Literature DB >> 19934086

Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism.

Anja K Arbeiter1, Birgitta Kranz, Anne-Margret Wingen, Klaus-Eugen Bonzel, Christian Dohna-Schwake, Ludwig Hanssler, Ulrich Neudorf, Peter F Hoyer, Rainer Büscher.   

Abstract

BACKGROUND: Newborns with inborn errors of metabolism often present with hyperammonaemic coma, requiring prompt diagnosis and specific medical therapy, nutritional support and efficient toxin removal. Little information regarding the efficacy and safety of continuous venovenous haemodialysis (CVVHD) as an option for extracorporal ammonia detoxification in children is available.
METHODS: Twenty-one patients with hyperammonaemia [19 neonates (mean age 4.1 +/- 2.4 days) and two children 1 and 7 years of age, respectively] were admitted to our hospital for dialysis between 1996 and 2008. Seventeen children (15 neonates), received CVVHD. Four neonates received continuous peritoneal dialysis (CPD). All started medical treatment with sodium benzoate, l-arginine hydrochloride and carnitine as well as protein-restricted parenteral diets with high caloric intake before dialysis.
RESULTS: Plasma ammonia levels (range 464-7267 microg/dl before dialysis and 27-3317 microg/dl after dialysis) were significantly reduced by 50% within 4.7 +/- 2.5 h with CVVHD compared with 13.5 +/- 6.2 h with CPD (P < 0.0001). Plasma ammonia levels <200 microg/dl critical range were achieved within 22.4 +/- 18.1 h in CVVHD patients compared with 35.0 +/- 24.1 h with CPD. Depending on the weight and blood pressure stability of the patients, mean blood flow velocities of 9.8 +/- 3.4 ml/kg/min and mean dialysate flow rates of 3925 +/- 2398 ml/min/1.73 m(2) were employed. Blood and dialysate flows significantly correlated with ammonia clearance and decay of ammonia in vivo. Because of the severe underlying disease, 18% of CVVHD patients died compared with 50% undergoing CPD. In total, 82% of CVVHD patients survived the first 6 months after dialysis. Among these, 43% were without sequelae, 43% developed moderate mental retardation, and two (14%) developed severe mental retardation.
CONCLUSION: CVVHD effectively and quickly eliminates plasma ammonia. To optimize long-term mental outcome, rapid identification and appropriate treatment of the underlying disease as well as starting dialysis early are of enormous therapeutic value.

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Year:  2009        PMID: 19934086     DOI: 10.1093/ndt/gfp595

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


  15 in total

1.  A biphasic dialytic strategy for the treatment of neonatal hyperammonemia.

Authors:  Mark Hanudel; Sonal Avasare; Eileen Tsai; Ora Yadin; Joshua Zaritsky
Journal:  Pediatr Nephrol       Date:  2014-02       Impact factor: 3.714

2.  Veno-Venous Extracorporeal Membrane Oxygenation for Continuous Renal Replacement in a Neonate with Propionic Acidemia.

Authors:  Jeffrey W Gander; Erika T Rhone; William G Wilson; John P Barcia; Melissa J Sacco
Journal:  J Extra Corpor Technol       Date:  2017-03

3.  Improvement of hepatic encephalopathy by application of peritoneal dialysis in a patient with non-end-stage renal disease.

Authors:  C Pipili; A Polydorou; K Pantelias; P Korfiatis; F Nikolakopoulos; E Grapsa
Journal:  Perit Dial Int       Date:  2013 Mar-Apr       Impact factor: 1.756

4.  Flow-through peritoneal dialysis in neonatal enema-induced hyperphosphatemia.

Authors:  Dusan Kostic; Andre Broggin Dutra Rodrigues; Antônio Leal; Camila Metran; Meire Nagaiassu; Andréia Watanabe; Maria Esther Ceccon; Uenis Tannuri; Vera Hermina Koch
Journal:  Pediatr Nephrol       Date:  2010-06-06       Impact factor: 3.714

5.  Efficacy and safety of intermittent hemodialysis in infants and young children with inborn errors of metabolism.

Authors:  I-Jung Tsai; Wuh-Liang Hwu; Shu-Chien Huang; Ni-Chung Lee; En-Ting Wu; Yin-Hsiu Chien; Yong-Kwei Tsau
Journal:  Pediatr Nephrol       Date:  2013-09-08       Impact factor: 3.714

6.  Short-term survival of hyperammonemic neonates treated with dialysis.

Authors:  Stefano Picca; Carlo Dionisi-Vici; Andrea Bartuli; Tommaso De Palo; Francesco Papadia; Giovanni Montini; Marco Materassi; Maria Alice Donati; Enrico Verrina; Maria Cristina Schiaffino; Carmine Pecoraro; Emilia Iaccarino; Enrico Vidal; Alberto Burlina; Francesco Emma
Journal:  Pediatr Nephrol       Date:  2014-09-04       Impact factor: 3.714

7.  Continuous Renal Replacement Therapy for Treatment of Severe Attacks of Inborn Errors of Metabolism.

Authors:  Ayse Filiz Yetimakman; Selman Kesici; Murat Tanyildiz; Benan Bayrakci
Journal:  J Pediatr Intensive Care       Date:  2019-03-27

Review 8.  Advances and challenges in the treatment of branched-chain amino/keto acid metabolic defects.

Authors:  Ina Knerr; Natalie Weinhold; Jerry Vockley; K Michael Gibson
Journal:  J Inherit Metab Dis       Date:  2011-02-03       Impact factor: 4.982

9.  Acute treatment of hyperammonemia by continuous renal replacement therapy in a newborn patient with ornithine transcarbamylase deficiency.

Authors:  Hyo Jeong Kim; Se Jin Park; Kook In Park; Jin Sung Lee; Ho Sun Eun; Ji Hong Kim; Jae Il Shin
Journal:  Korean J Pediatr       Date:  2011-10-31

Review 10.  The Role of RRT in Hyperammonemic Patients.

Authors:  Shruti Gupta; Andrew Z Fenves; Robert Hootkins
Journal:  Clin J Am Soc Nephrol       Date:  2016-05-19       Impact factor: 8.237

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