Early initiation of continuous renal replacement therapy improves survival of elderly patients with acute kidney injury: a multicenter prospective cohort study
- Jae Yoon Park1,
- Jung Nam An3, 6,
- Jong Hyun Jhee4,
- Dong Ki Kim2,
- Hyung Jung Oh4,
- Sejoong Kim5,
- Kwon Wook Joo2,
- Yun Kyu Oh6,
- Chun-Soo Lim6,
- Shin-Wook Kang4,
- Yon Su Kim2,
- Jung Tak Park†4Email author and
- Jung Pyo Lee†6Email author
© The Author(s). 2016
Received: 8 April 2016
Accepted: 26 July 2016
Published: 16 August 2016
Continuous renal replacement therapy (CRRT) is essential in the management of critically ill patients with acute kidney injury (AKI). However, the optimal timing for initiating CRRT remains controversial, especially in elderly patients. Therefore, we investigated the outcomes of early CRRT initiation in elderly patients with AKI.
A total of 607 patients ≥65 years of age who started CRRT due to AKI between August 2009 and December 2013 were prospectively enrolled. They were divided into two groups based on the median 6-hour urine output immediately before CRRT initiation. Propensity score matching was used to compare the overall survival rate, CRRT duration, and hospitalization duration.
The median age of both groups was 73.0 years, and 60 % of the patients were male. The most common cause of AKI was sepsis. In the early CRRT group, the mean arterial pressure was higher, but the prothrombin time and total bilirubin, aspartate aminotransferase, and alanine aminotransferase levels were lower. The overall cumulative survival rate was higher in the early CRRT group (log-rank P < 0.01). Late CRRT initiation was associated with a higher mortality rate than early initiation after adjusting for age, sex, the Charlson comorbidity index, systolic arterial pressure, prothrombin time, the total bilirubin, aspartate aminotransferase, and alanine aminotransferase levels, cumulative fluid balance and diuretic use (hazard ratio, 1.35; 95 % confidence interval 1.06, 1.71, P = 0.02). Following propensity score matching, patient survival was significantly better in the early CRRT group than in the late CRRT group (P < 0.01). The total duration of hospitalization from the start of CRRT was shorter among the survivors when CRRT was started earlier (26.7 versus 39.1 days, P = 0.04).
A better prognosis can be expected if CRRT is applied early in the course of AKI in critically ill, elderly patients.
KeywordsElderly patients Survival Continuous renal replacement therapy Acute kidney injury Propensity score matching
Elderly people (aged ≥65 years) are currently the fastest-growing sector of the general population in developed countries. They are more prone to developing acute kidney injury (AKI) because of structural and functional alterations in the kidney [1, 2], comorbidities (e.g., arteriosclerosis, hypertension, diabetes mellitus, and heart failure), and polypharmacy for the treatment of comorbidities, which increase in prevalence with age. Accordingly, an increasing number of elderly patients can be expected to develop AKI [3–5].
For more than a decade, continuous renal replacement therapy (CRRT) has been essential in the management of critically ill patients with AKI [6, 7]. The generally accepted indications for initiating CRRT in AKI include persistent hyperkalemia, severe acidosis and hypervolemia that are unresponsive to adequate medical management, and overt uremic symptoms or signs (e.g., uremic bleeding, pericarditis, and encephalopathy) [8–10].
Although the optimal timing of CRRT initiation remains controversial, recent studies comparing early and late initiation have suggested that early initiation may have a beneficial impact on survival [11–14]. However, elderly patients are more susceptible to hemodynamic complications during dialysis, such as intradialytic hypotension and arrhythmia, because of decreased autonomic function and cardiovascular reserve, bleeding problems, and neurological complications resulting from rapid changes in serum electrolytes and osmolarity [15, 16]. Additionally, because short-term and long-term survival following CRRT are expected to be lower in elderly patients compared with the general population , therapeutic decisions, including use of CRRT, tend to be more conservative for patients in this age group, especially in intensive care. Nevertheless, few studies have specifically examined CRRT in older individuals with AKI. Therefore, although previous studies have demonstrated that early initiation of CRRT could be beneficial in the general population, it is not clear whether it could also benefit elderly patients.
In the present study, we aimed to investigate the outcomes of early versus late initiation of CRRT using propensity score matching (PSM) in a multicenter, prospective CRRT cohort of elderly individuals.
All patients aged ≥18 years who received CRRT for AKI at Seoul National University Hospital, Seoul National University Boramae Hospital, and Yonsei University Severance Hospital were initially screened (n = 1471). The patients were prospectively enrolled between August 2009 and December 2013. We excluded 724 patients who were younger than 65 years of age and 140 who were on chronic dialysis. A total of 607 patients were included in the analyses. They were divided into two groups based on the body-weight-adjusted median 6-h urine output immediately before administration of CRRT.
The definition of AKI was based on the Kidney Disease: Improving Global Outcomes (KDIGO) clinical practice guidelines for AKI and was defined as the presence of at least one of the following criteria: an increase in the serum creatinine level ≥0.3 mg/dL (≥26.5 μmol/L) within 48 h; an increase in the serum creatinine level to ≥1.5 times the baseline level that was known or was presumed to have occurred within the previous 7 days; or urine volume <0.5 mL/kg/h for 6 h. For the diagnosis of systemic inflammatory response syndrome, the presence of at least two of the following criteria were required: core temperature ≥38 °C or ≤36 °C; heart rate ≥90 beats per minute; respiratory rate ≥20 breaths per minute and PCO2 ≤ 32 mmHg or mechanical ventilation; and peripheral leukocyte count ≥12,000/mm3 or ≤4000/mm3 . Septic AKI was defined as systemic inflammatory response syndrome combined with an infectious episode and AKI.
