Timing of renal replacement therapy initiation by AKIN classification system
© Leite et al.; licensee BioMed Central Ltd. 2013
Received: 14 January 2013
Accepted: 26 March 2013
Published: 2 April 2013
Previous studies using Acute Kidney Injury Network (AKIN)/RIFLE criteria to classify early initiation of renal replacement therapy (RRT) have defined it as the therapy started in less severe AKIN/RIFLE stages. Generally, these studies failed in demonstrating measurable benefits.
We compared RRT initiation in critically ill patients and defined early or late RRT in reference to timing after stage 3 AKIN was met: patients beginning RRT within 24 hours after acute kidney injury (AKI) stage 3 were considered early starters. AKIN criteria were evaluated by both urine output (UO) and serum creatinine (sCr) and patients with acute-on-chronic kidney disease were excluded. A propensity score methodology was used to control variables.
A total of 358 critically ill patients were submitted to RRT. Only 150 patients with pure AKI at stage 3 were analyzed. Mortality was lower in the early RRT group (51.5 vs. 77.9%, P = 0.001). After achieving balance between the groups using a propensity score, there was a significant 30.5 (95% confidence interval [CI] 14.4 to 45.2%, P = 0.002) relative decrease of mortality in the early RRT group. Moreover, patients on the early RRT group had lower duration of mechanical ventilation, time on RRT and a trend to lower intensive care unit (ICU) length of stay.
For the first time, AKIN was used with UO criterion to evaluate early and late RRT. Using a time-based approach could be a better parameter to access the association between RRT initiation and outcomes in patients with AKI.
Acute kidney injury is a common occurrence in critically ill patients, with incidence rates of occurrence varying from 5 to 60% [1, 2] and a trend towards higher rates (30 to 60%) when using the risk, injury, failure, loss of kidney function, end stage renal failure (RIFLE) or Acute Kidney Injury (AKI) Network (AKIN) classification. Acute kidney injury is an independent risk factor for increased morbidity and mortality [3, 4]. Renal replacement therapy (RRT) is necessary in about 6% of critically ill patients, according to a large multinational, multicenter survey . Generally, RRT is provided as supportive treatment to AKI patients, preventing additional disorders (hypervolemia, metabolic acidosis, progressive uremia, and hyperkalemia).
Data from mainly observational studies have suggested that early RRT in critically ill patients with AKI may have a beneficial impact on survival [5, 6]. However, in addition to the lack of large randomized clinical trials assessing early dialysis indication, there is a broad variation in the criteria used to classify early or late RRT. In a review of 16 studies comparing early vs late dialysis, metabolic markers (serum urea or hyperkalemia) were the most frequently used parameters (n = 8) [7–13]. Reduced urine output (n = 3) [14–16] or timing from ICU admission to RRT start (n = 2) [17, 18] have also been used to define early dialysis. RIFLE criteria have been used in three other studies to define early dialysis [19–21].
Although the RIFLE criteria were developed and validated for AKI diagnosis and evaluation of severity, and not a parameter to guide RRT initiation, some observational studies [19–21] have investigated whether initiating RRT in less severe renal injury (that is, RIFLE classification -0 or R) can be associated with a better survival rate. Although one study that analyzed AKI after major abdominal surgery demonstrated benefits , two others studies evaluating mainly patients with sepsis demonstrated similar outcomes with either early or late RRT [19, 21]. However, two problems can make the analysis of survival benefits in early dialysis difficult when using this definition: (1) patients at less severe AKI stages initiating RRT may have severe metabolic disorders (that is, metabolic acidosis, or hyperkalemia) in spite of limited renal injury, or even no AKI (RIFLE classification -0); (2) when using RIFLE/AKIN criteria, patients with chronic kidney disease (CKD) must have significant metabolic disorders to require RRT before classification with the maximum severity grade, as opposed to those with previous normal previous renal function. Moreover, no study has evaluated urinary output (UO), making the degree of AKI severity largely dependent on baseline serum creatinine (sCr), and there is no information on the timing of RRT initiation after diagnosis of severe AKI.
In the present study, a different approach using AKI severity classification was used. Our objective was to determine whether the timing of RRT earlier or later than 24 hours after classification as AKIN stage 3, is associated with hospital mortality in critically ill patients. Moreover, we excluded acute-on-chronic kidney injury (AKI-CKD) patients.
