Article

lock Open Access lock Peer-Reviewed

238

Views

ORIGINAL ARTICLE

Predictors of Postoperative Acute Kidney Injury after Coronary Artery Bypass Graft Surgery

Christian Ortega-LoubonI; Manuel Fernández-MolinaI; Lucía Pañeda-DelgadoI; Pablo Jorge-MonjasII; Yolanda CarrascalI

DOI: 10.21470/1678-9741-2017-0251

ABSTRACT

Objective: The aims of this study were to identify the risk factors associated with acute kidney injury (AKI) after isolated surgical revascularization with cardiopulmonary bypass and to develop a model to predict the appearance of postoperative AKI.
Methods: A total of 435 adult patients who underwent primary isolated coronary artery bypass graft (CABG) surgery, from 2012 to 2016, in the Clinic University Hospital of Valladolid (Spain) were enrolled. AKI was defined according to the risk, injury, failure, loss, and end-stage (RIFLE) criteria. Data were collected from hospital electronic medical records. Multiple logistic regression analysis was used to identify risk factors.
Results: The prevalence of AKI was 12.4%. Multivariate analysis identified age (odds ratio [OR], 1.056; 95% confidence interval [CI], 1.016-1.098; P=0.005), hypertension (OR, 3.078; 95% CI, 1.151-8.230; P=0.018), low ejection fraction (EF) (OR, 6.785; 95% CI, 2.080-22.135; P=0.001), estimated glomerular filtration rate (eGFR) (OR, 1.017; 95% CI, 1.005-1.028; P=0.014), EuroSCORE II (OR, 1.049; 95% CI, 1.004-1.096; P=0.033), and no intake of calcium-channel blockers (CCB) (OR, 4.892; 95% CI, 1.496-16.025; P=0.022) as risk factors for AKI. These risk factors were included in a model to predict postoperative AKI with an area under a receiver operating characteristic curve of 0.783±0.036 (95% CI, 0.713-0.854; P<0.0001).
Conclusion: Age, hypertension, low EF, eGFR, EuroSCORE II, and no intake of CCB were independent risk factors for postoperative AKI. These factors provide an easy and accurate model to predict postoperative AKI in patients undergoing cardiac surgery.

ABBREVIATIONS AND ACRONYMS

ACEF = Age, creatinine, ejection fraction

AKI = Acute kidney injury

AKICS = Acute kidney injury following cardiac surgery

BMI = Body mass index

CABG = Coronary artery bypass graft

CAD = Coronary artery disease

CCB = Calcium-channel blockers

CI = Confidence interval

COPD = Chronic obstructive pulmonary disease

CPB = Cardiopulmonary bypass

EF = Ejection fraction

eGFR = Estimated glomerular filtration rate

Hct = Hematocrit

ICU = Intensive care unit

IQR = Interquartile range

NYHA = New York Heart Association

OR = Odds ratio

RIFLE = Risk, injury, failure, loss, and end-stage

ROC = Receiver operating characteristic

RRT = Renal replacement therapy

SCr = Serum creatinine

SRI = Simplified renal index

INTRODUCTION

The development of postoperative acute kidney injury (AKI) is a recognized complication in patients undergoing cardiac surgery[1]. It has a dramatic impact on operative mortality, intensive care unit (ICU) resources, and hospital length of stay. Approximately 20% of cardiac surgical patients will develop postoperative AKI[2]. The risk of AKI increases 4.8 fold for each 88 µmol/L increment in serum creatinine (SCr) levels[3-5]. AKI severe enough to require renal replacement therapy (RRT) is infrequent, but the operative mortality in these patients ranges from 40% to 80%[6]. This emphasizes the crucial importance of taking any step possible to preserve renal function in the perioperative period, especially in patients at increased risk[3,7-9].

