Literature DB >> 12808177

Nutritional effects of increasing dialysis dose by adding an icodextrin daytime dwell to Nocturnal Intermittent Peritoneal Dialysis (NIPD) in children.

Koen J M van Hoeck1, Esther Rusthoven, Linda Vermeylen, Annemie Vandesompel, Bart Marescau, Marc Lilien, Cornelis H Schroder.   

Abstract

BACKGROUND: To assess the need to adapt dietary prescriptions, we studied potential effects of increasing the dialysis dose by adding a daytime icodextrin dwell, in children on Nocturnal Intermittent Peritoneal Dialysis (NIPD), on peritoneal amino acids (AA) and albumin loss, AA, albumin, cholesterol and fibrinogen plasma levels and nutritional intake.
METHODS: A cross-over study in eight children (age 2-12 years) on NIPD at baseline (week 1). INTERVENTION: to increase dialysis dose we added a daytime dwell with 1100 ml/m(2) icodextrin solution for a week (week 2). MAIN OUTCOME MEASURES: peritoneal albumin loss (quantified by nephelometry) and AA loss (quantified by liquid chromatography mass spectrometry) in the last 72 h dialysate collections of weeks 1 and 2. On days 7 and 14, morning blood sample was taken for urea, creatinine, plasma AA levels, serum albumin, cholesterol and fibrinogen determination. Nutritional intake diaries were kept throughout the study period.
RESULTS: Weekly dialysis creatinine clearance increased from 35 to 65 l/1.73 m(2) (P<0.0001) and Kt/V from 1.99 to 2.54 (P<0.01). Peritoneal albumin loss did not change significantly (2.4+/-0.4 to 2.4+/-0.3 g/m(2)/24 h) nor did serum albumin (3.25+/-0.52 to 3.21+/-0.25 g/dl), cholesterol (216+/-73 to 240+/-61 mg/dl) and fibrinogen (385+/-40 to 436+/-64 mg/dl). There was a significant increase in loss of essential (EAA) [1122+/-200 to 2104+/-417 mg/m(2)/week (P<0.0001)] and non-essential amino acids (NEAA) [6160+/-1341 to 10406+/-2899 mg/m(2)/week (P<0.001)]. Plasma AA levels did not change significantly except for a drop in histidine and glutamine. Dietary protein intake did not change from 43+/-12 to 41+/-8 g/m(2)/day, caloric intake from 73+/-21 to 70+/-24 kcal/kg/day.
CONCLUSIONS: Increasing dialysis dose by introducing a daytime icodextrin dwell during a week does not affect peritoneal albumin loss, serum albumin, cholesterol and fibrinogen levels nor dietary intake on a short term. There is a significant increase in EAA and NEAA loss without change in plasma levels. We suggest monitoring dietary intake when adding a daytime icodextrin dwell in children.

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Year:  2003        PMID: 12808177     DOI: 10.1093/ndt/gfg120

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  12 in total

1.  Icodextrin re-absorption varies with age in children on automated peritoneal dialysis.

Authors:  Allison Dart; Janusz Feber; Hubert Wong; Guido Filler
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2.  Kt/V and nPNA in pediatric peritoneal dialysis: a clinical or a mathematical association?

Authors:  F Cano; M Azocar; G Cavada; A Delucchi; V Marin; E Rodriguez
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Review 3.  Nutritional management and growth in children with chronic kidney disease.

Authors:  Lesley Rees; Helen Jones
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4.  Impact of fill volume on ultrafiltration with icodextrin in children on chronic peritoneal dialysis.

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5.  Nutritional status and volume control in adolescents on chronic hemodialysis.

Authors:  Fabio Paglialonga; Silvia Consolo; Marta Brambilla; Olga Caporale; Alejandro Cruz Gual; Maria Rosa Grassi; Giovanni Montini
Journal:  Pediatr Nephrol       Date:  2021-05-14       Impact factor: 3.714

6.  Icodextrin improves the serum potassium profile with the enhancement of nutritional status in continuous ambulatory peritoneal dialysis patients.

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Review 7.  Selection of modalities, prescription, and technical issues in children on peritoneal dialysis.

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Journal:  Pediatr Nephrol       Date:  2008-06-03       Impact factor: 3.714

Review 8.  Nutrition in children with CRF and on dialysis.

Authors:  Lesley Rees; Vanessa Shaw
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9.  Biphasic Regulation of Lipid Metabolism: A Meta-Analysis of Icodextrin in Peritoneal Dialysis.

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Review 10.  Malnutrition in Chronic Kidney Disease.

Authors:  Franca M Iorember
Journal:  Front Pediatr       Date:  2018-06-20       Impact factor: 3.418

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