Defining priorities in the transition from paediatric to adult healthcare for rare bone disease patients: a dialogic approach

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
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引用次数: 0

Abstract

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.

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。
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。
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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.
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