AbstractBackgroundThe 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.MethodsFour centres with large CF clinics from London (UK), Minneapolis (USA), Toronto (Canada) and Verona (Italy) identified 366 patients who had survived 40years and longer.ResultsAt 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 ΔF508 homozygous patients varied between 47% in London and 45% in Minneapolis to only 26% in Toronto and 9% in Verona.Average FEV1 and BMI values of the surviving pop...
We evaluated a multivariable logistic regression model predicting 5-year survival derived from a 199...
This paper describes the Data Registry System of the Cystic Fibrosis Foundation. Through this system...
SUMMARY Life tables were calculated for 273 British children with cystic fibrosis for the period 197...
AbstractBackgroundThe lifespan of patients with cystic fibrosis (CF) is increasing significantly. Th...
SummaryBackgroundThe proportion of patients with cystic fibrosis (CF) who are middle-aged is increas...
AbstractBackgroundIt is unclear why cystic fibrosis (CF) survival has improved. We wished to quantif...
Background: It is unclear why cystic fibrosis (CF) survival has improved. We wished to quantify incr...
Background—The UK has published ob-served cohort survival figures for subjects with cystic fibrosis ...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
AbstractBackgroundComparing international estimates of survival can be a useful way of highlighting ...
tinue to extend survival. An updated estimate of survival is needed for better prognostication and t...
Cystic fibrosis (CF) is the one of the most common inherited diseases. It affects around 10,000 peop...
AbstractA total of 53 national cystic fibrosis (CF) patient registry studies published between July ...
Background and aims To specify the prevalence of patients diagnosed with CF at age of ≥60 year-old a...
Background: Median survival for cystic fibrosis (CF) patients in Europe is unknown and is likely to ...
We evaluated a multivariable logistic regression model predicting 5-year survival derived from a 199...
This paper describes the Data Registry System of the Cystic Fibrosis Foundation. Through this system...
SUMMARY Life tables were calculated for 273 British children with cystic fibrosis for the period 197...
AbstractBackgroundThe lifespan of patients with cystic fibrosis (CF) is increasing significantly. Th...
SummaryBackgroundThe proportion of patients with cystic fibrosis (CF) who are middle-aged is increas...
AbstractBackgroundIt is unclear why cystic fibrosis (CF) survival has improved. We wished to quantif...
Background: It is unclear why cystic fibrosis (CF) survival has improved. We wished to quantify incr...
Background—The UK has published ob-served cohort survival figures for subjects with cystic fibrosis ...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
AbstractBackgroundComparing international estimates of survival can be a useful way of highlighting ...
tinue to extend survival. An updated estimate of survival is needed for better prognostication and t...
Cystic fibrosis (CF) is the one of the most common inherited diseases. It affects around 10,000 peop...
AbstractA total of 53 national cystic fibrosis (CF) patient registry studies published between July ...
Background and aims To specify the prevalence of patients diagnosed with CF at age of ≥60 year-old a...
Background: Median survival for cystic fibrosis (CF) patients in Europe is unknown and is likely to ...
We evaluated a multivariable logistic regression model predicting 5-year survival derived from a 199...
This paper describes the Data Registry System of the Cystic Fibrosis Foundation. Through this system...
SUMMARY Life tables were calculated for 273 British children with cystic fibrosis for the period 197...