Sign In
Individual Sign In
Create an Account
Institutional Sign In
OpenAthens Shibboleth
September 2002

Acute Kidney FailureA Pediatric Experience Over 20 Years

Author Affiliations

From the Departments of Pediatrics (Drs Williams, Sreedhar, Mickell, and Chan) and Biochemistry Molecular Biophysics (Dr Chan), Virginia Commonwealth University, Richmond. Dr Chan is now with The Barbara Bush Children's Hospital, Maine Medical Center, Portland, and the Department of Pediatrics, University of Vermont College of Medicine, Burlington.


Copyright 2002 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.2002

Arch Pediatr Adolesc Med. 2002;156(9):893-900. doi:10.1001/archpedi.156.9.893

Background  Acute kidney failure in children is a catastrophic, life-threatening event.

Objective  To compare and contrast 2 decades of data, analyzing the underlying causes, associated multiple organ system failures, outcome of dialysis procedures, and other variables of interest.

Design  Retrospective examination of clinical data collected between January 1, 1979, and December 31, 1998.

Setting  Regional health care center in the mid-Atlantic area.

Participants  Two hundred twenty-eight patients, aged from 1 day to 18 years, had acute kidney failure and were referred to a pediatric nephrology service.

Main Outcome Measures  Characteristics, percentage of mortality, intensive care unit admission, procedures, and other variables and causes of acute renal failure.

Results  The total number of cases analyzed represented 7% of all patients presented to the pediatric nephrology service. Sex distribution, ethnicity, and survival statistics were unchanged between both decades. The overall survival rate was 73%. One hundred fifty-four patients (68%) were admitted to the pediatric intensive care unit. The following 106 acute extracorporeal procedures were performed on 93 patients (41%): 12 patients received extracorporeal membrane oxygenation, 52 patients underwent peritoneal dialysis, 32 underwent hemodialysis, 3 patients received continuous venovenous hemofiltration, and 7 patients received continuous arteriovenous hemofiltration. Sepsis and burns, other leading causes of acute renal failure in the first decade, are replaced in the second decade by hematologic-oncologic complications and pulmonary failure.

Conclusions  Acute kidney failure following repair of cardiac lesions remains unchanged as a leading risk factor of mortality in both decades. Three organ system failures were associated with more than a 50% mortality rate. Predialysis low serum albumin concentrations emerged as a significant copredictor of mortality.

ACUTE KIDNEY failure is an abrupt cessation of kidney function, with life-threatening consequences in children worldwide.1 Given the fact that acute kidney failure is sometimes associated with significant multiple organ system failure (MOSF)2 and constitutes an important population admitted to pediatric intensive care units (ICUs),3 it seems logical that the various risk factors of this catastrophic event are issues of great importance in terms of tangible and intangible costs to the well-being of patients and their families. We share a 20-year experience at a single center with care provided by the same attendings in critical care, nephrology, and neonatology. This study will analyze the underlying diseases leading to acute kidney failure, the outcome of MOSFs, and other variables associated with mortality in the first decade compared with the second decade. Recently, hypoalbuminemia has been shown to be a singular predictor of nutrition failure and presence of systemic disease in children receiving chronic renal replacement therapy.4 We will examine whether it is also a co-mortality risk factor in acute kidney failure.

This study has particular relevance in the light of advancing technology, including the increase of extracorporeal membrane oxygenation in neonates,5 and the widespread and earlier use of acute renal replacement therapy.6


Between January 1979 and December 1998, 228 consecutive pediatric cases of acute renal failure were diagnosed and treated at the Medical College of Virginia Hospital, Richmond, a regional health care center in the mid-Atlantic area. All medical data were entered prospectively each day on standard forms ("the yellow sheets" advocated by Frederic C. Bartter, MD*) under direction of the same pediatric nephrologist (J.C.M.C.).

These forms remained unchanged in the 2 decades of the study and were intended for future review as well as for clinical use as a flow sheet. We obtained institutional review board approval for this study.

