Effects of Social Determinants of Health on Clinical Outcomes in Pediatric Cystic Fibrosis Patients

Jinan Ayub, Mary De Laosa, Sarah Bilinski, James F. Chmiel, Don B. Sanders
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Abstract

Background and Objective:  Advances in the treatment of cystic fibrosis (CF) with cystic fibrosis transmembrane regulator modulators have improved morbidity and mortality, however, clinical outcomes vary among genetically similar patients due to contributions of social determinants of health (SDOH). Pancreatic insufficiency, CF-related diabetes (CFRD), Pseudomonas infections, and lower BMI increase risk of severe lung disease, measured by forced expiratory volume in 1 second (FEV1). This project aims to identify socially vulnerable patients and evaluate the impact of SDOH on clinical outcomes.  Methods:  From January to July 2023, SDOH screeners were distributed to families of children with CF at Riley Hospital for Children, documenting transportation, housing, food insecurity, insurance, and medication costs. Clinical outcomes for each patient including FEV1% predicted, BMI/WFL percentile, CFRD, hospitalizations, respiratory infections with Pseudomonas aeruginosa, and pancreatic insufficiency within the past 12 months were recorded. Patients were categorized by SDOH vulnerability, and associations with poor clinical outcomes were analyzed using the Chi-squared test of independence.  Results:  A total of 193 screeners were analyzed: males represented 52.6% of the cohort, 2.60% identified as non-white race, and 3.65% reported Hispanic ethnicity. Overall, 51.8% screened positive for at least one SDOH (SDOH+) and 48.1% screened negative (SDOH-). The average FEV1% predicted decline among SDOH+ patients was 5.79% and 3.51% among SDOH- patients. SDOH+ patients were more likely to have at least a 5% decline in FEV1% predicted (p=0.037) and to be hospitalized due to exacerbations of CF lung disease at least once in the past 12 months (p=0.030). Although low BMI percentile, Pseudomonas infection, and CFRD were not significantly associated with SDOH, socially vulnerable patients demonstrated higher rates of these clinical outcomes.  Conclusion and Clinical Implications:  SDOH impact CF clinical outcomes. Screeners are effective in identifying socially vulnerable patients and serve as the first step in addressing unmet social needs. 
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健康的社会决定因素对小儿囊性纤维化患者临床结果的影响
背景和目的: 使用囊性纤维化跨膜调节器调节剂治疗囊性纤维化(CF)的进展改善了发病率和死亡率,然而,由于健康的社会决定因素(SDOH)的影响,基因相似的患者的临床结果各不相同。胰腺功能不全、CF 相关糖尿病(CFRD)、假单胞菌感染和较低的体重指数(BMI)会增加严重肺部疾病的风险(以 1 秒用力呼气容积(FEV1)衡量)。本项目旨在确定社会弱势患者,并评估 SDOH 对临床结果的影响。 方法: 从 2023 年 1 月到 7 月,向莱利儿童医院的 CF 患儿家庭发放 SDOH 筛查表,记录交通、住房、食品不安全、保险和药物费用。记录了每位患者的临床结果,包括预测 FEV1%、BMI/WFL 百分位数、CFRD、住院治疗、铜绿假单胞菌呼吸道感染以及过去 12 个月内的胰腺功能不全。根据 SDOH 易感性对患者进行分类,并使用卡方检验分析其与不良临床结果的关系。 结果 共对 193 名筛查者进行了分析:其中男性占 52.6%,2.60% 为非白人,3.65% 为西班牙裔。总体而言,51.8%的筛查者对至少一项 SDOH(SDOH+)呈阳性,48.1%的筛查者对一项 SDOH(SDOH-)呈阴性。SDOH+患者的平均预测 FEV1% 下降率为 5.79%,SDOH-患者的平均预测 FEV1% 下降率为 3.51%。SDOH+ 患者的 FEV1% 预测值至少下降 5%(P=0.037),且在过去 12 个月中至少因 CF 肺病加重住院一次(P=0.030)的可能性更大。虽然低体重指数百分位数、假单胞菌感染和 CFRD 与 SDOH 无显著相关性,但社会弱势患者出现这些临床结果的比例更高。 结论和临床意义: SDOH 对 CF 临床结果有影响。筛查人员可有效识别社会弱势患者,并作为解决未满足的社会需求的第一步。
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