Materials and methods
This is a retrospective analysis of a prospective cohort of consecutive critically ill adult patients (> 18 years of age) undergoing renal replacement therapy. The study was carried out at referral centers (General Hospital of Fortaleza and Haroldo Juaçaba Hospital) in Fortaleza, Brazil. These hospitals comprise four ICUs with a total of 43 beds. All patients needing RRT from January 2010 to December 2011 were initially included. We excluded patients undergoing maintenance RRT, with renal transplantation, with RRT initiated before ICU admission, those who needed RRT before being classified as AKIN stage 3 and with an ICU stay of less than 24 h. Patients who did not have sCr less than or equal to 1.4 mg/dL during their hospital stay were considered as having previous CKD and were excluded. This definition was used instead of glomerular filtration rate (GFR) because it is the highest level where AKI stage 3 could be diagnosed by a three-fold increase in reference sCr and not by an acute increment of 0.5 mg/dL in patients with sCr more than or equal to 4.0 mg/dL, as discussed below. All data, including UO at each 6-hour interval, were prospectively collected during the ICU stay by a group of attendant physicians and nurses after a standardized database record was implemented. Data preceding ICU admission were obtained from medical records. We did not have access to UO data before ICU admission. The Institutional Ethical Committee of the Hospital Geral de Fortaleza approved the analysis of data and agreed that informed consent was unnecessary due to the purely observational and non-interventional nature of this study (Resolução CNS 196/96).
Clinical and laboratory parameters
Data variables included demographic characteristics, comorbidities, surgical or medical ICU admission and the indications for RRT. Biochemistry data such as complete blood cell count, serum urea (sUr), sCr, blood gas analyses, serum total bilirubin and serum potassium were recorded upon ICU admission and RRT initiation. The clinical parameters and severity score were also recorded. The clinical parameters included heart rate, systolic and diastolic blood pressure, partial pressure of arterial blood gas oxygen and fraction of inspired oxygen. Urine output was measured each 2-hour interval during the ICU stay. Severity scores included the Glasgow Coma Scale (GCS), Acute Physiology and Chronic Health Evaluation II (APACHE II) score and Simplified Acute Physiology Score III (SAPS III). The use of mechanical ventilation and need for vasopressor drugs were recorded. Definitions were made as follows: hypertension was defined as blood pressure above 140/90 mmHg or use of anti-hypertension agents; diabetes was defined as previous use of insulin or oral hypoglycemic agents; sepsis was defined as the presence of both infection and systemic inflammatory response syndrome . All sCr levels measured from hospital admission until the start of RRT were recorded. At hospital discharge, the GFR of survivors was estimated by the CKD-Epidemiology Collaboration (EPI) equation.
The indications for RRT were: (1) azotemia (sUr > 150 mg/dL) with uremic symptoms; (2) oligoanuria (urine output < 100 ml every twelve hours) refractory to diuretics; (3) hyperkalemia (sK+ > 5.5 mmol/L) refractory to medical treatment, and (4) metabolic acidosis (pH < 7.2 and serum bicarbonate < 16 m Eq/L in arterial blood gas).
Acute kidney injury classification
Diagnosis and severity of AKI was defined by the AKIN classification system, using the worst criteria (sCr increment or reduced UO). The reference sCr was the lowest achieved during hospital stay before RRT start. Time from AKI stage 3 diagnosis to RRT start was recorded. Patients with more than one AKI episode during their hospital stay had only the first RRT-related AKI episode recorded. Patients initiating RRT less than 24 h after reaching AKIN stage 3 were included in the early RRT group and those after 24 h were included in the late RRT group.
Renal replacement therapy modality
Prescription and initiation of RRT was performed by two groups of nephrologists who did not work with the present researchers. When patients were receiving vasopressor drugs, sustained low efficiency RRT (SLED) was performed; otherwise, conventional intermittent hemodialysis was performed. For SLED, the blood flow and dialysate flow rates were 200 ml/minute and 300 ml/minute, respectively, and the duration was 8 h. Conventional intermittent hemodialysis was performed for 4 h with a dialysate flow of 500 ml/minute, and blood flow of 300 ml/minute. As hemodynamics changed during the ICU stay, patients changed between RRT modalities.
The endpoint of this study was in-hospital mortality. The survival period was calculated from RRT initiation to mortality in non-survivors or to hospital discharge in survivors. Secondary endpoints included ICU length of stay (LOS), days on mechanical ventilation and time on RRT.
