B. Frederiksen et al., IMPROVED SURVIVAL IN THE DANISH CENTER-TREATED CYSTIC-FIBROSIS PATIENTS - RESULTS OF AGGRESSIVE TREATMENT, Pediatric pulmonology, 21(3), 1996, pp. 153-158
We report survival data for Danish center-treated cystic fibrosis (CF)
patients, covering the period 1974-1993 and using cross-sectional cum
ulative survival probability based on annual age-specific mortality ra
tes. Analyses by age and by years after diagnosis were made. No signif
icant differences were noted in the survival probability when patients
were grouped according to sex or absence/presence of meconium ileus.
The annual mortality rate for 1989-1993 was 0-1.2%. Using the age-spec
ific mortality rate for 1989-1993, we were unable to calculate the med
ian survival probability because the curve did not fall below 50% (age
up to 45 years); however, it was possible to show that the survival p
robability for a newborn CF child to reach his 45th birthday was 80.4%
(confidence interval 76.5-84.6%). The median age at diagnosis was 0.6
3 years with no sex difference. The probability of surviving 40 years
after the diagnosis of CF was made was 83.3% (confidence interval 80.1
-86.6%). This is considerably higher than any other published survival
probability. An early anti-Pseudomonas aeruginosa treatment regimen s
eemed important in achieving the observed improved survival. Pediatr P
ulmonol. 1996; 21:153-158. (C) 1996 Wiley-Liss, Inc.