- Open Access
Cardiovascular and renal effects of carperitide and nesiritide in cardiovascular surgery patients: a systematic review and meta-analysis
Critical Care volume 15, Article number: R258 (2011)
Acute kidney injury (AKI) following cardiovascular surgery is a common disease process and is associated with both morbidity and mortality. The aim of our study was to evaluate the cardiovascular and renal effects of an atrial natriuretic peptide (ANP, carperitide) and a B-type (or brain) natriuretic peptide (BNP, nesiritide) for preventing and treating AKI in cardiovascular surgery patients.
Electronic databases, including PubMed, EMBASE and references from identified articles were used for a literature search.
Data on the infusion of ANP or BNP in cardiovascular surgery patients was collected from fifteen randomized controlled trials and combined. The infusion of ANP or BNP increased the urine output and creatinine clearance or glomerular filtration rate, and reduced the use of diuretics and the serum creatinine levels. A meta-analysis showed that ANP infusion significantly decreased peak serum creatinine levels, incidence of arrhythmia and renal replacement therapy. The meta-analysis also showed that ANP or BNP infusion significantly decreased the length of ICU stay and hospital stay compared with controls. However, the combined data were insufficient to determine how ANP or BNP infusion during the perioperative period influences long-term outcome in cardiovascular surgery patients.
The infusion of ANP or BNP may preserve postoperative renal function in cardiovascular surgery patients. A large, multicenter, prospective, randomized controlled trial will have to be performed to assess the therapeutic potential of ANP or BNP in preventing and treating AKI in the cardiovascular surgical setting.
Even with the latest advances in surgical and anesthetic techniques and postoperative intensive care, patients undergoing cardiovascular surgery for left ventricular dysfunction still have a fairly high mortality [1, 2]. The mortality for severe left ventricular dysfunction in patients undergoing coronary artery bypass grafting is 4.6% to 5.6% and 22.3% to 31% at 30-days and 5 years, respectively, whereas the mortality for normal left ventricular function is 1.1% to 1.9% and 5.5% to 7% at 30 days and 5 years, respectively[1, 2]. These cardiovascular surgery patients spend prolonged periods in the ICU and hospital, and their survival is strongly dependent on their pre-operative left ventricular ejection fraction . Cardiorenal syndrome is another serious concern, as patients with left ventricular dysfunction also tend to suffer from acute kidney injury (AKI) . AKI is a common complication in all patients undergoing cardiovascular surgery. A small percentage (0.7% to 3.4%) of patients who develop AKI after cardiovascular surgery require renal replacement therapy, and renal replacement therapy-dependent AKI is an independent risk factor for early mortality following cardiovascular surgery [4–6]. To make matters worse, AKI considerably increases postoperative costs following cardiovascular surgery . The associated mortality risk is additive in non-overlapping patients groups; the hazard ratio for AKI only is 1.41 and for left ventricular dysfunction only is 1.71. In patients in whom both are present, hazard ratio is 3.23 . In any case, interventions to prevent or improve AKI during the perioperative period are clearly needed for cardiovascular surgery patients.
Atrial natriuretic peptide (ANP), a 28-amino-acid peptide hormone synthesized by the cardiac atria, is a potent natriuretic, diuretic, and vasorelaxant substance . ANP increases the pressure within the glomerular capillaries by dilating afferent renal arterioles and constricting efferent renal arterioles , resulting in an increase in glomerular filtration. ANP has also been shown to improve renal function in animal models of acute ischemic renal failure [10, 11]. B-type (or brain) natriuretic peptide (BNP), a 32-amino-acid peptide initially isolated from porcine brain, was identified as a hormone primarily derived from the cardiac ventricles . The synthesis, secretion and clearance of ANP are different from those of BNP, suggesting discrete pathophysiological roles of ANP and BNP in a dual natriuretic peptide system. ANP is secreted in response to an acute increase in atrial stretch and/or pressure, while BNP is regulated at the gene expression level and responds to increased atrial/ventricular pressure [13, 14]. The plasma half-life of ANP is 3 minutes and that of BNP is 20 minutes.