The pathogenesis of AKI after cardiac surgery is not completely understood. It is very unlikely that a single etiologic factor will cause postoperative renal injury[3]. AKI is the consequence of multiple kidney aggressions occurring during the preoperative, intraoperative, and postoperative periods[3].

Coronary artery disease (CAD) is one of the main causes of death in developed countries and coronary artery bypass graft (CABG) is the most common cardiovascular procedure performed worldwide[10,11]. Every interventional approach has a different impact on the onset of renal injury, but a greater risk of renal dysfunction is inevitable after cardiopulmonary bypass (CPB)[12]. Unlike valve surgery, which is an independent risk factor for postoperative AKI, coronary surgery is not directly related to renal dysfunction[13].

Despite the fact that multiple AKI risk factors have been already identified, postoperative AKI still remains as the strongest risk factor for death after cardiac surgery[1]. Various predictive models have been developed to predict AKI, such as the acute kidney injury following cardiac surgery (AKICS) score, Cleveland Clinic score, Mehta score, and simplified renal index (SRI) score[14]. Nevertheless, their predictive value combining discrimination and calibration were barely satisfactory and not convincible[14]. Therefore, it is crucial to recognize these risk factors promptly and to develop a model to predict AKI's appearance, which allows appropriate measures to be taken to reduce its incidence.

This study aimed to identify the risk factors associated with AKI after isolated revascularization surgery with CPB and to make an accurate and predictive model for AKI after cardiac surgery. Such predictive model would be highly valuable for clinical practices because AKI is a well-established predictor of all-cause mortality in patients receiving CABG.

METHODS

Study Design

We performed an observational retrospective study of 435 consecutive patients undergoing CABG under CPB, from January 2012 to December 2016, at the Clinic University Hospital of Valladolid. All patients undergoing elective or urgent isolated primary CABG surgery under CPB were included. Those with prior renal insufficiency, off-pump surgery, prior cardiac intervention, or CABG combined with heart valve replacement or other surgical procedures were excluded.

The primary outcome variable was the development of AKI after cardiac procedure. AKI was defined according to the risk, injury, failure, loss, and end-stage (RIFLE) criteria[15]. The baseline SCr level was determined using the most recent level measured (mean of 1.0 ± 1.0 days) before surgery and the estimated glomerular filtration rate (eGFR) derived from the Cockcroft-Gault formula.

Secondary outcomes were need of RRT, ICU length of stay, and 30-day mortality.

Clinical and Laboratory Variables

Preoperative variables were age at time of surgery, gender, weight, height, body mass index (BMI), personal history [i.e., smoking, hypertension, peripheral vascular disease, diabetes mellitus, dyslipidemia, chronic obstructive pulmonary disease (COPD), and stroke], New York Heart Association (NYHA) classification, left ventricular function <30%, emergency surgery, need of RRT, long-term medical treatment, time elapsed between angiography and surgery, EuroSCORE I, EuroSCORE II, hemoglobin, hematocrit (Hct), SCr levels on preoperative laboratory testing, and eGFR.

Intraoperative variables were CPB and aortic cross-clamp times. Postoperative variables included AKI, need of RRT, days of stay at ICU, and 30-day mortality.

All data were obtained from electronic medical records and the cardiovascular surgery database at the medical center.

Statistical Analysis

Data were analyzed using IBM SPSS Statistics for Windows, version 20.0, software (IBM Corp., Armonk, NY, USA).

Qualitative variables are reported as frequency and percentage and quantitative variables are reported as mean ± standard deviation or median (interquartile range - IQR) as appropriate.

Associations between AKI and other variables were identified using χ2 or Fisher's exact test for qualitative analysis; Student's t-test or Mann-Whitney U test was used for quantitative analysis, according to normality criteria.

All variables were included in multivariate logistic regression analyses; bootstrapping was performed to derive 95% confidence intervals (CI) for estimates. Multicollinearity was assessed using variance inflation factor. Logistic regression was repeated with variables that had been significant in previous analysis. The model was further developed and validated using the bootstrap approach, which is the method most widely advocated by experts for model development and internal validation[16].

