-onset HF within 12 months after randomization. Participants, clinicians, and outcome assessors were blinded to treatment allocation throughout the study period. RESULTS: . A total of 379 patients were included in the primary analysis (mean age 61.6 years; 78.1% male). The incidence of HF was significantly lower in the NXT group than in the placebo group (5.98%vs. 14.06%; HR 0.41, 95% CI 0.21-0.81; p = 0.01). The incidence of MACEs was also reduced with NXT (7.97%vs. 14.84%; HR 0.52, 95% CI 0.28-0.98; p = 0.04). The rates of serious adverse events (7.97%vs. 14.84%; p = 0.042) and any adverse events (7.97%vs. 21.09%; p < 0.001) were lower in the NXT group. No other significant between-group differences were observed for secondary outcomes or adverse event subtypes. CONCLUSION: . NXT, administered in addition to standard GDMT, significantly reduced the 12-month risk of HF and MACEs in reperfused AMI patients, with a favourable safety profile. These findings support NXT as a promising complementary strategy for secondary prevention after AMI.
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