Literature DB >> 29095391

Acute Illness Protocol for Maple Syrup Urine Disease.

Lance H Rodan, Saud H Aldubayan, Gerard T Berry, Harvey L Levy.   

Abstract

Inborn errors of metabolism (IEMs) are genetic disorders that disrupt enzyme activity, cellular transport, or energy production. They are individually rare but collectively have an incidence of 1:1000. Most patients with IEMs are followed up by a physician with expertise in biochemical genetics (metabolism), but may present outside this setting. Because IEMs can present acutely with life-threatening crises that require specific interventions, it is critical for the emergency medicine physician, pediatrician, internist, and critical care physician as well as the biochemical geneticist to have information on the initial assessment and management of patients with these disorders. Appropriate early care can be lifesaving. This protocol is not designed to replace the expert consultation of a biochemical geneticist, but rather to improve early care and increase the level of comfort of the acute care physician with initial management of maple syrup urine disease until specialty consultation is obtained.

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Year:  2018        PMID: 29095391     DOI: 10.1097/PEC.0000000000001299

Source DB:  PubMed          Journal:  Pediatr Emerg Care        ISSN: 0749-5161            Impact factor:   1.454


  4 in total

1.  Intravenous administration of a branched-chain amino-acid-free solution in children and adults with acute decompensation of maple syrup urine disease: a prospective multicentre observational study.

Authors:  Jean-Meidi Alili; Marie-Pierre Berleur; Marie-Caroline Husson; Karine Mention; Manuel Schiff; Jean-Baptiste Arnoux; Anaïs Brassier; Anne-Sophie Guemman; Coraline Grisel; Sandrine Dubois; Marie-Thérèse Abi-Wardé; Christine Broissand; Aude Servais; Myriam Dao; Pascale de Lonlay
Journal:  Orphanet J Rare Dis       Date:  2022-05-16       Impact factor: 4.303

2.  Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency department.

Authors:  Yılmaz Yıldız; Leman Akcan Yıldız; Ali Dursun; Ayşegül Tokatlı; Turgay Coşkun; Özlem Tekşam; Hatice Serap Sivri
Journal:  Eur J Pediatr       Date:  2020-02-11       Impact factor: 3.183

3.  Intravenous branched-chain amino-acid-free solution for the treatment of metabolic decompensation episodes in Spanish pediatric patients with maple syrup urine disease.

Authors:  Paula Sánchez-Pintos; Silvia Meavilla; María Goretti López-Ramos; Ángeles García-Cazorla; Maria L Couce
Journal:  Front Pediatr       Date:  2022-08-15       Impact factor: 3.569

4.  A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single-center study and the generation of www.emergencyprotocol.net.

Authors:  Alessandro Rossi; Irene J Hoogeveen; Charlotte M A Lubout; Foekje de Boer; Marieke J Fokkert-Wilts; Iris L Rodenburg; Esther van Dam; Sarah C Grünert; Diego Martinelli; Maurizio Scarpa; Hanka Dekker; Sebastiaan T Te Boekhorst; Francjan J van Spronsen; Terry G J Derks
Journal:  J Inherit Metab Dis       Date:  2021-05-04       Impact factor: 4.982

  4 in total

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