Literature DB >> 18715831

An international/multicentre report on patients with cystic fibrosis (CF) over the age of 40 years.

Margaret E Hodson1, Nicholas J Simmonds, Warren J Warwick, Elizabeth Tullis, Carlo Castellani, Baroukh Assael, John A Dodge, Mary Corey.   

Abstract

BACKGROUND: The lifespan of patients with cystic fibrosis (CF) is increasing significantly. The objective of this international pilot study was to study the characteristics of these long-term survivors.
METHODS: Four centres with large CF clinics from London (UK), Minneapolis (USA), Toronto (Canada) and Verona (Italy) identified 366 patients who had survived 40 years and longer.
RESULTS: At all centres males survived longer than females. There were more pancreatic sufficient patients in Verona (60%) and Toronto (40%) than in London (16%) and Minneapolis (21%). The percentage of DeltaF508 homozygous patients varied between 47% in London and 45% in Minneapolis to only 26% in Toronto and 9% in Verona. Average FEV(1) and BMI values of the surviving population appeared to stabilise after 40 years of age. FEV(1) was on average 12% higher in patients who were pancreatic sufficient (p > 0.0001). There was no difference in survival between the centres. The overall median survival after the age of 40 was 13 years. The estimated annual death rate was approximately 3.4% from the age of 40-60 years.
CONCLUSIONS: Significant numbers of patients are now surviving to 40 years or more, and it is hoped that an in-depth study of these patients may identify the factors contributing to longer survival.

Entities:  

Mesh:

Year:  2008        PMID: 18715831     DOI: 10.1016/j.jcf.2008.06.003

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  18 in total

1.  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

2.  Improving transition from paediatric to adult cystic fibrosis care: programme implementation and evaluation.

Authors:  Megumi J Okumura; Thida Ong; Diana Dawson; Dennis Nielson; Nancy Lewis; Martha Richards; Claire D Brindis; Mary Ellen Kleinhenz
Journal:  BMJ Qual Saf       Date:  2014-01-10       Impact factor: 7.035

3.  Analysis of the bacterial communities present in lungs of patients with cystic fibrosis from American and British centers.

Authors:  Franziska A Stressmann; Geraint B Rogers; Erich R Klem; Andrew K Lilley; Scott H Donaldson; Thomas W Daniels; Mary P Carroll; Nilesh Patel; Benjamin Forbes; Richard C Boucher; Matthew C Wolfgang; Kenneth D Bruce
Journal:  J Clin Microbiol       Date:  2010-11-10       Impact factor: 5.948

4.  Phenotypes of California CF Newborn Screen-Positive Children with CFTR 5T Allele by TG Repeat Length.

Authors:  Danieli Barino Salinas; Colleen Azen; Suzanne Young; Thomas G Keens; Martin Kharrazi; Richard B Parad
Journal:  Genet Test Mol Biomarkers       Date:  2016-07-22

Review 5.  Managing the underlying cause of cystic fibrosis: a future role for potentiators and correctors.

Authors:  Luis J V Galietta
Journal:  Paediatr Drugs       Date:  2013-10       Impact factor: 3.022

6.  Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007.

Authors:  P M George; W Banya; N Pareek; D Bilton; P Cullinan; M E Hodson; N J Simmonds
Journal:  BMJ       Date:  2011-02-28

7.  Comparison of Nutrition and Lung Function Outcomes in Patients with Cystic Fibrosis Living in Canada and the United States.

Authors:  Christopher H Goss; Jenna Sykes; Sanja Stanojevic; Bruce Marshall; Kristofer Petren; Josh Ostrenga; Aliza Fink; Alexander Elbert; Bradley S Quon; Anne L Stephenson
Journal:  Am J Respir Crit Care Med       Date:  2018-03-15       Impact factor: 30.528

8.  The adult cystic fibrosis airway microbiota is stable over time and infection type, and highly resilient to antibiotic treatment of exacerbations.

Authors:  Anthony A Fodor; Erich R Klem; Deirdre F Gilpin; J Stuart Elborn; Richard C Boucher; Michael M Tunney; Matthew C Wolfgang
Journal:  PLoS One       Date:  2012-09-26       Impact factor: 3.240

9.  Chronic disease management in children based on the five domains of health.

Authors:  Wing Lung Alvin So
Journal:  Case Rep Pediatr       Date:  2013-04-09

10.  Reference percentiles for FEV(1) and BMI in European children and adults with cystic fibrosis.

Authors:  Pierre-Yves Boëlle; Laura Viviani; Pierre-Francois Busson; Hanne V Olesen; Sophie Ravilly; Martin Stern; Baroukh M Assael; Celeste Barreto; Pavel Drevinek; Muriel Thomas; Uros Krivec; Meir Mei-Zahav; Jean-François Vibert; Annick Clement; Anil Mehta; Harriet Corvol
Journal:  Orphanet J Rare Dis       Date:  2012-09-07       Impact factor: 4.123

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