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2007-2018 年全国健康访谈调查(NHIS)分析:研究美国镰状细胞病儿童的神经系统并发症。

Analysis of the 2007-2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States.

机构信息

Global Health Program, Department of Social and Behavioral Sciences, ISEE Lab, NYU School of Global Public Health, 708 Broadway, 4th FL, New York, NY 10003, USA.

Department of Biostatistics, NYU School of Global Public Health, 708 Broadway, New York, NY 10003, USA.

出版信息

Int J Environ Res Public Health. 2023 Jun 15;20(12):6137. doi: 10.3390/ijerph20126137.

Abstract

This study compared neurological complications among a national sample of United States children with or without sickle cell disease (SCD) and evaluated health status, healthcare and special education utilization patterns, barriers to care, and association of SCD status and demographics/socioeconomic status (SES) on comorbidities and healthcare utilization. Data was acquired from the National Health Interview Survey (NHIS) Sample Child Core questionnaire 2007-2018 dataset that included 133,542 children. An affirmation from the guardian of the child determined the presence of SCD. Regression analysis was used to compare the associations between SCD and demographics/SES on neurological conditions at < 0.05. Furthermore, adjusted odds ratios (AORs) were estimated for having various neurological conditions. Of the 133,481 children included in the NHIS, the mean age was 8.5 years (SD: 0.02) and 215 had SCD. Of the children with SCD, the sample composition included male ( = 110), and Black ( = 82%). The SCD sample had higher odds of having neuro-developmental conditions ( < 0.1). Families of Black children (55% weighted) reported household incomes < 100% of federal poverty level. Black children were more likely to experience longer wait times to see the doctor (AOR, 0.3; CI 0.1-1.1). Compared to children without SCD, those with SCD had a greater chance of seeing a medical specialist within 12 months (AOR 2.3; CI 1.5-3.7). This representative sample of US children with SCD shows higher odds of developing neurological complications, increased healthcare and special education services utilization, with Black children experiencing a disproportionate burden. This creates the urgency to address the health burden for children with SCD by implementing interventions in healthcare and increasing education assistance programs to combat neurocognitive impairments, especially among Black children.

摘要

这项研究比较了美国全国样本中患有或不患有镰状细胞病(SCD)的儿童的神经并发症,并评估了健康状况、医疗保健和特殊教育利用模式、护理障碍,以及 SCD 状况和人口统计学/社会经济地位(SES)对合并症和医疗保健利用的影响。数据来自 2007 年至 2018 年国家健康访谈调查(NHIS)样本儿童核心问卷数据集,其中包括 133,542 名儿童。儿童监护人的确认决定了 SCD 的存在。回归分析用于比较 SCD 与人口统计学/SES 对神经疾病的关联,差异具有统计学意义( < 0.05)。此外,还估计了患有各种神经疾病的调整优势比(AOR)。在纳入 NHIS 的 133,481 名儿童中,平均年龄为 8.5 岁(标准差:0.02),215 名患有 SCD。在患有 SCD 的儿童中,样本构成包括男性( = 110)和黑人( = 82%)。SCD 样本患有神经发育状况的几率更高( < 0.1)。黑人儿童的家庭(55%加权)报告家庭收入低于联邦贫困线的 100%。黑人儿童更有可能经历更长的就医等待时间(AOR,0.3;CI 0.1-1.1)。与没有 SCD 的儿童相比,患有 SCD 的儿童在 12 个月内看医生的机会更大(AOR 2.3;CI 1.5-3.7)。这项代表美国 SCD 儿童的样本显示,他们出现神经并发症的几率更高,利用医疗保健和特殊教育服务的几率更高,而黑人儿童的负担不成比例。这迫切需要通过在医疗保健中实施干预措施和增加教育援助计划来解决 SCD 儿童的健康负担,以对抗神经认知障碍,特别是在黑人儿童中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa4e/10298081/a2cf91aa4b89/ijerph-20-06137-g001.jpg

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