Literature DB >> 9266382

Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine disease.

P Jouvet1, F Poggi, D Rabier, J L Michel, P Hubert, M Sposito, J M Saudubray, N K Man.   

Abstract

Maple syrup urine disease results in accumulation of leucine and its metabolites, which may lead in the long term to neurological dysfunction. In acute neonatal crises, large amounts of leucine may be removed by continuous venovenous haemofiltration. This extracorporeal technique has its risks and hazards, which increase with duration of treatment. We report three neonates in life-threatening conditions due to maple syrup urine disease, treated for not more than 12 h with various continuous venovenous techniques: continuous haemofiltration, haemodiafiltration and haemodialysis. The efficiency of and tolerance to these techniques was evaluated. For all three patients, plasma leucine levels decreased dramatically from 2186, 3818 and 2536 mumol/L to 1131, 1275 and 488 mumol/L, respectively. Leucine clearance obtained was 4.28 ml/min in haemodiafiltration. Their patients' neurological status improved rapidly and they have a normal developmental quotient at 22 months, 13 months, and 11 months of age, respectively. Tolerance was good except for hypothermia and drop in haematocrit in all cases. Haemodiafiltration management was more cumbersome and time consuming because it required continual adjustment of the substitution fluid flow rate to precisely balance inflow and outflow rates. We recommend continuous venovenous haemodialysis as the therapy of choice. It might be anticipated that improvement of this technique, by increasing dialysate flow rate and blood flow rate, will allow leucine concentration to be decreased below 1000 mumol/L within 6-8 h, whatever the initial level.

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Year:  1997        PMID: 9266382     DOI: 10.1023/a:1005314025760

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  16 in total

1.  Continuous venovenous haemofiltration in the acute treatment of inborn errors of metabolism.

Authors:  P Jouvet; F Poggi; J M Saudubray
Journal:  Pediatr Nephrol       Date:  1995-02       Impact factor: 3.714

2.  Intellectual outcome in children with maple syrup urine disease.

Authors:  P Kaplan; A Mazur; M Field; J A Berlin; G T Berry; R Heidenreich; M Yudkoff; S Segal
Journal:  J Pediatr       Date:  1991-07       Impact factor: 4.406

3.  Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolism.

Authors:  G N Thompson; W W Butt; F A Shann; D M Kirby; R D Henning; D W Howells; A Osborne
Journal:  J Pediatr       Date:  1991-06       Impact factor: 4.406

4.  Continuous arteriovenous hemofiltration in critically ill children with acute renal failure.

Authors:  G Zobel; M Trop; E Ring; H M Grubbauer
Journal:  Crit Care Med       Date:  1987-07       Impact factor: 7.598

5.  Hudson memorial lecture. Neonatal management of organic acidurias. Clinical update.

Authors:  J M Saudubray; H Ogier; C Charpentier; E Depondt; F X Coudé; A Munnich; G Mitchell; F Rey; J Rey; J Frézal
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

6.  Removal of branched-chain amino acids by peritoneal dialysis, continuous arteriovenous hemofiltration, and continuous arteriovenous hemodialysis in rabbits: implications for maple syrup urine disease treatment.

Authors:  J B Gouyon; J Desgres; C Mousson
Journal:  Pediatr Res       Date:  1994-03       Impact factor: 3.756

7.  Continuous arteriovenous hemofiltration after cardiac operations in infants and children.

Authors:  G Paret; A J Cohen; D J Bohn; H Edwards; R Taylor; D Geary; W G Williams
Journal:  J Thorac Cardiovasc Surg       Date:  1992-11       Impact factor: 5.209

8.  Continuous venovenous hemodiafiltration in infants and children.

Authors:  T E Bunchman; N J Maxvold; D B Kershaw; A B Sedman; J R Custer
Journal:  Am J Kidney Dis       Date:  1995-01       Impact factor: 8.860

Review 9.  Continuous renal replacement therapies for the treatment of acute renal failure in intensive care patients.

Authors:  C Ronco
Journal:  Clin Nephrol       Date:  1993-10       Impact factor: 0.975

Review 10.  Effects of alterations of oxygen transport on the neonate.

Authors:  G Lister; G Moreau; M Moss; N S Talner
Journal:  Semin Perinatol       Date:  1984-07       Impact factor: 3.300

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  6 in total

1.  Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the disease.

Authors:  E Simon; R Fingerhut; J Baumkötter; V Konstantopoulou; R Ratschmann; U Wendel
Journal:  J Inherit Metab Dis       Date:  2006-08       Impact factor: 4.982

2.  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

3.  Continuous renal replacement therapy in neonates weighing less than 3 kg.

Authors:  Young Bae Sohn; Kyung Hoon Paik; Hee Yeon Cho; Su Jin Kim; Sung Won Park; Eun Sun Kim; Yun Sil Chang; Won-Soon Park; Yoon-Ho Choi; Dong-Kyu Jin
Journal:  Korean J Pediatr       Date:  2012-08-23

4.  A technique for rapid exchange of continuous renal replacement therapy.

Authors:  Peter Yorgin; Marlys Ludlow; Annabelle Chua; Steve Alexander
Journal:  Pediatr Nephrol       Date:  2006-03-14       Impact factor: 3.714

Review 5.  Animal models of maple syrup urine disease.

Authors:  K J Skvorak
Journal:  J Inherit Metab Dis       Date:  2009-03-09       Impact factor: 4.982

Review 6.  Emergency management of inherited metabolic diseases.

Authors:  V Prietsch; M Lindner; J Zschocke; W L Nyhan; G F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2002-11       Impact factor: 4.982

  6 in total

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