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1.
Przegl Lek ; 49(1-2): 61-5, 1992.
Artigo em Polonês | MEDLINE | ID: mdl-1280842

RESUMO

Recombinant human erythropoietin (EPO) was administered to 12 children aged 8-17 years subjected to hemodialysis for a mean period of 16 (S.D. 19.7) months prior to EPO treatment. The hormone was administered thrice weekly at an intravenous dose of 25-75 u/kg until hemoglobin value of 100 g/l was obtained, and subsequently at maintenance doses for mean period of 7 (S.D. 4.0) months. The urea kinetic modeling (UKM) algorithms allowed to compute dialysis index KT/V for each patient in modeling sessions performed once a month. The analysis included the effect of EPO upon: peripheral whole blood count; individual UKM parameters; selected laboratory data (predialysis potassium, phosphorus, creatinine, total blood protein and albumin levels) in three randomized groups according to the value of KT/V: I. KT/V less than or equal to 1.0--underdialyzed, II. KT/V (1.0-1.4)--adequately dialyzed, III. KT/V greater than 1.4--overdialyzed. The results from 188 pre-EPO modeling sessions and 78 sessions in the course of EPO treatment were compared. All the three groups revealed increased Hb, Ht and erythrocyte count in cu mm, statistically significant in Groups II and III. EPO administration resulted in an improvement of dialysis adequacy, increasing the number of adequate modeling sessions from 66 up to 90% and simultaneously reducing the number of sessions in Groups I and III from 9.5 to 2.5% and from 24.5 to 7.5%, respectively. The 2.4% decrease of dialysis index observed after EPO administration was due to increased urea distribution volume.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Eritropoetina/administração & dosagem , Falência Renal Crônica/terapia , Diálise Renal/métodos , Terapia Assistida por Computador , Adolescente , Criança , Terapia Combinada , Creatinina/sangue , Esquema de Medicação , Eritropoetina/genética , Feminino , Hematócrito , Hemoglobinas/análise , Humanos , Injeções Intravenosas , Falência Renal Crônica/sangue , Masculino , Cuidados Paliativos , Ureia/sangue
2.
Przegl Lek ; 49(1-2): 55-60, 1992.
Artigo em Polonês | MEDLINE | ID: mdl-1455008

RESUMO

Recombinant human erythropoietin (EPO) was administered to 12 children with terminal renal failure aged 8-17 years subjected to hemodialysis for a mean period of 16 (S.D. = 19.7) month prior to EPO utilisation. The hormone was administered thrice weekly at an intravenous dose of 25-75 u/kg until Hb value of 100 g/l was obtained, and subsequently at maintenance doses for mean period of 7 (S.D. = 4.0) month. The urea kinetic modeling (UKM) algorithms allowed to compute protein catabolic rate (pcr) for each patient in modeling sessions performed once a month. The analysis included the effect of EPO upon: 1. peripheral whole blood count; 2. individual UKM parameters; 3. selected lab data describing the metabolic status of the patient (predialysis potassium, phosphorus, creatinine, total blood protein and albumin--and iron levels), in three randomized groups according to the value of pcr. Group I presented pcr less than 1.0 g protein/kg/day typical for malnutrition; group II--pcr = 1.0-1.4 g protein/kg/day--with appropriate protein catabolism; group III--pcr greater than 1.4 g protein/kg/day--hypercatabolic. The results from 188 pre-EPO modeling sessions and 78 sessions in the course of EPO treatment were compared. All the three groups revealed statistically significant increased Hb, Ht and erythrocyte count after EPO administration, which also resulted an increase of protein catabolism what is manifested in a decrease in the number of sessions by 26.1% in Group I and a corresponding increase by 13.5% and 12.6% in Groups II and III, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Eritropoetina/administração & dosagem , Falência Renal Crônica/terapia , Diálise Renal , Adolescente , Proteínas Sanguíneas/análise , Criança , Terapia Combinada , Creatinina/sangue , Contagem de Eritrócitos/efeitos dos fármacos , Eritropoetina/genética , Feminino , Hematócrito , Hemoglobinas/análise , Humanos , Falência Renal Crônica/sangue , Assistência de Longa Duração , Masculino , Recombinação Genética , Ureia/sangue
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