Accuracy was measured by the area under the receiver operating characteristic (ROC) curve analysis.

Odds ratio (OR) with 95% CI and P-value were reported. P-values <0.05 were considered statistically significant.

RESULTS

Fifty-four (12.4%) patients developed postoperative AKI. Compared to patients without AKI, those who developed AKI were older, underwent operations in an urgent/emergency basis, and had higher frequency of hypertension, lower ejection fraction (EF), lower level of hemoglobin, lower Hct, higher levels of SCr, lower eGFR, longer CPB time, longer cross-clamp time, and shorter time elapsed between angiography and surgery (Table 1).

Table 1 - Preoperative, intraoperative, and postoperative variables according to the presence of acute kidney injury (AKI).
Variables n = 435 (%) Non-AKI (381) AKI (54) P-value
Age (years) 66.8±9.2 66.2±9.1 70.8±8.6 0.001
Female 91 (20.9) 82 (21.5) 9 (16.7) 0.460
BMI (kg/m2) 27.7±3.8 27.6±3.8 28.5±4.0 0.114
    Patients with BMI <18 3 (0.7) 2 (0.2) 1 (1.9) 0.235
    Patients with BMI 18-24 108 (24.8) 100 (26.2) 8 (14.8)
    Patients with BMI 25-29 214 (49.2) 187 (49.1) 27 (50)
    Patients with BMI >30 110 (25.3) 92 (24.1) 18 (33.3)
Smoking 247 (56.8) 215 (56.4) 32 (59.3) 0.695
Hypertension 327 (75.2) 279 (73.2) 48 (88.9) 0.013
Peripheral vascular disease 194 (44.6) 172 (45.4) 22 (40.7) 0.519
Diabetes mellitus 160 (36.8) 142 (37.3) 18 (33.3) 0.574
Dyslipidemia 295 (67.8) 261 (68.5) 34 (63.0) 0.415
COPD 33 (7.6) 28 (7.3) 5 (9.3) 0.585
Stroke 20 (4.6) 17 (4.5) 3 (5.6) 0.726
NYHA III-IV 86 (19.8) 74 (19.4) 12 (22.3) 0.291
Sinus rhythm 349 (80.2) 310 (81.4) 39 (72.2) 0.250
Severe left ventricular dysfunction (LVEF <30%) 22 (5.1) 13 (3.4) 9 (16.7) 0.001
Emergency surgery 59 (13.6) 45 (11.8) 14 (25.9) 0.005
Cardiogenic shock 10 (2.3) 5 (1.3) 5 (9.3) 0.047
AMI 47 (10.8) 36 (9.4) 11 (20.4) 1.000
Long-term treatment        
    β-blockers 215 (49.4) 195 (51.2) 20 (37.0) 0.052
    CCB 66 (15.2) 62 (16.3) 4 (7.4) 0.089
    Diuretics 96 (22.1) 76 (19.9) 20 (37.0) 0.005
    ACE inhibitors 192 (44.1) 164 (43.0) 28 (51.9) 0.223
Hemoglobin (g/L) 130±42.3 131±42.2 124±42.9 0.010
Hct (proportion of 1.0) 0.38±0.08 0.38±0.08 0.37±0.06 0.009
SCr (µmol/L) 106.1±221.0 101.7±238.7 114.0±53.0 0.001
eGFR (mL/min/m2) 87.8±34.3 90.3±34.2 70.3±29.2 0.001
Patients with eGFR >30 (mL/min/m2) 426 (97.9) 375 (98.4) 51 (94.4) 0.088
Patients with eGFR <30 (mL/min/m2) 9 (2.1) 6 (1.6) 3 (5.6)
Time elapsed between angiography and surgery (days) 21.9±51.3 22.7±53.2 16.0±34.0 0.086
EuroSCORE I 6.3±7.3 5.6±6.0 11.1±12.1 0.001
EuroSCORE II 3.8±5.7 3.3±4.7 7.1±9.4 0.001
Intraoperative        
    CPB time (min) 99.4±41.7 98.0±41.9 109.2±39.5 0.030
    Cross-clamp time (min) 64.0±26.6 63.32±26.3 69.1±28.6 0.204
Postoperative        
    RRT 4 (0.9) 0 4 (7.4) 0.001
    Days of stay at ICU 2 (IQR 0-55) 2.7±2.2 7.4±9.3 0.001
    30-day mortality 22 (5.1) 12 (3.1) 10 (18.5) 0.001

