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Article
February 1975

Dietary Supplement and Nutrition in Children With Cystic Fibrosis

Author Affiliations

From the Children's Hospital (Drs. Kellogg and Ingberg, and Mss. Richter and Gutjahr); Children's Hospital Research Foundation (Mss. Berry and Hunt); and the Department of Pediatrics, University of Cincinnati College of Medicine (Mss. Berry and Hunt, and Drs. Kellogg and Ingberg).

Am J Dis Child. 1975;129(2):165-171. doi:10.1001/archpedi.1975.02120390009003
Abstract

Assessment of nutritional status of patients with cystic fibrosis of the pancreas (CFP) showed that poor growth was associated with low concentrations of albumin, urea nitrogen, and cholesterol in serum and with elevated white blood cell (WBC) counts. Patients with CFP maintained weight approximately 1 standard deviation below the mean until age 8 years, after which there was a progressive decline in growth rate compared to normal. A complete dietary supplement consisting of a beef serum hydrolysate, a glucose polymer, and medium-chain triglycerides was given to 15 patients for a year. Patients who received the diet showed significant gains in weight, significant increase in clinical score, significant increase in serum albumin level, and a significant drop in the WBC count compared to control patients who did not receive the supplement.

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