Literature DB >> 12162107

Monitoring early inflammation in CF. Infant pulmonary function testing.

Jack K Sharp1.   

Abstract

Infant pulmonary function tests (iPFTs) have primarily been used as research tools to further define physiologic pulmonary abnormalities in infants and young children with cystic fibrosis (CF). Methodologies used to measure pulmonary function in infants are described, with particular relevance to CF. A comprehensive review of studies and findings in CF infants using iPFTs is presented. Further goals in improving methodologies and in defining pulmonary disease in CF are presented.

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Year:  2002        PMID： 12162107     DOI： 10.1385/CRIAI:23:1:059

Source DB:  PubMed          Journal:  Clin Rev Allergy Immunol        ISSN： 1080-0549            Impact factor:   8.667


  54 in total

Review 1.  Methods of testing lung function in early childhood.

Authors:  C S Beardsmore
Journal:  Pediatr Allergy Immunol       Date:  1998       Impact factor: 6.377

2.  Bronchodilator responsiveness in infants and young children with cystic fibrosis.

Authors:  P Hiatt; H Eigen; P Yu; R S Tepper
Journal:  Am Rev Respir Dis       Date:  1988-01

3.  Effects of maternal smoking during pregnancy and a family history of asthma on respiratory function in newborn infants.

Authors:  S M Stick; P R Burton; L Gurrin; P D Sly; P N LeSouëf
Journal:  Lancet       Date:  1996-10-19       Impact factor: 79.321

4.  Total respiratory system compliance in asymptomatic infants with cystic fibrosis.

Authors:  R S Tepper; P W Hiatt; H Eigen; J Smith
Journal:  Am Rev Respir Dis       Date:  1987-05

Review 5.  Respiratory mechanics in infants: physiologic evaluation in health and disease. American Thoracic Society/European Respiratory Society.

Authors: 
Journal:  Am Rev Respir Dis       Date:  1993-02

6.  Improved detection of abnormal respiratory function using forced expiration from raised lung volume in infants with cystic fibrosis.

Authors:  D J Turner; C J Lanteri; P N LeSouef; P D Sly
Journal:  Eur Respir J       Date:  1994-11       Impact factor: 16.671

7.  Effects of viral lower respiratory tract infection on lung function in infants with cystic fibrosis.

Authors:  P W Hiatt; S C Grace; C A Kozinetz; S H Raboudi; D G Treece; L H Taber; P A Piedra
Journal:  Pediatrics       Date:  1999-03       Impact factor: 7.124

8.  Lung function and bronchial challenges in infants: repeatability of histamine and comparison with methacholine challenges.

Authors:  S M Stick; D J Turner; P N LeSouëf
Journal:  Pediatr Pulmonol       Date:  1993-09

9.  Serial lung function studies in cystic fibrosis in the first 5 years of life.

Authors:  S Godfrey; M Mearns; G Howlett
Journal:  Arch Dis Child       Date:  1978-01       Impact factor: 3.791

10.  Longitudinal evaluation of pulmonary function in infants and very young children with cystic fibrosis.

Authors:  R S Tepper; G L Montgomery; V Ackerman; H Eigen
Journal:  Pediatr Pulmonol       Date:  1993-08
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  2 in total

1.  The "Goldilocks effect" in cystic fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse.

Authors:  J Craig Cohen; Lennart K A Lundblad; Jason H T Bates; Michael Levitzky; Janet E Larson
Journal:  BMC Genet       Date:  2004-07-27       Impact factor: 2.797

2.  Glucocorticoids Distinctively Modulate the CFTR Channel with Possible Implications in Lung Development and Transition into Extrauterine Life.

Authors:  Mandy Laube; Miriam Bossmann; Ulrich H Thome
Journal:  PLoS One       Date:  2015-04-24       Impact factor: 3.240
  2 in total

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