TY - JOUR
T1 - Management of anemia in children receiving chronic peritoneal dialysis
AU - Borzych-Duzalka, Dagmara
AU - Bilginer, Yelda
AU - Soo Ha, Il
AU - Bak, Mustafa
AU - Rees, Lesley
AU - Cano, Francisco
AU - Loza Munarriz, Reyner
AU - Chua, Annabelle
AU - Pesle, Silvia
AU - Emre, Sevinc
AU - Urzykowska, Agnieszka
AU - Quiroz, Lily
AU - Ruscasso, Javier Darío
AU - White, Colin
AU - Pape, Lars
AU - Ramela, Virginia
AU - Printza, Nikoleta
AU - Vogel, Andrea
AU - Kuzmanovska, Dafina
AU - Simkova, Eva
AU - Müller-Wiefel, Dirk E.
AU - Sander, Anja
AU - Warady, Bradley A.
AU - Schaefer, Franz
PY - 2013/3/29
Y1 - 2013/3/29
N2 - Little information exists regarding the efficacy,modifiers, and outcomes of anemiamanagement in children with CKDor ESRD.Weassessed practices, effectors, and outcomes of anemiamanagement 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. Theweekly ESAdose inversely correlatedwith agewhen scaled to weight but did not correlatewith age when normalized to body surface area. ESA sensitivity was positively associatedwith 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 serumalbumin and was inversely associated with ESAdose. 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.
AB - Little information exists regarding the efficacy,modifiers, and outcomes of anemiamanagement in children with CKDor ESRD.Weassessed practices, effectors, and outcomes of anemiamanagement 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. Theweekly ESAdose inversely correlatedwith agewhen scaled to weight but did not correlatewith age when normalized to body surface area. ESA sensitivity was positively associatedwith 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 serumalbumin and was inversely associated with ESAdose. 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.
UR - https://www.scopus.com/pages/publications/84875724009
U2 - 10.1681/ASN.2012050433
DO - 10.1681/ASN.2012050433
M3 - Article
C2 - 23471197
AN - SCOPUS:84875724009
SN - 1046-6673
VL - 24
SP - 665
EP - 676
JO - Journal of the American Society of Nephrology
JF - Journal of the American Society of Nephrology
IS - 4
ER -