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奈西立肽对射血分数保留的失代偿性心力衰竭患者肾功能及其他临床参数的影响。

The effect of nesiritide on renal function and other clinical parameters in patients with decompensated heart failure and preserved ejection fraction.

作者信息

Kelesidis Iosif, Mazurek Jeremy, Khullar Pankaj, Saeed Wajeeha, Vittorio Timothy, Zolty Ronald

机构信息

Department of Cardiology, Albert Einstein College of Medicine, Bronx, NY 10467, USA.

出版信息

Congest Heart Fail. 2012 May-Jun;18(3):158-64. doi: 10.1111/j.1751-7133.2011.00272.x. Epub 2011 Nov 27.

DOI:10.1111/j.1751-7133.2011.00272.x
PMID:22497779
Abstract

The role of nesiritide in patients with decompensated heart failure with preserved ejection fraction (dHFpEF) has not been previously studied. In this investigation, the authors retrospectively analyzed the effect of nesiritide on renal function and clinical outcomes in patients admitted with dHFpEF. Of the 658 patients included, 328 were treated with nesiritide while 330 patients were treated with standard diuretic therapy. In both the nesiritide and no nesiritide groups, there was a significant change in mean glomerular filtration rate (GFR) and creatinine at 72 hours as well as at day of discharge (P<.001). This trend did not progress at 1 month in the nesiritide group, although it did in the no nesiritide group. At 1 month after therapy, however, there was a significant difference between the two groups in the mean change of GFR and creatinine (P<.001). There was no significant difference in >25% decrease of GFR anytime through day 30 (25% vs 29.69%, P=.236) between the two groups. On multivariate analysis, nesiritide was an important predictor of renal function at 1 month (P<.05). Thus, nesiritide can be administered safely without negatively impacting long-term renal function in patients admitted with dHFpEF.

摘要

奈西立肽在射血分数保留的失代偿性心力衰竭(dHFpEF)患者中的作用此前尚未得到研究。在本研究中,作者回顾性分析了奈西立肽对因dHFpEF入院患者肾功能及临床结局的影响。纳入的658例患者中,328例接受奈西立肽治疗,330例接受标准利尿剂治疗。在奈西立肽组和非奈西立肽组中,72小时及出院时平均肾小球滤过率(GFR)和肌酐均有显著变化(P<0.001)。奈西立肽组在1个月时这一趋势未继续进展,而非奈西立肽组则继续进展。然而,治疗1个月后,两组间GFR和肌酐的平均变化存在显著差异(P<0.001)。两组在第30天内任何时间GFR下降>25%的情况无显著差异(25%对29.69%,P = 0.236)。多因素分析显示,奈西立肽是1个月时肾功能的重要预测因素(P<0.05)。因此,对于因dHFpEF入院的患者,使用奈西立肽是安全的,不会对长期肾功能产生负面影响。

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The effect of nesiritide on renal function and other clinical parameters in patients with decompensated heart failure and preserved ejection fraction.奈西立肽对射血分数保留的失代偿性心力衰竭患者肾功能及其他临床参数的影响。
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Effects of standard heart failure therapy and concomitant treatment with intravenous furosemide or inotropes (dobutamine, dopamine, and/or milrinone) on renal function and mortality in patients treated with nesiritide.奈西立肽治疗患者中标准心力衰竭治疗以及静脉注射呋塞米或正性肌力药物(多巴酚丁胺、多巴胺和/或米力农)联合治疗对肾功能和死亡率的影响。
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Effect of nesiritide infusion duration on renal function in acutely decompensated heart failure patients.奈西立肽输注持续时间对急性失代偿性心力衰竭患者肾功能的影响。
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Effect of nesiritide in patients with acute decompensated heart failure.奈西立肽治疗失代偿性心力衰竭的疗效。
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Intermittent outpatient nesiritide infusion reduces hospital admissions in patients with advanced heart failure.间歇性门诊输注奈西立肽可减少晚期心力衰竭患者的住院次数。
J Cardiovasc Pharmacol Ther. 2007 Sep;12(3):232-6. doi: 10.1177/1074248407303657.

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