Descriptive statistics are expressed as mean ± SD, or as absolute frequency and percentage, according to continuous or categorical data, respectively. All variables were tested for normal distribution using the Kolmogorov-Smirnov test. The unpaired Student's t-test was applied to compare continuous variables and normally distributed data when appropriate. Categorical data were tested using the chi-square test.
Kaplan-Meier curves obtained with the log-rank test were plotted to demonstrate the differences in patient survival between the two groups (early RRT vs late RRT). A propensity score methodology was used to control for bias due to selection of patients placed on early RRT, using the inverse probability of treatment weighting (IPTW) method. This method has been shown to have superior performance in estimation of risk differences in observational studies . First, a propensity score model included demographic, clinical and laboratory data at ICU admission and at the day of RRT start that could have influenced the decision of placement on early RRT. This estimated the probability for each study subject to be placed on early RRT. Then, the contribution of each subject was weighted by 1/propensity score for the early RRT group, and by 1/(1-propensity score) for the delayed late RRT group. These weights assured that for each combination of the covariates used in the propensity score model, the sum of the contributions of all subjects was equal. All pre-RRT variables were balanced between groups. Covariate balance after the IPTW weighting was assessed by computing their standardized differences, and groups were considered balanced if the standardized differences of all covariates were < 0.25  and no further adjustment was required for the outcome analysis. Short-term outcome variables were compared using IPTW-weighted regression models. Results were expressed as absolute and relative average treatment effect. Statistical significance was set at P < 0.05. Analyses were performed with SPSS 19.0 for Windows and R software version 2.10.1 for Windows, using the Design and Survey packages .
Patients' characteristics before and after inverse probability weighting
After inverse probability of treatment weighting
( n = 150)
( n = 64)
( n = 86)
55.5 ± 19.1
54.6 ± 19.7
56.2 ± 18.4
Sex, male, n (%)
Diabetes mellitus, n (%)
Hypertension, n (%)
Lower sCr, mg/dL
0.90 ± 0.30
0.96 ± 0.30
0.87 ± 0.29
Surgical ICU admission, n (%)
Sepsis diagnosed, n (%)
Data at ICU admission
Vasoactive drugs, n (%)
Systolic blood pressure, mmHg
101.0 ± 22.9
91.8 ± 20.2
108.6 ± 22.5
Diastolic blood pressure, mmHg
59.4 ± 14.9
55.5 ± 13.4
62.5 ± 15.3
Heart rate, bpm
101.1 ± 23.5
104.7 ± 21.5
99.3 ± 24.8
10.1 ± 2.2
9.8 ± 2.4
10.5 ± 2.1
White blood cells, x103/mm3
17.0 ± 8.6
15.9 ± 6.6
17.5 ± 7.4
Platelet count, x103/mm3
230.4 ± 121.7
235.3 ± 131.2
226.4 ± 120.2
2.11 ± 1.22
2.0 ± 0.9
1.7 ± 0.8
78.7 ± 43.1
82.7 ± 44.1
75.4 ± 41.8
4.4 ± 2.1
4.7 ± 1.4
4.2 ± 0.9
17.7 ± 5.7
16.7 ± 5.5
18.5 ± 5.9
12.8 ± 2.7
12.8 ± 3.1
12.8 ± 2.5
APACHE II score
18.8 ± 6.1
19.2 ± 6.3
18.7 ± 5.9
SAPS III score
61.1 ± 11.9
62.1 ± 11.7
60.2 ± 12.0
Data at RRT start
2.93 ± 1.82
2.7 ± 1.1
2.8 ± 1.5
106.7 ± 64.8
100.1 ± 54.9
108.2 ± 55.6
5.3 ± 2.0
4.9 ± 1.9
5.1 ± 2.1
16.2 ± 4.4
14.4 ± 3.9
17.2 ± 4.3
APACHE II score
20.2 ± 6.3
20.3 ± 6.8
20.1 ± 6.2
SAPS III score
62.6 ± 12.3
63.2 ± 11.8
62.7 ± 11.6
Indications for dialysis
Azotemia, n (%)
Oligoanuria, n (%)
Metabolic acidosis, n (%)
Hyperkalemia, n (%)
Short-term outcome among the early and delayed RRT groups, before and after inverse probability weighting of treatment
After IPTW weighting
( n = 64)
( n = 86)
Average treatment effect
Duration of mechanical ventilation, days
12.5 ± 9.8
18.0 ± 13.7
12.8 ± 7.8
18.9 ± 9.4
-6.02 (-11.50 to -0.54)
Length of ICU stay, days
18.7 ± 12.5
24.7 ± 17.3
19.4 ± 11.5
25.4 ± 10.9
-5.97 (-12.91 to 0.976)
Time on RRT, days
6.9 ± 4.6
8.9 ± 4.6
6.7 ± 4.9
9.7 ± 6.1
-2.95 (-5.77 to -0.125)
In-hospital mortality, n (%)
-30.5 (-14.4 to -45.2)
Propensity score analysis
Variables included in the propensity score model along with their estimates and standard errors
Lowest sCr pre-RRT, mg/d)
Systolic blood pressure at ICU admission, mmHg
