Disparities in cystic fibrosis survival in Mexico: Impact of socioeconomic status

被引:10
作者
Bustamante, Adriana E. [1 ]
Fernandez, Lucia T. [2 ]
Rivas, Lissette C. [1 ]
Mercado-Longoria, Roberto [1 ]
机构
[1] Hosp Univ Dr Jose E Gonzalez, Dept Pneumol, Monterrey, Nuevo Leon, Mexico
[2] Hosp Univ Dr Jose E Gonzalez, Dept Internal Med, Monterrey, Nuevo Leon, Mexico
关键词
disparities; low‐ income countries; median survival age;
D O I
10.1002/ppul.25351
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
引用
收藏
页码:1566 / 1572
页数:7
相关论文
共 36 条
  • [1] Association between socioeconomic status, sex, and age at death from cystic fibrosis in England and Wales (1959 to 2008): cross sectional study
    Barr, Helen L.
    Britton, John
    Smyth, Alan R.
    Fogarty, Andrew W.
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2011, 343
  • [2] Microbiology of Cystic Fibrosis Airway Disease
    Blanchard, Ana C.
    Waters, Valerie J.
    [J]. SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2019, 40 (06) : 727 - 736
  • [3] Disparities in cystic fibrosis survival in Mexico: Impact of socioeconomic status
    Bustamante, Adriana E.
    Fernandez, Lucia T.
    Rivas, Lissette C.
    Mercado-Longoria, Roberto
    [J]. PEDIATRIC PULMONOLOGY, 2021, 56 (06) : 1566 - 1572
  • [4] Bustamante AE, 2020, ACTA PEDIATR MEX, V41, P159
  • [5] Diabetes as a Determinant of Mortality in Cystic Fibrosis
    Chamnan, Parinya
    Shine, Brian S. F.
    Haworth, Charles S.
    Bilton, Diana
    Adler, Amanda I.
    [J]. DIABETES CARE, 2010, 33 (02) : 311 - 316
  • [6] Chávez-Saldaña M, 2010, REV INVEST CLIN, V62, P546
  • [7] Cystic Fibrosis Foundation, 2019, PATIENT REGISTRY ANN
  • [8] Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis
    Emerson, J
    Rosenfeld, M
    McNamara, S
    Ramsey, B
    Gibson, RL
    [J]. PEDIATRIC PULMONOLOGY, 2002, 34 (02) : 91 - 100
  • [9] Are Measures of Body Habitus Associated With Mortality in Cystic Fibrosis?
    Fogarty, Andrew W.
    Britton, John
    Clayton, Andy
    Smyth, Alan R.
    [J]. CHEST, 2012, 142 (03) : 712 - 717
  • [10] Dantés OG, 2011, SALUD PUBLICA MEXICO, V53, pS220