Improving cystic fibrosis survival as a result of management in a specialized Center with 10-year follow-up
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Keywords

Cystic Fibrosis
Cystic Fibrosis Center
Survival
Mortality
Pneumonology
Epidemiology and Public Health
Survival Analysis

How to Cite

1.
Lentini N. E, López-Millán A, Lores L. AM, Pesciullesi B. MR, Ituarte R. LM, Viera C. TB. Improving cystic fibrosis survival as a result of management in a specialized Center with 10-year follow-up. Andes pediatr [Internet]. 2014 Jun. 6 [cited 2025 Oct. 22];85(3):281-7. Available from: https://andespediatrica.cl/index.php/rchped/article/view/3119

Abstract

Introduction: Cystic fibrosis (CF), the most common genetic disease among whites, is a multisystem disease that requires a coordinated multidisciplinary approach to get better results regarding survival and quality of life. This is why a Cystic Fibrosis Center (CFC) was held in Mendoza, Argentina, with the assumption that the organization and management of CF, according to international standards would improve survival. 

Patients and Method: 106 patients with CF have been evaluated since 1975 in this Center. Patients were grouped for follow-up monitoring as the 1999, 2002, 2005 and 2008 cohort studies. The chi-square test was used to compare survival rates and the nonparametric Mann-Whitney test was used to calculate the median age of the population. 

Results: In 2008, survival at 17 years old was 80% compared with 45% for the same age in 1999 (p < 0,001). The median age of the total CF population increased from 4 (1985) to 12 years old (2008) (p < 0,003). 

Conclusions: A multidisciplinary standardized approach of this condition in a CF Center can significantly increase survival.

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