Socioeconomic differences in access to scoliosis care in the pediatric population.

IF 1.6 Q3 CLINICAL NEUROLOGY
Spine deformity Pub Date : 2024-11-01 Epub Date: 2024-06-19 DOI:10.1007/s43390-024-00912-0
Steven M Garcia, Kian Niknam, Faith Sumandea, Ishaan Swarup
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引用次数: 0

Abstract

Purpose: Adolescent idiopathic scoliosis (AIS) is a common spinal deformity affecting pediatric patients, with up to 10% requiring surgical intervention. Studies have shown disparities in these patients associated with race, ethnicity, and insurance type, but there is limited information on disparities that exist based on geographical parameters. In this study, we aim to explore the disparities in the care for AIS by looking at differences in the rates of readmission, infection, and revision between patients residing in rural and urban environments.

Methods: This is a retrospective cohort study utilizing the Pediatric Health Information System. Pediatric patients that underwent posterior spinal fusion (PSF) for AIS from October 2015 to July 2022 were included. Diagnoses and procedures were identified based on ICD-10 codes and internal tools built into the database. Descriptive statistics were used to summarize the data, including demographics, infection rates, readmission rates, and revision rates. T tests, Chi-squared tests, and logistic regression were used to assess differences between the rural and urban populations. We utilized STATA/SE 15.1 for all data analysis.

Results: 15,318 patients were included in the final cohort. Demographics and baseline characteristics were similar between the rural and urban patients, although more rural patients used Medicaid over commercial insurance (41.5% vs. 32.7%, p < 0.01), median household income was lower in rural patients (p < 0.01), and there was a higher proportion of Hispanic patients in the urban patient cohort (13.9% vs. 6.4%, p < 0.01). Complication rates were not significantly different between the urban and rural patient cohorts, although rural patients did have a significantly higher 90-day readmission rate (7.3% vs. 6.1%, p = 0.03) and higher rates of instrumentation removal (7.7% vs. 4.9%, p = 0.01).

Conclusions: The surgical outcomes between rural and urban pediatric AIS patients undergoing PSF are comparable, although 90-day readmission rates and rates of instrumentation removal were higher in rural patients. Insurance status is likely a significant driver for the differences observed in this study. Future research is needed to better understand the reasons for these differences and to develop strategies to improve outcomes.

Level of evidence: Retrospective cohort study, Level III.

小儿脊柱侧凸治疗的社会经济差异。
目的:青少年特发性脊柱侧凸(AIS)是影响儿童患者的一种常见脊柱畸形,高达 10% 的患者需要手术治疗。研究表明,这些患者的差异与种族、人种和保险类型有关,但基于地理参数的差异信息却很有限。在本研究中,我们旨在通过观察居住在农村和城市环境中的患者在再入院率、感染率和翻修率方面的差异,探讨 AIS 护理方面的差异:这是一项利用儿科健康信息系统进行的回顾性队列研究。研究纳入了2015年10月至2022年7月期间因AIS接受后路脊柱融合术(PSF)的儿科患者。根据 ICD-10 编码和数据库内置工具确定诊断和手术。描述性统计用于总结数据,包括人口统计学、感染率、再入院率和翻修率。我们使用 T 检验、卡方检验和逻辑回归来评估农村和城市人口之间的差异。我们使用 STATA/SE 15.1 进行所有数据分析:15,318 名患者被纳入最终队列。农村和城市患者的人口统计学特征和基线特征相似,但更多的农村患者使用医疗补助而非商业保险(41.5% 对 32.7%,P 结论:农村和城市儿童的手术结果存在差异:接受 PSF 治疗的农村和城市儿科 AIS 患者的手术效果相当,但农村患者的 90 天再入院率和器械拆除率较高。保险状况可能是造成本研究中观察到的差异的重要原因。未来的研究需要更好地了解这些差异的原因,并制定改善结果的策略:回顾性队列研究,III 级。
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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来源期刊
CiteScore
3.20
自引率
18.80%
发文量
167
期刊介绍: Spine Deformity the official journal of the?Scoliosis Research Society is a peer-refereed publication to disseminate knowledge on basic science and clinical research into the?etiology?biomechanics?treatment?methods and outcomes of all types of?spinal deformities. The international members of the Editorial Board provide a worldwide perspective for the journal's area of interest.The?journal?will enhance the mission of the Society which is to foster the optimal care of all patients with?spine?deformities worldwide. Articles published in?Spine Deformity?are Medline indexed in PubMed.? The journal publishes original articles in the form of clinical and basic research. Spine Deformity will only publish studies that have institutional review board (IRB) or similar ethics committee approval for human and animal studies and have strictly observed these guidelines. The minimum follow-up period for follow-up clinical studies is 24 months.
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