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Debate continues about whether intravenous magnesium sulfate improves outcomes in AMI. A study in Cardiovascular Drugs and Therapy evaluated how timing of magnesium administration relates to short- and long-term mortality in the contemporary percutaneous coronary intervention (PCI) era.

The retrospective observational cohort included 4,610 patients with acute type 1 myocardial infarction identified from the MIMIC-IV database. Patients were grouped by the interval between diagnosis and magnesium initiation: Q1 (no magnesium), Q2 (≤2 hours), Q3 (2–6 hours), Q4 (6–12 hours), and Q5 (≥12 hours). The primary outcome was 28-day all-cause mortality, and the secondary outcome was one-year all-cause mortality. Overall 28-day mortality was 18.5%.

Adjusted Kaplan-Meier analyses showed an association between intravenous magnesium sulfate and lower long-term mortality across all timing groups. Landmark analysis demonstrated a stronger association before 28 days (p<0.001). Restricted mean survival time analyses supported the consistency of these results.

Although the findings suggest a possible survival advantage, the single-center observational design cannot confirm causality. Well-designed randomized controlled trials are needed to determine whether intravenous magnesium sulfate improves outcomes in patients with AMI.

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Key highlights
  • Early and late intravenous magnesium use showed consistent associations with survival trends.
  • Mortality patterns varied across treatment timing groups but moved in similar directions.
  • Findings highlight the need for randomized trials to define the therapeutic role of magnesium in acute myocardial infarction (AMI).
Source

Sun Y, Xue X, Zhang W, et al. Association of Intravenous Magnesium Sulfate With Mortality in Patients With Myocardial Infarction: A Retrospective Cohort Study. Cardiovasc Drugs Ther. Published online December 9, 2025. doi:10.1007/s10557-025-07823-w

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Intravenous Magnesium in Acute MI Linked to Improved Survival Patterns
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Analysis of 4,610 patients showed lower long-term mortality across all treatment windows, with stronger associations observed within the first 28 days

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