The primary outcome was the patient survival rate after CRRT initiation. The secondary outcomes were mortality on the 28th day of CRRT, the durations of CRRT and total renal replacement therapy (RRT), and the durations of total hospitalization and stay in the intensive care unit (ICU) from CRRT initiation.
At the time of CRRT initiation, demographic, clinical, and laboratory data were collected. For the assessment of disease severity, the Charlson comorbidity index (CCI), sequential organ failure assessment (SOFA) score, and acute physiology and chronic health evaluation (APACHE) II score were calculated at the time of dialysis initiation [19, 20]. All available intake and output data for 3 days immediately before CRRT initiation were used to calculate the cumulative fluid balance. The estimated glomerular filtration rate (eGFR) was also calculated using the modification of diet in renal disease equation . The patients were stratified into two groups (patients with early or late CRRT) based on the body-weight-adjusted median 6-h urine output before CRRT initiation.
Categorical variables described as frequencies and proportions were compared using the chi-squared test. Following a test for normality, the non-normally distributed variables were expressed as the median (25–75th percentiles) and were compared using the Mann–Whitney U or Kruskal-Wallis test. The normally distributed variables were presented as the mean ± standard deviation. Patient survival was estimated by Kaplan-Meier curves and multivariate Cox regression models based on the body-weight-adjusted median 6-h urine output immediately before CRRT initiation. Propensity scores were estimated by multiple logistic regression analysis with adjustments for patient age, sex, the CCI, systolic arterial pressure, prothrombin time, and the total bilirubin level. After calculation of the propensity scores, we matched patients in the early and late CRRT groups with similar propensity scores at a 1:1 ratio using the nearest neighbor method, no replacement, and a 0.2 caliper width. PSM was used to increase the precision of the estimated effect without increasing bias due to the presence of variables potentially associated with survival . The characteristics of both the early and late CRRT groups were compared before and after PSM. Kaplan-Meier survival curves and life tables were generated for the two groups after PSM.
All statistical tests were evaluated using a two-tailed 95 % confidence interval (CI), and a P value <0.05 was considered statistically significant. All descriptive and survival analyses were performed using SPSS for Windows, version 21.0 (IBM, Armonk, NY, USA). R software (version 2.14.2) was used for PSM.
Baseline characteristics of the subjects
Baseline characteristics of the two groups stratified by median pre-CRRT 6-h urine output before and after propensity score matching at the time of CRRT initiation
Before propensity score matching
After propensity score matching
Early CRRT (N = 303)
Late CRRT (N = 304)
Early CRRT (N = 241)
Late CRRT (N = 241)
Sex, male (n (%))
180 (59.4 %)
185 (60.9 %)
145 (60.2 %)
145 (60.2 %)
Body mass index (kg/m2)
Cause of acute kidney injury (n (%))
138 (45.5 %)
137 (45.1 %)
116 (48.1 %)
116 (48.1 %)
27 (8.9 %)
18 (5.9 %)
20 (8.3 %)
12 (5.0 %)
49 (16.2 %)
63 (20.7 %)
37 (15.4 %)
46 (19.1 %)
34 (11.2 %)
25 (8.2 %)
26 (10.8 %)
21 (8.7 %)
55 (18.2 %)
61 (20.1 %)
42 (17.4 %)
46 (19.1 %)
Time from ICU admission to CRRT initiation (h)
Charlson comorbidity index
11.6 ± 3.7
12.5 ± 3.4
11.8 ± 3.6
12.4 ± 3.4
APACHE II score
28.5 ± 7.4
29.6 ± 7.1
29.2 ± 7.4
29.5 ± 7.1
Mechanical ventilation needs (n (%))
251 (82.8 %)
253 (83.5 %)
203 (84.2 %)
200 (83.0 %)
Systolic blood pressure (mmHg)
115.1 ± 24.7
109.3 ± 24.8
111.9 ± 22.0
109.7 ± 24.7
Diastolic blood pressure (mmHg)
61.8 ± 14.0
61.0 ± 15.0
61.2 ± 13.1
61.8 ± 15.1
Mean arterial pressure (mmHg)
79.6 ± 15.6
77.1 ± 16.3
78.1 ± 14.1
77.8 ± 16.3
Six-hour urine volume before CRRT initiation (mL)
Cumulative fluid balance (mL)
Diuretics use (n (%))
209 (69.0 %)
194 (63.8 %)
164 (68.0 %)
148 (61.4 %)
Target clearance (mL/kg/h)
Dialysate flow rate (mL/h)
Replacement flow rate (mL/h)
Blood flow rate (mL/min)
White blood cells (n/μL)
2.7 ± 0.5
2.7 ± 0.6
2.6 ± 0.5
2.7 ± 0.6
Total bilirubin (mg/dL)
Aspartate aminotransferase (IU/L)
Alanine aminotransferase (IU/L)
Blood urea nitrogen (mg/dL)
Before PSM, 303 patients were in the early CRRT group, and 304 were in the late CRRT group. Sepsis (45.3 %) was the most common cause of AKI, followed by ischemia (18.5 %) and postoperative (9.7 %) and nephrotoxic (7.4 %) causes. The median 6-h urine output before CRRT initiation was 0.24 mL/kg/h. The patients were divided into two groups based on the median 6-hour urine output: early (≥0.24 mL/kg/h) and late (<0.24 mL/kg/h) CRRT groups. The 6-hour urine volumes before CRRT initiation were 230.0 (150.0–432.0) mL in the early CRRT group and 20.0 (0.0–40.0) mL in the late CRRT group. There was no difference in cumulative fluid balance or diuretic use between the two groups. The time from ICU admission to CRRT initiation was 6.8 (1.5–31.1) h in the early CRRT group and 7.9 (1.7–37.8) h in the late CRRT group (P = 0.30). The CCI, SOFA score, and APACHE II score did not differ between the two groups. The number of patients who required mechanical ventilation and the fraction of inspired oxygen (0.5 (0.4-0.5) versus 0.5 (0.4–0.5), P = 0.76) also did not differ between the two groups. The systolic blood pressure (SBP) and mean arterial pressure were higher in the early CRRT group. However, the target clearance and initial blood flow rate for CRRT did not differ between the groups. The serum creatinine level, eGFR, white blood cell count, hemoglobin concentration, and platelet count also did not differ between the groups. The prothrombin time-international normalized ratio (PT-INR) and serum total bilirubin, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) levels were higher in the late CRRT group.
