Literature DB >> 19157942

A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency.

Georgianne L Arnold1, Johan Van Hove, Debra Freedenberg, Arnold Strauss, Nicola Longo, Barbara Burton, Cheryl Garganta, Can Ficicioglu, Stephen Cederbaum, Cary Harding, Richard G Boles, Dietrich Matern, Pranesh Chakraborty, Annette Feigenbaum.   

Abstract

INTRODUCTION: Very long chain acyl-CoA dehydrogenase (VLCAD) deficiency is a disorder of oxidation of long chain fat, and can present as cardiomyopathy or fasting intolerance in the first months to years of life, or as myopathy in later childhood to adulthood. Expanded newborn screening has identified a relatively high incidence of this disorder (1:31,500), but there is a dearth of evidence-based outcomes data to guide the development of clinical practice protocols. This consensus protocol is intended to assist clinicians in the diagnosis and management of screen-positive newborns for VLCAD deficiency until evidence-based guidelines are available.
METHOD: The Oxford Centre for Evidence-based Medicine system was used to grade the literature review and create recommendations graded from A (evidence level of randomized clinical trials) to D (expert opinion). Delphi was used as the consensus tool. A panel of 14 experts (including clinicians, diagnostic laboratory directors and researchers) completed three rounds of survey questions and had a face-to-face meeting. RESULT: Panelists reviewed the initial evaluation of the screen-positive infant, diagnostic testing and management of diagnosed patients. Grade C and D consensus recommendations were made in each of these three areas. The panel did not reach consensus on all issues, particularly in the dietary management of asymptomatic infants diagnosed by newborn screening.

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Year:  2009        PMID: 19157942      PMCID: PMC3219055          DOI: 10.1016/j.ymgme.2008.09.008

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  24 in total

Review 1.  The Delphi technique: myths and realities.

Authors:  Catherine Powell
Journal:  J Adv Nurs       Date:  2003-02       Impact factor: 3.187

2.  Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism.

Authors:  D S Millington; N Kodo; D L Norwood; C R Roe
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.

Authors:  J C Wood; M J Magera; P Rinaldo; M R Seashore; A W Strauss; A Friedman
Journal:  Pediatrics       Date:  2001-07       Impact factor: 7.124

4.  Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children.

Authors:  D Bonnet; D Martin; E Villain; P Jouvet; D Rabier; M Brivet; J M Saudubray
Journal:  Circulation       Date:  1999-11-30       Impact factor: 29.690

Review 5.  Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.

Authors:  N Gregersen; B S Andresen; M J Corydon; T J Corydon; R K Olsen; L Bolund; P Bross
Journal:  Hum Mutat       Date:  2001-09       Impact factor: 4.878

6.  Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program.

Authors:  T H Zytkovicz; E F Fitzgerald; D Marsden; C A Larson; V E Shih; D M Johnson; A W Strauss; A M Comeau; R B Eaton; G F Grady
Journal:  Clin Chem       Date:  2001-11       Impact factor: 8.327

7.  Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype.

Authors:  D S Roe; C Vianey-Saban; S Sharma; M T Zabot; C R Roe
Journal:  Clin Chim Acta       Date:  2001-10       Impact factor: 3.786

8.  MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency.

Authors:  Ute Spiekerkoetter; Bin Sun; Thomas Zytkovicz; Ronald Wanders; Arnold W Strauss; Udo Wendel
Journal:  J Pediatr       Date:  2003-09       Impact factor: 4.406

9.  A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency.

Authors:  Georgianne L Arnold; Dwight D Koeberl; Dietrich Matern; Bruce Barshop; Nancy Braverman; Barbara Burton; Stephen Cederbaum; Annette Fiegenbaum; Cheryl Garganta; James Gibson; Stephen I Goodman; Cary Harding; Stephen Kahler; David Kronn; Nicola Longo
Journal:  Mol Genet Metab       Date:  2007-12-21       Impact factor: 4.797

10.  Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress.