Heart rate at ICU admission, bpm
Bicarbonate at ICU admission, mEq/L
Potassium at ICU admission, mEq/L
SCr pre-RRT, mg/dL
The propensity score model had good discrimination to predict early RRT, c-index = 0.856, good validation (Hosmer-Lemeshow statistics, P = 0.429), and explained 45% of the variability in the data set (R2 = 0.45). All demographic, clinical and laboratory variables pre-RRT were well balanced between groups after IPTW, as shown in Table 1. Thus, groups were rendered comparable with regard to all these covariates, and no further adjustment was required for the outcome analysis. In-hospital mortality, ICU LOS and duration of mechanical ventilation were the outcome variables that were comparable between the groups after IPTW weighting. There was a significant 37.3% relative decrease in in-hospital mortality in the early RRT group compared with the late RRT group (Table 2). Moreover, a significant reduction was observed in the duration of mechanical ventilation on a 6-day average, fewer days on RRT-dependence and a trend toward a decrease in ICU LOS in the early RRT group.
In this study, we evaluated the impact of early RRT on mortality in critically ill AKI patients. While previous studies generally used serum urea [8–13] or time from ICU admission to RRT initiation to characterize early RRT [17, 18], some recent studies have attempted to define the timing of RRT initiation using RIFLE/AKIN criteria [19–21]. These recent studies have defined early RRT started during the initial stages of RIFLE/AKIN classification. The present study has significant differences from other studies in evaluating early RRT. First, we defined early RRT by time (RRT initiating earlier or later than 24 hours after AKI was diagnosed at its worst stage). Secondly, we studied a highly homogeneous population, excluding patients with AKI-CKD, and performed analysis only considering patients who had achieved AKI stage 3 before initiating RRT. Lastly, AKIN criteria were evaluated by either sCr and/or UO criteria. Using this approach, there was a significant (37.3%) relative decrease in the mortality rate in patients subjected to early RRT.
Several studies have used sUr to define early RRT, with controversial results. In the present study, overall, pre-RRT sUr was similar to levels among patients in early RRT in other studies, suggesting all patients were started relatively early on RRT. Shiao et al.  demonstrated better survival in patients undergoing abdominal surgery who were submitted to early RRT, defined by the RIFLE criteria. In the aforementioned study, there was a trend towards higher blood urea nitrogen (BUN) in the late RRT group. In the present study, there was no difference in mean sUr levels between patients with early or late RRT (Table 2). This finding demonstrates that early RRT can be associated with better mortality, regardless of pre-RRT urea levels.
To the best of our knowledge, only three studies have evaluated early RRT using the AKIN/RIFLE approach [19–21]. While the previously cited study of patients undergoing abdominal surgery demonstrated a difference in survival rates, the two others, which predominantly included septic patients, were unable to shown any survival benefits of early RRT. When early RRT is defined only as RRT started at earlier AKI stages (that is, RIFLE classification -0 or R), these studies can present some interpretation bias. First, patients with no AKI might be included. As AKI is associated with poor prognosis in critically ill patients, the inclusion of these patients can influence the results. Secondly, patients can achieve a more severe AKI stage by the UO criterion and erroneously remain in the early RRT group. Finally, patients with previous CKD may need RRT earlier during the evolution of an AKI episode due to serious metabolic disorders, mainly when only sCr is available. This can explain the higher prevalence of CKD patients in the groups initiating RRT at RIFLE stages -0 or R [20, 21]. In our data, fewer patients starting RRT were classified as AKI stage 3 by sCr. If the UO criterion was not considered, these patients would be classified at earlier AKI stages.
