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Vol. 34. Issue 2.
Pages 247-248 (June 2016)
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Vol. 34. Issue 2.
Pages 247-248 (June 2016)
Erratum
DOI: 10.1016/j.rppede.2016.04.004
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Erratum to “In time: averting the legacy of kidney disease – focus on childhood” [Rev. Paul. Pediatr. 34 (1) (2016) 5–10]
Errata do “Em tempo: evitando as consequências da doença renal – foco na infância” [Rev Paul Pediatr 2016;34(1):5–10]
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Julie R. Ingelfingera,
Corresponding author
myriam@worldkidneyday.org

Corresponding author.
, Kamyar Kalantar-Zadehb, Franz Schaeferc, on behalf of the World Kidney Day Steering Committee 1
a Massachusetts General Hospital, Boston, USA
b University of California, Irvine, USA
c Heidelberg University Hospital, Heildelberg, Germany
Related content
Rev Paul Ped. 2016;34:5-1010.1016/j.rppede.2015.12.001
Julie R. Ingelfinger, Kamyar Kalantar-Zadeh, Franz Schaefer
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In the editorial Erratum of “In time: averting the legacy of kidney disease − focus on childhood” [Rev Paul Pediatr. 2016;34(1):5-10], in the Table 2, which reads:

Table 2 Etiology of chronic kidney disease in children.2

DRCDRET
Etiology  Percentage (range)  Etiology  Percentage (range) 
CAKUT  48-59%  CAKUT  34-43% 
GN  5-14%  GN  15-29% 
HN  10-19%  HN  12-22% 
HUS  2-6%  HUS  2-6% 
Cystic  5-9%  Cystic  6-12% 
Ischemic  2-4%  Ischemic  2% 

CKD, chronic kidney disease; ESRD, childhood onset end-stage renal disease; CAKUT, congenital anomalies of the kidney and urinary tract; GN, glomerulonephritis; HN, hypertension; HUS, hemolytic uremic syndrome. Rare causes include congenital NS, metabolic diseases, cystinosis. Miscellaneous causes depend on how such entities are classified.

Chronic Kidney Disease data are from North American Pediatric Renal Trials and Collaborative Studies, the Italian Registry and the Belgian Registry. Childhood onset end-stage renal disease data are from ANZDATA, ESPN/ERA-EDTA, UK Renal Registry and the Japanese Registry.

It should read:

Table 2 Etiology of chronic kidney disease in children.2

DRCDRET
Etiology  Percentage (range)  Etiology  Percentage (range) 
CAKUT  48-59%  CAKUT  34-43% 
GN  5-14%  GN  15-29% 
HN  10-19%  HN  12-22% 
HUS  2-6%  HUS  2-6% 
Cystic  5-9%  Cystic  6-12% 
Ischemic  2-4%  Ischemic  2% 

CKD, chronic kidney disease; ESRD, childhood onset end-stage renal disease; CAKUT, congenital anomalies of the kidney and urinary tract; GN, glomerulonephritis; HN, hereditary nephropathy; HUS, hemolytic uremic syndrome. Rare causes include congenital NS, metabolic diseases, cystinosis. Miscellaneous causes depend on how such entities are classified.

Chronic Kidney Disease data are from North American Pediatric Renal Trials and Collaborative Studies, the Italian Registry and the Belgian Registry. Childhood onset end-stage renal disease data are from ANZDATA, ESPN/ERA-EDTA, UK Renal Registry and the Japanese Registry.

Philip Kam Tao Li, Guillermo Garcia-Garcia, William G. Couser, Timur Erk, Julie R. Ingelfinger, Kamyar Kalantar-Zadeh, Charles Ker-nahan, Charlotte Osafo, Miguel C. Riella, Luca Segantini, Elena Zakharova.

Copyright © 2016. Sociedade de Pediatria de São Paulo
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