All of the patients in the two groups were matched by propensity scores for the timing of initiation of CRRT using the following covariates: age, sex, the CCI, SBP, the PT-INR, and the total bilirubin level. After PSM, 482 patients (241 in each group) remained. The distributions of the propensity scores before and after matching are shown in the supplementary data section (Additional file 1: Figure S1). Almost all of the baseline parameters, including age, sex, body mass index (BMI), the cause of AKI, time from ICU admission to CRRT initiation, the CCI, SOFA score, APACHE II score, mechanical ventilation requirements, arterial pressures, CRRT setting, and biochemical data, except for the AST, ALT, and creatinine levels, were similar between the propensity score-matched patients in the early and late CRRT groups. In addition, the propensity scores of the matched patients did not differ between the groups.
Survival analyses stratified by timing of CRRT initiation
Multivariate analysis of risk factors for mortality in elderly patients with severe acute kidney injury in the group with late initiation of continuous renal replacement therapy (CRRT) compared to the group with early initiation of CRRT group, using Cox regression models and a propensity score-matched model
95 % Confidence interval
Duration of RRT and hospitalization
Comparison of duration of dialysis and hospital stay before and after propensity score matching
Before propensity score matching
After propensity score matching
Early CRRT (N = 303)
Late CRRT (N = 304)
Early CRRT (N = 75)
Late CRRT (N = 41)
Early CRRT (N = 241)
Late CRRT (N = 241)
Early CRRT (N = 59)
Late CRRT (N = 40)
Duration of CRRT (days)
Duration of total RRT (days)
Duration of ICU stay from CRRT initiation (days)
Total duration of hospitalization from CRRT initiation (days)
After PSM, there was no significant difference in the duration of CRRT or total RRT between all of the patients and the survivors. Although the duration of ICU stay from CRRT initiation was longer in the early CRRT group (6.2 (1.7–11.0) versus 3.9 (1.3–9.1), P = 0.02), among the survivors there was no difference between the groups. Further, while the total duration of hospitalization did not differ between the groups, it was shorter among the survivors in the early CRRT group (26.7 (16.1–38.2) versus 39.1 (27.7–79.3) days, P = 0.04).
In the present study, we compared the outcomes of CRRT among elderly patients according to the timing of CRRT initiation, with stratification by the median 6-h urine output immediately before initiation, using prospective data from 607 patients aged ≥65 years who started CRRT due to AKI between 2009 and 2013 at three centers. The results indicated a survival benefit of early CRRT initiation.
The question of when to initiate dialysis in patients with AKI has been debated almost as long as hemodialysis has been an integral part of the treatment of patients with AKI in clinical medicine. In general, CRRT has been indicated for patients with severe AKI presenting with intractable metabolic derangement or uremic complications. Additionally, many factors must be considered in deciding when to initiate CRRT, including the patient’s demographic data, socio-economic status, and clinical circumstances [8–10, 23]. Therefore, the optimal timing of CRRT initiation has been difficult to investigate and varies substantially among clinical practitioners.
“Early” or “prophylactic” RRT was first introduced in the 1950s. Early literature published in the 1960s and 1970s suggests that early initiation of RRT may improve survival [24–30]. These studies defined early initiation of dialysis as blood urea nitrogen (BUN) ranging from approximately <100 mg/dL to 150 mg/dL and late initiation as BUN ranging from approximately 160 mg/dL to >200 mg/dL. However, those studies had poor experimental design, including inadequate, small sample sizes and the use of arbitrary definitions for early initiation of RRT. In one randomized controlled trial (RCT) that analyzed the outcomes of 34 patients with AKI in the 1980s, dialysis was performed to maintain predialysis BUN at <60 mg/dL in an intensive treatment arm and at 100 mg/dL in a non-intensive arm . Although survival was lower in the intensively treated group, this difference was not significant because of the small sample size.
