Key result
Early metoprolol in ICU CHF patients linked to ~2% higher 30-day mortality.
Why the study?
The risk-benefit balance of early metoprolol administration in critically ill ICU patients with CHF remains controversial, and high-quality causal clinical evidence is lacking.
Does early metoprolol use increase 30-day mortality in ICU patients with congestive heart failure?
Observational (n=3,934)
No
Does early metoprolol use increase 30-day mortality in ICU patients with congestive heart failure?
Effect estimate: ATE 0.02 (95% CI 0.0004-0.0396)
p-value: p=0.045
Early administration of metoprolol within 24 hours of ICU admission in patients with congestive heart failure is associated with increased 30-day mortality, particularly in hemodynamically unstable and elderly patients.
Early metoprolol was associated with higher 30-day mortality in ICU heart failure; leaves open causation and requires randomized confirmation.
Background The risk-benefit balance of early metoprolol administration in critically ill patients with congestive heart failure (CHF) admitted to the intensive care unit (ICU) remains controversial. However, high-quality causality clinical evidence is still lacking. This study utilized real-world data and causal forest algorithm to investigate the average treatment effect (ATE) of early metoprolol use on 30-day mortality in ICU patients with CHF. We also explored the heterogeneity of individual treatment effects (ITE) to identify clinical characteristics across different treatment-effect populations. Method Study population and their clinical characteristics were obtained from the MIMIC-IV database (version 3.1). Propensity score matching (PSM) was performed to balance baseline confounders. Causal forest models estimated the ATE and ITE. Variable importance, conditional average treatment effect (CATE), and ITE-based quartile analysis were performed to identify heterogeneity and clinical characteristics of patients. Results A total of 5,758 patients were included in the initial cohort, with 3,934 patients entering the final analysis after PSM. The causal forest model indicated that early metoprolol use increased the risk of 30-day ICU mortality by 2% compared with no use group (ATE = 0.02, 95% CI: 0.0004–0.0396, P = 0.045). APSIII, age, and SOFA were the top three variables contributing to the ATE. The causal forest model estimated the conditional average treatment effects for every variable. Individual treatment effects exhibited a right-skewed distribution. The highest ITE percentile was associated with APSIII >64, age >78 years, SOFA >8, WBC >13.95 × 10 9 /L, and BUN >43.06 mg/dL. Conclusion Early metoprolol use within 24 h of ICU admission in CHF patients is associated with increased 30-day mortality. Therapeutic effects were heterogeneous, with the adverse effects being particularly pronounced in patients with high APSIII, advanced age, elevated SOFA, high white blood cell counts, and elevated blood urea nitrogen levels. These findings suggest careful consideration should be given to the early use of metoprolol in high-risk patients.
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Chen et al. (2026) conducted an observational in Congestive heart failure (n=3,934). Early metoprolol vs. No metoprolol use was evaluated on 30-day all-cause mortality (ATE 0.02, 95% CI 0.0004-0.0396, p=0.045). Early metoprolol use within 24 hours of ICU admission in patients with congestive heart failure increased the risk of 30-day mortality by 2%.
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