In our study, we attempted to eliminate these pitfalls by separately analyzing only patients in whom CKD could be excluded (patients with baseline sCR < 1.5 mg/dL). Moreover, only patients achieving AKI stage 3 were included, thus selecting a population with the same degree of AKI severity. Finally, we applied both sCr and UO criteria. Recorded urine output disclosed that only 25/240 patients were submitted to RRT before AKI stage 3 was reached. In the study performed by Maccariello et al. , 52% of patients initiated RRT at RIFLE stages -R or I. In both studies by the National Taiwan University Surgical ICU Associated Renal Failure (NSARF) study group [20, 21], approximately half of the patients initiated RRT at RIFLE stages -0 or R. It is probable that these patients would have had more severe AKI stages if the UO criterion had been applied.
We have defined CKD as an inability to achieve sCr ≤ 1.4 mg/dL before RRT. This cutoff was chosen because it is the highest reference level where AKI stage 3 can be achieved only by a three-fold increase in sCr criteria and not by the acute increase of 0.5 mg/dL. This strategy insured that time from renal insult to worst AKI stage is similar in patients with comparable injury severity, according to creatinine kinetics as suggested by Waikar and Bonventre .
Timing to RRT was measured after patients achieved AKIN stage 3. We have chosen this method instead of AKI diagnosis at earlier stages because it seems a more practical approach. Not all patients with AKI will need RRT or even progress to AKI stage 3, but it is more likely patients achieving AKIN stage 3 will need RRT. As stated by Lameire et al. , 'interpretation of studies about early or late dialysis is complicated because there is a loss of the semantic significance of a time-related event' and that 'conclusions on the impact of early versus late initiation of dialysis would be only justified when, at the moment patients fulfilled the criteria for dialysis, one group started RRT immediately while for the other group dialysis was delayed.' In the present methodology, all patients achieved AKI at stage 3 and RRT was a time-related event. We suggest that one parameter used to initiate RRT in critically ill patients can be when stage 3 is reached and renal function recuperation within a short time has been ruled out. This does not eliminate the possibility of starting RRT at early stages when associated with severe metabolic disorders and/or refractory hypervolemia.
Although showing promising results in terms of performing early RRT in critically ill patients, this study evaluated only AKIN stage 3, so the influence of RRT on AKI earlier stages was not evaluated. This limitation is counterbalanced by considering UO. When using the UO criterion, many patients classified AKIN 3 would be otherwise classified AKIN 1 or 2, using only sCr alone. Including UO criteria could explain why a minority of patients needed RRT before achieving AKIN stage 3. A second limitation is that excluding patients who could not achieve a sCr lower than 1.4 mg/dL, might mean that patients with community-acquired AKI have been considered as having CKD. In these patients, it would not be possible to precisely determine when AKI reached stage 3, making it difficult to classify them into early or late RRT groups. Another limitation is the lack of data on fluid balance, making it especially difficult to explore reasons for reduced mechanical ventilation time in early RRT patients. Although it is a retrospective study, we have tried to balance all variables that could influence the decision to initiate RRT earlier, using the propensity score and the IPTW method to balance variables. Finally, the relatively small number of patients is counterbalanced by the homogeneity of this population, including only patients with pure AKI.
Using a time-based approach from AKIN stage 3 by UO or sCr to RRT initiation, this study demonstrated a reduced mortality rate and reduced need for mechanical ventilation among critically ill AKI patients receiving RRT in the first 24 h after diagnosis of AKI stage 3, by applying both sCr and UO criteria. Patients with AKI-CKD can influence results of studies that use AKIN/RIFLE classification to define early RRT. We suggest that in patients with stage 3 AKI, RRT must be considered in less than 24 h.
Urinary output is an important criterion for staging AKI and can be useful in determining the timing of RRT.
Patients with previous CKD can influence the results of studies when classifying early RRT by AKI stage.
Performing RRT in the first 24 h of AKIN stage 3 diagnosis reduced in-hospital mortality and mechanical ventilation time.
acute-on-chronic kidney disease
Acute Kidney Injury Network
- APACHE II:
Acute Physiology and Chronic Health Evaluation II
chronic kidney disease
chronic kidney disease epidemiology collaboration
Glasgow Coma Scale
glomerular filtration rate
inverse probability of treatment weighting
length of stay
National Taiwan University Surgical ICU Associated Renal Failure
risk, injury, failure, loss of kidney function, end stage renal failure
renal replacement therapy
- SAPS III:
Simplified Acute physiology Score III
sustained low efficiency dialysis
To the administration and ICU professionals of the General Hospital of Fortaleza and the Cancer Institute of Ceará.
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