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左西孟旦或重组人脑利钠肽对急性失代偿性心力衰竭患者心肾功能影响的对比研究 被引量:8

Comparison of clinical outcomes between levosimendan and recombinant B-type natriuretic peptide for heart and renal function in acute decompensated heart failure patients
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摘要 目的探讨静脉滴注左西孟旦(Levo)或重组人脑利钠肽(rhBNP)对急性失代偿性心力衰竭(ADHF)患者心肾功能的影响。方法 50例ADHF患者(纽约心脏病学会心功能分级Ⅲ或Ⅳ级)纳入研究,随机分入Levo组(静脉滴注Levo 0.1μg·kg-1·min-1)和rhBNP组(静脉滴注rhBNP 0.01μg·kg-1·min-1),每组25例。观察两组治疗后24h的24h尿量、收缩压的变化,治疗后48h的血清肌酐(sCr)水平、估算的肾小球滤过率(eGFR)的变化,治疗后7d的左心室射血分数(LVEF)、血浆脑利钠肽(BNP)水平的变化。进一步比较治疗前收缩压≤95mmHg(1mmHg=0.133kPa)且LVEF<0.35的患者治疗前后的收缩压和LVEF。结果两组在治疗后24、48、72h的24h尿量均较同组治疗前显著增多(P值均<0.01)。两组在治疗后24h的收缩压与同组治疗前的差异均无统计学意义(P值均>0.05)。两组在治疗后24、48、72h和7d的sCr水平均较同组治疗前显著下降(P值均<0.01),eGFR均较同组治疗前显著升高(P值均<0.01)。两组在治疗后7d的血浆BNP水平均较同组治疗前显著降低(P值均<0.01),LVEF均较同组治疗前显著改善(P值均<0.05)。两组间治疗后各时间的24h尿量、收缩压、eGFR和sCr、血浆BNP水平的差异均无统计学意义(P值均>0.05),Levo组在治疗后7d的LVEF显著高于rhBNP组同时间(P<0.01)。Levo组中治疗前收缩压≤95mmHg且LVEF<0.35的ADHF患者(12例)治疗前后收缩压的差异无统计学意义(P>0.05),治疗后7d的LVEF较治疗前显著提高(P<0.01);rhBNP组中治疗前收缩压≤95mmHg且LVEF<0.35的ADHF患者(9例)治疗前后的收缩压和LVEF与治疗前的差异均无统计学意义(P值均>0.05)。结论 ADHF患者静脉滴注Levo较rhBNP能更好地改善左心室的收缩功能,两者均具有肾脏保护作用。对于低心排量伴收缩压降低的患者更倾向于选择Levo。 Objective To compare the effects between levosimendan (Levo) and recombinant human B- type natriuretic peptide (rhBNP) on heart and renal function in patients suffered from acute decompensated heart failure (ADHF). Methods Fifty patients with ADHF (New York Heart Association heart function classification standard 11[ or ]V) were enrolled in this study and randomly divided into Levo group (n=25, 0. 1μg·kg-1·min-1 Levo was intravenously given) and rhBNP group (n = 25, 0.01 μg·kg-1·min-1 rhBNP was intravenously given). Urine volume, systolic blood pressure (SBP), serum creatinine (sCr), estimated glomerular filtration rate (eGFR), left ventricular ejection fraction (LVEF) and serum BNP were measured before and after treatment. Subgroup analyses were performed for patients with LVEF^0.35 and SBP^95 mmHg (1 mmHg = 0. 133 kPa). Results Compared with the parameters before treatment, 24 h urine volume, eGFR and LVEF were significantly increased, while sCr and BNP were significantly decreased after treatment (P〈0.01 or P〈0.05). There was nosignificant difference between preoperative and postoperative SBP in all patients (P〉0.05). After treatment, there was no significant difference in terms of 24 h urine volume, SBP, sOr, eGFR or BNP between two groups (all P〉0.05). LVEF in Levo group was significantly higher than that in rhBNP group on day 7 after surgery (P〈 0.01). Subgroup analysis showed that SBP level was not significantly decreased (P〉0. 05) and LVEF was significantly increased after treatment (P〈0.05) in Levo group, while there was no significant difference in SBP or LVEF in rhBNP group (both P〉0.05). Conclusion Compared with rhBNP therapy, intravenous Levo therapy may effectively improve LVEF in ADHF patients. Both Levo and rhBNP can protect renal function. Therefore, it is prone to choose Levo in patients those with low-output heart failure, especially those with low blood pressure.
出处 《上海医学》 CAS CSCD 北大核心 2013年第11期915-919,共5页 Shanghai Medical Journal
基金 上海市卫生局局级科研项目资助(20114324)
关键词 左西孟旦 重组人脑利钠肽 急性失代偿性心力衰竭 心功能 .肾功能 Levosimendan Recombinant B-type natriuretic peptide~ Acute decompensated heart failure^Heart function~ Renal function
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参考文献19

