Literature DB >> 3115682

Improved exercise tolerance with long-term parenteral nutrition in cystic fibrosis.

B Skeie1, J Askanazi, M M Rothkopf, S H Rosenbaum, V Kvetan, E Ross.   

Abstract

Two cystic fibrosis (CF) patients with severe pulmonary disease and malnutrition were followed during a course of long-term home total parenteral nutrition (TPN), which included iv fat emulsion. They gained 7 and 12 kg in body weight, respectively, and their ability to participate in daily activities increased. Progressive exercise testing before and during TPN showed a marked increase in maximal work load: 100% and 30%, respectively. At any given work load, oxygen uptake was increased while the respiratory quotient remained lower after the course of TPN. We believe that the lower respiratory quotient and greater oxygen consumption during exercise were due to a reduction in anaerobic metabolism after TPN.

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Year:  1987        PMID: 3115682     DOI: 10.1097/00003246-198710000-00014

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  3 in total

1.  Percutaneous endoscopic gastrostomy feeding in patients with cystic fibrosis.

Authors:  S G Williams; F Ashworth; A McAlweenie; S Poole; M E Hodson; D Westaby
Journal:  Gut       Date:  1999-01       Impact factor: 23.059

Review 2.  Exercise recommendations for individuals with cystic fibrosis.

Authors:  S R Boas
Journal:  Sports Med       Date:  1997-07       Impact factor: 11.136

Review 3.  Growth hormone and exercise tolerance in patients with cystic fibrosis.

Authors:  Matthias Hütler; Ralph Beneke
Journal:  Sports Med       Date:  2004       Impact factor: 11.136

  3 in total

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