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Acute management of propionic acidemia

Authors :
Chapman, Kimberly A.
Gropman, Andrea
MacLeod, Erin
Stagni, Kathy
Summar, Marshall L.
Ueda, Keiko
Mew, Nicholas Ah
Franks, Jill
Island, Eddie
Matern, Dietrich
Pena, Loren
Smith, Brittany
Sutton, V. Reid
Urv, Tiina
Venditti, Charles
Chakrapani, Anupam
Source :
Molecular Genetics & Metabolism. Jan2012, Vol. 105 Issue 1, p16-25. 10p.
Publication Year :
2012

Abstract

Abstract: Propionic acidemia or aciduria is an intoxication-type disorder of organic metabolism. Patients deteriorate in times of increased metabolic demand and subsequent catabolism. Metabolic decompensation can manifest with lethargy, vomiting, coma and death if not appropriately treated. On January 28–30, 2011 in Washington, D.C., Children''s National Medical Center hosted a group of clinicians, scientists and parental group representatives to design recommendations for acute management of individuals with propionic acidemia. Although many of the recommendations are geared toward the previously undiagnosed neonate, the recommendations for a severely metabolically decompensated individual are applicable to any known patient as well. Initial management is critical for prevention of morbidity and mortality. The following manuscript provides recommendations for initial treatment and evaluation, a discussion of issues concerning transport to a metabolic center (if patient presents to a non-metabolic center), acceleration of management and preparation for discharge. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
10967192
Volume :
105
Issue :
1
Database :
Academic Search Index
Journal :
Molecular Genetics & Metabolism
Publication Type :
Academic Journal
Accession number :
70234839
Full Text :
https://doi.org/10.1016/j.ymgme.2011.09.026