Two synthetic natriuretic peptides are available for use as therapeutic agents in patients with acute heart failure: recombinant human ANP, carperitide (HANP®, Daiichisankyo Co., Ltd, Tokyo, Japan) and recombinant human BNP, nesiritide (Natrecor®, Scios Inc., Sunnyvale, CA, USA). ANP (carperitide) is commercially available in Japan and has been used in the treatment of acute heart failure. BNP (nesiritide) is available in USA, Switzerland, Argentina, Columbia and Israel [15, 16] and has been used in the treatment of fluid-overloaded patients with acute heart failure [17, 18].
With these points in mind, we reviewed the literature on the cardiovascular and renal effects of ANP  and BNP in cardiovascular surgery patients in order to gain insight into potential postoperative treatment for AKI.
Materials and methods
We report our study's findings in accordance with the criteria of the PRISMA Group . Electronic databases, including PubMed, EMBASE and references from identified articles between January 1994 and January 2011 were used for a literature search relating to the effects of ANP or BNP on hemodynamics and renal function in cardiovascular surgery patients. The following key words were searched: atrial natriuretic peptide or carperitide, B-type (or brain) natriuretic peptide or nesiritide, acute kidney injury or acute renal failure, left ventricular dysfunction or heart failure, cardiac surgery or cardiovascular surgery. The methodological quality of each study was assessed. Studies were excluded if they were duplicated studies, reviews, retrospective studies, not cardiovascular surgery, not infusion of ANP or BNP, and did not use a control group. We have evaluated the funding source of the individual studies.
Concerning meta-analysis, we calculated the odds ratio (OR) and 95% confidence intervals (CI) between the ANP or BNP group and the control group for need for hemodialysis, incidence of arrhythmias, and mortality. We also calculated weighted difference in means and 95% CI between the ANP or BNP group and the control group for peak serum creatinine levels and length of ICU stay and hospital stay, by the general variance-based method.
Of the 893 references screened, 15 randomized controlled trials (RCTs) of the infusion of ANP or BNP in cardiovascular surgery patients were included in systematic review and 9 studies for meta-analysis (Figure 1). Most of the studies described single-center studies with small samples sizes. Tables 1 and 2 show the respective effects of ANP and BNP on hemodynamics, renal function, and other parameters in cardiovascular surgery patients. The methodological quality of the included studies was as follows. The patients were randomly allocated in all studies. Allocation concealment was adequate in 11 studies [21–31], which blinded the participants and the investigators, and unclear in the remaining studies. Four studies [[25, 27] to ] excluded withdrawals after randomization, but the remaining eleven studies did not have withdrawals. Completeness of follow up was adequate in all studies. There was no relationship between funding source and ANP or BNP in these studies. The main results of the meta-analysis were as follows: ANP infusion significantly decreased peak serum creatinine levels, incidence of arrhythmia and need for renal replacement therapy (Figure 2), and ANP or BNP infusion significantly decreased the length of ICU stay and hospital stay compared with controls, but not mortality compared with controls (Figures 3 and 4).
ANP infusion decreased the mean pulmonary arterial pressure [32, 33], pulmonary capillary wedge pressure [32, 34], central venous pressure or right atrial pressure [21, 32, 34], systemic vascular resistance index [21, 34], and pulmonary vascular resistance index [21, 33], but did not change the heart rate or mean arterial pressure [22, 33]. There is some disagreement in the reported effects of ANP on cardiac index. Bergman et al.  showed a decrease in cardiac index after ANP infusion, whereas Hayashi et al.  and Hayashida et al.  showed an increase in cardiac index. A meta-analysis showed that ANP infusion significantly decreased the incidence of arrhythmias compared with controls [23, 27] (Figure 2). ANP infusion increased urine output [21, 22, 24, 34, 35], increased creatinine clearance or glomerular filtration rate (GFR) [21, 22, 25–27, 35], decreased serum creatinine levels [24, 26, 27, 35], and decreased the furosemide dosage [21, 24, 32], compared with controls. ANP infusion also decreased the incidence of renal replacement therapy compared with controls [25, 26]. The meta-analysis showed that ANP infusion significantly decreased peak serum creatinine levels and the need for renal replacement therapy compared with controls (Figure 2). ANP infusion increased plasma cyclic guanosine 3',5'-monophosphate (cGMP) levels [21, 34] but decreased plasma BNP levels [23, 24, 27], compared with controls. ANP infusion decreased renin and aldosterone [21, 32] and pleural effusion  compared with controls. ANP infusion increased renal replacement therapy-free survival at 21 days compared with controls . The meta-analysis showed that ANP infusion significantly reduced the length of ICU stay and hospital stay, but not mortality compared with controls (Figure 3).