The diagnosis of acute kidney failure was made by the same attending nephrologist (J.C.M.C.) using the following criteria: a sudden cessation of kidney function characterized by oliguria, less than 0.5 mL/kg per hour, confirmed by rising levels of serum urea nitrogen and creatinine to double that of normal for age.1,6 Patients with preexisting chronic kidney diseases4 were excluded. The criteria for admission to the ICU was determined by the same 2 attendings (S.S.S. and J.J.M.), and were as follows: (1) the requirement of close monitoring of critically ill patients, such as those who were recovering from postcardiac surgery; (2) patients requiring invasive monitoring, that is, arterial lines, ventriculostomies, and others; (3) those in congestive heart failure or respiratory failure requiring intubation; and (4) patients with MOSFs7 requiring invasive monitoring. The established criteria for MOSF were adjusted for age.7,8 The race, age, and other clinical characteristics of the children are summarized in Table 1.

Table 1. 
Image not available
Clinical Characteristics of 228 Cases of Pediatric Acute Renal Failure

In the patients described herein, univariant analysis was used on all variables of interest in survivors and nonsurvivors. Fisher exact and χ2 tests were used to compare data between the 2 decades (ie, decade 1, 1979-1988; decade 2, 1989-1998). A Kaplan-Meier survival plot for serum albumin concentrations was used. All values were expressed as mean ± SD. P<.05 denotes statistical significance.


The 228 patients with acute kidney failure represented 7% of all inpatient and outpatient referrals made to the pediatric nephrology service over these 2 decades.9 The clinical characteristics were as follows: slightly more male than female patients (60% vs 40% and 57% vs 43%, respectively). Comparing the first (1979-1988) and second (1989-1998) decades, the ethnic distribution was, respectively, 53% and 54% white; 38% and 33% black; and 9% and 13% others. No statistically significant differences were noted between the first and the second decade in these patient characteristics as given in Table 1.

Between the 2 decades, patient survival was 71% and 74%, respectively, for an overall survival rate of 73%. The mortality rates between the 2 decades were not significantly different as well, at 29% and 26%, respectively (Table 1). Table 2 lists the age of patients in relationship to mortality.

Table 2. 
Image not available
Mortality in Acute Renal Failure in Association With Age

Among the survivors, the order of underlying causes for acute kidney failure hardly change between the 2 decades. (Table 3) Hemolytic uremic syndrome (HUS)9 in the survivors was the leading cause of acute kidney failure in both decades, 38% and 22%, respectively. There was 1 death from HUS in the 2 decades, of a total of 49 patients, making the mortality rate 2% for this condition. Twenty-one percent and 57% of these patients required dialysis in their respective decades.

Table 3. 
Image not available
Underlying Cause and Outcome of Pediatric Acute Renal Failure

Postcardiac surgery remained the leading cause of acute kidney failure among the nonsurvivors in both decades. However, sepsis as a cause of acute kidney failure dropped significantly from 23% (1979-1988) to 3% (1989-1998) (P<.001). Figure 1 shows the organisms responsible for sepsis in each decade. Also, extensive burns precipitating acute kidney failure accounted for 13% of acute kidney failure in the first decade, but dropped significantly to 0% in the second decade. Pulmonary causes of acute kidney failure among the nonsurvivors increased between the 2 decades, 7% to 12%, but this did not reach statistical significance. Hematologic-oncologic causes of acute kidney failure among the nonsurvivors also increased from 10% in the first decade to 22% in the second decade, in association with bone marrow transplant rejections, leukemia, tumor lysis, hyperuricemia, and other complications (Figure 2). While tumor lysis was an important cause of death in the first decade (Figure 2), it was not so in the second, where the mortality rate from this cause was 0%. "Anticipatory" intervention is prevalent and the improved results may be attributed to this. The use of peritoneal dialysis (PD) dropped from 60% of all acute renal replacement therapy in the first decade to 44% in the second decade (Table 4). The use of hemodialysis, continuous venovenous hemofiltration (CVVH), and continuous arteriovenous hemofiltration (CAVH) increased to 43% of acute renal replacement therapy in the second decade. Also, the interval between renal consultation for acute kidney failure to the initiation of acute renal replacement therapy was 2.0 ± 1.8 days vs 1.9 ± 1.4 days, respectively, between the 2 decades.

