Mortalidad por fibrosis quística en Chile (1997-2003)

• Jaime Cerda L ^[1] ; Gonzalo Valdivia C ^[1] ; Ernesto Guiraldes C ^[1] ; Ignacio Sánchez D ^[1]
  1. [1] Pontificia Universidad Católica de Chile

     Pontificia Universidad Católica de Chile

     Santiago, Chile

     
• Localización: Revista Médica de Chile, ISSN-e 0034-9887, Vol. 136, Nº. 2, 2008, págs. 157-162
• Idioma: español
• Títulos paralelos:
  • Cystic fibrosis mortality in Chile between 1997 and 2003
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• Resumen

  • Cystic fibrosis (CF) is the most common lethal autosomic recessive disease among Caucasians. In Chile, its incidence is estimated in 1/4,000 newborns and it is possibly underestimated. Aim: To analyze CF mortality in Chile during the period 1997-2003. Material and methods: Demographic and CF mortality data reported by the National Institute of Statistics during the period 1997-2003 were recorded, according to sex and age. Overall mortality rate for each year was estimated, as well as the average mortality rate during the same period in patients younger than 1 year, 1-4 years, 5-9 years, 10-14 years and older than 15 years. Results: One hundred and three deaths (56 females) due to CF occurred during 1997-2003. Sixty-eight deaths corresponded to patients younger than 15years (66.0%). Overall mortality rate ranged from 0.82 to 1.33 per 10(6) inhabitants in 1997 and 1999, respectively. Average mortality rate ranged from 0.46 to 9.81 per ^inhabitants among patients older than 15 years and younger than 1 year, respectively. Conclusions: Most CF deaths occurred in the pediatric age group