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Disparities in cystic fibrosis survival in Mexico: Impact of socioeconomic status.
Bustamante, Adriana E; Fernández, Lucía T; Rivas, Lissette C; Mercado-Longoria, Roberto.
Affiliation
  • Bustamante AE; Pneumology Department, Hospital Universitario Dr. José E. González, Monterrey, Nuevo León, México.
  • Fernández LT; Internal Medicine Department, Hospital Universitario Dr. José E. González, Monterrey, Nuevo León, México.
  • Rivas LC; Pneumology Department, Hospital Universitario Dr. José E. González, Monterrey, Nuevo León, México.
  • Mercado-Longoria R; Pneumology Department, Hospital Universitario Dr. José E. González, Monterrey, Nuevo León, México.
Pediatr Pulmonol ; 56(6): 1566-1572, 2021 06.
Article in En | MEDLINE | ID: mdl-33656284
BACKGROUND: Median survival age in cystic fibrosis (CF) has increased in developed countries. Scarce literature exists about survival in Latin America, especially in Mexico. The aim of our study was to assess the median age of survival in CF patients and the impact of risk factors in Mexico over a 20-year period. METHODS: We conducted a retrospective study with all patients registered and followed in the CF Center in Monterrey, Mexico from 2000 to 2020. Median survival age was the primary outcome, assessed with Kaplan-Meier analysis. The influence of clinical, biological, and demographic factors on survival was analyzed with Cox regression model. RESULTS: Two-hundred five patients were included. Median survival for the cohort was 21.37 years (95% confidence interval [CI], 17.20-25.55). In the multivariate Cox regression model, low socioeconomic status (hazard ratio [HR], 4.21; 95% CI, 2.43-7.27), chronic Pseudomonas aeruginosa infection at 6 years (HR, 10.45; 95% CI, 5.66-19.28), and pancreatic insufficiency (HR, 3.13; 1.38-7.13) were independent risk factors for mortality. CONCLUSION: Median survival in Mexican patients with CF is lower than in high-income countries, and socioeconomic status plays a conspicuous role in the disparity. To increase patient survival for those residing in low-middle income countries, public health authorities must design policies that fully cover diagnosis and treatment strategies for the CF population.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Determinantes_sociais_saude Limits: Humans Country/Region as subject: Mexico Language: En Journal: Pediatr Pulmonol Journal subject: PEDIATRIA Year: 2021 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Determinantes_sociais_saude Limits: Humans Country/Region as subject: Mexico Language: En Journal: Pediatr Pulmonol Journal subject: PEDIATRIA Year: 2021 Document type: Article Country of publication: United States