Management of Anemia in Children Receiving Chronic Peritoneal Dialysis

Dagmara Borzych–Dużałka(Heidelberg University), Yelda Bilginer(Hacettepe University), Il Soo Ha(Seoul National University Children's Hospital), Mustafa Bak(Dr. Behçet Uz Çocuk Hastalıkları Hastanesi), Lesley Rees(Great Ormond Street Hospital), Francisco Cano(Hospital Luis Calvo Mackenna), Reyner Loza Munarriz(Hospital Nacional Cayetano Heredia), Annabelle N. Chua(Texas Children's Hospital), Silvia Pesle, Sevinç Emre(Istanbul University), Agnieszka Urzykowska(Children's Memorial Health Institute), Lily Quiroz(Hospital Roberto del Rio), Javier Ruscasso(Hospital de Niños Superiora Sor María Ludovica), Colin White(BC Children's Hospital), Lars Pape(Medizinische Hochschule Hannover), Virginia Ramela, Nikoleta Printza(Aristotle University of Thessaloniki), Andrea Vogel(Pontificia Universidad Católica de Chile), Dafina Kuzmanovska(PHI University Psychiatric Clinic - Skopje), Eva Šimková(Dubai Hospital), Dirk E. Müller‐Wiefel(Universität Hamburg), Anja Sander(Heidelberg University), Bradley A. Warady(Children's Mercy Hospital), Franz Schaefer(Heidelberg University)
Journal of the American Society of Nephrology
March 8, 2013
Cited by 89Open Access
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Abstract

Little information exists regarding the efficacy, modifiers, and outcomes of anemia management in children with CKD or ESRD. We assessed practices, effectors, and outcomes of anemia management in 1394 pediatric patients undergoing peritoneal dialysis (PD) who were prospectively followed in 30 countries. We noted that 25% of patients had hemoglobin levels below target (<10 g/dl or <9.5 g/dl in children older or younger than 2 years, respectively), with significant regional variation; levels were highest in North America and Europe and lowest in Asia and Turkey. Low hemoglobin levels were associated with low urine output, low serum albumin, high parathyroid hormone, high ferritin, and the use of bioincompatible PD fluid. Erythropoiesis-stimulating agents (ESAs) were prescribed to 92% of patients, and neither the type of ESA nor the dosing interval appeared to affect efficacy. The weekly ESA dose inversely correlated with age when scaled to weight but did not correlate with age when normalized to body surface area. ESA sensitivity was positively associated with residual diuresis and serum albumin and inversely associated with serum parathyroid hormone and ferritin. The prevalence of hypertension and left ventricular hypertrophy increased with the degree of anemia. Patient survival was positively associated with achieved hemoglobin and serum albumin and was inversely associated with ESA dose. In conclusion, control of anemia in children receiving long-term PD varies by region. ESA requirements are independent of age when dose is scaled to body surface area, and ESA resistance is associated with inflammation, fluid retention, and hyperparathyroidism. Anemia and high ESA dose requirements independently predict mortality.


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