Literature DB >> 24122260

A biphasic dialytic strategy for the treatment of neonatal hyperammonemia.

Mark Hanudel, Sonal Avasare, Eileen Tsai, Ora Yadin, Joshua Zaritsky.   

Abstract

BACKGROUND: Neonates with inborn errors of metabolism (IEM) often develop hyperammonemia which, if not corrected quickly, may result in poor neurologic outcomes. As pharmacologic therapy cannot rapidly lower ammonia levels, dialysis is frequently required. Both hemodialysis (HD) and standard-dose continuous renal replacement therapy (CRRT) are effective; however, HD may be followed by post-dialytic ammonia rebound, and standard-dose CRRT may not effect a rapid enough decrease in ammonia levels. CASE-DIAGNOSIS/TREATMENT: We present two cases of IEM-associated neonatal hyperammonemia in which we employed a biphasic, high-dose CRRT treatment strategy, initially using dialysate flow rates of 5,000 mL/h (approximately 40,000 mL/h/1.73 m(2)) in order to rapidly decrease ammonia levels, then decreasing the dialysate flow rates to 500 mL/h (approximately 4,000 mL/h/1.73 m(2)) in order to prevent ammonia rebound.
CONCLUSIONS: This biphasic dialytic treatment strategy for neonatal hyperammonemia effected rapid ammonia reduction without rebound and accomplished during a single dialysis run without equipment changes.

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Mesh:

Year:  2014        PMID: 24122260      PMCID: PMC5922760          DOI: 10.1007/s00467-013-2638-x

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  15 in total

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2.  Phenylacetate and benzoate clearance in a hyperammonemic infant on sequential hemodialysis and hemofiltration.

Authors:  Timothy E Bunchman; Gina-Marie Barletta; John W Winters; John J Gardner; Teri L Crumb; Kevin D McBryde
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3.  Renal replacement therapy in the treatment of confirmed or suspected inborn errors of metabolism.

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4.  Dialysis in neonates with inborn errors of metabolism.

Authors:  F Schaefer; E Straube; J Oh; O Mehls; E Mayatepek
Journal:  Nephrol Dial Transplant       Date:  1999-04       Impact factor: 5.992

Review 5.  Hyperammonemia in review: pathophysiology, diagnosis, and treatment.

Authors:  Ari Auron; Patrick D Brophy
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6.  Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism.

Authors:  Anja K Arbeiter; Birgitta Kranz; Anne-Margret Wingen; Klaus-Eugen Bonzel; Christian Dohna-Schwake; Ludwig Hanssler; Ulrich Neudorf; Peter F Hoyer; Rainer Büscher
Journal:  Nephrol Dial Transplant       Date:  2009-11-23       Impact factor: 5.992

7.  Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.

Authors:  M Msall; M L Batshaw; R Suss; S W Brusilow; E D Mellits
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8.  High-dose continuous renal replacement therapy for neonatal hyperammonemia.

Authors:  Joann M Spinale; Benjamin L Laskin; Neal Sondheimer; Sarah J Swartz; Stuart L Goldstein
Journal:  Pediatr Nephrol       Date:  2013-03-08       Impact factor: 3.714

9.  Regional citrate anticoagulation for hemodialysis: calcium-free vs. calcium containing dialysate - a randomized trial.

Authors:  J Buturovic-Ponikvar; S Cerne; J Gubensek; R Ponikvar
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10.  Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.

Authors:  Gregory M Enns; Susan A Berry; Gerard T Berry; William J Rhead; Saul W Brusilow; Ada Hamosh
Journal:  N Engl J Med       Date:  2007-05-31       Impact factor: 91.245

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  10 in total

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