Figure 1.
Image not available

Organisms responsible for sepsis in acute renal failure.

Figure 2.
Image not available

Hematologic-oncologic complications associated with acute renal failure.

Table 4. 
Image not available
Need for ECMO, PD, HD, and CVVH*

Figure 3 shows the data on mortality in acute kidney failure in association with other organ failures. In the first decade, 27% of the patients died with 2 MOSFs; 3 MOSFs, 57%; and 4 MOSFs, 100%. However, in the second decade of this study, 2 MOSFs had a mortality rate of 13%; 3 MOSFs, 68%; and 4 MOSFs, 88%.

Figure 3.
Image not available

Mortality in association with multiple organ system failure.

Examination of all serum variables on the comprehensive metabolic profile, for example, sodium, potassium, chloride, carbon dioxide, cholesterol, calcium, glucose, and others, obtained immediately before acute kidney replacement therapy did not show significant differences between survivors and nonsurvivors, with the exception of the serum albumin concentrations (Figure 4). The serum albumin concentrations were 2.6 ± 0.7 g/dL in nonsurvivors vs 3.3 ± 0.9 g/dL in survivors (P<.05). Figure 5 shows a survival distribution plot for serum albumin concentration. Hypoalbuminemia was significantly associated with the nonsurvivors.

Figure 4.
Image not available

Mean ± SD serum albumin concentration obtained before acute renal replacement therapy.

Figure 5.
Image not available

Hypoalbuminemia as a significant risk factor of mortality. Kaplan-Meier survival curve for serum albumin concentration shows that 20% of the patients with hypoalbuminemia died by day 5 and 40% died by day 30.


We reviewed all English-language published reports since 1977 of acute kidney failure with 50 children or more (Table 5). It was surprising to find a persisting scarcity of published data specifically addressing acute kidney failure and its risk factors and morbidity and mortality in the pediatric population. In regard to our patient data on morbidity and mortality and critical illness, our criteria for ICU admission were (1) the requirement of close monitoring of critically ill patients, such as those who were recovering from cardiac surgery; (2) patients requiring invasive monitoring, that is, arterial lines, ventriculostomies, and others; (3) those in congestive heart failure or respiratory failure requiring intubation; and (4) patients with MOSFs, as established previously, requiring invasive monitoring. Similar criteria for ICU admission were used by Moghal et al7 resulting in 48% of their 227 children (1984-1991) with acute kidney failure admitted to their ICU compared with the 68% ICU admission rate in our present series. If criteria for admission to the ICU are to be taken as life-threateningly ill, our patients can be considered at least as critical as those in the other series (Table 5). Also, the overall mortality rate of 27% in our study compares favorably with the other published series, despite the persistent requirement of ICU admissions for this disease.

Table 5. 
Image not available
Critically Ill Pediatric Patients With Acute Renal Failure*1015,1,7,8,16

Smoyer et al17 and Zobel et al18 indicated that pediatric patients with acute kidney failure with MOSF, even when treated with continuous kidney replacement therapy, sustained a 60% to 100% mortality rate. In further review of the pediatric literature (Table 5), we noted that few studies examined the number of organ failures in relationship to mortality rate in acute kidney failure.1924 Our data (Figure 3) show that the mortality rate between the 2 decades dropped, even with 4 organs failing. The mortality rate fell from 100% to 88% in the second decade (1989-1998), possibly related to advances in antibiotics, earlier therapy, and better volume control in the recent decade. The examination by Shaw et al25 and Meeks and Sims26 examination of 831 children with MOSFs did not provide specific data on the 5% of their patients who developed kidney failure. However, our data of 57% to 68% mortality with 3 MOSFs are lower than the 89% mortality reported by Shaw et al25 and Meeks and Sims,26 again verifying that advances in technology appear to have allowed us to improve our management of this particular risk factor.