BNP infusion did not change the pulmonary arterial pressure . Over the first 24 hours after surgery, BNP infusion significantly attenuated the peak increase in serum creatinine, significantly attenuated the fall in GFR, and increased urine output, compared with controls . BNP infusion decreased plasma cystatin levels and maintained creatinine clearance, compared with controls . BNP infusion decreased the incidence of AKI, decreased serum creatinine levels, and increased GFR, compared with controls, but there were no differences between the BNP and control groups in mortality or the incidence of renal replacement therapy . In one study, the urine output and furosemide dosage were not significantly different between the BNP and control groups . BNP infusion increased plasma cGMP levels  and decreased plasma ANP levels  compared with controls. Time to extubation and PaO2/FIO2 ratio at 48 hours were not significantly different between the BNP group and the control group . One study showed a shorter ICU stay and reduced 180-day mortality in the BNP group compared with the control group . The meta-analysis showed that BNP infusion significantly reduced the length of ICU stay and hospital stay, but not mortality compared with controls (Figure 4).
AKI after cardiac surgery is associated with an increased risk of morbidity, mortality, and length of ICU and hospital stay [4–6]. In a retrospective study of 2,973 patients, long-term mortality after cardiothoracic surgery was proportional to severity of AKI, as defined by RIFLE (Risk, Injury, Failure, Loss, and End stage) classification . In addition, duration of AKI is associated with long-term mortality after cardiac surgery . Therefore, severity and duration of AKI have important implications for patient care. The predominant causes of AKI in patients undergoing cardiovascular surgery are hypoperfusion and inflammation because of cardiopulmonary bypass (CPB). The nonpulsatile flow during CPB has been shown to cause AKI by inducing vasoconstriction and ischemic renal injury . There appear to be other mechanisms responsible for AKI, however, as even patients who undergo surgery off CPB (off-pump) are at risk for AKI. The pathophysiology of AKI is multifactorial. Cardiac-surgery-associated AKI is caused by exogenous and endogenous toxins, metabolic factors, ischemia and reperfusion, neurohormonal activation, inflammation, and oxidative stress . Similar to cardiac surgery, AKI is the most common complication in patients undergoing pararenal aortic aneurysm repair. Suprarenal aortic cross-clamping is associated with a significant postoperative decline in renal function . Even infrarenal aortic cross-clamping is associated with an increase in renal vascular resistance and a decrease in renal blood flow . Therefore, in addition to cardiac surgery, we have included abdominal aortic aneurysm repair as one of cardiovascular surgery. The risk of AKI can therefore be reduced by maintaining adequate hemodynamics and an adequate metabolic state, avoiding nephrotoxic drugs, and inhibiting neurohormonal activation and inflammation during perioperative periods.
Furosemide is frequently used to facilitate fluid and electrolyte management of AKI. However, meta-analysis has shown that furosemide is not associated with any significant clinical benefits in the prevention and treatment of AKI and high doses may even be detrimental .
The cardiovascular effects of ANP or BNP are vasodilation and a reduced sympathetic tone in the peripheral vasculature . ANP and BNP bind to natriuretic peptide receptor A, which increases cGMP and dilates veins and arteries , and thereby reduces preload and afterload. ANP, meanwhile, decreases pulmonary capillary wedge pressure, central venous pressure, mean pulmonary arterial pressure, pulmonary vascular resistance index, and systemic vascular resistance index [21, 32–34]. The ANP patient group also had a reduced incidence of arrhythmias compared with controls [23, 27]. The reduction of arrhythmia may be attributable to stable serum potassium levels, as the dose of furosemide and rate of KCl correction are lower in the ANP groups than in the controls [23, 32]. However, arrhythmias may be caused by many different factors, including hypomagnesemia, myocardial injury from surgical handling, inflammation after cardiac surgery, acute atrial enlargement from volume overload, inadequate cardioprotection during CPB, and hyperadrenergic state. Although the true mechanism is unknown, we surmise that the anti-arrhythmic effects of ANP are due to prevention of volume overload and suppression of the sympathetic nervous system except for potassium levels.
