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Risk of persistent growth impairment after alternate-day prednisone treatment in children with cystic fibrosis

Article Abstract:

Boys who received prednisone to treat some complications of cystic fibrosis may be shorter than normal as adults. This was the conclusion of a study that followed 224 children with cystic fibrosis, 151 of whom had taken prednisone to treat lung disease but had stopped six or seven years prior to the study. By the time of the study, 68% were 18 years old or older. Catch-up growth began two years after the drug was stopped, but boys who had taken prednisone were still shorter than boys who had not. Girls were not affected by the drug as much as boys.

Author: Lai, Hui-Chuan, FitzSimmons, Stacey C., Allen, David B., Kosorok, Michael R., Rosenstein, Beryl J., Campbell, Preston W., Farrell, Philip M.
Publisher: Massachusetts Medical Society
Publication Name: The New England Journal of Medicine
Subject: Health
ISSN: 0028-4793
Year: 2000
Causes of, Complications and side effects, Drug therapy, Growth disorders, Prednisone

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Nutritional benefits of neonatal screening for cystic fibrosis

Article Abstract:

Testing newborn infants for cystic fibrosis may identify affected babies early and allow them to be treated to prevent any nutritional deficiencies. At one hospital, 650,341 newborn infants were tested between 1985 and 1994, which resulted in 56 infants being diagnosed with cystic fibrosis at an average age of 12 weeks. Their nutritional outcome was compared to 40 children who were diagnosed at an average age of 72 weeks. The early-diagnosis group was longer and heavier than the late-diagnosis group both at the time of diagnosis and 10 years later.

Author: Kosorok, Michael R., Farrell, Philip M., Laxova, Anita, Mischler, Elaine H., Splaingard, Mark, Shen, Guanghong, Koscik, Rebecca E., Bruns, W. Theodore
Publisher: Massachusetts Medical Society
Publication Name: The New England Journal of Medicine
Subject: Health
ISSN: 0028-4793
Year: 1997
Evaluation, Food and nutrition, Infants (Newborn), Newborn infants, Medical screening, Health screening

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Longitudinal development of mucoid pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis

Article Abstract:

A study is conducted to investigate the epidemiology of Pseudomonas aeruginosa infection and its impact on cystic fibrosis (CF) pulmonary morbidity. The conclusion suggests that early prevention and detection of nonmucoid and mucoid P aeruginosa are critical because of early acquisition and prevalence.

Author: Kosorok, Michael R., Farrell, Philip M., Laxova, Anita, Zhanhai Li, West, Susan E. H., Splaingard, Mark L., Rock, Michael J., Collins, Jannette, Green, Christopher G.
Publisher: American Medical Association
Publication Name: JAMA, The Journal of the American Medical Association
Subject: Health
ISSN: 0098-7484
Year: 2005
United States, Research and Development in the Physical, Engineering, and Life Sciences, Research and Testing Services, Medical Research, Epilepsy & Muscle Disease R&D, Administration of Public Health Programs, Health Research Programs, Risk factors, Pseudomonas aeruginosa infections, Medicine, Experimental

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Subjects list: Cystic fibrosis, Diagnosis
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