Doses of Disparity: Gaps in the Management of Crohn’s Disease

IF 2.3 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Sean J.L. Parker BS, FA, Ryan A. Mitchell BS, Samrawit Zinabu MD, Miriam Michael MD
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引用次数: 0

Abstract

Introduction

Crohn’s Disease (CD) is a chronic inflammatory bowel disease commonly treated with biologics (e.g., infliximab, adalimumab), immunomodulators (e.g., azathioprine, methotrexate), aminosalicylates (e.g. mesalamine), corticosteroids or, when severe, surgical intervention. While studies suggest that African Americans have a lower incidence of CD than European Americans, the incidence of CD is on the rise among African American populations, with these patients often presenting with more severe disease at diagnosis. Socioeconomic barriers, provider bias, and healthcare disparities may contribute. This study examines whether African American patients are more or less likely to receive biologics or immunomodulators before surgery compared to European American patients.

Methods

We conducted a retrospective cohort study using the TriNetX Global Network, a de-identified electronic health record-based database, encompassing 33,802 patients from 140 healthcare organizations. CD patients were identified using International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) codes. Two cohorts were defined based on ethnic identification— European American and African American—and were matched 1:1 using propensity score matching for age, sex, comorbidities, literacy and socioeconomic factors. Baseline data were extracted from the 12 months preceding the index event, with the data spanning a period of 20 years. The primary outcomes were the proportions of patients prescribed traditional corticosteroids, aminosalicylates, immunomodulators, or biologics as determined by RxNorm codes. Group differences were evaluated using Z-tests and Kaplan–Meier survival analysis.

Results

After matching, each cohort comprised 33,802 patients with comparable demographics (mean age 40.5 ± 18.3 years; 58.4% female, 41.6% male). While African American patients had higher corticosteroid utilization when compared to European Americans (40.8% vs 37%), notable differences emerged in the other treatment modalities. African American patients had lower utilization rates of aminosalicylates (13.4% vs 14.3%) immunomodulators (8.9% vs 11.3%), and biologics (16.7% vs 17.8%). All the results were statistically significant.

Conclusion

.These findings reveal meaningful disparities in therapeutic treatment patterns of CD despite established guidelines for standard of care. The observed differences in non-surgical approaches may contribute to divergent long-term outcomes, potentially leading to higher rates of surgical intervention in African American patients. This illustrates the need for further studies to investigate whether these discrepancies lead to higher rates of surgical intervention in African American patients and underscores the importance of early pharmacological interventions to ensure equitable care across ethnic groups in the United States.
剂量差异:克罗恩病管理的差距
克罗恩病(CD)是一种慢性炎症性肠病,通常用生物制剂(如英夫利昔单抗、阿达木单抗)、免疫调节剂(如硫唑嘌呤、甲氨蝶呤)、氨基水杨酸盐(如美沙拉胺)、皮质类固醇或严重时的手术干预治疗。虽然研究表明非洲裔美国人的乳糜泻发病率低于欧洲裔美国人,但非洲裔美国人的乳糜泻发病率呈上升趋势,这些患者在诊断时往往表现出更严重的疾病。社会经济障碍、提供者偏见和医疗保健差异可能是原因之一。这项研究调查了非裔美国患者在手术前接受生物制剂或免疫调节剂的可能性比欧裔美国患者高还是低。方法我们使用TriNetX全球网络(一个基于去识别电子健康记录的数据库)进行了一项回顾性队列研究,包括来自140个医疗机构的33,802名患者。采用《国际疾病分类第十版临床修改》(ICD-10-CM)编码对CD患者进行鉴定。根据种族认同定义了两个队列——欧裔美国人和非裔美国人,并使用年龄、性别、合并症、识字和社会经济因素的倾向评分进行1:1匹配。基线数据是从指数事件发生前的12个月提取的,数据跨度为20年。主要结果是处方传统皮质类固醇、氨基水杨酸盐、免疫调节剂或生物制剂的患者比例,由RxNorm代码确定。采用z检验和Kaplan-Meier生存分析评估组间差异。结果匹配后,每个队列包括33,802例具有相似人口统计学特征的患者(平均年龄40.5±18.3岁,女性58.4%,男性41.6%)。虽然非裔美国患者的皮质类固醇使用率高于欧裔美国患者(40.8% vs 37%),但在其他治疗方式上出现了显著差异。非裔美国患者对氨基水杨酸盐(13.4% vs 14.3%)、免疫调节剂(8.9% vs 11.3%)和生物制剂(16.7% vs 17.8%)的使用率较低。结论:这些发现表明,尽管制定了标准治疗指南,但乳糜泻的治疗模式存在显著差异。观察到的非手术方法的差异可能导致不同的长期结果,可能导致非裔美国患者的手术干预率更高。这说明需要进一步的研究来调查这些差异是否导致非裔美国患者的手术干预率更高,并强调早期药物干预的重要性,以确保美国各种族群体的公平护理。
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来源期刊
CiteScore
4.80
自引率
3.00%
发文量
139
审稿时长
98 days
期刊介绍: Journal of the National Medical Association, the official journal of the National Medical Association, is a peer-reviewed publication whose purpose is to address medical care disparities of persons of African descent. The Journal of the National Medical Association is focused on specialized clinical research activities related to the health problems of African Americans and other minority groups. Special emphasis is placed on the application of medical science to improve the healthcare of underserved populations both in the United States and abroad. The Journal has the following objectives: (1) to expand the base of original peer-reviewed literature and the quality of that research on the topic of minority health; (2) to provide greater dissemination of this research; (3) to offer appropriate and timely recognition of the significant contributions of physicians who serve these populations; and (4) to promote engagement by member and non-member physicians in the overall goals and objectives of the National Medical Association.
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