Despite the tremendous advances in the last decade of both critical care management and kidney replacement therapy, however, the significant finding in our study was the persistently high mortality rate of critically ill patients after cardiac surgery. Patients frequently developed acute kidney failure as a result of poor perfusion and hypoxia secondary to prolonged pump time during surgery for congenital heart disease, 27% in the first decade, 44% in the second decade among the nonsurvivors. The younger the patient, the poorer the prognosis, especially in patients younger than 1 year (Table 2). It is also possible that the difference is due to changes in the attending surgeons, increased complexity of patients with heart disease in the second decade, and differences in techniques.

Although mortality from acute kidney failure secondary to an underlying cardiac diagnosis did not appear to have changed significantly when data between the 2 decades were compared, there was a shift in other underlying diagnoses. In the first decade, acute kidney failure associated with cardiac surgery was the major cause of mortality, followed by sepsis (Table 3), burns, pulmonary, and hematologic-oncologic complications. Among nonsurvivors, sepsis-associated acute kidney failure dropped from 23% in the first decade to 3% in the second decade (P<.001) presumably, again, because of advances in antibiotic therapy and better management of fluid volume control. Although the organisms causing sepsis did not change in the 2 decades (Figure 1), there was an increased emergence of methicillin-resistant Staphylococcus aureus in the first decade and of penicillin-resistant Streptococcus pneumoniae in the second decade. Despite these changes in sensitivity, we managed to have better outcomes in the second decade.

Also, in the second decade, the noncardiac causes of death shifted to hematologic-oncologic complications, for example, leukemic-tumor lysis, hyperuricemia, bone marrow transplantation (Figure 2), and respiratory failure. The incidence of hematologic-oncologic complications associated with death in acute kidney failure increased in the second decade possibly because of the increase in aggressive chemotherapy, management, and bone marrow transplantation availability. The latter procedure was unavailable in the first decade of this study (Figure 2).

The significant drop in burns as a cause of acute kidney failure in the second decade may be partly due to a change in burn care management, as the care of pediatric burn patients was taken over by a newly developed burn unit independent of the pediatric ICU in the second decade. It would also appear that burn prevention and management have improved to a degree that the hypovolemia of burns is successfully eliminated as a significant cause of acute kidney failure in the second decade.

Another important and significant risk factor for mortality was age. The youngest patients showed a higher mortality rate. Most published studies of acute kidney failure in early life are small series1926 of fewer than 25 patients, yet the mortality rate is high.1926 In our study, neonates and infants, aged 1 day to 1 year, represented 57% of the total nonsurvivor group (Table 2), and they composed a very large part of the postcardiac acute kidney failure group. In addition, the 12 patients requiring extracorporeal membrane oxygenation were all in the neonatal age group. Extracorporeal membrane oxygenation, in turn, led to the choice of CVVH or CAVH over PD in all of these infants because of the availability of dialysis access. These observations in morbidity and mortality are in accord with the observations of Gong et al16 that coma, hypovolemia, respiratory failure, and acute tubular necrosis in infants younger than 1 year remain significant mortality risk factors. Acute kidney failure in neonates and infants1927 also represents a special clinical and technical challenge, because of the tiny body size of the patients. Finally, the higher mortality rate in this age group could possibly be due to other associated congenital anomalies.1927

Our data indicated that in the more recent decade (1989-1998), the use of acute PD had decreased significantly (Table 4). Acute hemodialysis, CVVH, CAVH, and renal replacement procedures were used more frequently than before, with a corresponding decrease in the use of PD. This trend of moving away from acute PD in favor of acute hemodialysis, CVVH, or CAVH in renal replacement therapy in acute kidney failure was first suggested by a questionnaire survey of pediatric nephrologists by Warady and Bunchman.28 Our data over the span of 20 years substantiated this trend. Acute PD, of course, will still be done via Tenckhoff cannula, especially for our younger patients. However, CVVH and CAVH will probably be preferred, especially whenever extracorporeal membrane oxygenation is used with its need to limit the risk of infection from PD in this particular group, as well as dialysis access availability.

