Pediatric Nephrology

, 24:431

Hemoglobin target in chronic kidney disease: a pediatric perspective

Editorial Commentary


Erythropoietin has transformed the treatment of the anemia of chronic kidney disease (CKD) by preventing the need for blood transfusions and improving the quality of life in all patients, including children. Anemia in children, in the age group 1–19 years, may be defined as hemoglobin (Hgb) levels < 12.1–13.5 g/dl for boys and < 11.4–11.5 g/dl for girls, based on the National Health and Nutrition Examination Survey (NHANES) norms. The prevalence of anemia in children ranges from 31.2% in stage 1 CKD to 93.3% in stages 4 and 5 CKD. The recent publication of trials evaluating the optimal hemoglobin level in adult CKD patients has generated considerable uncertainty about the target Hgb level in children with CKD. It is unclear whether generalizing of results from these trials in adults to children is appropriate. Adequately powered, randomized, controlled studies have not been conducted on children, and none to our knowledge are currently planned. The Food and Drug Administration (FDA) offers scant guidance on the Hgb target level for children, other than implying that it should be no different from that for adults. The purpose of this editorial is to critically scrutinize whether there is a benefit to the normalization of anemia in children with CKD and whether adoption of the results from adult studies is appropriate.


Erythropoietin Anemia CKD Pediatric Hemoglobin 

The benefits and risks of normalizing the hemoglobin level for children with chronic kidney disease

Proponents of the normalization of hemoglobin levels in chronic kidney disease (CKD) have argued for the diverse benefits of correcting anemia in children. These benefits include improvements in quality of life, cognitive function, exercise capacity, scholastic performance, growth and nutrition, and cardiovascular function [1]. Quality of life (QOL) and its components have frequently been used as surrogate outcome measures for children, since they influence physical performance, exercise tolerance, and even school attendance. However, studies demonstrating these benefits have largely been small in sample size, non-randomized in design, of short duration, and have used non-validated instruments [2, 3, 4, 5]. In a multi-center interventional trial that evaluated intelligence quotient (IQ) using the Weschler intelligence test, treatment of anemia was associated with a significant increase in IQ [6]. However, the design was limited by a single-arm and a sample size of only 22 children with CKD. With respect to growth, many trials have demonstrated a lack of effect of anemia correction on growth in children with CKD [1]. Recent studies have not only demonstrated a high prevalence of growth retardation in children with chronic kidney disease but have also suggested that initial hemoglobin (Hgb) level and early treatment with erythropoietin is associated with improved growth [7]. While these studies have limitations, including retrospective design and small numbers (47 children), they have been influential in supporting normalization of Hgb level in children with CKD. The evidence for improvement in cardiovascular co-morbidity in children with treatment of anemia rests on the results of a single, randomized, placebo-controlled trial comprised of only 11 children undergoing dialysis. In that study, patients were assigned to therapy with erythropoiesis-stimulating agents (ESAs) or to placebo for 24 weeks. ESA therapy was associated with partial correction of an elevated cardiac index at 6 months and a significant reduction in left ventricular mass at 12 months [8]. The subjects in that study were severely anemic, with baseline Hgb of 7.3 g/dl. It was suggested that these data were concordant with those from two observational studies providing further resonance to the importance of anemia treatment [9]. A recent study examined 677 adolescents on hemodialysis for the relationship between Hgb level and the risk for death or hospitalization [10]. Patients with Hgb ≥11 g/dl consistently demonstrated a 60% to 70% decrease in the risk of death. However, mortality was similar for patients with Hgb levels of 11 g/dl to 12 g/dl and > 12 g/dl when compared with those with Hgb < 10 g/dl, and no significant difference in risk for hospitalization was observed between the various Hgb categories. Warady and Ho, using data from the North American Pediatric Renal Transplant Cooperative Study (NAPRTCS), reported an association between a baseline hematocrit less than 33% at 30 days after initiation of dialysis and increased risk for prolonged hospitalization and death in patients with incident end-stage renal disease (ESRD) who were younger than 18 years of age [11]. A study by Furth et al. suggested an association of greater decline in glomerular filtration rate (GFR) with hematocrit less than 36%, reiterating the importance of correction of anemia [12].

Balanced against the potential benefits of epoetin in correcting CKD are the risks of hypertension, thrombosis and atherosclerosis [13]. Exacerbation of hypertension has been reported by several authors in both non-dialysis CKD and children on dialysis [14, 15, 16, 17, 18, 19]. However, many of the studies excluded children with moderate or uncontrolled hypertension, either before or during the trial period. Vaziri and co-workers, in both humans and animal models, have explored the mechanism of hypertension. Vaziri has suggested that erythropoietin-induced hypertension is a nitric oxide-mediated complication [20]. Consequently, the use of lower doses of epoetin (approximately 150 U/kg per week) is recommended. In light of studies supporting a prothrombotic potential of epoetin in children, it has been suggested that epoetin administration be deferred for at least 2 weeks after surgery for arteriovenous (AV) fistula to prevent fistula thrombosis [13, 14, 21].

The mechanism by which epoetin might increase cardiovascular risk remains unclear, even though studies in the adult CKD and dialysis population demonstrate either no benefit or increased cardiac events and mortality when higher doses of epoetin are used to achieve a higher Hgb concentration [22, 23, 24]. The reason for the higher incidence of adverse events remains obscure; however, the presence of erythropoietin receptors in organs other than the bone marrow, such as the vascular endothelium, the myocardium, the kidneys, and the central nervous system, raises the possibility that there may be non-erythropoetic effects of erythropoietin that might explain the adverse risk [20, 25].