  • 1ABRAHAM W T, LOWES B D, FERGUSON D A, et al. Systemic hemodynamic, neurohormonal, and renal effects of a steady-state infusion of human brain natriuretic peptide in patients with hemodynamically decompensated heart failure [J]. J Card Fail, 1998, 4(1): 37-44.
  • 2BURGER A J. A review of the renal and neurohormonal effects of B-type natriuretic peptide[J]. Congest Heart Fail, 2005, 11(1): 30-38.
  • 3Publication Committee for the VMAC Investigators ( Vasodilatation in the management of acute CHF ). Intravenous nesiritide vs nitroglycerin for treatment of decompensated congestive heart failure: a randomized controlled trial[J]. JAMA, 2002, 287(12) : 1531-1540.
  • 4PEACOCK W F 4th, HOLLAND R, GYARMATHY R, et al. Observation unit treatment of heart failure with nesiritide: results from the proaction trial [J]. J Emerg Med, 2005, 29(3): 243-252.
  • 5COLUCCI W S, ELKAYAM U, HORTON D P, et al. Intravenous nesiritide, a natriuretic peptide, in the treatment of decompensated congestive heart failure. Nesiritide Study Group[J]. N Engl J Med, 2000, 343(4): 246-253.
  • 6COLUCCI W S. Nesirinde for the treatment of decompensated heart failure[J]. J Card Fail, 2001, 7 (1) 92-100.
  • 7MEBAZAA A, NIEMINEN M S, PACKER M, et al. Levosimendan vs dobutamine for patients with acute decompensated heart failure: the SURVIVE randomized trial [J]. JAMA, 2007, 297(17): 1883-1891.
  • 8FARMAKIS D, PARISSIS J T, BISTOLA V, et al. Plasma B-type natriuretic peptide reduction predicts long-term response to levosimendan therapy in acutely decompensated chronic heart failure[J]. Int J Cardiol, 2010, 139 (1): 75-79.
  • 9DELANEY A, BRADFORD C, MCCAFFREY J, et al. Levosimendan for the treatment of acute severe heart failure: a meta-analysis of randnmised controlled trials[J]. Int J Cardiol, 2010, 138(3), 281-289.
  • 10ZHANG J, FU X, JIA X, et al. B-type natriuretic peptide for prevention of contrast-induced nephropathy in patients with heart failure undergoing primary percutaneous coronary intervention[J]. Acta Radiol, 2010, 51(6): 641-648.

二级参考文献12

  • 1Mcmurray J, Pfeffer MA. New therapy options in congestive heart failure [ J ]. Circulation, 2002,105 ( 17 ) : 2099 - 2106.
  • 2Chung P, Hermann L. Acute decompensated heart failure: formulating an evidence -based approach to diagnosis and treatment( part I) [J]. MtSinai J Med, 2006,73(2) :506-515.
  • 3Spinarova L, Vitovec J. Neurohumoral changes in chronic heart failure[ J]. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub, 2007,151 (2) :201-207.
  • 4Keating GM, Goa KL. Nesiritide: a review of its use in acute decompensated heart failure [J]. Drugs,2003,63 ( 1 ) :47 - 70.
  • 5Taylor JA, Christenson RH, Rao K, et al. B - type natriuretic peptide and N - terminal pro B - type natriuretic peptide are depressed in obesity despite higher left ventricular end diastolic pressures [ J ]. Am Heart J, 2006,152 (6) :1071 -1076.
  • 6Weeks SG. Nesiritide: the clinical experience [ J]. Can J Cardiol, 2008,24 : 19B-21B.
  • 7Charles C J, Rademaker MT, Richards AM. Hemodynamic, hormonal, and renal actions of adrenomedullin - 2 in normal conscious sheep Endocrinology [ J ]. 2006,147 (4) : 1871 - 1877.
  • 8Abraham WT, Cheng ML, Smoluk G, et al. Vasodilation in the Management of Acute Congestive Heart Failure (VMAC) Study Group. Clinical and bemodynamic effects of nesiritide( B - type natriuretic peptide) in patients with decompensated heart failure receiving beta blockers [ J ]. Congest Heart Fail, 2005,11 (2) :59 - 64.
  • 9Hunt SA, Abraham WT, Chin MH, et al. ACC/AHA 2005 Guideline Update for the Diagnosis and Management of Chronic Heart Failure in the Adult - Summary Article [ J]. Circulation, 2005, 112 (12) :54-235.
  • 10Owan TE, Chen HH, Frantz RP, et al. The effects of nesiritide on renal function and diuretic responsiveness in acutely decompensated heart failure patients with renal dysfunction [ J ]. J Card Fail,2008, 14(4) :267 N275.

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