P285 Lower residual fat malabsorption and improved growth in children with cystic fibrosis treated with a novel oral lipid technology supplement

2020 ◽  
Vol 19 ◽  
pp. S135-S136
Author(s):  
V. Stallings ◽  
A. Tindall ◽  
A. Maqbool ◽  
M. Mascarenhas ◽  
J. Schall
2011 ◽  
Vol 10 (3) ◽  
pp. 150-158 ◽  
Author(s):  
M. Wouthuyzen-Bakker ◽  
F.A.J.A. Bodewes ◽  
H.J. Verkade

PEDIATRICS ◽  
1971 ◽  
Vol 48 (3) ◽  
pp. 483-487
Author(s):  
Lloyd J. Filer ◽  
Lewis A. Barness ◽  
Richard B. Goldbloom ◽  
Malcolm A. Holliday ◽  
Robert Miller ◽  
...  

Certain milk substitute infant formulas, particularly meat-based and casein hydrolysate based formulas, may be low in vitamin K content in relation to the needs of the infants receiving them. Studies are reviewed of a few infants in which inadequate dietary supply of vitamin K from such sources may have been one factor in the development of hypoprothrombinemia, though this could not be established with certainty. On theoretical grounds it seems reasonable to increase the level of vitamin K1 in milk substitute formulas to 100 µg/l, particularly because these products are often used in treatment of clinical conditions which are associated with diminished absorption of this vitamin. Vitamin K1 (phylloquinone) would seem the most appropriate form to be used for supplementation of formulas. In clinical situations associated with malabsorption of fat, e.g., cystic fibrosis of the pancreas or biliary atresia, and prolonged diarrhea or starvation, vitamin K supplementation of feedings or periodic parenteral administration of vitamin K is recommended. When parenteral vitamin K is necessary, intravenous administration is rarely indicated. Subcutaneous or intramuscular injection is preferred.


1999 ◽  
Vol 70 (5) ◽  
pp. 943-944 ◽  
Author(s):  
Jane Murphy ◽  
Kirsi Laiho ◽  
Steve Wootton

Gut ◽  
1986 ◽  
Vol 27 (9) ◽  
pp. 1043-1048 ◽  
Author(s):  
Z Weizman ◽  
P R Durie ◽  
H R Kopelman ◽  
S M Vesely ◽  
G G Forstner

2004 ◽  
Vol 19 (4) ◽  
pp. 448-453 ◽  
Author(s):  
MARC A RITZ ◽  
ROBERT J FRASER ◽  
ADDOLORATA C DI MATTEO ◽  
HUGH GREVILLE ◽  
ROSS BUTLER ◽  
...  

2017 ◽  
Vol 18 (1-2) ◽  
pp. 11
Author(s):  
Suharjono Suharjono ◽  
Sunoto Sunoto ◽  
Aswitha Budiarso ◽  
Titut S. Pusponegoro ◽  
W.A.F.J. Tumbelaka

I. Problems of malabsorption syndrome in developing countries like lndonesia are associated especially with :(1) Protein Calorie Malnutrition(2) Low Birth Weight(3) Gastroenteritis(4) Post bowel surgery(5) Being unused to drink milk after weaning.They show a big difference with those in developed countries where they usually are correlated with a.o. coeliac disease, cystic fibrosis, etc.II. Solving the problems :a. Since in diarrhoeal patients, with or without PCM, sugar intolerance and or fat malabsorption usually occur, a formula consisting of low or freelactose with easily absorbable fats i.e. MCT or UFA, might be the best solution as a refeeding regimen.b. Besides treating the malabsorption syndrome, other measures are much more important i.e correction of fluid and electrolyte imbalance and treatment of predisposing condition.


2021 ◽  
Vol 8 ◽  
Author(s):  
Andrea M. Coverstone ◽  
Thomas W. Ferkol

Cystic fibrosis is the most common life-shortening genetic disease affecting Caucasians, clinically manifested by fat malabsorption, poor growth and nutrition, and recurrent sinopulmonary infections. Newborn screening programs for cystic fibrosis are now implemented throughout the United States and in many nations worldwide. Early diagnosis and interventions have led to improved clinical outcomes for people with cystic fibrosis. Newer cystic fibrosis transmembrane conductance regulator potentiators and correctors with mutation-specific effects have increasingly been used in children, and these agents are revolutionizing care. Indeed, it is possible that highly effective modulator therapy used early in life could profoundly affect the trajectory of cystic fibrosis lung disease, and primary prevention may be achievable.


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