Since there have been no large randomized controlled trials in children, the correction of the risk of anemia in children is largely based on extrapolation from adult randomized controlled trials (RCTs). Two RCTs have been cited by the Food and Drug Administration (FDA) in their black box warning: one in hemodialysis patients—the Normal Hematocrit study (NHS), and the other in non-dialysis patients—the Correction of Hgb and Outcomes in Renal Insufficiency (CHOIR) study. The NHS trial randomly assigned 1,223 symptomatic hemodialysis patients to a hematocrit of 42% versus 30% with high-dose and lower-dose epoetin treatment, respectively [24]. Patients were considered to be at high risk of cardiovascular disease, because they were required to have congestive heart failure or ischemic heart disease on enrollment. The primary endpoint was the length of time to death or a first non-fatal myocardial infarction. The study was terminated early by the data monitoring committee, at the third interim analysis, because of the higher risk observed in patients randomly assigned to the higher hematocrit arm of the trial. The study demonstrated increased risk for patients assigned to the higher hematocrit [relative risk (RR) of 1.3]. The study also reported a higher rate of vascular thrombosis in patients treated to the higher hematocrit. However, the study did not address the benefit or harm of maintaining hematocrit between 30% and 42%. The CHOIR study was an open-label, randomized trial that studied 1,432 patients with non-dialysis CKD across 131 centers in the USA; 715 patients were randomly assigned to receive epoetin alpha targeted to achieve an Hgb level of 13.5 g/dl, and 717 were randomly selected to receive epoetin alpha targeted to achieve an Hgb level of 11.3 g/dl [22]. Eligibility criteria included age > 18 years and an estimated GFR of 15–50 ml/min per 1.73 m2 body surface area. The primary endpoint was a composite of death, myocardial infarction, congestive heart failure (CHF) hospitalization (excluding hospitalization during which renal replacement therapy occurred) and stroke. Secondary endpoints included the components of the primary endpoint, as well as cardiovascular and total hospitalizations, QOL and the time-to-dialysis. There were 222 composite events: 125 in the high Hgb group and 97 in the low Hgb group [P = 0.03, hazard ratio (HR) 1.34; with 95% confidence interval of 1.03 and 1.74]. The higher rate of composite events was explained largely by a higher rate of death (48% higher risk, P = 0.07) or CHF hospitalization (41%, P = 0.07). The QOL improved in both groups but did not differ significantly. These trials were supported by a recent meta-analysis that concluded that, when an Hgb level > 12 g/d is aimed for, there is a 17% higher risk of mortality. The higher mortality was attributed to higher risk of cardiovascular complications [26]. Despite these studies in adults, higher doses of epoetin are being used in children to achieve normalization of hematocrit based on data from the NAPRTCS 2001 and 2004 registry reports [27]. In this report, younger children are being given higher doses of erythropoietin (EPO), with infants requiring the highest dose, ranging from 275 U/kg per week to 350 U/kg per week [28].

Recommendations for the optimal Hgb level in children

Based on RCTs in adults and largely observational studies in children, an opinion-based minimum Hgb level of 11 g/dl has been recommended by the European Pediatric Peritoneal Dialysis Working Group (EPPWG) and National Kidney Foundation Kidney Disease Outcome Quality Initiative (NKF-K/DOQI) with the rationale of improved quality of life and better survival [2, 29, 30]. In addition, the EPPWG has recommended the use of iron as an adjunct to epoetin in the treatment of anemia. Studies of adults have also suggested that, among adult patients suffering inflammation and on permanent hemodialysis, when an increase in the dose of epoetin is contemplated, administration of 1 g of ferric gluconate is effective in improving hemoglobin levels [31, 32]. The EPPWG did not recommend an upper limit for the Hgb level, while NKF-K/DOQI has most recently suggested that Hgb levels should be 11 to 12 g/dl [29, 30]. The FDA has most recently stated that the optimal Hgb level in adults (and children) with CKD should be in the 10 g/dl to 12 g/dl range. The optimal target level of Hgb in children is compounded by the age-related variation in defining the normal Hgb concentration and, consequently, the anemic range [33]. Additionally, the variability in Hgb concentration—a phenomenon called Hgb cycling—results in quite considerable difficulty in maintaining Hgb targets between 11 g/dl and 12 g/dl. Hgb cycling is defined as a non-physiological oscillation or periodic fluctuation in the Hgb level by more than 1.5 g/dl from an equilibrium point. Over 90% of adult hemodialysis patients demonstrate at least one Hgb cycle in a year [34]. To our knowledge, hemoglobin cycling has not been studied in children.

In conclusion, there are limited data that address the hemoglobin target levels in children with CKD. Since children have important physiologic differences from adults, and since the effects of the complications of CKD, including anemia, may be different in children than in adults, RCTs in children are desperately needed. However, until randomized controlled studies of children with CKD are conducted, adult studies should help guide the decision in children. At this point we recommend aiming for an Hgb level of 10 g/dl to 12 g/dl in children, commensurate with the FDA guidelines.


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Copyright information

© IPNA 2008

Authors and Affiliations

  1. 1.Renal DivisionBrigham and Women’s Hospital and Harvard Medical SchoolBostonUSA
  2. 2.Dialysis ServicesBrigham and Women’s HospitalBostonUSA

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