Key result
High-dose methylprednisolone administered within 24 hours after transmural myocardial infarction in rats significantly decreased infarct wall thickness to 0.99 mm compared to 1.35 mm with saline (P<0.001).
Why the study?
Does methylprednisolone administration after myocardial infarction worsen early infarct expansion in a rat model?
Population
Rats undergoing either transmural infarction by left coronary ligation or sham operation
Comparison
Methylprednisolone 50 mg/kg i.p. x 4 within 24 h… vs Saline treatment
Design
Preclinical, Randomized
Follow-up
Up to 7 days
Authors
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High-dose methylprednisolone may promote early infarct expansion in rat MI models; leaves open relevance to human postinfarction remodeling.
Does methylprednisolone administration after myocardial infarction worsen early infarct expansion in a rat model?
Absolute Event Rate: 0.99% vs 1.35%
p-value: p=<0.001
High-dose methylprednisolone given within 24 hours after myocardial infarction promotes early infarct expansion by increasing the slippage of necrotic myocytes before collagen deposition begins.
Mannisi et al. (1987) studied Myocardial infarction (n=128). Methylprednisolone vs. Saline placebo was evaluated on Infarct wall thickness at 3 days (mm) (p=<0.001). High-dose methylprednisolone administered within 24 hours after transmural myocardial infarction in rats significantly decreased infarct wall thickness to 0.99 mm compared to 1.35 mm with saline (P<0.001).
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