Literature DB >> 10451398

Normal growth in cystic fibrosis associated with a specialised centre.

C E Collins1, L MacDonald-Wicks, S Rowe, E V O'Loughlin, R L Henry.   

Abstract

OBJECTIVE: To assess the impact of lifetime continuous care within the John Hunter Hospital cystic fibrosis (CF) clinics on growth and lung function.
DESIGN: A cross sectional survey of variables affecting nutritional status in CF was undertaken for 1993 and 1997. Data were retrieved from medical records and grouped into 5 year age bands. MAIN OUTCOME MEASURES: Change in height z-score, weight centile, and forced expiratory volume in one second (FEV(1)) between patient cohorts receiving specialised care for different lengths of time.
RESULTS: Improved mean height z-score (-0.880 v -0.047) and weight centile (28.3% v 48.1%) for the 10-15 year age group in 1997, who had received continuous lifetime care within the clinic, compared with the same age group in 1993, for whom continuous medical care started at an older age. There was no corresponding improvement in FEV(1), as an indicator of lung function, in this group (81.6% predicted v 89.5% predicted).
CONCLUSIONS: This study suggests that lifetime continuous care within a specialised CF centre is associated with improved growth but not improved lung function.

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Mesh:

Year:  1999        PMID: 10451398      PMCID: PMC1718083          DOI: 10.1136/adc.81.3.241

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  19 in total

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Journal:  J Pediatr       Date:  1982-06       Impact factor: 4.406

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  8 in total

Review 1.  Growth and growth charts in cystic fibrosis.

Authors:  Leena Patel; Moira Dixon; T J David
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Review 2.  Shared care--is it worth it for the patient?

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3.  TNF-alpha polymorphisms as a potential modifier gene in the cystic fibrosis.

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4.  Effects of gender and age at diagnosis on disease progression in long-term survivors of cystic fibrosis.

Authors:  Jerry A Nick; Cathy S Chacon; Sara J Brayshaw; Marion C Jones; Christine M Barboa; Connie G St Clair; Robert L Young; David P Nichols; Jennifer S Janssen; Gwen A Huitt; Michael D Iseman; Charles L Daley; Jennifer L Taylor-Cousar; Frank J Accurso; Milene T Saavedra; Marci K Sontag
Journal:  Am J Respir Crit Care Med       Date:  2010-05-06       Impact factor: 21.405

5.  Association between socioeconomic status, sex, and age at death from cystic fibrosis in England and Wales (1959 to 2008): cross sectional study.

Authors:  Helen L Barr; John Britton; Alan R Smyth; Andrew W Fogarty
Journal:  BMJ       Date:  2011-08-23

6.  A cross-sectional study of growth, nutritional status and body proportions in children and adolescents at a medical center specializing in the treatment of cystic fibrosis in Poland.

Authors:  Dorota Sands; Wioleta Umławska; Anna Zielińska
Journal:  Arch Med Sci       Date:  2015-03-14       Impact factor: 3.318

7.  Do children with cystic fibrosis receiving outreach care have poorer clinical outcomes than those treated at a specialist cystic fibrosis centre?

Authors:  Heinrich C Weber; Philip F Robinson; Nicole Saxby; Sean A Beggs; Ingrid Els; Rodney I Ehrlich
Journal:  Aust J Rural Health       Date:  2016-11-17       Impact factor: 1.662

8.  The Effect of Timing of Mandibular Distraction Osteogenesis on Weight Velocity in Infants Affected by Severe Robin Sequence.

Authors:  Zhe Mao; Ricardo Battaglino; Jiawei Zhou; Yingqiu Cui; Mayank Shrivastava; Gabriel Tian; Faezeh Sahebdel; Liang Ye
Journal:  Children (Basel)       Date:  2022-02-28
  8 in total

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