Measuring the impact of rare diseases in Tasmania, Australia.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Philippa Scanlon, Garry Ridler, Genevieve Say, Miranda Kellett, Jac Charlesworth, Amanda Neil, Joanne L Dickinson, Kathryn Burdon, Matthew Jose, Mathew Wallis
{"title":"Measuring the impact of rare diseases in Tasmania, Australia.","authors":"Philippa Scanlon, Garry Ridler, Genevieve Say, Miranda Kellett, Jac Charlesworth, Amanda Neil, Joanne L Dickinson, Kathryn Burdon, Matthew Jose, Mathew Wallis","doi":"10.1186/s13023-024-03343-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>An ongoing challenge with rare diseases is limited data and, consequently, limited knowledge about the collective prevalence and impact of these conditions on individuals, families, and the health system, particularly in rural and regional areas. Using existing datasets, this project aimed to examine the epidemiology of and hospital activity for Tasmanians with rare diseases.</p><p><strong>Methods: </strong>Rare diseases were defined as non-infectious diseases with a prevalence of less than 1 in 2000. An initial resource set of 1028 ICD-10-AM diagnostic codes was used to identify a cohort of Tasmanians with rare diseases in Tasmanian Health datasets (1 January 2007 until 31 December 2020). Validating the resource set using a small group with known rare diseases revealed limitations in ascertainment, and so an expanded set of 1940 ICD-10-AM diagnostic codes was developed by cross-referencing ICD-10-AM codes with Orphanet data. Cohort hospital activity and admission costs were compared to statewide data for the final year of the study, 01 January 2020 to 31 December 2020.</p><p><strong>Results: </strong>Using the resource set of 1028 ICD-10-AM diagnostic codes, the period prevalence of rare diseases in Tasmania across all age groups was estimated at 3.5%, with a point prevalence of 1.5% in December 2020. In 2020, 3384 individuals within the Tasmanian rare disease cohort, representing 0.6% of the Tasmanian population, accessed the public hospital system and accounted for 5.6% of all admissions. The mean length of stay for rare disease-related hospital admissions was 5.0 days, compared to 3.3 days for non-rare disease-related admissions. The mean cost per admission for the rare disease cohort was AUD$11,310, compared to AUD$6475 for all admissions statewide. In 2020, using the expanded resource set, the total cost of public hospital admissions in Tasmania was estimated to be AUD$979 million, with rare disease-related hospital admissions accounting for 9.1% of this cost, increasing to 19.0% when the costs for all admissions for the rare disease patients were included.</p><p><strong>Conclusions: </strong>Patients with rare diseases had more admissions, longer length of stay, and a higher average cost per admission. Patients with rare diseases have a disproportionate impact on statewide hospital activity and costs in Tasmania.</p>","PeriodicalId":19651,"journal":{"name":"Orphanet Journal of Rare Diseases","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11514960/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Orphanet Journal of Rare Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13023-024-03343-2","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: An ongoing challenge with rare diseases is limited data and, consequently, limited knowledge about the collective prevalence and impact of these conditions on individuals, families, and the health system, particularly in rural and regional areas. Using existing datasets, this project aimed to examine the epidemiology of and hospital activity for Tasmanians with rare diseases.

Methods: Rare diseases were defined as non-infectious diseases with a prevalence of less than 1 in 2000. An initial resource set of 1028 ICD-10-AM diagnostic codes was used to identify a cohort of Tasmanians with rare diseases in Tasmanian Health datasets (1 January 2007 until 31 December 2020). Validating the resource set using a small group with known rare diseases revealed limitations in ascertainment, and so an expanded set of 1940 ICD-10-AM diagnostic codes was developed by cross-referencing ICD-10-AM codes with Orphanet data. Cohort hospital activity and admission costs were compared to statewide data for the final year of the study, 01 January 2020 to 31 December 2020.

Results: Using the resource set of 1028 ICD-10-AM diagnostic codes, the period prevalence of rare diseases in Tasmania across all age groups was estimated at 3.5%, with a point prevalence of 1.5% in December 2020. In 2020, 3384 individuals within the Tasmanian rare disease cohort, representing 0.6% of the Tasmanian population, accessed the public hospital system and accounted for 5.6% of all admissions. The mean length of stay for rare disease-related hospital admissions was 5.0 days, compared to 3.3 days for non-rare disease-related admissions. The mean cost per admission for the rare disease cohort was AUD$11,310, compared to AUD$6475 for all admissions statewide. In 2020, using the expanded resource set, the total cost of public hospital admissions in Tasmania was estimated to be AUD$979 million, with rare disease-related hospital admissions accounting for 9.1% of this cost, increasing to 19.0% when the costs for all admissions for the rare disease patients were included.

Conclusions: Patients with rare diseases had more admissions, longer length of stay, and a higher average cost per admission. Patients with rare diseases have a disproportionate impact on statewide hospital activity and costs in Tasmania.

衡量罕见疾病对澳大利亚塔斯马尼亚州的影响。
背景:罕见病一直面临的一个挑战是数据有限,因此,人们对这些疾病的集体患病率及其对个人、家庭和医疗系统的影响了解有限,尤其是在农村和地区。本项目利用现有数据集,旨在研究塔斯马尼亚罕见病的流行病学和医院活动:罕见病的定义是发病率低于 2000 年 1 例的非传染性疾病。初始资源集包含 1028 个 ICD-10-AM 诊断代码,用于识别塔斯马尼亚州卫生数据集中患有罕见疾病的塔斯马尼亚人群组(2007 年 1 月 1 日至 2020 年 12 月 31 日)。使用一小群已知罕见病患者对资源集进行验证后发现,该资源集在确认方面存在局限性,因此通过将 ICD-10-AM 诊断代码与 Orphanet 数据进行交叉比对,开发出了一套包含 1940 个 ICD-10-AM 诊断代码的扩展资源集。将队列医院活动和住院费用与研究最后一年(2020 年 1 月 1 日至 2020 年 12 月 31 日)的全州数据进行了比较:使用包含 1028 个 ICD-10-AM 诊断代码的资源集,塔斯马尼亚各年龄组的罕见病患病率估计为 3.5%,2020 年 12 月的点患病率为 1.5%。2020 年,塔斯马尼亚罕见病队列中有 3384 人(占塔斯马尼亚人口的 0.6%)进入公立医院系统,占所有入院人数的 5.6%。罕见病相关住院病人的平均住院时间为 5.0 天,而非罕见病相关住院病人的平均住院时间为 3.3 天。罕见病群组每次入院的平均费用为 11310 澳元,而全州所有入院的平均费用为 6475 澳元。2020 年,利用扩大的资源集,塔斯马尼亚州公立医院的住院总成本估计为 9.79 亿澳元,其中罕见病相关住院成本占 9.1%,如果将罕见病患者的所有住院成本计算在内,则这一比例将增至 19.0%:罕见病患者的入院次数更多、住院时间更长、每次入院的平均费用更高。罕见病患者对塔斯马尼亚州全州的医院活动和成本产生了不成比例的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信