Mortality from sickle cell disease in Brazil.

IF 2.5
PLOS global public health Pub Date : 2025-07-24 eCollection Date: 2025-01-01 DOI:10.1371/journal.pgph.0002066
Paula Fraiman Blatyta Caselli, Claudia Di Lorenzo Oliveira, Isabel Gomes, Tassila Salomon, Ester Cerdeira Sabino, Ligia Capuani, Dahra Teles Cruz, Claudia Maximo, Miriam Veronica Flor-Park, Rosimere Afonso Mota, Daniela de Oliveira Werneck Rodrigues, Carla Luana Dinardo, Cesar de Almeida Neto, Brian Custer, Shannon Kelly
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Abstract

Despite early diagnosis through neonatal screening and improved access to vaccines, antibiotics, and disease-modifying therapies, many individuals with sickle cell disease (SCD) die before age 60. This study evaluated causes and independent predictors of mortality in a Brazilian SCD population using data from the multicenter REDS-III cohort [2013-2018], which included six centers. Eligible patients were randomly enrolled during routine visits. Clinical and laboratory data were abstracted from medical records, and deaths were confirmed via chart review and linkage to the national death certificate database. Key variables were compared between deceased and surviving adults using Chi-square and Mann-Whitney tests. A multivariable Cox regression model identified independent predictors of mortality. Children were excluded from regression analysis due to low pediatric mortality. Among 2,793 participants, 1,558 (55.8%) were under 18. By the end of follow-up, 159 (5.7%) had died-142 adults and 17 children. Median life expectancy was 65.7 years. Infection was the leading cause of death (33.3%), followed by non-infectious pulmonary conditions (25.2%) and neurologic disease (14.5%). Cause of death was unknown in 3.1% of cases. In adults, independent predictors of mortality were older age [HR 1.03; 95% CI 1.01-1.04], iron overload [HR 1.68; 95% CI 1.09-2.60], and prior hospital admissions [HR 1.68; 95% CI 1.10-2.56]. The mortality burden in SCD is shifting toward adults, particularly in the third and fourth decades of life. Individuals with SCD in Brazil die about 10 years earlier than the general population. The main causes of death in our cohort were infections, acute chest syndrome and stroke, highlighting the need for prompt recognition and treatment of these complications. Screening and treatment for iron overload and closer monitoring and consideration of disease modifying therapies for patients with frequent hospital admissions are important as both were identified as independent predictors of mortality.

巴西镰状细胞病的死亡率。
尽管通过新生儿筛查进行早期诊断,并改善获得疫苗、抗生素和疾病改善疗法的机会,但许多镰状细胞病(SCD)患者在60岁之前死亡。本研究使用多中心red - iii队列[2013-2018]的数据评估了巴西SCD人群的死亡原因和独立预测因素,该队列包括6个中心。在常规访问中随机招募符合条件的患者。从医疗记录中提取临床和实验室数据,并通过图表审查和与国家死亡证明数据库的链接确认死亡。使用卡方检验和曼-惠特尼检验比较死亡和幸存成人的关键变量。多变量Cox回归模型确定了死亡率的独立预测因子。由于儿童死亡率低,儿童被排除在回归分析之外。在2793名参与者中,有1558名(55.8%)未满18岁。随访结束时,159人(5.7%)死亡,其中成人142人,儿童17人。平均预期寿命为65.7岁。感染是导致死亡的主要原因(33.3%),其次是非传染性肺部疾病(25.2%)和神经系统疾病(14.5%)。3.1%的病例死亡原因不明。成人死亡率的独立预测因子为年龄较大[HR 1.03;95% CI 1.01-1.04],铁超载[HR 1.68;95% CI 1.09-2.60]和既往住院情况[HR 1.68;95% ci 1.10-2.56]。SCD的死亡率负担正在向成年人转移,特别是在生命的第三和第四个十年。巴西SCD患者的死亡时间比一般人群早10年左右。在我们的队列中,主要死亡原因是感染、急性胸综合征和中风,这突出了及时识别和治疗这些并发症的必要性。筛选和治疗铁超载以及密切监测和考虑对频繁住院的患者进行疾病修饰治疗是重要的,因为两者都被确定为死亡率的独立预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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