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Argentinian clinical genomics in a leukodystrophies and genetic leukoencephalopathies cohort: Diagnostic yield in our first 9 years.阿根廷临床基因组学在白质营养不良症和遗传性脑白质病队列中的应用:我们前 9 年的诊断收益。
Ann Hum Genet. 2020 Jan;84(1):11-28. doi: 10.1111/ahg.12345. Epub 2019 Aug 16.
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A model for geographic and sociodemographic access to care disparities for adults with congenital heart disease.先天性心脏病成人患者在地理和社会人口学方面获得医疗服务差异的模型。
Congenit Heart Dis. 2019 Sep;14(5):752-759. doi: 10.1111/chd.12819. Epub 2019 Jul 30.
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Association of Diagnosis of Leukodystrophy With Race and Ethnicity Among Pediatric and Adolescent Patients.儿科和青少年患者的脑白质营养不良诊断与种族和民族的关联。
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Socioeconomic Mediators of Racial and Ethnic Disparities in Congenital Heart Disease Outcomes: A Population-Based Study in California.社会经济因素在先天性心脏病结局中的种族和民族差异的中介作用:加利福尼亚州的一项基于人群的研究。
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Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease.遗传诊断对先前未确诊疾病患者的影响。
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The BabySeq project: implementing genomic sequencing in newborns.婴儿测序项目:在新生儿中实施基因组测序
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Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy.脊髓性肌萎缩症的单剂量基因治疗。
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Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy.用于脑型肾上腺脑白质营养不良的造血干细胞基因治疗
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美国儿科脑白质营养不良诊断中的地理和专业差异

Geographic and Specialty Access Disparities in US Pediatric Leukodystrophy Diagnosis.

机构信息

Departments of Sociology, University of Utah, Salt Lake City, UT.

Department of Sociology & Anthropology. University of Texas at El Paso, El Paso, TX.

出版信息

J Pediatr. 2020 May;220:193-199. doi: 10.1016/j.jpeds.2020.01.063. Epub 2020 Mar 3.

DOI:10.1016/j.jpeds.2020.01.063
PMID:32143930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7186149/
Abstract

OBJECTIVE

To examine disparities in the diagnosis of leukodystrophies including geographic factors and access to specialty centers.

STUDY DESIGN

Retrospective cohort study of pediatric patients admitted to Pediatric Health Information System hospitals. Patients with leukodystrophy were identified with International Classification of Diseases, Tenth Revision, Clinical Modification diagnostic codes for any of 4 leukodystrophies (X-linked adrenoleukodystrophy, Hurler disease, Krabbe disease, and metachromatic leukodystrophy). We used 3-level hierarchical generalized logistic modeling to predict diagnosis of a leukodystrophy based on distance traveled for hospital, neighborhood composition, urban/rural context, and access to specialty center.

RESULTS

We identified 501 patients with leukodystrophy. Patients seen at a leukodystrophy center of excellence hospital were 1.73 times more likely to be diagnosed than patients at non-center of excellence hospitals. Patients who traveled farther were more likely to be diagnosed than those who traveled shorter. Patients living in a Health Professionals Shortage Area zip code were 0.86 times less likely to be diagnosed than those living in a non-Health Professionals Shortage Area zip code.

CONCLUSIONS

Geographic factors affect the diagnosis of leukodystrophies in pediatric patients, particularly in regard to access to a center with expertise in leukodystrophies. Our findings suggest a need for improving access to pediatric specialists and possibly deploying specialists or diagnostic testing more broadly.

摘要

目的

研究包括地理因素和获得专业中心机会在内的白质营养不良诊断方面的差异。

研究设计

儿科健康信息系统医院住院患儿的回顾性队列研究。通过国际疾病分类第 10 次修订临床修正版诊断代码,确定任何 4 种白质营养不良(X 连锁肾上腺脑白质营养不良、粘多糖贮积症 I 型、克雅氏病和异染性脑白质营养不良)的患者。我们使用 3 级分层广义逻辑模型,根据前往医院的距离、社区构成、城乡环境以及获得专业中心的机会,预测白质营养不良的诊断。

结果

我们确定了 501 名白质营养不良患者。在白质营养不良卓越中心医院就诊的患者被诊断为白质营养不良的可能性是在非卓越中心医院就诊的患者的 1.73 倍。前往较远医院就诊的患者比前往较近医院就诊的患者更有可能被诊断为白质营养不良。居住在卫生专业人员短缺地区邮政编码的患者被诊断为白质营养不良的可能性比居住在非卫生专业人员短缺地区邮政编码的患者低 0.86 倍。

结论

地理因素影响儿科患者白质营养不良的诊断,特别是在获得白质营养不良专业知识中心的机会方面。我们的研究结果表明,需要改善儿科专家的就诊机会,并可能更广泛地部署专家或诊断测试。