Authors:  U Spiekerkoetter; C Tokunaga; U Wendel; E Mayatepek; V Exil; M Duran; F A Wijburg; R J A Wanders; A W Strauss
Journal:  Eur J Clin Invest       Date:  2004-03       Impact factor: 4.686

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  63 in total

1.  Variability in the clinical management of fatty acid oxidation disorders: results of a survey of Canadian metabolic physicians.

Authors:  Beth K Potter; Julian Little; Pranesh Chakraborty; Jonathan B Kronick; Jessica Evans; Julia Frei; Sarah C Sutherland; Kumanan Wilson; Brenda J Wilson
Journal:  J Inherit Metab Dis       Date:  2011-06-01       Impact factor: 4.982

2.  Expanded newborn screening: reducing harm, assessing benefit.

Authors:  Bridget Wilcken
Journal:  J Inherit Metab Dis       Date:  2010-05-04       Impact factor: 4.982

3.  Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.

Authors:  Marcus J Miller; Lindsay C Burrage; James B Gibson; Meghan E Strenk; Edward J Lose; David P Bick; Sarah H Elsea; V Reid Sutton; Qin Sun; Brett H Graham; William J Craigen; Victor Wei Zhang; Lee-Jun C Wong
Journal:  Mol Genet Metab       Date:  2015-09-02       Impact factor: 4.797

4.  Adult-onset very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD).

Authors:  F Fatehi; A A Okhovat; Y Nilipour; M Mroczek; V Straub; A Töpf; A Palibrk; S Peric; V Rakocevic Stojanovic; H Najmabadi; S Nafissi
Journal:  Eur J Neurol       Date:  2020-07-24       Impact factor: 6.089

5.  MCT oil-based diet reverses hypertrophic cardiomyopathy in a patient with very long chain acyl-coA dehydrogenase deficiency.

Authors:  Muhammad Ali Pervaiz; Fran Kendal; Madhuri Hegde; Rani H Singh
Journal:  Indian J Hum Genet       Date:  2011-01

6.  Lethal Undiagnosed Very Long-Chain Acyl-CoA Dehydrogenase Deficiency with Mild C14-Acylcarnitine Abnormalities on Newborn Screening.

Authors:  U Spiekerkoetter; M Mueller; M Sturm; M Hofmann; D T Schneider
Journal:  JIMD Rep       Date:  2012-02-26

7.  Rhabdomyolysis as a manifestation of a metabolic disease: a case report.

Authors:  Marta Sousa Moniz; Maria Inês Mascarenhas; Carlos Escobar; Pedro Nunes; Clara Abadesso; Helena Loureiro; Helena Almeida
Journal:  Rev Bras Ter Intensiva       Date:  2017 Jan-Mar

8.  Development of a Tandem Mass Spectrometry Method for Rapid Measurement of Medium- and Very-Long-Chain Acyl-CoA Dehydrogenase Activity in Fibroblasts.

Authors:  Damien Bouvier; Christine Vianey-Saban; Séverine Ruet; Cécile Acquaviva
Journal:  JIMD Rep       Date:  2016-12-10

9.  Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiency.

Authors:  Manuel Schiff; Al-Walid Mohsen; Anuradha Karunanidhi; Elizabeth McCracken; Renita Yeasted; Jerry Vockley
Journal:  Mol Genet Metab       Date:  2013-02-13       Impact factor: 4.797

10.  A novel tandem mass spectrometry method for rapid confirmation of medium- and very long-chain acyl-CoA dehydrogenase deficiency in newborns.

Authors:  Frank ter Veld; Martina Mueller; Simone Kramer; Ulrike Haussmann; Diran Herebian; Ertan Mayatepek; Maurice D Laryea; Sonja Primassin; Ute Spiekerkoetter
Journal:  PLoS One       Date:  2009-07-30       Impact factor: 3.240

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