In addition, acute kidney replacement therapy was initiated within 1.9 ± 1.4 days in the more recent decade (1989-1998) compared with 2.0 ± 1.8 days in the previous decade (1979-1988) between the renal consultation and the start of acute kidney dialysis. Our data begin with our initial consultation, which naturally affects our initiation of dialysis. Thus, together, our data suggest more favorable outcomes with earlier, rather than later, time lags of 4.2 to 4.8 days between the onset of kidney failure and the start of dialysis as reported by Arora et al.1

An interesting finding in our analysis was that HUS29 represented the largest group of survivors, without differences between the 2 decades. There was only 1 death in our group of 49 patients with HUS, a 2½-year-old, resulting in a 2% mortality rate. This conforms to the decrease in HUS mortality from 40% in the past to 5% in recent years.30 Although we used the same criteria for initiation of dialysis in acute kidney failure throughout the 2 decades, we were more aggressive in using dialysis in the recent decade. For example, we used dialysis in 57% of the patients with HUS in the second decade compared with 21% in the first decade. The improved survival in HUS in our study may be related to our more aggressive dialysis therapy. These findings contrast with the current 68% mortality rate in India. In this series of 25 patients with HUS reported by Arora et al,1 late referral resulting in more critically ill patients was the reason given for the higher mortality rate. This is understandable with the persistence of significant differences in availability of medical care and gross national income between the United States and India. This continuing difference also has a greater significant effect on both chronic and acute kidney diseases and the long-term survival of children in India.

In long-term dialysis for end-stage kidney disease,4,3134 hypoalbuminemia is shown to be an index of malnutrition and a predictor of mortality. Although Obialo et al35 showed that hypoalbuminemia (<3.5 g/dL) can be a useful predictor of mortality in adults with acute kidney failure, this had not been examined in children. Our data (Figure 4) showed that there is a significantly lower serum albumin predialysis level between nonsurvivors (2.6 ± 0.7 g/dL) and survivors (3.3 ± 0.9 g/dL) (P<.05). In addition, the cumulative survival data (Figure 5) clearly established that hypoalbuminemia could discriminate between the survivors and the nonsurvivors, with 40% dying by day 30. Thus, our data ascertain the efficacy of using serum albumin concentration as a copredictor of mortality in pediatric acute kidney failure. Obialo et al35 also suggested that low albumin concentrations in adult patients may be correlated with the activation of inflammatory mediators. Studies on a molecular basis of these observations may illuminate new avenues to improve survival in these patients.


We have seen that postcardiac surgery36 associated with acute kidney failure remains the leading mortality risk factor. Hematologic-oncologic complications have become a more frequent cause of acute kidney failure in the recent decade because of advances in care management. Sepsis as an associated cause of acute kidney failure dropped from 23% to 3% in the last 2 decades although the organisms responsible for the sepsis did not change. Our data on acute dialysis indicated less PD being done in the recent decade, a trend previously suggested in a questionnaire survey.28 Also, although mortality risks increase significantly with MOSFs in association with acute kidney failure in adults,37 our data in this study suggest a slightly better prognosis in children.38,39 Another significant comorbid risk factor is young age (ie, <1 year), combined with the need for extracorporeal membrane oxygenation due to respiratory failure secondary to problems in fluid management. Finally, our data suggest that hypoalbuminemia is a copredictor of mortality in pediatric acute kidney failure.

Back to top
Article Information

Accepted for publication April 4, 2002.

This study was supported by grants T32 DK07761 and R01 DK50419 from the National Institutes of Health, Bethesda, Md (Dr Chan).

We thank Sung C. Choi, PhD, for statistical support; Karl S. Roth, MD, and K. C. Lin, MSc, for review; and Betty Timozek for secretarial assistance.

This study was presented as a poster at the World Congress of Nephrology American Society of Nephrology/International Society of Nephrology, San Francisco, Calif, October 14-17, 2001.

*Frederic C. Bartter, possibly the longest serving branch chief of the National Heart, Lung, and Blood Institute at the National Institutes of Health, always advocated the use of the National Institutes of Health's data forms, referred by generations of clinical associates as "the yellow sheets," to keep patient data and to plan research studies.