In the late 1990s and early 2000s, several studies evaluating the impact of the timing of CRRT initiation also addressed the potential survival benefit of early dialysis. Survival was better with early CRRT initiation (39 % versus 20 %) in a study conducted in 1999, involving retrospective analysis of 100 patients who received CRRT to treat post-traumatic AKI . However, in this study the definition of the timing of initiation of dialysis was arbitrary and multivariate analysis was not performed to correct for possible confounders, such as age and serum albumin level. Similar data were reported in the 2000s in three retrospective analyses of the timing of CRRT initiation in patients following cardiac surgery [33, 34] and in oliguric patients with sepsis . In the two former post-cardiac-surgery studies, oliguria, defined as urine volume of <100 mL over 8 h despite furosemide administration, was used as an initiation criterion for early CRRT and azotemia (serum creatinine >5 mg/dL  or BUN ≥84 mg/dL and serum creatinine ≥2.8 mg/dL ) and hyperkalemia (serum potassium >5.5 mEq/L  or >6.0 mEq/L ) as a criterion for late CRRT. Both studies demonstrated better survival in the early dialysis group. In the latter study of patients with oliguria and sepsis, there were also more favorable survival outcomes in the group that with early initiation of CRRT. Similar to many previous studies, BUN was used in this study as a surrogate marker for the extent of AKI. However, BUN is suboptimal for estimating renal function because it is affected not only by glomerular filtration but also by renal tubular control, protein intake, protein catabolism, various clinical conditions (e.g., gastrointestinal bleeding), and pharmacological therapy (e.g., corticosteroids) .
The timing of RRT in critically ill patients with AKI is still the subject of controversy despite recent RCTs. Two RCTs evaluating the effects of early versus late initiation of RRT in critically ill patients with AKI have been published in 2016 [37, 38]. One single-center RCT from Germany included 231 critically ill patients with KDIGO stage 2 AKI and plasma neutrophil gelatinase-associated lipocalin (NGAL) >150 ng/Ml, and defined early RRT as initiation within 8 h of diagnosis of stage 2 AKI and delayed RRT as initiation within 12 h of stage 3 AKI . The researchers reported that early RRT initiation reduced mortality during the first 90 days.
Another multicenter RCT from France included 619 patients with severe AKI classified as KDIGO stage 3, who required mechanical ventilation, catecholamine infusion, or both, and did not have a potentially life-threatening complication directly related to renal failure . The researchers defined early RRT as initiation immediately after randomization and late RRT as initiation in patients with at least one of the following criteria: severe hyperkalemia, metabolic acidosis, pulmonary edema, BUN > 112 mg/dL, and/or oliguria for more than 72 h after randomization. They concluded that there was no significant difference in 60-day mortality between the early and late groups.
In the present study, we defined the elderly population as individuals ≥65 years of age. Global life expectancy at any age has increased, and the size of the population above 65 years of age is rapidly increasing in developed countries . Along with the increasing size of the elderly population, the incidence of AKI is also rising [40–42]. Because of structural and functional changes in the kidneys, the presence of multiple comorbidities, and the resulting medication use, the elderly population is less able to adapt to rapid hemodynamic changes and alterations in electrolyte levels and osmolality [1–5]. Moreover, as with other life-sustaining therapies, economic and ethical concerns must be considered in making decisions on the initiation of RRT in the elderly population [43, 44].
According to previous studies involving intermittent hemodialysis, elderly patients with AKI generally tolerate hemodialysis well, despite their increased fragility . Further, a critical care study has demonstrated that although elderly individuals have increased mortality risk, intensive care in this population is generally cost-effective . Although several previous studies have reported a survival benefit of early CRRT in relatively older patients with AKI [33, 46, 47], it does not seem appropriate to use these data to predict the outcomes of elderly patients. In 2004, in two studies that included 64 and 61 AKI patients who required CRRT after cardiac surgery respectively [33, 46], the conclusions was that early CRRT initiation is beneficial. However, the ages of the patients in these studies were younger than in our study. In particular, the study performed in Turkey included over 80 % of patients younger than 70 years of age , while 74 % of the participants in our study were over 70 years of age, and the youngest patient was 65. Further, a study published in 2013 included patients with a mean age of 61 years. However, the standard deviation was relatively large, indicating that most of the patients were under 65 years of age . In addition, that study reported short-term outcome (28-day survival) only. In contrast, we presented both short-term and long-term outcomes, along with the duration of CRRT, RRT, ICU stay and hospitalization, which they did not report. Recently, a study published in 2015, in which 32,045 patients were stratified between July 2000 and October 2008 according to the KDIGO definition and classification of AKI, reported that patients who met both the serum creatinine level and urine output criteria for AKI were at the greatest risk of death or RRT . However, the researchers investigated the outcomes of patients at various stages of AKI (only approximately 30 % of the patients required RRT) and of those without AKI with a mean age below 60 years. In contrast, we investigated the outcomes of critically ill, elderly patients with a median age of approximately 75 years, who had severe AKI and required CRRT.
In this study, we used the body-weight-adjusted median 6-h urine output immediately before CRRT initiation as the criterion for CRRT initiation. The early CRRT group had significantly better survival than the late CRRT group, even after multivariate analyses of risk factors. We chose the quantity of urine as a threshold for CRRT initiation for several reasons. First, urine output has long been used as a marker of AKI and for guiding renal resuscitation in critically ill patients [49–52]. In several previous studies urine output was also used as an indication to start CRRT, with reported survival benefit consistent with ours [33, 34, 46, 47]. Second, researchers have questioned whether BUN is an appropriate biomarker for determining when to initiate dialysis . Urine output markers other than BUN have been reported to be potentially more suitable for prediction of the survival of critically ill patients with AKI [31, 47]. One RCT conducted in 1986 reported that urine output was a significant factor for survival. However, this study did nto demonstrate the utility of BUN as an indicator for starting dialysis . A study performed in 2013 that compared BUN and urine output as criteria for the timing of CRRT initiation in critically ill patients with AKI concluded that urine quantity, but not the BUN concentration, was significantly associated with prognosis . Third, although some novel biomarkers have been recently introduced as potentially better predictors of AKI, their applicability as markers of severity remain limited in clinical practice, especially in emergency departments and ICUs.