The natriuretic and diuretic actions of ANP and BNP are caused by renal hemodynamic and direct tubular actions . ANP increases transcapillary filtration pressure within the glomerulus , and this then translates to an increase in GFR. The protective effect of ANP for the kidney may take place via the ANP-induced increases in the medullary vasa recta blood flow , an action that may protect against medullary ischemia. In one study, the urinary N-acetyl-β-D-glucosaminidase (NAG)/creatinine ratio, an index of renal tubular damage, was significantly lower in the ANP group than in the control group .
ANP or BNP infusion increased urine volume, creatinine clearance and GFR and decreased serum creatinine in patients with normal renal function [22, 26]. ANP or BNP infusion also attenuated serum creatinine increase and maintained creatinine clearance and GFR in patients with preoperative renal dysfunction , in patients with AKI after cardiac surgery  and in patients with left ventricular ejection fraction (LVE F) ≤40% . Especially, Mentzer et al.  have shown that the beneficial effects of BNP on postoperative renal dysfunction were prominent in patients with renal dysfunction at baseline serum creatinine (Cr) > 1.2 mg/dl. In these patients, BNP significantly inhibited serum creatinine increase and GFR decrease compared with those of normal renal function. Therefore, the renal effects of ANP and BNP may depend on degree of underlying renal function.
Although 10 of 15 studies did not mentioned fluid balance, some of the studies suggest that the control groups were given more volume. This may be relevant to recent studies on AKI and volume loading , which have shown that adequate volume repletion is of major importance for prevention of AKI.
ANP and BNP also suppress the renin-angiotensin-aldosterone axis , thereby counterbalancing the vasoconstrictive effects of these neurohormones. In fact, two clinical studies have shown that ANP infusion decreases renin and aldosterone compared with controls [21, 32]. The effects of ANP in preserving the peritubular capillary blood flow and suppressing the renin-angiotensin system may protect against renal tubular damage after cardiovascular surgery. The cardiovascular and renal effects of ANP and BNP and the action of these natriuretic peptides in manipulating the renin-angiotensin-aldosterone axis may help to prevent serious AKI in the management of patients with cardio-renal syndrome.
The major site of ANP synthesis is the atrium, and ANP mRNA levels are considerably higher in the atrium than in the ventricles. However, ventricular ANP expression is re-induced in heart failure. Although concentrations of BNP and BNP mRNA are much lower in the ventricle than in the atrium, the total content of BNP and BNP mRNA in the ventricle accounts for 30% and 70% of that in the whole heart, respectively. In patients with congestive heart failure, concentrations of myocardial BNP mRNA and circulating BNP are increased more than are those of ANP, suggesting that BNP plays the role of an emergency hormone against ventricular overload. The characteristic feature of BNP mRNA that is different from ANP mRNA is a conserved sequence consisting of repeated AUUUA units in the 3' untranslated region. The presence of this sequence accelerates the degradation of BNP mRNA. Therefore, BNP gene expression is regulated differently from ANP gene expression and is thought to dynamically change, depending on the physiological and pathophysiological conditions . While ANP and BNP seem to play discrete pathophysiological roles in a dual natriuretic peptide system [14, 15], their roles may also be compensatory in relation to each other. ANP and BNP bind to the same natriuretic peptide receptor A  and this may lead to mutual biological invasion of ANP and BNP. ANP infusion decreases plasma BNP levels in patients undergoing cardiovascular surgery, while BNP infusion decreases plasma ANP levels in the same patients [23, 24, 31, 34]. This tells us that ANP and BNP are closely related.
There are many natriuretic peptide receptors A in the body. If there are some unoccupied natriuretic receptors A on the various target cells, exogenous ANP (or BNP) may bind to these receptors, leading to biological effects. In fact, in patients with high plasma BNP levels (> 230 pg/ml), the effect of ANP infusion on left ventricular contractility was blunted but its beneficial effects on left ventricular diastolic function and left ventricular-arterial coupling remained . Thus, ANP infusion may improve left ventricular diastolic function even in patients with high plasma levels. Taken together, extra ANP (or BNP) are likely to confer benefit, even if the endogenous system is at full capacity.
