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Clinical Research of Milrinone in Treatment to Refractory Heart Failure |
People’s Hospital of Dongguan City, Dongguan 523000, China |
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Abstract Objective: To investigate the effectiveness and safety of milrinone in treatment to refractory heart failure. Method: During January 2012 to June 2014, 60 patients with refractory heart failure were divided into sodium nitroprusside group( n=30) and milrinone group(n=30). The dosage of sodium nitroprusside and milrinone were 0.5-3 μg/(kg·min)min and 0.5 μg/(kg·min), which the time of duration was 3 days. Result: 28 patients in sodium nitroprusside group and 25 patients in milrinone group were included in the analysis. 7-day effectiveness of the milrinone group was significantly higher than that of the sodium nitroprusside group( P<0.05). BNP of the milrinone group after
treatment was significantly lower than that of the sodium nitroprusside group( P<0.05). There were significant differences in LVEF, E/A, SV, CI between the two groups( P<0.05). There was no significant difference in incidence of adverse events between the two groups. Conclusion: Milrinone can improve the success rate of rescue in patients with Refractory heart failure.
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