ACE=angiotensin-converting enzyme; AMI=acute myocardial infarction; BMI=body mass index; CCB=calcium-channel blockers; COPD=chronic obstructive pulmonary disease; CPB=cardiopulmonary bypass; eGFR=estimated glomerular filtration rate; Hct=hematocrit; ICU=intensive care unit; IQR=interquartile range; NYHA=New York Heart Association; RRT=renal replacement therapy; SCr=serum creatinine

Table 1 - Preoperative, intraoperative, and postoperative variables according to the presence of acute kidney injury (AKI).

Mean EuroSCORE I and EuroSCORE II were higher in the AKI group (11.1±12.1 and 7.1±9.4, respectively). Twenty-two (5.1%) patients died within 30 days of operation, with a significantly higher mortality rate in the AKI group than in the non-AKI group (18.5% vs. 3.1%; P=0.001). In addition, patients in the AKI group also had longer length of stay in the ICU (Table 1).

After incorporating the variables into the multiple logistic regression analysis with stepwise selection, age, hypertension, EF <30%, eGFR, and EuroSCORE II were independently associated with risk of postoperative AKI. Not taking calcium-channel blockers (CCB) medication was also a risk factor for the development of postoperative AKI (OR, 4.892; 95%CI, 1.496-16.025; P=0.022). These variables were then analyzed using bootstrap approach for the internal model validation for binary clinical risk prediction models (Table 2).

Table 2 - Multiple logistic regression analysis for acute kidney injury (AKI) (validated with bootstrap approach).
Risk factors B-coefficient CI (95%) SE OR CI (95%) P-value
Age (years) 0.055 0.180-0.100 0.020 1.056 1.016-1.098 0.005
Hypertension 1.124 0.292-2.496 1.135 3.078 1.151-8.230 0.018
EF <30% 1.915 0.696-3.107 0.603 6.785 2.080-22.135 0.001
eGFR (mL/min/m2) 0.017 0.004-0.030 0.007 1.017 1.005-1.028 0.014
EuroSCORE II 0.048 0.011-0.127 0.030 1.049 1.004-1.096 0.033
No CCB intake 1.588 0.306-4.160 2.814 4.892 1.496-16.025 0.022
Constant -9.031 -17.495 - -5.333 3.751 0.000 NA 0.001

CCB=calcium-channel blockers; CI=confidence interval; EF=ejection fraction; eGFR=estimated glomerular filtration rate; NA=not applicable; OR=odds ratio; SE=standard error

Table 2 - Multiple logistic regression analysis for acute kidney injury (AKI) (validated with bootstrap approach).

These variables, when combined, gave us a model that accurately predicts postoperative AKI with ROC curve of 0.783±0.036 (95%CI, 0.713-0.854; P<0.001) (Table 3, Figure 1).

