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Erschienen in: Pediatric Nephrology 10/2004

01.10.2004 | Original Article

Two different therapeutic regimes in patients with sequelae of hemolytic-uremic syndrome

verfasst von: María Gracia Caletti, Horacio Lejarraga, Diana Kelmansky, Mabel Missoni

Erschienen in: Pediatric Nephrology | Ausgabe 10/2004

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Abstract

Renal disease is the most important long-term complication of hemolytic-uremic syndrome (HUS). A comparative study of renal function was carried out in two groups of patients. Group 1 included 19 children followed for a median of 11 years, 1960–1980, with a low-sodium diet, antihypertensive drugs, and a restricted protein intake in the end stage of renal disease. Group 2 included 26 children treated for a median of 9 years, 1988–2002, on a low-sodium diet, early restriction of protein intake according to recommendations, and angiotensin converting enzyme inhibitors (ACEi). Long-term renal function was assessed by the inverse of the plasma creatinine concentration (1/[Cr]) over time. Linear regression lines were fitted to individual values of 1/[Cr] for each child. Regression coefficients of children in group 1 were all negative, ranging from −0.031 to −0.00043; 7 were significantly different from zero, indicating a linear fall in renal function over time. In contrast, children from group 2 had 11 negative slopes (only 1 significant) and 15 positive slopes, ranging from 0.17893 to −0.3899. Fisher’s exact test showed that group 1 had significantly more children with negative slopes than group 2. This comparatively better long-term outcome of renal function in children under contemporary treatment was probably associated with early restriction of protein and use of ACEi.
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Metadaten
Titel
Two different therapeutic regimes in patients with sequelae of hemolytic-uremic syndrome
verfasst von
María Gracia Caletti
Horacio Lejarraga
Diana Kelmansky
Mabel Missoni
Publikationsdatum
01.10.2004
Verlag
Springer-Verlag
Erschienen in
Pediatric Nephrology / Ausgabe 10/2004
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-004-1516-y

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