Abstract
Nearly all children who require renal replacement therapy develop anemia because endogenous renal erythropoietin (EPO) production is inadequate to sustain a normal number of circulating erythrocytes. Anemic children may have compensatory changes in heart rate and respiration, impaired cognition, fatigue with exertion, left ventricular hypertrophy, anorexia, and a lower satisfaction with life when compared to non-anemic children. Prior to the availability of recombinant human erythropoietin (rHuEPO) therapy, children with end-stage renal disease (ESRD) were dependent on red blood cell transfusions to ameliorate the effects of severe anemia. Erythropoietin therapy has dramatically improved outcomes in children with ESRD by avoiding the morbidity associated with red blood cell transfusions, including iron overload, viral infections, and human leukocyte antigen (HLA) sensitization. Despite the improvement in outcomes, there is still room for improvement as anemia is still under-recognized and under-treated.
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Yorgin, P.D., Al-Uzri, A. (2004). Management of renal anemia. In: Warady, B.A., Schaefer, F.S., Fine, R.N., Alexander, S.R. (eds) Pediatric Dialysis. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-1031-3_19
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DOI: https://doi.org/10.1007/978-94-007-1031-3_19
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