What This Paper Adds

There is a scarcity of up-to-date published data specifically addressing acute kidney failure in children. Studies involving large numbers of children with this disorder are also rare. Because it can be such a catastrophic, life-threatening event, it is important for community pediatricians to recognize the clinical features of this disease with regard to morbidity and mortality. We report a 20-year experience of 228 children at the same institution with the same intensivists and nephrologist.

The results of our analysis suggest that although we have improved in most areas of care and management, we still fared poorly with our patients in infancy. The data also provided evidence that during the first decade, burns and sepsis were major comorbid factors, but not so in the second decade. In addition, more CVVH, CAVH, and less PD were done in the recent decade compared with the earlier decade. We conclude that acute kidney failure in childhood continues to carry significant mortality risks, especially in the presence of other organ failures. Finally hypoalbuminemia, rather than elevated levels of serum urea nitrogen or creatinine, at the start of dialysis is a significant copredictor of mortality.

Corresponding author and reprints: James C. M. Chan, MD, The Barbara Bush Children's Hospital, Maine Medical Center, 22 Bramhall St, Portland, ME 04102-3175 (e-mail:

Arora  PKher  VRai  PKSinghal  MKGulati  SGupta  A Prognosis of acute renal failure in children: a multivariate analysis. Pediatr Nephrol. 1997;11153- 155Article
Wilkinson  JDPollack  MMRuttimann  UEGlass  NLYeh  TS Outcome of pediatric patients with multiple organ system failure. Crit Care Med. 1986;14271- 274Article
Wilkinson  JDPollack  MMGlass  NLKanter  RKKatz  RWSteinhart  CM Mortality associated with multiple organ system failure and sepsis in pediatric intensive care unit. J Pediatr. 1987;111324- 328Article
Gulati  SStephens  DBalfe  JASecker  DHarvey  EBalfe  JW Children with hypo-albuminemia on continuous peritoneal dialysis are at risk for technique failure. Kidney Int. 2001;592361- 2367Article
Swaniker  FKolla  SMoler  F  et al.  Extracorporeal life support outcome for 128 pediatric patients with respiratory failure. J Pediatr Surg. 2000;35197- 202Article
Gettings  LGReynolds  HNScalea  T Outcome in post-traumatic acute renal failure when continuous renal replacement therapy is applied early vs late. Intensive Care Med. 1999;25805- 813Article
Moghal  NEBrocklebank  JTMeadow  SR A review of acute renal failure in children: incidence, etiology and outcome. Clin Nephrol. 1998;4991- 95
Lowrie  LH Renal replacement therapies in pediatric multiorgan dysfunction syndrome. Pediatr Nephrol. 2000;146- 12Article
Chan  JCM Lessons from 20 years of leading a pediatric nephrology program. Nephron. 1998;78378- 388Article
Counahan  RCameron  JSOgg  CS  et al.  Presentation, management, complications, and outcome of acute renal failure in childhood: five years' experience. BMJ. 1977;1599- 602Article
Hodson  EMKjellstrand  CMMauer  SM Acute renal failure in infants and children: Outcome of 53 patients requiring hemodialysis treatment. J Pediatr. 1978;93756- 761Article
Elzouki  AYAmin  FJaiswal  OP Prevalence and pattern of renal disease in eastern Libya. Arch Dis Child. 1983;58106- 109Article
Niaudet  PHaj-Ibrahim  MGagnadoux  MFBroyer  M Outcome of children with acute renal failure. Kidney Int Suppl. 1985;17S148- S151
Reznik  VMGriswold  WRPeterson  BMRodarte  AFeris  MEMendoza  SA Peritoneal dialysis for acute renal failure in children. Pediatr Nephrol. 1991;5715- 717Article
Gallego  NGallego  APascual  JLiano  FEstepa  ROrtuno  J Prognosis of children with acute renal failure: a study of 138 cases. Nephron. 1993;64399- 404Article