Numerous studies have explored the utilization of early biomarkers of AKI, such as NGAL and the recent combination of tissue inhibitor of metalloproteinase-2 and urine insulin-like growth factor-binding protein 7, in critically ill patients during the last decade [53–59]. However, for critically ill patients with AKI, biomarkers that reflect their ever-changing states are needed, and there is limited time to wait for test results. Urine output can be monitored very easily and allows for continuous measurements. Therefore, it could be used as a general tool for managing patients with AKI, including initial screening, risk assessment, diagnosis, treatment decisions, and assessment of prognosis. In our study, the time from ICU admission to CRRT initiation did not significantly differ between the groups (6.8 (1.5–31.1) hours in the early CRRT group versus 7.9 (1.7–37.8) hours in the late CRRT group, P = 0.30). This non-significant difference is in conflict with recent RCTs demonstrating significant differences in the time from ICU admission to RRT initiation [37, 38].
These discrepant results between our study and previous studies may be attributed to the use of different definitions of CRRT onset time [37, 38], in addition to differences in clinical practice policies. A trend toward admitting patients to the ICU at earlier time points could have decreased the difference in the time between CRRT initiation and ICU admission between the groups. A previous study conducted at our institute demonstrated that the time from ICU admission to CRRT initiation did not significantly differ between patients with high and low urine output at CRRT initiation, supporting the notion that institutional policy characteristics may be partly responsible for our non-significant findings .
To the best of our knowledge, this is the largest study to show a survival benefit of early CRRT initiation in critically ill, elderly patients with AKI. Our results were obtained from a multicenter, prospective observational study. Despite the increasing emphasis on the importance of care for the elderly population and increase in general medical management as care evolves, few studies have specifically examined CRRT in older individuals. Our data justify starting CRRT earlier in the course of severe AKI in elderly patients. Although the worse outcomes in the late CRRT group can be expected considering the univariate analysis results because of their lower blood pressure and higher PT-INR, total bilirubin, AST and ALT, the survival benefit of early CRRT initiation remained, even after multivariate risk factor analyses using the multivariate Cox regression model and PSM with adjustments for significant factors for mortality. We showed a significant survival benefit of early initiation of CRRT in the elderly before and after PSM (Figs. 1 and 2) and also demonstrated survival benefit in multivariate analyses with adjustments for various factors that influence the survival of patients with AKI (Table 2; model 3: HR 1.35, 95 % CI 1.06, 1.71, P = 0.02). The adjusted factors that influence survival in univariate analyses included age, sex, the CCI, SBP, prothrombin time, the total bilirubin, AST, and ALT levels, cumulative fluid balance, and use of diuretics. The significance of these results was maintained even after comparison with the propensity score-matched control group (Table 2; model 4: HR 1.32, 95 % CI 1.08, 1.61, P < 0.01). Additionally, on subgroup analysis of survivors, the total duration of hospitalization from CRRT initiation was shorter when CRRT was started earlier in the course of AKI (Table 3; 26.7 (16.1–38.2) versus 39.1 (27.7–79.3) days, P = 0.04). Although the duration of CRRT, total RRT, and the ICU stay from the start of CRRT did not differ based on the timing of CRRT initiation, our data may be used to guide clinicians in making difficult decisions about the management of critically ill, elderly patients with AKI.
Our study had several limitations. First, even after adjusting for multiple confounders and selection effects, subjects who possibly did not require CRRT may have been included in the early initiation group. Second, the quantity of urine is also an imperfect surrogate for renal function. It is affected by not only glomerular filtration but also volume status, urinary tract obstruction, and pharmacological therapy. However, our aim was not to find an indicator of kidney function but rather to identify a clinically useful marker that could predict the survival of patients with AKI. Third, our data are limited by the definition of the timing of CRRT initiation. In this study, urine output was the only variable that divided the study population in terms of the timing of dialysis initiation; several previous studies have used serum creatinine  or BUN [31, 36, 47] as a marker along with urine output. However, as stated previously, the use of BUN has been challenged in many recent studies investigating the association between the timing of dialysis initiation and mortality [36, 47], and to the best of our knowledge, no study has assessed the superiority of serum creatinine over urine output as a marker for determining the timing of dialysis initiation. Fourth, because the arterial partial pressure of oxygen was not known for the participants in this cohort, we were unable to determine the ratio of the arterial oxygen concentration to the fraction of inspired oxygen.
In conclusion, a better prognosis can be expected if CRRT is applied early in the course of AKI in critically ill, elderly patients. Although well-designed RCTs are still necessary, our results contribute to the determination of whether early CRRT initiation yields a better survival benefit in elderly patients with severe AKI.