Limitations of this meta-analysis
First, few studies use the same protocols and the end points are vastly different. The primary endpoints in most of the studies were continuous changes in serum creatinine and creatinine clearance or GFR. The clinically important endpoints of renal replacement therapy and/or mortality were considered primary outcomes in only seven of the studies [23, 25–30], and most of the studies lacked the robustness to demonstrate beneficial effects of ANP or BNP on mortality. Second, the included studies had patients with different renal functions and differed significantly in doses, timing of initiation and duration of ANP or BNP treatments. These facts restrict comparing these studies with each other and the reliability of our findings. Third, since there were no standard indications for renal replacement therapy, the decision to initiate renal replacement therapy was dependent on the participating doctors. Therefore, there may be a wide variation in the incidence of renal replacement therapy. Fourth, four out of eleven studies were performed by the same group of investigators in the same institution. Accordingly, the results may be biased more slightly toward the studies of this group. Finally, as a marker of renal function there are some shortcomings of creatinine because serum creatinine is affected by age, gender, muscle mass, nutritional status and analytical interference, although AKI has been defined largely by changes in creatinine. Estimated GFR formulae based on serum creatinine, age, sex and weight are used in daily clinical practice, but their accuracy is debatable. In addition, a 24 hour urine creatinine clearance has been commonly employed for the detection of AKI. However, since a substantial fraction of urinary creatinine is derived from tubular secretion, creatinine clearance regularly overestimates GFR . Accordingly, we have to interpret the results carefully by considering the shortcomings of creatinine.
Even so, ANP and BNP have cardiovascular and renal effects as well as effects in manipulating the renin-angiotensin-aldosterone axis. On these grounds, we speculate that ANP and BNP may be able to prevent or treat for AKI in cardiovascular surgery patients. The infusion of ANP or BNP in these patients should be investigated more thoroughly.
The infusion of ANP or BNP may preserve renal function after cardiovascular surgery. Only seven studies have researched the incidence of renal replacement therapy and the longer-term outcome in patients after cardiovascular surgery. The meta-analysis showed that ANP infusion significantly decreased peak serum creatinine levels, incidence of arrhythmia and renal replacement therapy, and ANP or BNP infusion significantly decreased the length of ICU stay and hospital stay compared with controls. A large, muticenter, prospective, randomized controlled trial will have to be performed to assess the therapeutic potential of ANP or BNP in preventing and treating AKI in the cardiovascular surgical setting.
Data on infusion of ANP and BNP in cardiovascular surgery patients was collected from fifteen RCTs and combined.
ANP infusion increased urine output and the creatinine clearance or GFR, and reduced the use of diuretics and the serum creatinine levels compared with controls.
The meta-analysis showed that ANP infusion significantly decreased peak serum creatinine levels, the incidence of arrhythmia and hemodialysis, and ANP or BNP infusion significantly decreased the length of ICU stay and hospital stay compared with controls.
The combined data were insufficient to determine how ANP or BNP infusion during the perioperative period affect the long-term outcome in cardiovascular surgery patients.
acute kidney injury
atrial natriuretic peptide
B-type (or brain) natriuretic peptide
blood urea nitrogen
cyclic guanosine 3',5'-monophosphate
glomerular filtration rate
left ventricular ejection fraction
randomized controlled trials.
Appoo J, Norris C, Merali S, Graham MM, Koshal A, Knudtson ML, Ghali WA: Long-term outcome of isolated coronary artery bypass surgery in patients with severe left ventricular dysfunction. Circulation 2004,110(Suppl II):13-17.
