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本文引用的文献

1
Estimates of the excess cost burden of Ehlers-Danlos syndromes: a United States MarketScan® claims database analysis.估计埃勒斯-当洛斯综合征的超额成本负担:美国 MarketScan®索赔数据库分析。
Front Public Health. 2024 Jul 3;12:1365712. doi: 10.3389/fpubh.2024.1365712. eCollection 2024.
2
Phenotypic Clusters and Multimorbidity in Hypermobile Ehlers-Danlos Syndrome.可弯曲性埃勒斯-当洛综合征的表型聚类与共病现象
Mayo Clin Proc Innov Qual Outcomes. 2024 May 15;8(3):253-262. doi: 10.1016/j.mayocpiqo.2024.04.001. eCollection 2024 Jun.
3
The Impact of Chronic Diseases on Mental Health: An Overview and Recommendations for Care Programs.慢性病对心理健康的影响:护理方案概述与建议。
Curr Psychiatry Rep. 2024 Jul;26(7):394-404. doi: 10.1007/s11920-024-01510-7. Epub 2024 May 20.
4
Looking back and beyond the 2017 diagnostic criteria for hypermobile Ehlers-Danlos syndrome: A retrospective cross-sectional study from an Italian reference center.回顾和超越 2017 年的弹性过度综合征诊断标准:来自意大利参考中心的回顾性横断面研究。
Am J Med Genet A. 2024 Feb;194(2):174-194. doi: 10.1002/ajmg.a.63426. Epub 2023 Sep 29.
5
The psychological burden associated with Ehlers-Danlos syndromes: a systematic review.Ehlers-Danlos 综合征相关的心理负担:系统评价。
J Osteopath Med. 2022 Apr 14;122(8):381-392. doi: 10.1515/jom-2021-0267.
6
The national economic burden of rare disease in the United States in 2019.2019 年美国罕见病的国家经济负担。
Orphanet J Rare Dis. 2022 Apr 12;17(1):163. doi: 10.1186/s13023-022-02299-5.
7
Patients with Ehlers-Danlos syndrome on the diagnostic odyssey: Rethinking complexity and difficulty as a hero's journey.患有埃勒斯-当洛斯综合征的患者在诊断的探索之旅中:重新思考复杂性和困难,将其视为英雄的旅程。
Am J Med Genet C Semin Med Genet. 2021 Dec;187(4):416-424. doi: 10.1002/ajmg.c.31935. Epub 2021 Sep 15.
8
Are patients with hypermobile Ehlers-Danlos syndrome or hypermobility spectrum disorder so different?患有可活动型埃勒斯-当洛斯综合征或高活动度谱系障碍的患者有那么大的不同吗?
Rheumatol Int. 2021 Oct;41(10):1785-1794. doi: 10.1007/s00296-021-04968-3. Epub 2021 Aug 16.
9
Ending the Diagnostic Odyssey-Is Whole-Genome Sequencing the Answer?终结诊断之旅——全基因组测序是答案吗?
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Diagnosed prevalence of Ehlers-Danlos syndrome and hypermobility spectrum disorder in Wales, UK: a national electronic cohort study and case-control comparison.英国威尔士埃勒斯-丹洛斯综合征和关节活动过度谱系障碍的诊断患病率:一项全国性电子队列研究及病例对照比较
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2022年埃勒斯-丹洛斯综合征对美国患者的经济影响。

The Financial Impact of Ehlers-Danlos Syndromes on Patients in the United States in 2022.

作者信息

Schubart Jane R, Schaefer Eric W, Mills Susan E, Knight Dacre R T, Shen Chan, Francomano Clair A

机构信息

Department of Surgery, Penn State College of Medicine, Hershey, PA.

Department of Public Health Sciences, Penn State College of Medicine, Hershey, PA.

出版信息

Mayo Clin Proc Innov Qual Outcomes. 2024 Dec 14;9(1):100586. doi: 10.1016/j.mayocpiqo.2024.11.003. eCollection 2025 Feb.

DOI:10.1016/j.mayocpiqo.2024.11.003
PMID:39790860
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11713486/
Abstract

OBJECTIVE

To determine the financial impact of Ehlers-Danlos syndromes (EDS) on patients in the United States by examining the medical expenses incurred by patients.

PATIENTS AND METHODS

We used a convenience sample approach and disseminated a self-reported survey questionnaire to individuals with EDS via patient advocacy organizations and support groups across the country, social media, and health professionals from April 1, 2023, to December 31, 2023. The survey focused on the out-of-pocket medical expenses incurred by patients.

RESULTS

The final analytic data set included 884 responses. Responses were received from individuals in all 50 states and the District of Columbia. More than 50% reported individual income less than $25,000, and more than 30% reported household income less than $50,000. More than 80% of respondents had some type of commercial insurance and 29% reported receiving Medicaid. Respondents received more financial assistance from their family and friends than from government sources. The total median out-of-pocket financial cost by our analysis was $13,450 (IQR: $6500-$25,800). Of the 838 who responded to the question, "Did the affected person receive the health care they needed?", 19% answered "no", 51% answered "yes, sometimes", and 30% answered "yes, most of the time".

CONCLUSION

The factors contributing to financial impact include both direct and indirect costs of accessing and receiving medical care. Our study findings highlight the magnitude of the burden of health care spending on patients with EDS.

摘要

目的

通过检查患者产生的医疗费用,确定埃勒斯-当洛综合征(EDS)对美国患者的经济影响。

患者与方法

我们采用便利抽样法,于2023年4月1日至2023年12月31日,通过全国患者权益倡导组织、支持团体、社交媒体以及医疗专业人员,向患有EDS的个体发放了一份自我报告调查问卷。该调查聚焦于患者的自付医疗费用。

结果

最终分析数据集包含884份回复。收到了来自美国所有50个州和哥伦比亚特区的个体的回复。超过50%的人报告个人收入低于25,000美元,超过30%的人报告家庭收入低于50,000美元。超过80%的受访者拥有某种类型的商业保险,29%的人报告接受医疗补助。受访者从家人和朋友那里获得的经济援助多于从政府渠道获得的援助。根据我们的分析,自付费用的总中位数为13,450美元(四分位距:6500美元至25,800美元)。在回答“受影响的人是否获得了他们所需的医疗保健?”这一问题的838人中,19%回答“否”,51%回答“是,有时”,30%回答“是,大部分时间”。

结论

造成经济影响的因素包括获取和接受医疗护理的直接和间接成本。我们的研究结果凸显了医疗保健支出对EDS患者造成的负担程度。