Association of Unmet Social Needs With Disease-Related Outcomes in Pediatric Patients With Sickle Cell Disease

IF 2.4 3区 医学 Q2 HEMATOLOGY Pediatric Blood & Cancer Pub Date : 2024-12-09 DOI:10.1002/pbc.31478
Molly Sonenklar, Sarah Marks, Cerelia Donald, Cecelia Valrie, Wally Smith, India Sisler
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Abstract

Background

Social determinants of health (SDoH) are socioeconomic factors that influence health and well-being, though when unmet can greatly contribute to health disparities. Individuals with sickle cell disease (SCD) are at increased risk of mortality, disability, and healthcare utilization. However, there are limited data linking specific social needs with disease outcomes in this population. Therefore, we sought to identify the unmet needs in one institution and their association with healthcare utilization.

Methods

Children with SCD and their guardians answered demographic and SDoH questionnaires during routine Sickle Cell Clinic appointments. We defined an unmet social need as any positive answer to the SDoH questionnaire. Disease outcome variables were electronic health record (EHR)-documented emergency department (ED) visits, hospitalizations, clinic appointment attendance, and guardian-reported acute SCD events in the previous year.

Results

A total of 114 parent–guardian dyads participated, with 103 having complete data to analyze. In all, 52% of subjects reported at least one unmet social need with food insecurity (36%), trouble paying utility bills (28%), and unemployment (16%) being the most prevalent. Subjects with at least one unmet need had two times the rate of ED visits and/or hospitalizations and were 1.15 times more likely to have an SCD event in the past year. However, only the association with ED visits was statistically significant (p = 0.03).

Conclusion

Over half of subjects reported at least one unmet need; the most common being reliable access to food, which has the potential to impact health outcomes of sickle cell patients. Furthermore, unmet social needs are linked to healthcare utilization and SCD-related complications, supporting routine screening for SDoH in this population.

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儿童镰状细胞病患者未满足的社会需求与疾病相关结局的关系
背景:健康的社会决定因素(SDoH)是影响健康和福祉的社会经济因素,但如果没有得到满足,可能会极大地造成健康差距。患有镰状细胞病(SCD)的个体在死亡、残疾和医疗保健利用的风险增加。然而,在这一人群中,将特定的社会需求与疾病结果联系起来的数据有限。因此,我们试图确定一个机构未满足的需求及其与医疗保健利用的关系。方法:SCD患儿及其监护人在镰状细胞门诊例行就诊时填写人口统计和SDoH问卷。我们将未满足的社会需求定义为对SDoH问卷的任何积极回答。疾病结局变量为电子健康记录(EHR)记录的急诊科(ED)就诊次数、住院次数、门诊预约出勤率和监护人报告的前一年急性SCD事件。结果:共114对家长-监护人参与调查,其中103对有完整数据可供分析。总的来说,52%的受试者报告至少有一种未满足的社会需求,其中食品不安全(36%)、支付水电费困难(28%)和失业(16%)是最普遍的。至少有一项需求未得到满足的受试者ED就诊和/或住院率是其两倍,在过去一年中发生SCD事件的可能性是其1.15倍。然而,只有与ED就诊有统计学意义(p = 0.03)。结论:超过一半的受试者报告至少有一项需求未得到满足;最常见的是获得食物的可靠途径,这有可能影响镰状细胞患者的健康结果。此外,未满足的社会需求与医疗保健利用和scd相关并发症有关,支持在该人群中进行SDoH常规筛查。
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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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