Ahmed WA, Tully PJ, Baker RA, Knight JL: Survival after isolated coronary artery bypass grafting in patients with severe left ventricular dysfunction. Ann Thorac Surg 2009, 87: 1106-1112. 10.1016/j.athoracsur.2008.12.081
Ronco C, Haapio M, House AA, Anavekar N, Bellomo R: Cardiorenal syndrome. J Am Coll Cardiol 2008, 52: 1527-1539. 10.1016/j.jacc.2008.07.051
Loef BG, Epema AH, Navis G, Ebels T, Stegeman CA: Postoperative renal dysfunction and preoperative left vetricular dysfunction predispose patients to increased long-term mortality after coronary bypass graft surgery. Br J Anaesth 2009, 102: 749-755. 10.1093/bja/aep088
Karkouti K, Wijeysundera DN, Yau TM, Callum JL, Cheng DC, Crowther M, Dupuis J-Y, Fremes SE, Kent B, Laflamme C, Lamy A, Legare J-F, Mazer CD, McCluskey SA, Rubens FD, Sawchuk C, Beattie WS: Acute kidney injury after cardiac surgery; focus on modifiable risk factors. Circulation 2009, 119: 495-502. 10.1161/CIRCULATIONAHA.108.786913
Thakar CV, Worley S, Arrigain S, Yared J-P, Paganini EP: Influence of renal dysfunction on mortality after cardiac surgery: modifying effect of preoperative renal function. Kidney Int 2005, 67: 1112-1119. 10.1111/j.1523-1755.2005.00177.x
Dasta JF, Kane-Gill SL, Durtschi AJ, Pathak DS, Kellum JA: Costs and outcomes of acute kidney injury (AKI) following cardiac surgery. Nephrol Dial Transplant 2008, 23: 1970-1974. 10.1093/ndt/gfm908
Levin ER, Gardner DG, Samson WK: Natriuretic peptides. N Engl J Med 1998, 339: 321-328. 10.1056/NEJM199807303390507
Marin-Grez M, Fleming JT, Steinhausen M: Atrial natriuretic peptide causes pre-glomerular vasodilatation and post-glomerular vasoconstriction in rat kidney. Nature 1986, 324: 473-476. 10.1038/324473a0
Shaw SG, Weidmann P, Hodler J, Zimmermann A, Patemostro A: Atrial natriuretic peptide protects against acute ischemic renal failure in the rat. J Clin Invest 1987, 80: 1232-1237. 10.1172/JCI113197
Hirata Y, Habuka K, Narumi Y, Yokoyama K, Makita K, Imai T: Atrial natriuretic peptide infusion improves ischemic renal failure after suprarenal abdominal aortic cross-clamping in dogs. Crit Care Med 2003, 31: 2205-2210. 10.1097/01.CCM.0000080487.20304.2E
Rademaker MT, Richards AM: Cardiac natriuretic peptide for cardiac health. Clin Sci 2005, 108: 23-36. 10.1042/CS20040253
Kuhn M: Cardiac and intestinal natriuretic peptides: insights from genetically modified mice. Peptides 2005, 26: 1078-1085. 10.1016/j.peptides.2004.08.031
Houben AJ, van der Zander K, de Leeuw PW: Vascular and renal actions of brain natriuretic peptide in man: physiology and pharmacology. Fundam Clin Pharmacol 2005, 19: 411-419. 10.1111/j.1472-8206.2005.00336.x
Abassi Z, Karram T, Ellaham S, Winaver J, Hoffman A: Implications of the natriuretic peptide system in the pathogenesis of heart failure: diagnostic and therapeutic importance. Pharmacol Ther 2004, 102: 223-241. 10.1016/j.pharmthera.2004.04.004
D'Souza SP, Davis M, Baxter GF: Autocrine and paracrine actions of natriuretic peptides in the heart. Pharmacol Ther 2004, 101: 113-129. 10.1016/j.pharmthera.2003.11.001
Colucci WS, Elkayam U, Horton DP, Abraham WT, Bouge RC, Johnson AD, Wagoner LE, Givertz MM, Liang C-S, Neibaur M, Haught H, LeJemtel TH, for the Nesiritide Study Group: Intravenous nesiritide, a natriuretic peptide, in the treatment of decompensated congestive heart failure. N Engl J Med 2000, 343: 246-253. 10.1056/NEJM200007273430403
Publication Committee for the VMAC Investigators (Vasodilation in the Management of Acute CHF): Intravenous nesiritide vs. nitroglycerin for treatment of decompensated congestive heart failure: a randomized controlled trial. JAMA 2002, 287: 1531-1540. 10.1001/jama.287.12.1531
Mitaka C, Kudo T, Haraguchi G: Effects of atrial natriuretic peptide on renal function in patients undergoing cardiovascular surgery. J Jpn Soc Intensive Care Med 2011, 18: 201-206. (in Japanese) 10.3918/jsicm.18.201
Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group: Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PloS Med 2009, 6: e1000097. 10.1371/journal.pmed.1000097