AKI, acute kidney injury; ALT, alanine aminotransferase; APACHE II score, acute physiology and chronic health evaluation II score; AST, aspartate aminotransferase; BUN, blood urea nitrogen; CCI, Charlson comorbidity index; CI, confidence interval; CRRT, continuous renal replacement therapy; eGFR, estimated glomerular filtration rate; HR, hazard ratio; ICU, intensive care unit; KDIGO, Kidney Disease: Improving Global Outcomes; PSM, propensity score matching; PT-INR, prothrombin time-international normalized ratio; RCT, randomized controlled trial; SBP, systolic blood pressure; SOFA score, sequential organ failure assessment score
JYP designed and carried out the study, collected the data, analyzed and interpreted the results, and drafted the manuscript. JNA and JHJ participated in acquisition and analysis of the data and reviewed critical revisions. DKK participated in acquisition, processing, and analysis of the data. HJO, SK, KWJ, YKO, CSL, and SWK participated in acquisition and interpretation of the data. YSK participated in acquisition and interpretation of the data and reviewed critical revisions. JTP conceived the study, participated in its design, and helped to draft the manuscript. JPL conceived the study, participated in its design and coordination, and helped to draft the manuscript. All the authors took part in the manuscript writing and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
We obtained consent to publish from the participants for the reporting of individual patient data.
Ethics approval and consent to participate
The study protocol complied with the Declaration of Helsinki and received full approval from the institutional review boards of Seoul National University Hospital, Seoul National University Boramae Hospital, and Yonsei University Severance Hospital. We obtained informed consent from the participants prior to enrollment in the present study.
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- Epstein M. Effects of aging on the kidney. Fed Proc. 1979;38:168–71.PubMedGoogle Scholar
- Pascual J, Liano F, Ortuno J. The elderly patient with acute renal failure. J Am Soc Nephrol. 1995;6:144–53.PubMedGoogle Scholar
- Coca SG. Acute kidney injury in elderly persons. Am J Kidney Dis. 2010;56:122–31.View ArticlePubMedPubMed CentralGoogle Scholar
- Abdel-Kader K, Palevsky PM. Acute kidney injury in the elderly. Clin Geriatr Med. 2009;25:331–58.View ArticlePubMedPubMed CentralGoogle Scholar
- Hsu CY, McCulloch CE, Fan D, Ordonez JD, Chertow GM, Go AS. Community-based incidence of acute renal failure. Kidney Int. 2007;72:208–12.View ArticlePubMedPubMed CentralGoogle Scholar
- Lins RL, Elseviers MM, Van der Niepen P, Hoste E, Malbrain ML, Damas P, et al. Intermittent versus continuous renal replacement therapy for acute kidney injury patients admitted to the intensive care unit: results of a randomized clinical trial. Nephrol Dial Transplant. 2009;24:512–8.View ArticlePubMedGoogle Scholar
- Hyman A, Mendelssohn DC. Current Canadian approaches to dialysis for acute renal failure in the ICU. Am J Nephrol. 2002;22:29–34.View ArticlePubMedGoogle Scholar
- Bellomo R, Ronco C. Indications and criteria for initiating renal replacement therapy in the intensive care unit. Kidney Int Suppl. 1998;66:S106–9.PubMedGoogle Scholar
- Mehta RL. Indications for dialysis in the ICU: renal replacement vs. renal support. Blood Purif. 2001;19:227–32.View ArticlePubMedGoogle Scholar
- Palevsky PM. Renal replacement therapy I: indications and timing. Crit Care Clin. 2005;21:347–56.View ArticlePubMedGoogle Scholar
- Seabra VF, Balk EM, Liangos O, Sosa MA, Cendoroglo M, Jaber BL. Timing of renal replacement therapy initiation in acute renal failure: a meta-analysis. Am J Kidney Dis. 2008;52:272–84.View ArticlePubMedGoogle Scholar
- Karvellas CJ, Farhat MR, Sajjad I, Mogensen SS, Leung AA, Wald R, et al. A comparison of early versus late initiation of renal replacement therapy in critically ill patients with acute kidney injury: a systematic review and meta-analysis. Crit Care. 2011;15:R72.View ArticlePubMedPubMed CentralGoogle Scholar
- Lee J, Cho JH, Chung BH, Park JT, Lee JP, Chang JH, et al. Classical indications are useful for initiating continuous renal replacement therapy in critically ill patients. Tohoku J Exp Med. 2014;233:233–41.View ArticlePubMedGoogle Scholar
- Oh HJ, Shin DH, Lee MJ, Koo HM, Doh FM, Kim HR, et al. Early initiation of continuous renal replacement therapy improves patient survival in severe progressive septic acute kidney injury. J Crit Care. 2012;27:743. e9–18.View ArticlePubMedGoogle Scholar
- Phillips PA, Johnston CI, Gray L. Disturbed fluid and electrolyte homoeostasis following dehydration in elderly people. Age Ageing. 1993;22:S26–33.View ArticlePubMedGoogle Scholar