Table 3 - Prediction model of acute kidney injury (AKI) using the risk factors resulted from the multiple logistic regression analysis.
Risk factors ROC curve* SE CI (95%) P-value
Age 0.660 0.039 0.584-0.736 <0.001
Hypertension 0.579 0.038 0.504-0.654 0.059
EF <30% 0.566 0.045 0.478-0.654 0.116
eGFR 0.690 0.041 0.610-0.770 <0.001
EuroSCORE II 0.686 0.036 0.615-0.758 <0.001
No CCB intake 0.542 0.040 0.464-0.620 0.314
Model 0.783 0.036 0.713-0.854 <0.001

* Hosmer-Lemeshow (H-L) value=0.720

CCB=calcium-channel blockers; CI=confidence interval; EF=ejection fraction; eGFR=estimated glomerular filtration rate; ROC=receiver operating characteristic; SE=standard error

Table 3 - Prediction model of acute kidney injury (AKI) using the risk factors resulted from the multiple logistic regression analysis.

Fig. 1 - ROC curves using hypertension, EuroSCORE II, EF, eGFR, age, and CCB intake for predicting postoperative AKI.
AKI=acute kidney injury; CCB=calcium-channel blockers; CI=confidence interval; EF=ejection fraction; eGFR=estimated glomerular filtration rate; ROC=receiver operating characteristic

DISCUSSION

AKI is a well-known major complication associated with cardiac surgery and its incidence ranges from 8.9% to 42.5%, depending on the definition[17-19]. The incidence of AKI following CABG in our population is fairly consistent with the incidence reported in the published data, which was described from 12% to 48.5%[19-21], with an associated mortality of 12.6%. Furthermore, several studies have demonstrated that 3.8%-7% of patients would require RRT[22]. Our reported mortality was slightly higher (18.5%) and may be related to the older age of our patient population, compared with reported series of younger patients with postoperative AKI[20].

The development of AKI is tied to poor postoperative outcomes and high mortality rates in patients undergoing isolated CABG. There are multiple mechanisms involved with AKI development, including ischemic reperfusion lesion, nephrotoxin release, hemolysis, oxidative stress, and cytokine secretion, which produce systemic inflammatory responses, endothelial lesion, and tubular cell damage[23].

Patients who developed AKI were older and had higher BMI, hypertension, severe left ventricular dysfunction, and worse preoperative renal function. Our findings aligned with the current data which report the etiology of AKICS as multifactorial[24-26], correlating with advanced age, preexisting kidney disease, and left ventricular impairment, which are some of the important predictors of AKI development[20].

Decreased left ventricle EF and increased SCr levels are risk factors for major complications and high mortality after cardiac surgery; they also contribute to the development of postoperative AKI[23]. Indeed, as our findings demonstrate, severely decreased left ventricle EF is one of the strongest risk factors related to postoperative AKI.

Optimizing cardiac function could be a good strategy to minimize the risk of postoperative AKI, according to Leppikangas et al.[27]. They reported that the use of preoperative calcium sensitizer infusion could be a good strategy to improve left ventricular EF in patients with high-risk cardiac surgery[27].

Coronary angiography with iodinated contrast media is usually performed before cardiac operations to define the extent and severity of CAD. The use of iodinated contrast media is associated with contrast-induced nephropathy, a common and important potential complication after coronary angiography[28].

Another factor that influences the risk of AKI is the time elapsed between cardiac catheterization and CABG; in case of urgent surgeries, it is not possible to delay the surgery after the angiography. Recent reports focused on the time interval between coronary angiography and cardiac operation as the main determinant of postoperative renal failure[29]. The notion that a 'double hit' on renal function in close succession may increase the risk of AKI provides the basis for the recommendation to wait before exposing the kidneys to a second insult[28]. However, there is no consensus for a specific time delay between cardiac catheterization and CABG operation.

Mehta et al.[30] recently reported that the risk of post-CABG AKI development was "inversely and modestly related to the time between cardiac catheterization and CABG", with the highest incidence occurring in patients operated on ≤1 day after cardiac catheterization. This contrasts with our findings; we found no statistical difference between the time interval from catheterization to CABG and the development of postoperative AKI[30].

Identification and categorization of these high-risk patients allow for optimal decision-making for earlier interventions and better management strategies.