Sezai A, Shiono M, Orime Y, Hata H, Hata M, Negishi N, Sezai Y: Low-dose continuous infusion of human atrial natriuretic peptide during and after cardiac surgery. Ann Thorac Surg 2000, 69: 732-738. 10.1016/S0003-4975(99)01305-3
Bergman A, Odar-Cederlόf I, Westman L, Ohqvist G: Effects of human atrial natriuretic peptide in patients after coronary artery bypass surgery. J Cardiothorac Vasc Anesth 1996, 10: 490-496. 10.1016/S1053-0770(05)80010-2
Sezai A, Hata M, Wakui S, Niino T, Takayama T, Hirayama A, Saito S, Minami K: Efficacy of continuous low-dose hANP administration in patients undergoing emergent coronary artery bypass grafting for acute coronary syndrome. Circ J 2007, 71: 1401-1407. 10.1253/circj.71.1401
Mitaka C, Kudo T, Jibiki M, Sugano N, Inoue Y, Makita K, Imai T: Effects of human natriuretic peptide on renal function in patients undergoing abdominal aortic aneurysm repair. Crit Care Med 2008, 36: 745-751. 10.1097/CCM.0B013E3181659118
Swärd K, Valsson F, Odencrants P, Samuelsson O, Ricksten S-E: Recombinant human atrial natriuretic peptide in ischemic acute renal failure: a randomized placebo-controlled trial. Crit Care Med 2004, 32: 1310-1315. 10.1097/01.CCM.0000128560.57111.CD
Sezai A, Hata M, Niino T, Yoshitake I, Unosawa S, Wakui S, Osaka S, Takayama T, Kasamaki Y, Hirayama A, Minami K: Influence of continuous infusion of low-dose human atrial natriuretic peptide on renal function during cardiac surgery. J Am Coll Cardiol 2009, 54: 1058-1064. 10.1016/j.jacc.2009.05.047
Sezai A, Hata M, Niino T, Yoshitake I, Unosawa S, Wakui S, Fujita K, Takayama T, Kasamaki Y, Hirayama A, Minami K: Continuous low-dose infusion of human atrial natriuretic peptide in patients with left ventricular dysfunction undergoing coronary artery bypass grafting. J Am Coll Cardiol 2010, 55: 1844-1851. 10.1016/j.jacc.2009.11.085
Mentzer RM, Oz MC, Sladen RN, Graeve AH, Hebeler RF, Luber JM Jr, Smedira NG, on behalf of the NAPA Investigators: Effects of perioperative nesiritide in patients with left ventricular dysfunction undergoing cardiac surgery. J Am Coll Cardiol 2007, 49: 716-726. 10.1016/j.jacc.2006.10.048
Chen HH, Sundt TM, Cook DJ, Heublein DM, Burnett JC Jr: Low dose nesiritide and the preservation of renal function in patients with renal dysfunction undergoing cardiopulmonary-bypass surgery. A double-blind placebo-controlled pilot study. Circulation 2007,116(suppl I):134-138.
Ejaz AA, Martin TD, Johson RJ, Winterstein AG, Klodell CT, Hess PJ Jr, Ali AK, Whidden EM, Staples NL, Alexander JA, House-Fancher MA, Beaver TM: Prophylactic nesiritide does not prevent dialysis or all-cause mortality in patients undergoing high-risk cardiac surgery. J Thorac Cardiovasc Surg 2009, 138: 959-964. 10.1016/j.jtcvs.2009.05.014
Beaver TM, Winterstein A, Hess PJ Jr, Martin TD, Arnaoutakis GJ, Peng YG, Ejaz AA: Nesiritide following maze and mitral valve surgery. J Card Surg 2008, 23: 431-436. 10.1111/j.1540-8191.2007.00552.x
Hayashi Y, Ohtani M, Hiraishi T, Kobayashi Y, Nakamura T: Synthetic human α-atrial natriuretic peptide infusion in management after open heart operations. ASAIO Journal 2003, 49: 320-324. 10.1097/01.MAT.0000065370.44623.6E
Sumi K, Iida H, Yamaguchi S, Fukuoka N, Shimabukuro K, Dohi S: Human atrial natriuretic peptide prevents the increase in pulmonary artery pressure associated with aortic unclamping during abdominal aortic aneurysmectomy. J Cardiothorac Vasc Anesth 2008, 22: 204-209. 10.1053/j.jvca.2007.07.016
Hayashida N, Chihara S, Kashikie H, Tayama E, Yokose S, Akasu K, Aoyagi S: Effects of intraoperative administration of atrial natriuretic peptide. Ann Thorac Surg 2000, 70: 1319-1326. 10.1016/S0003-4975(00)01658-1
Izumi K, Eishi K, Yamachika S, Hashizume K, Tada S, Yamane K, Takai H, Tanigawa K, Miura T, Nakaji S: The efficacy of human atrial natriuretic peptide in patients with renal dysfunction undergoing cardiac surgery. Ann Thorac Cardiovasc Surg 2008, 14: 294-302.