- Schepkens H, Vanholder R, Billiouw JM, Lameire N. Life-threatening hyperkalemia during combined therapy with angiotensin-converting enzyme inhibitors and spironolactone: an analysis of 25 cases. Am J Med. 2001;110:438–41.View ArticlePubMedGoogle Scholar
- Allegretti AS, Steele DJ, David-Kasdan JA, Bajwa E, Niles JL, Bhan I. Continuous renal replacement therapy outcomes in acute kidney injury and end-stage renal disease: a cohort study. Crit Care. 2013;17:R109.View ArticlePubMedPubMed CentralGoogle Scholar
- Zahar JR, Timsit JF, Garrouste-Orgeas M, Francais A, Vesin A, Descorps-Declere A, et al. Outcomes in severe sepsis and patients with septic shock: pathogen species and infection sites are not associated with mortality. Crit Care Med. 2011;39:1886–95.View ArticlePubMedGoogle Scholar
- Vincent JL, Moreno R, Takala J, Willatts S, De Mendonca A, Bruining H, et al. The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med. 1996;22:707–10.View ArticlePubMedGoogle Scholar
- Knaus WA, Draper EA, Wagner DP, Zimmerman JE. APACHE II: a severity of disease classification system. Crit Care Med. 1985;13:818–29.View ArticlePubMedGoogle Scholar
- Levey AS, Coresh J, Greene T, Stevens LA, Zhang YL, Hendriksen S, et al. Using standardized serum creatinine values in the modification of diet in renal disease study equation for estimating glomerular filtration rate. Ann Intern Med. 2006;145:247–54.View ArticlePubMedGoogle Scholar
- Brookhart MA, Schneeweiss S, Rothman KJ, Glynn RJ, Avorn J, Sturmer T. Variable selection for propensity score models. Am J Epidemiol. 2006;163:1149–56.View ArticlePubMedPubMed CentralGoogle Scholar
- Vasudevan A, Iyengar A, Phadke K. Modality of choice for renal replacement therapy for children with acute kidney injury: results of a survey. Indian J Nephrol. 2012;22:121–4.View ArticlePubMedPubMed CentralGoogle Scholar
- Salisbury PF. Timely versus delayed use of the artificial kidney. Arch Intern Med. 1958;101:690–701.View ArticleGoogle Scholar
- Teschan PE, Baxter CR, O'Brien TF, Freyhof JN, Hall WH. Prophylactic hemodialysis in the treatment of acute renal failure. Ann Intern Med. 1960;53:992–1016.View ArticlePubMedGoogle Scholar
- Parsons FM, Hobson SM, Blagg CR, Mc CB. Optimum time for dialysis in acute reversible renal failure. Description and value of an improved dialyser with large surface area. Lancet. 1961;1:129–34.View ArticlePubMedGoogle Scholar
- Fischer RP, Griffen Jr WO, Reiser M, Clark DS. Early dialysis in the treatment of acute renal failure. Surg Gynecol Obstet. 1966;123:1019–23.PubMedGoogle Scholar
- Bosteels V, Verberckmoes R, Vandenbroucke J, Michielsen P. Importance of early and frequent dialysis for the prognosis of postoperative and post-traumatic anuria. J Urol Nephrol (Paris). 1970;76:797–800.Google Scholar
- Kleinknecht D, Jungers P, Chanard J, Barbanel C, Ganeval D. Uremic and non-uremic complications in acute renal failure: evaluation of early and frequent dialysis on prognosis. Kidney Int. 1972;1:190–6.View ArticlePubMedGoogle Scholar
- Conger JD. A controlled evaluation of prophylactic dialysis in post-traumatic acute renal failure. J Trauma. 1975;15:1056–63.View ArticlePubMedGoogle Scholar
- Gillum DM, Dixon BS, Yanover MJ, Kelleher SP, Shapiro MD, Benedetti RG, et al. The role of intensive dialysis in acute renal failure. Clin Nephrol. 1986;25:249–55.PubMedGoogle Scholar
- Gettings LG, Reynolds HN, Scalea T. Outcome in post-traumatic acute renal failure when continuous renal replacement therapy is applied early vs. late. Intensive Care Med. 1999;25:805–13.View ArticlePubMedGoogle Scholar
- Elahi MM, Lim MY, Joseph RN, Dhannapuneni RR, Spyt TJ. Early hemofiltration improves survival in post-cardiotomy patients with acute renal failure. Eur J Cardiothorac Surg. 2004;26:1027–31.View ArticlePubMedGoogle Scholar
- Piccinni P, Dan M, Barbacini S, Carraro R, Lieta E, Marafon S, et al. Early isovolaemic haemofiltration in oliguric patients with septic shock. Intensive Care Med. 2006;32:80–6.View ArticlePubMedGoogle Scholar
- Liu KD, Himmelfarb J, Paganini E, Ikizler TA, Soroko SH, Mehta RL, et al. Timing of initiation of dialysis in critically ill patients with acute kidney injury. Clin J Am Soc Nephrol. 2006;1:915–9.View ArticlePubMedGoogle Scholar
- Waikar SS, Bonventre JV. Can we rely on blood urea nitrogen as a biomarker to determine when to initiate dialysis? Clin J Am Soc Nephrol. 2006;1:903–4.View ArticlePubMedGoogle Scholar
- Zarbock A, Kellum JA, Schmidt C, Van Aken H, Wempe C, Pavenstadt H, et al. Effect of early vs delayed initiation of renal replacement therapy on mortality in critically ill patients with acute kidney injury: the ELAIN randomized clinical trial. JAMA. 2016;315:2190–9.View ArticlePubMedGoogle Scholar
- Gaudry S, Hajage D, Schortgen F, Martin-Lefevre L, Pons B, Boulet E, et al. Initiation strategies for renal-replacement therapy in the intensive care unit. N Engl J Med. 2016;375(2):122–33.View ArticlePubMedGoogle Scholar
