确定罕见骨病患者从儿科向成人医疗保健过渡的优先事项。对话方式。

IF 1.6 4区 医学 Q3 GENETICS & HEREDITY
D. Scognamiglio , M. Boarini , M.C. la Forgia , E. Grippa , S. Forni , A. Sergi , A. Romeo , G. Massa , L. Sangiorgi
{"title":"确定罕见骨病患者从儿科向成人医疗保健过渡的优先事项。对话方式。","authors":"D. Scognamiglio ,&nbsp;M. Boarini ,&nbsp;M.C. la Forgia ,&nbsp;E. Grippa ,&nbsp;S. Forni ,&nbsp;A. Sergi ,&nbsp;A. Romeo ,&nbsp;G. Massa ,&nbsp;L. Sangiorgi","doi":"10.1016/j.ejmg.2023.104891","DOIUrl":null,"url":null,"abstract":"<div><p>The Italian patient association for Multiple Osteochondromas, Ollier Disease, and Maffucci Syndrome, Associazione Conto Alla Rovescia-ACAR Aps, conducted a mixed-methods study at its 2023 annual conference. The study included the Open Dialogue Approach and a feedback survey to identify the main priorities in the transitioning process from paediatric to adult healthcare for patients with Multiple Osteochondromas, Ollier Disease, and Maffucci Syndrome.</p><p>The common needs identified by patients, families, caregivers, and healthcare professionals were coordination and continuity of care, patient empowerment and communication, social and practical support, and transition planning and support.</p><p>This experience fostered a sense of collaboration and cooperation among stakeholders, helping to build trust and create a shared vision for improving the quality of care for these patients. Furthermore, it could be considered a starting point for other patient associations interested in using different approaches to identify the needs of their members and actively involve all stakeholders.</p></div>","PeriodicalId":11916,"journal":{"name":"European journal of medical genetics","volume":"67 ","pages":"Article 104891"},"PeriodicalIF":1.6000,"publicationDate":"2023-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1769721223001970/pdfft?md5=e60faf7e0501489ecf8d70674fd7f82e&pid=1-s2.0-S1769721223001970-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients: a dialogic approach\",\"authors\":\"D. Scognamiglio ,&nbsp;M. Boarini ,&nbsp;M.C. la Forgia ,&nbsp;E. Grippa ,&nbsp;S. Forni ,&nbsp;A. Sergi ,&nbsp;A. Romeo ,&nbsp;G. Massa ,&nbsp;L. Sangiorgi\",\"doi\":\"10.1016/j.ejmg.2023.104891\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The Italian patient association for Multiple Osteochondromas, Ollier Disease, and Maffucci Syndrome, Associazione Conto Alla Rovescia-ACAR Aps, conducted a mixed-methods study at its 2023 annual conference. The study included the Open Dialogue Approach and a feedback survey to identify the main priorities in the transitioning process from paediatric to adult healthcare for patients with Multiple Osteochondromas, Ollier Disease, and Maffucci Syndrome.</p><p>The common needs identified by patients, families, caregivers, and healthcare professionals were coordination and continuity of care, patient empowerment and communication, social and practical support, and transition planning and support.</p><p>This experience fostered a sense of collaboration and cooperation among stakeholders, helping to build trust and create a shared vision for improving the quality of care for these patients. Furthermore, it could be considered a starting point for other patient associations interested in using different approaches to identify the needs of their members and actively involve all stakeholders.</p></div>\",\"PeriodicalId\":11916,\"journal\":{\"name\":\"European journal of medical genetics\",\"volume\":\"67 \",\"pages\":\"Article 104891\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2023-11-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1769721223001970/pdfft?md5=e60faf7e0501489ecf8d70674fd7f82e&pid=1-s2.0-S1769721223001970-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European journal of medical genetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1769721223001970\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of medical genetics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1769721223001970","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

意大利多发性骨软骨瘤、肝脏疾病和马夫齐综合征患者协会(Associazione Conto Alla Rovescia-ACAR Aps)在其2023年年会上进行了一项混合方法研究。该研究包括开放对话方法和一项反馈调查,以确定多发性骨软骨瘤、脂肪肝疾病和马夫奇综合征患者从儿科向成人医疗保健过渡过程中的主要优先事项。患者、家属、护理人员和医疗保健专业人员确定的共同需求是护理的协调和连续性、患者赋权和沟通、社会和实际支持以及过渡规划和支持。这一经验培养了利益相关者之间的协作与合作意识,有助于建立信任,并为改善这些患者的护理质量创造共同的愿景。此外,它可以被视为其他有兴趣使用不同方法来确定其成员需求并积极参与所有利益相关者的患者协会的起点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients: a dialogic approach

The Italian patient association for Multiple Osteochondromas, Ollier Disease, and Maffucci Syndrome, Associazione Conto Alla Rovescia-ACAR Aps, conducted a mixed-methods study at its 2023 annual conference. The study included the Open Dialogue Approach and a feedback survey to identify the main priorities in the transitioning process from paediatric to adult healthcare for patients with Multiple Osteochondromas, Ollier Disease, and Maffucci Syndrome.

The common needs identified by patients, families, caregivers, and healthcare professionals were coordination and continuity of care, patient empowerment and communication, social and practical support, and transition planning and support.

This experience fostered a sense of collaboration and cooperation among stakeholders, helping to build trust and create a shared vision for improving the quality of care for these patients. Furthermore, it could be considered a starting point for other patient associations interested in using different approaches to identify the needs of their members and actively involve all stakeholders.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.10
自引率
0.00%
发文量
193
审稿时长
66 days
期刊介绍: The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.
×
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