One of our main findings was that the use of CCB drugs has a possible nephroprotective effect in patients undergoing myocardial revascularization with extracorporeal circulation, similarly to the findings reported by Passaroni et al.[31]. They found that patients who did not receive CCB medications presented a higher percentage of AKI development after CABG with CPB. The nephroprotection effect is due to inhibition of glomerular vasoconstriction, producing vasodilatation of the arterioles and increasing the natriuretic effect[31].

Predictors

Preoperative, intraoperative, and postoperative periods are all important for the development of AKI, but the use of traditional markers such as SCr levels to diagnose AKI can limit and even delay its diagnosis[32]; there could already exist an acute renal lesion with a normal SCr value. This occurs in addition to the hemodilution in the first postoperative hours after cardiac surgery. Thus, there would not be an increase in SCr levels and the diagnosis of AKI could be delayed[33].

To prevent CABG-related AKI, predictive risk scores based on preoperative variables have been developed, such as the Cleveland Clinic score, Mehta score, SRI score, AKICS score, and age, creatinine, EF (ACEF) score[32]. However, there is still no consensus to recommend the use of a specific score to predict AKI before CABG[32].

The ACEF score was first described in 2009 in a publication for quick bedside evaluations[34]. According to Chen et al.[23], "the ACEF score may be the best and easiest tool to guide preventive and early therapeutic strategies for AKI to improve patient clinical outcomes" with a ROC curve of 0.781±0.027 (95%CI, 0.729-0.834; P=0.001).

Moreover, we found that the combination of factors such as hypertension, EF <30, eGFR, EuroSCORE II, and lack of CCB intake could bring us a model with a better ROC curve (0.783±0.036; 95%CI, 0.713-0.854; P<0.001). This scoring system may be an applicable model to predict postoperative AKI development because it uses clinical data, which can be readily and rapidly obtained, making it very appropriate for elective or urgent surgery[23]. More effort is required to develop and validate different prediction models to identify postoperative AKI in an easy-to-use, accurate pattern.

CONCLUSION

AKI following isolated CABG surgery occurs with some frequency and it is of great clinical importance, related with poor postoperative outcomes, prolonged ICU stay, and high mortality rates. Independent risk factors for developing postoperative AKI consist of age, hypertension, EF <30%, eGFR, EuroSCORE II, and no intake of CCB drugs. These factors provide an easy and accurate model to predict postoperative AKI in patients undergoing cardiac surgery.

REFERENCES

1. Najafi M. Serum creatinine role in predicting outcome after cardiacsurgery beyond acute kidney injury. World J Cardiol.2014;6(9):1006-21.

2. Bojar RM. Fluid management, renal, metabolic, and endocrineproblems. In: Bojar RM, ed. Manual of perioperative care in adult cardiacsurgery. 5th ed. Boston: Wiley-Blackwell; 2011.p.583-628.

3. Gaffney AM, Sladen RN. Acute kidney injury in cardiac surgery. CurrOpin Anaesthesiol. 2015;28(1):50-9.

4. Ortega-Loubon C, Fernández-Molina M, Carrascal-Hinojal Y,Fulquet-Carreras E. Cardiac surgery-associated acute kidney injury. Ann CardAnaesth. 2016;19(4):687-98. [MedLine]

5. Machado MN, Nakazone MA, Maia LN. Acute kidney injury based on KDIGO(Kidney Disease Improving Global Outcomes) criteria in patients with elevatedbaseline serum creatinine undergoing cardiac surgery. Rer Bras Cir Cardiovasc.2014;29(3):299-307.

6. Felicio ML, Andrade RR, Castiglia YM, Silva MA, Vianna PT, MartinsAS. Cystatin C and glomerular filtration rate in the cardiac surgery withcardiopulmonary bypass. Rev Bras Cir Cardiovasc.2009;24(3):305-11.