- Akposso K, Hertig A, Couprie R, Flahaut A, Alberti C, Karras GA, et al. Acute renal failure in patients over 80 years old: 25-years' experience. Intensive Care Med. 2000;26:400–6.View ArticlePubMedGoogle Scholar
- Feest TG, Round A, Hamad S. Incidence of severe acute renal failure in adults: results of a community based study. BMJ. 1993;306:481–3.View ArticlePubMedPubMed CentralGoogle Scholar
- Pascual J, Liano F. Causes and prognosis of acute renal failure in the very old. Madrid Acute Renal Failure Study Group. J Am Geriatr Soc. 1998;46:721–5.View ArticlePubMedGoogle Scholar
- Prescott GJ, Metcalfe W, Baharani J, Khan IH, Simpson K, Smith WC, et al. A prospective national study of acute renal failure treated with RRT: incidence, aetiology and outcomes. Nephrol Dial Transplant. 2007;22:2513–9.View ArticlePubMedGoogle Scholar
- Somogyi-Zalud E, Zhong Z, Hamel MB, Lynn J. The use of life-sustaining treatments in hospitalized persons aged 80 and older. J Am Geriatr Soc. 2002;50:930–4.View ArticlePubMedGoogle Scholar
- Cosmos A. Cost-effectiveness of providing quality ICU care to elderly patients. ICU Management. 2009;9:6–7.Google Scholar
- Bonello M, Petras D, Ricci Z, Zamperetti N, Ronco C. Acute renal failure in the elderly critically ill patient. In: Ronco C, Bellomo R, Kellum JA, editors. Critical Care Nephrology. Philadelphia: Saunders, Elsevier; 2009. p. 1675–80.Google Scholar
- Demirkilic U, Kuralay E, Yenicesu M, Caglar K, Oz BS, Cingoz F, et al. Timing of replacement therapy for acute renal failure after cardiac surgery. J Card Surg. 2004;19:17–20.View ArticlePubMedGoogle Scholar
- Oh HJ, Shin DH, Lee MJ, Ko KI, Kim CH, Koo HM, et al. Urine output is associated with prognosis in patients with acute kidney injury requiring continuous renal replacement therapy. J Crit Care. 2013;28:379–88.View ArticlePubMedGoogle Scholar
- Kellum JA, Sileanu FE, Murugan R, Lucko N, Shaw AD, Clermont G. Classifying AKI by urine output versus serum creatinine level. J Am Soc Nephrol. 2015;26:2231–8.View ArticlePubMedGoogle Scholar
- Legrand M, Payen D. Understanding urine output in critically ill patients. Ann Intensive Care. 2011;1:13.View ArticlePubMedPubMed CentralGoogle Scholar
- Md Ralib A, Pickering JW, Shaw GM, Endre ZH. The urine output definition of acute kidney injury is too liberal. Crit Care. 2013;17:R112.View ArticlePubMedPubMed CentralGoogle Scholar
- Mehta RL. Acute kidney injury: urine output in AKI—the canary in the coal mine? Nat Rev Nephrol. 2013;9:568–70.View ArticlePubMedGoogle Scholar
- Zhang Z, Xu X, Ni H, Deng H. Urine output on ICU entry is associated with hospital mortality in unselected critically ill patients. J Nephrol. 2014;27:65–71.View ArticlePubMedGoogle Scholar
- Schmidt-Ott KM, Mori K, Li JY, Kalandadze A, Cohen DJ, Devarajan P, et al. Dual action of neutrophil gelatinase-associated lipocalin. J Am Soc Nephrol. 2007;18:407–13.View ArticlePubMedGoogle Scholar
- Nickolas TL, O'Rourke MJ, Yang J, Sise ME, Canetta PA, Barasch N, et al. Sensitivity and specificity of a single emergency department measurement of urinary neutrophil gelatinase-associated lipocalin for diagnosing acute kidney injury. Ann Intern Med. 2008;148:810–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Devarajan P. Review: neutrophil gelatinase-associated lipocalin: a troponin-like biomarker for human acute kidney injury. Nephrology (Carlton). 2010;15:419–28.View ArticleGoogle Scholar
- de Geus HR, Bakker J, Lesaffre EM, le Noble JL. Neutrophil gelatinase-associated lipocalin at ICU admission predicts for acute kidney injury in adult patients. Am J Respir Crit Care Med. 2011;183:907–14.View ArticlePubMedGoogle Scholar
- Nickolas TL, Schmidt-Ott KM, Canetta P, Forster C, Singer E, Sise M, et al. Diagnostic and prognostic stratification in the emergency department using urinary biomarkers of nephron damage: a multicenter prospective cohort study. J Am Coll Cardiol. 2012;59:246–55.View ArticlePubMedPubMed CentralGoogle Scholar
- Bihorac A, Chawla LS, Shaw AD, Al-Khafaji A, Davison DL, Demuth GE, et al. Validation of cell-cycle arrest biomarkers for acute kidney injury using clinical adjudication. Am J Respir Crit Care Med. 2014;189:932–9.View ArticlePubMedGoogle Scholar
- Meersch M, Schmidt C, Van Aken H, Martens S, Rossaint J, Singbartl K, et al. Urinary TIMP-2 and IGFBP7 as early biomarkers of acute kidney injury and renal recovery following cardiac surgery. PLoS One. 2014;9:e93460.View ArticlePubMedPubMed CentralGoogle Scholar
- Bagshaw SM, Uchino S, Bellomo R, Morimatsu H, Morgera S, Schetz M, et al. Timing of renal replacement therapy and clinical outcomes in critically ill patients with severe acute kidney injury. J Crit Care. 2009;24:129–40.View ArticlePubMedGoogle Scholar