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Normal statural growth in 2 infants on chronic peritoneal dialysis: anecdotal or whole management-related
M Fischbach1, J Terzic, S Menouer
1Nephrology Dialysis Transplantation Children's Unit, University Hospital, Strasbourg, France. Michel.Fischbach@chru-strasbourg.fr
Insights
Normal growth in infants on chronic peritoneal dialysis (CPD) is achievable with optimized management. This includes careful vitamin D analogue use, maintaining hemoglobin, and high dialysis doses for children with renal hypodysplasia.
Area of Science:
- Pediatric Nephrology
- Renal Replacement Therapy
- Growth and Development
Background:
- Growth retardation is a common complication in children undergoing chronic peritoneal dialysis (CPD).
- Despite various interventions, achieving normal growth in infants on CPD remains challenging.
Observation:
- Two infants with renal hypodysplasia requiring CPD from an early age experienced normal growth over one year.
- Management involved oral nutrition, tidal peritoneal dialysis for high clearance, hemoglobin levels above 13 g/dl, and cautious use of vitamin D analogues.
Findings:
- Optimized management, including avoiding high-dose activated vitamin D, maintaining normal hemoglobin, and delivering high dialysis doses, facilitated normal statural growth.
- This approach contrasts with the typical growth issues seen in children on CPD.
Implications:
- The presented management strategy may be crucial for optimizing statural growth in infants on CPD.
- Further clinical evaluation is needed to establish these findings as clinical guidelines.
Aims:
Growth retardation is usual in children on chronic peritoneal dialysis (CPD). Despite attention to many contributing factors (nutrition, dialysis dose, hemoglobin level, adynamic bone disease, hyperparathyroidism or rickets, growth hormone resistance, etc.), normal growth is rarely obtained in infants on CPD.
Materials And Methods:
We had the chance to observe normal growth over a 1 year period in 2 consecutively treated infants on CPD. Louise (renal hypodysplasia) required CPD at the age of 1 month: creatinine 430 micromol/l; oliguric, creatinine clearance lower than 5 ml/min/1.73 m2. Nutrition was achieved orally with human milk during the first 6 months of life. Tidal peritoneal dialysis allowed a high dialysis dose Kt/V urea 3.8/week and Kcreatinine 105 l/week/1.73 m2. Hemoglobin was maintained over 13 g/dl and low levels of vitamin D analogue were prescribed to avoid adynamic bone disease. At the age of 1 year her height was 75 cm. i.e. in the normal range for age. Madeline (renal hypodysplasia) commenced on CPD at the age of 6 weeks and managed similarly. Her height at 1 year of age was 74 cm.
Results:
In our 20 years of experience with children on dialysis, these 2 cases of normal statural growth for age at 1 year warrant discussion. As well as nutritional support, the new and recent therapeutic options in our team were: firstly, to avoid high doses of activated vitamin D to control PTH, as high doses are able to induce both a risk of adynamic bone disease and a direct bone cartilage toxicity: secondly, to maintain normal hemoglobin level; and thirdly, to deliver a high dialysis dose (urea, creatinine clearance) based on an individually adapted prescription.
Conclusion:
We feel this management approach is necessary to achieve optimal statural growth in children on chronic peritoneal dialysis. But this management concept only based on clinical anecdotal observations needs further evaluation before its use in clinical guidelines.
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