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墨西哥囊性纤维化存活率的差异:社会经济地位的影响。

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

机构信息

Pneumology Department, Hospital Universitario Dr. José E. González, Monterrey, Nuevo León, México.

Internal Medicine Department, Hospital Universitario Dr. José E. González, Monterrey, Nuevo León, México.

出版信息

Pediatr Pulmonol. 2021 Jun;56(6):1566-1572. doi: 10.1002/ppul.25351. Epub 2021 Mar 13.

Abstract

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.

摘要

背景

在发达国家,囊性纤维化(CF)患者的中位生存年龄有所增加。关于拉丁美洲,尤其是墨西哥的生存情况,文献记载甚少。我们的研究旨在评估墨西哥 CF 患者 20 年来的中位生存年龄以及危险因素的影响。

方法

我们进行了一项回顾性研究,纳入了 2000 年至 2020 年在墨西哥蒙特雷 CF 中心登记和随访的所有患者。使用 Kaplan-Meier 分析评估中位生存年龄作为主要结局。使用 Cox 回归模型分析临床、生物学和人口统计学因素对生存的影响。

结果

共纳入 205 例患者。该队列的中位生存时间为 21.37 年(95%置信区间 [CI],17.20-25.55)。在多变量 Cox 回归模型中,低社会经济地位(危险比 [HR],4.21;95%CI,2.43-7.27)、6 岁时慢性铜绿假单胞菌感染(HR,10.45;95%CI,5.66-19.28)和胰腺功能不全(HR,3.13;95%CI,1.38-7.13)是死亡的独立危险因素。

结论

墨西哥 CF 患者的中位生存时间低于高收入国家,社会经济地位在差异中起着显著作用。为了提高中低收入国家患者的生存,公共卫生当局必须制定全面涵盖 CF 人群诊断和治疗策略的政策。

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