Gong  WKTan  THFoong  PPMurugasu  BYap  HK Eighteen years experience in pediatric acute dialysis: analysis of predictors of outcome. Pediatr Nephrol. 2001;16212- 215Article
Smoyer  WEMcAdams  CKaplan  BSSherbotie  JR Determinants of survival in pediatric continuous hemofiltration. J Am Soc Nephrol. 1995;61401- 1409
Zobel  GKuttnig  MRing  EGrubbauer  HM Clinical scoring systems in children with continuous extracorporeal renal support. Child Nephrol Urol. 1990;1014- 17
Ronco  CBrendolan  ABragantini  L  et al.  Treatment of acute renal failure in newborns by continuous arterio-venous hemofiltration. Kidney Int. 1986;29908- 915Article
Grylack  LMedani  CHultzen  C  et al.  Nonoliguric acute renal failure in the newborn: a prospective evaluation of diagnostic indexes. AJDC. 1982;136518- 520
Griffin  NKMcElnea  JBarratt  M Acute renal failure in early life. Arch Dis Child. 1976;51459- 462Article
Norman  MEAsadi  FK A prospective study of acute renal failure in the newborn infant. Pediatrics. 1979;63475- 479
Zobel  GRing  EMuller  W Continuous arteriovenous hemofiltration in premature infants. Crit Care Med. 1989;17534- 536Article
Aschinberh  LCZeis  PMHageman  JRVidyasagar  D Acute renal failure in the newborn. Crit Care Med. 1977;536- 42Article
Shaw  NJBrocklebank  JTDickinson  DFWilson  NWalker  DR Long-term outcome for children with acute renal failure following cardiac surgery. Int J Cardiol. 1991;31161- 166Article
Meeks  ACSims  DG Treatment of renal failure in neonates. Arch Dis Child. 1988;631372- 1376Article
Niaudet  BHaesner  MPrecht  K Prognosis of acute dialysis dependent renal failure [in German]. Z Urol Nephrol. 1990;83625- 628
Warady  BABunchman  T Dialysis therapy for children with acute renal failure: survey results. Pediatr Nephrol. 2000;1511- 13Article
Tonshoff  BSammet  ASanden  IMehls  OWaldherr  RScharer  K Outcome and prognostic determinants in hemolytic uremic syndrome in children. Nephron. 1994;6863- 70Article
Remuzzi  GRuggenenti  P The hemolytic uremic syndrome. Kidney Int. 1995;482- 19Article
Blake  PGFlowerdew  GBlake  RMOreopoulos  DG Serum albumin in patients on continuous ambulatory peritoneal dialysis: predictors and correlations with outcomes. J Am Soc Nephrol. 1993;31501- 1507
Struijk  DGKrediet  RTKoomen  GCBoeschoten  EWArisz  L The effect of serum albumin at the start of continuous ambulatory peritoneal dialysis treatment on patient survival. Perit Dial Int. 1994;14121- 126
Owen Jr  WFLew  NLLiu  YLowrie  EGLazarus  JM The urea reduction ratio and serum albumin concentration as predictors of mortality in patients undergoing hemodialysis. N Engl J Med. 1993;3291001- 1006Article
Teehan  BPSchleifer  CRBrown  JMSigler  MHRaimondo  J Urea kinetic analysis and clinical outcome on CAPD: a five year longitudinal study. Adv Perit Dial. 1990;6181- 185
Obialo  CIOkonofua  ECNzerue  MCTayade  ASRiley  LJ Role of hypoalbuminemia and hypocholesterolemia as copredictors of mortality in acute renal failure. Kidney Int. 1999;561058- 1063Article
Picca  SPrincipato  FMazzera  E  et al.  Risks of acute renal failure after cardiopulmonary bypass surgery in children: a retrospective 10-year case-control study. Nephrol Dial Transplant. 1995;10630- 636
Liano  FGarcia-Martin  FGallego  A  et al.  Easy and early prognosis in acute tubular necrosis: a forward analysis of 228 cases. Nephron. 1989;51307- 313Article
Ellis  DAvner  EDStarzl  TE Renal failure in children with hepatic failure undergoing liver transplantation. J Pediatr. 1986;108393- 398Article
Hand  MMAlexander  SRHarmon  WEBarratt  TMedAvner  EDedHarmon  WEed Intensive care. Pediatric Nephrology. Baltimore, Md Lippincott Williams & Wilkins1998;1135- 1150