Literature DB >> 626067

Relative underweight in cystic fibrosis and its prognostic value.

R Kraemer, A Rüdeberg, B Hadorn, E Rossi.   

Abstract

On the basis of observations in 117 children with cystic fibrosis, seen from January 1956 to June 1976, it is demonstrated that the relative underweight (weight loss corrected for height) is most pronounced in children with predominantly pulmonary sypmtoms. The degree of underweight closely correlates inversely with survival. Because of its prognostic value, it is recommended that this clinical parameter be included in the checkups which are periodically carried out on children suffering from cystic fibrosis.

Entities:  

Mesh:

Year:  1978        PMID: 626067     DOI: 10.1111/j.1651-2227.1978.tb16273.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  54 in total

1.  Normal growth in cystic fibrosis associated with a specialised centre.

Authors:  C E Collins; L MacDonald-Wicks; S Rowe; E V O'Loughlin; R L Henry
Journal:  Arch Dis Child       Date:  1999-09       Impact factor: 3.791

Review 2.  Energy balance and growth in cystic fibrosis.

Authors:  S A Wootton; J L Murphy; S A Bond; J E Ellis; A A Jackson
Journal:  J R Soc Med       Date:  1991       Impact factor: 5.344

Review 3.  A rational approach to the nutritional care of patients with cystic fibrosis.

Authors:  P R Durie; P B Pencharz
Journal:  J R Soc Med       Date:  1989       Impact factor: 5.344

4.  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

5.  Bone mineral content in cystic fibrosis patients: correlation with fat-free mass.

Authors:  F Salamoni; M Roulet; F Gudinchet; M Pilet; D Thiébaud; P Burckhardt
Journal:  Arch Dis Child       Date:  1996-04       Impact factor: 3.791

6.  Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis.

Authors:  Huichuan J Lai; Suzanne M Shoff; Philip M Farrell
Journal:  Pediatrics       Date:  2009-02       Impact factor: 7.124

7.  A double blind lipase for lipase comparison of a high lipase and standard pancreatic enzyme preparation in cystic fibrosis.

Authors:  I M Bowler; S P Wolfe; H M Owens; T A Sheldon; J M Littlewood; M P Walters
Journal:  Arch Dis Child       Date:  1993-02       Impact factor: 3.791

8.  Gender differences in habitual activity in children with cystic fibrosis.

Authors:  H C Selvadurai; C J Blimkie; P J Cooper; C M Mellis; P P Van Asperen
Journal:  Arch Dis Child       Date:  2004-10       Impact factor: 3.791

9.  Clinical outcome in relation to care in centres specialising in cystic fibrosis: cross sectional study.

Authors:  R Mahadeva; K Webb; R C Westerbeek; N R Carroll; M E Dodd; D Bilton; D A Lomas
Journal:  BMJ       Date:  1998-06-13

10.  Increasing calorie consumption in children with cystic fibrosis: replication with 2-year follow-up.

Authors:  L J Stark; L G Knapp; A M Bowen; S W Powers; E Jelalian; S Evans; M A Passero; M M Mulvihill; M Hovell
Journal:  J Appl Behav Anal       Date:  1993
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.