School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Department of Pediatrics, Children's Hospital of Richmond, Virginia Commonwealth University, Richmond, Virginia, USA.
Pediatr Pulmonol. 2021 May;56(5):883-890. doi: 10.1002/ppul.25192. Epub 2020 Dec 14.
Differences in socioenvironmental exposures influence overall child health, but their association with pediatric cystic fibrosis (CF) outcomes is less clear. This observational study investigated the relationship between area-level socioeconomic deprivation, state child health, and CF respiratory outcomes in a national cohort.
We assessed relationships between the 2015 area deprivation index, a composite measure of socioeconomic disadvantage; the 2016 child health index, a state-specific measure of overall child health; and CF respiratory outcomes in the 2016 CF Foundation Patient Registry.
The sample included 9934 individuals with CF, aged 6-18 years. In multiple regression analysis adjusted for demographic and clinical covariates, those residing in the worst tertile for area deprivation had 2.8% lower percent predicted forced expiratory volume in 1 s (ppFEV ; 95% confidence interval [CI]: -4.1 to -1.5), 1.2 more intravenous (IV) treatment nights (CI: 0.1-2.4), and 20% higher odds of ≥2 pulmonary exacerbations (odds ratio [OR]: 1.2, CI: 1.0-1.5) than best-tertile counterparts. Children with CF in states at the worst tertile for child health had 2.3% lower ppFEV (CI: -4.5 to -0.2), 2.2 more IV treatment nights (CI: 0.5-3.6), and 40% higher odds of ≥2 exacerbations (OR: 1.4, CI: 1.1-1.8) than best-tertile counterparts. State child health accounted for the association between area deprivation and multiple exacerbations and more IV treatment nights.
Both area socioeconomic characteristics and state child health play a role in pediatric CF outcomes. The residual association of the state child health with CF outcomes after controlling for area deprivation reflects the ability of state programs to mitigate the effect of poverty.
社会环境暴露的差异会影响儿童的整体健康,但它们与儿科囊性纤维化 (CF) 结局的关系尚不清楚。本观察性研究调查了全国队列中地区社会经济贫困程度、州儿童健康状况与 CF 呼吸系统结局之间的关系。
我们评估了 2015 年地区贫困指数(一种社会经济劣势综合衡量指标)与 2016 年儿童健康指数(一种特定于州的儿童整体健康衡量指标)之间的关系,以及 2016 年 CF 基金会患者登记处的 CF 呼吸系统结局。
样本包括 9934 名年龄在 6-18 岁的 CF 患者。在调整人口统计学和临床协变量的多元回归分析中,那些居住在地区贫困程度最差三分位的患者的预计用力呼气量百分比(ppFEV)低 2.8%(95%置信区间[CI]:-4.1 至-1.5),静脉(IV)治疗夜数多 1.2 个(CI:0.1-2.4),且发生≥2 次肺部恶化的几率高 20%(比值比[OR]:1.2,CI:1.0-1.5)。在儿童健康状况最差三分位的州的 CF 患儿的 ppFEV 低 2.3%(CI:-4.5 至-0.2),IV 治疗夜数多 2.2 个(CI:0.5-3.6),且发生≥2 次恶化的几率高 40%(OR:1.4,CI:1.1-1.8)。州儿童健康状况解释了地区贫困与多次恶化和更多 IV 治疗夜数之间的关联。
地区社会经济特征和州儿童健康状况都对儿科 CF 结局有影响。在控制地区贫困程度后,州儿童健康状况与 CF 结局之间的残余关联反映了州计划减轻贫困影响的能力。