| Update of nutrition management of MSUD |
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| Written by Rani Singh, PhD. | |
| Saturday, December 17 1994 06:32 | |
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Submitted by: Rani Singh, PhD. - Atlanta, Georgia MSUD is a genetic disorder. Children with this disorder cannot use the BCAA (branched-chain amino acids) in the normal way. The outcome in these children is affected by several factors. These include age of diagnosis, degree of enzyme impairment, time at which diet therapy is begun and adequacy of management. Management requires an aggressive protocol to reduce plasma BCAA to avoid central nervous system changes. Goals of long-term nutrition support are: a) Normal plasma amino acid concentrations b) Urine free of branched-chain keto acids (BCKA) c) Normal growth, development and status. Nutritional management requires initiation of nutrition support immediately with BCAA free medical foods (formula). Depending on clinical status, patients are fed by nipple, nasogastric (N-G) tube, intravenous infusion (IV), or a combination of these methods. When plasma leucine reaches the upper limit of treatment range, leucine is added back gradually using infant formula or whole cow's milk depending on the child's age. Over restriction or imbalance of BCAAs has adverse effects. These include anemia, desquamation (shedding of the skin) and failure to thrive. Free isoleucine and valine can be used to correct some imbalances. It is very important to provide protein-free sources to meet energy requirements. In addition 100 to 500 mg of oral thiamine per day may be provided for three months to evaluate the response. Guidelines used for fluid requirements in treating these children include:
It was emphasized that energy requirements during acute illness/surgery increase. Therefore aggressive nutrition support becomes necessary to prevent catabolism which could be caused by poor oral intake or the stress of infection itself. Suggested nutrition protocol during illness:
In conclusion, immediate adequate energy and fluid intake become important during acute episodes.
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