Literature DB >> 12006958

Effects of megestrol acetate on weight gain, body composition, and pulmonary function in patients with cystic fibrosis.

Valerie Eubanks1, Nicki Koppersmith, Nancy Wooldridge, J P Clancy, Raymond Lyrene, Ramin B Arani, Jeanette Lee, Lyle Moldawer, Joy Atchison, Eric J Sorscher, Christopher M Makris.   

Abstract

OBJECTIVES: Malnutrition is a negative prognostic indicator in patients with cystic fibrosis (CF) and may accentuate pulmonary decline. We tested whether megestrol acetate would have beneficial effects on growth in patients with CF and pancreatic insufficiency. STUDY
DESIGN: We performed a randomized, double-blind, placebo controlled study. All patients were taking replacement enzymes to compensate for pancreatic insufficiency. Patients (n = 17) were randomly assigned to receive either megestrol acetate or placebo.
RESULTS: The treatment group had a significant increase in weight-for-age z scores compared with placebo and reached 100% of their ideal body weight within 3 months of initiating therapy. Weight gain included both fat and fat-free mass. Improved pulmonary function (forced vital capacity and forced expiratory volume in 1 second) was noted in the treatment group compared with placebo (P <.04). Reversible adrenal suppression was observed in the majority of patients who received megestrol acetate.
CONCLUSIONS: Short-term use of megestrol acetate results in significant weight gain and improved pulmonary function in malnourished subjects with CF. Our study provides a controlled basis for this intervention, identifies important side effects, and provides the foundation for multiyear, longitudinal trials in a larger number of patients with CF.

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Year:  2002        PMID: 12006958     DOI: 10.1067/mpd.2002.121936

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  8 in total

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  8 in total

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