High-volume continuous venovenous hemofiltration as an effective therapy for acute management of inborn errors of metabolism in young children
Journal
Blood Purification
Journal Volume
25
Journal Issue
4
Pages
303-308
Date Issued
2007
Author(s)
Abstract
Background/Aim: Renal replacement therapies (RRTs) have been used for the acute management of inborn errors of metabolism. Hemodialysis is the most effective modality. The aim of this article is to demonstrate that high-volume hemofiltration can offer an alternative way to effectively remove small molecules. Methods: Eight patients presented with acute neurological deterioration due to ammonia or organic acid accumulation. Different RRTs were applied, including continuous venovenous hemofiltration (CVVH, n = 7), continuous arteriovenous hemofiltration (CAVH, n = 2), continuous venovenous hemodialysis (CVVHD, n = 1), intermittent hemodialysis (HD, n = 1), and peritoneal dialysis (PD, n = 2). Results: Ammonia 50% reduction time in HD was 1.7 h while in CVVH it was 2-14.5 h. The greater the ultrafiltration flow was, the sooner patients regained consciousness. CAVH, CVVHD or PD was not sufficient enough. Conclusion: CVVH also has a good clearance for organic acid and ammonia if applying high-volume hemofiltration (>35 ml/kg/h). It can be therefore be considered as an alternative therapy if infant HD is not available. Copyright ? 2007 S. Karger AG.
Subjects
Hemodialysis; Hemofiltration; Hyperammonemia; Organic acidemia; Peritoneal dialysis
SDGs
Other Subjects
ammonia; carboxylic acid; alternative medicine; article; child; clinical article; consciousness level; continuous hemodiafiltration; continuous hemofiltration; controlled study; female; hemodialysis; human; inborn error of metabolism; male; neurologic disease; newborn; peritoneal dialysis; priority journal; renal replacement therapy; ultrafiltration; Carbamoyl-Phosphate Synthase I Deficiency Disease; Child; Child, Preschool; Female; Hemofiltration; Humans; Hyperammonemia; Infant; Infant, Newborn; Infection; Male; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Methylmalonic Acid; Ornithine Carbamoyltransferase Deficiency Disease; Renal Replacement Therapy; Treatment Outcome
Type
journal article