Hobson CE, Yavas S, Segal MS, Schold JD, Tribble CG, Layon AJ, Bihorac A: Acute kidney injury is associated with increased long-term mortality after cardiothoracic surgery. Circulation 2009, 119: 2444-2453. 10.1161/CIRCULATIONAHA.108.800011
Brown JR, Kramer RS, Coca SG, Parikh CR: Duration of acute kidney injury impacts long-term survival after cardiac surgery. Ann Thorac Surg 2010, 90: 1142-1149. 10.1016/j.athoracsur.2010.04.039
Abu-Omar Y, Ratnatunga C: Cardiopulmonary bypass and renal injury. Perfusion 2006, 21: 209-213. 10.1191/0267659106pf870oa
Bellomo R, Auriemma S, Fabbri A, D'onofrio A, Katz N, McCullough PA, Ricci Z, Shaw A, Ronco C: The pathophysiology of cardiac surgery-associated acute kidney injury (CSA-AKI). Int J Artif Organs 2008, 31: 166-178.
Chong T, Nguyen L, Owens CD, Conte MS, Belkin M: Suprarenal aortic cross-clamping position: a reappraisal of its effects on outcomes for open abdominal aortic aneurysm repair. J Vasc Surg 2009, 49: 873-880. 10.1016/j.jvs.2008.10.057
Gelman S: The pathophysiology of aortic cross-clamping and unclamping. Anesthesiology 1995, 82: 1026-1060. 10.1097/00000542-199504000-00027
Ho KM, Sheridan D: Meta-analysis of frusemide to prevent or treat acute renal failure. BMJ 2006, 333: 420. 10.1136/bmj.38902.605347.7C
Kiberd BA, Larson TS, Robertson CR, Jamison RL: Effect of atrial natriuretic peptide on vasa recta blood flow in the rat. Am J Physiol 1987, 252: F1112-F1117.
Brochard L, Abroug F, Brenner M, Broccard AF, Danner RL, Ferrer M, Laghi F, Magder S, Papazian L, Pelosi P, Polderman KH, on behalf of the ATS/ERS/ESICM/SCCM/SRLF Ad Hoc Committee on Acute Renal Failure: An official ATS/ERS/ESICM/SCCM/SRLF statement: prevention and management of acute renal failure in the ICU patient. Am J Respir Crit Care Med 2010, 181: 1128-1155. 10.1164/rccm.200711-1664ST
Nishikimi T, Kuwahara K, Nakao K: Current biochemistry, molecular biology, and clinical relevance of natriuretic peptides. J Cardiol 2011, 57: 131-140. 10.1016/j.jjcc.2011.01.002
Nakajima K, Onishi K, Dohi K, Tanabe M, Kurita T, Yamanaka T, Ito M, Isaka N, Nobori T, Nakano T: Effects of human atrial natriuretic peptide on cardiac function and hemodynamics in patients with high plasma BNP levels. Int J Cardiol 2005, 104: 332-337. 10.1016/j.ijcard.2004.12.020
Perrone RD, Madias NE, Levey AS: Serum creatinine as an index of renal function: new insight into old concepts. Clin Chem 1992, 38: 1933-1953.
The authors declare that they have no competing interests.
CM conceived the study and wrote the manuscript. TK and GH conceived the study and conducted the literature search. MT performed the meta-analysis. All of the authors read and approved the final manuscript for publication.
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Mitaka, C., Kudo, T., Haraguchi, G. et al. Cardiovascular and renal effects of carperitide and nesiritide in cardiovascular surgery patients: a systematic review and meta-analysis. Crit Care 15, R258 (2011). https://doi.org/10.1186/cc10519
- acute kidney injury
- atrial natriuretic peptide
- B-type (or Brain) natriuretic peptide
- cardiovascular surgery
- heart failure
- renal function