7. Josephs SA, Thakar CV. Perioperative risk assessment, prevention,and treatment of acute kidney injury. Int Anesthesiol Clin.2009;47(4):89-105. [MedLine]

8. Chen TH, Chang CH, Lin CY, Jenq CC, Chang MY, Tian YC, et al. Acutekidney injury biomarkers for patients in a coronary care unit: a prospectivecohort study. PLoS One. 2012;7(2):e32328. [MedLine]

9. Lin CY, Tsai FC, Tian YC, Jenq CC, Chen YC, Fang JT, et al.Evaluation of outcome scoring systems for patients on extracorporeal membraneoxygenation. Ann Thorac Surg. 2007;84(4):1256-62.

10. Coppolino G, Presta P, Saturno L, Fuiano G. Acute kidney injury inpatients undergoing cardiac surgery. J Nephrol.2013;26(1):32-40. [MedLine]

11. Mejía OA, Lisboa LA, Puig LB, Moreira LF, Dallan LA, Jatene FB.On-pump or off-pump? Impact of risk scores in coronary artery bypass surgery.Rev Bras Cir Cardiovasc. 2012;27(4):503-11.

12. Alsabbagh MM, Asmar A, Ejaz NI, Aiyer RK, Kambhampati G, Ejaz AA.Update on clinical trials for the prevention of acute kidney injury in patientsundergoing cardiac surgery. Am J Surg. 2013;206(1):86-95. [MedLine]

13. Grayson AD, Khater M, Jackson M, Fox MA. Valvular heart operation isan independent risk factor for acute renal failure. Ann Thorac Surg.2003;75(6):1829-35.

14. Jiang W, Xu J, Shen B, Wang C, Teng J, Ding X. Validation of fourprediction scores for cardiac surgery-associated acute kidney injury in Chinesepatients. Braz J Cardiovasc Surg. 2017;32(6):481-6. [MedLine]

15. Nina VJ, Matias MM, Brito DJ, Figueiredo Neto JA, Coutinho LB,Rodrigues RF, et al. Acute kidney injury after coronary artery bypass grafting:assessment using RIFLE and AKIN criteria. Rev Bras Cir Cardiovasc.2013;28(2):231-7.

16. Collins GS, Ma J, Gerry S, Ohuma E, Odondi L, Trivella M, et al.Risk prediction models in perioperative medicine: methodological considerations.Curr Anesthesiol Rep. 2016;6(3):267-75.

17. Brown JR, Kramer RS, Coca SG, Parikh CR. Duration of acute kidneyinjury impacts long-term survival after cardiac surgery. Ann Thorac Surg.2010;90(4):1142-8.

18. Parolari A, Pesce LL, Pacini D, Mazzanti V, Salis S, Sciacovelli C,et al. Risk factors for perioperative acute kidney injury after adult cardiacsurgery: role of perioperative management. Ann Thorac Surg.2012;93(2):584-91.

19. Hiew KC, Sachithanandan A, Arif M, Badmanaban B, Muiz A, Faisal I,et al. Acute kidney injury following coronary artery bypass graft surgery in atertiary public hospital in Malaysia: an analysis of 1228 consecutive cases. MedJ Malaysia. 2016;71(3):126-30.

20. Benedetto U, Luciani R, Goracci M, Capuano F, Refice S, Angeloni E,et al. Miniaturized cardiopulmonary bypass and acute kidney injury in coronaryartery bypass graft surgery. Ann Thorac Surg.2009;88(2):529-35.

21. Gallagher S, Jones DA, Lovell MJ, Hassan S, Wragg A, Kapur A, et al.The impact of acute kidney injury on midterm outcomes after coronary arterybypass graft surgery: a matched propensity score analysis. J Thorac CardiovascSurg. 2014;147(3):989-95.

22. Holzmann MJ, Rydén L, Sartipy U. Acute kidney injury and long-termrisk of stroke after coronary artery bypass surgery. Int J Cardiol.2013;168(6):5405-10.

23. Chen SW, Chang CH, Fan PC, Chen YC, Chu PH, Chen TH, et al.Comparison of contemporary preoperative risk models at predicting acute kidneyinjury after isolated coronary artery bypass grafting: a retrospective cohortstudy. BMJ Open. 2016;6(6):e010176. [MedLine]

24. Savluk OF, Guzelmeric F, Yavuz Y, Cevirme D, Gurcu E, Ogus H, et al.N-acetylcysteine versus dopamine to prevent acute kidney injury after cardiacsurgery in patients with preexisting moderate renal insuficiency. Braz JCardiovasc Surg. 2017;32(1):8-14. [MedLine]

25. Taniguchi FP, Souza AR, Martins AS. Cardiopulmonary bypass time as arisk factor for acute renal failure. Rev Bras Cir Cardiovasc.2007;22(2):201-5.

26. Kocogullari CU, Kunt AT, Aksoy R, Duzyol C, Parlar H, Saskin H, etal. Hemoglobin A1c levels predicts acute kidney injury after coronary arterybypass surgery in non-diabetic patients. Braz J Cardiovasc Surg.2017;32(2):83-9. [MedLine]

27. Leppikangas H, Järvelä K, Sisto T, Maaranen P, Virtanen M, Lehto P,et al. Preoperative levosimendan infusion in combined aortic valve and coronarybypass surgery. Br J Anaesth. 2011;106(3):298-304. [MedLine]

28. McCullough PA. Contrast-induced acute kidney injury. J Am CollCardiol. 2008;51(15):1419-28.

29. Greason KL, Englberger L, Suri RM, Park SJ, Rihal CS, Pislaru SV, etal. Safety of same-day coronary angiography in patients undergoing electiveaortic valve replacement. Ann Thorac Surg. 2011;91(6):1791-6.

30. Mehta RH, Honeycutt E, Patel UD, Lopes RD, Williams JB, Shaw LK, etal. Relationship of the time interval between cardiac catheterization andelective coronary artery bypass surgery with postprocedural acute kidney injury.Circulation. 2011;124(11 Suppl):S149-55.

31. Passaroni AC, Silva MA, Martins AS, Kochi AC. Use of nefidipine andacute kidney injury incidence in postoperative of myocardial revascularizationsurgery with cardiopulmonary bypass. Rev Bras Cir Cardiovasc.2010;25(1):32-7.

32. Onk OA, Onk D, Ozcelik F, Gunay M, Turkmen K. Risk factors for acutekidney injury after coronary artery bypass surgery and its detection usingneutrophil gelatinase-associated lipocalin. Cardiorenal Med.2016;6(3):216-29.

33. Lassnigg A, Schmidlin D, Mouhieddine M, Bachmann LM, Druml W, BauerP, et al. Minimal changes of serum creatinine predict prognosis in patientsafter cardiothoracic surgery: a prospective cohort study. J Am Soc Nephrol.2004;15(6):1597-605.

34. Ranucci M, Castelvecchio S, Menicanti L, Frigiola A, Pelissero G.Risk of assessing mortality risk in elective cardiac operations: age,creatinine, ejection fraction, and the law of parsimony. Circulation.2009;119(24):3053-61.

No financial support.
No conflict of interest.

Authors' roles & responsibilities

COL Contribution to the design of the study; data collection; statistical analysis; discussion of results; manuscript writing; article review; final manuscript approval

MFM Article review; final manuscript approval

LPD Article review; final manuscript approval

PJM Contribution to the design of the study; statistical analysis; article review; final manuscript approval

YC Conception and design of the project; data collection; discussion of results; article review; final manuscript approval

Article receive on Tuesday, January 2, 2018

CCBY All scientific articles published at bjcvs.org are licensed under a Creative Commons license

Indexes

All rights reserved 2017 / © 2024 Brazilian Society of Cardiovascular Surgery DEVELOPMENT BY