Smit Marenka, Albanese Alberto, Benson Monika, Edwards Mark J, Graessner Holm, Hutchinson Michael, Jech Robert, Krauss Joachim K, Morgante Francesca, Pérez Dueñas Belen, Reilly Richard B, Tinazzi Michele, Contarino Maria Fiorella, Tijssen Marina A J
Expertise Centre Movement Disorders Groningen, Department of Neurology, University Medical Centre Groningen, Groningen, Netherlands.
Department of Neurology, Istituto di Ricovero e Cura a Carattere Scientifico Humanitas Research Hospital, Milan, Italy.
Front Neurol. 2021 Jun 3;12:646841. doi: 10.3389/fneur.2021.646841. eCollection 2021.
Improved care for people with dystonia presents a number of challenges. Major gaps in knowledge exist with regard to how to optimize the diagnostic process, how to leverage discoveries in pathophysiology into biomarkers, and how to develop an evidence base for current and novel treatments. These challenges are made greater by the realization of the wide spectrum of symptoms and difficulties faced by people with dystonia, which go well-beyond motor symptoms. A network of clinicians, scientists, and patients could provide resources to facilitate information exchange at different levels, share mutual experiences, and support each other's innovative projects. In the past, collaborative initiatives have been launched, including the , the which however only existed for a limited time), and the Dutch project. The European Reference Network on Rare Neurological Diseases includes dystonia among other rare conditions affecting the central nervous system in a dedicated stream. Currently, we aim to broaden the scope of these initiatives to a comprehensive European level by further expanding the DystoniaNet network, in close collaboration with the ERN-RND. In line with the ERN-RND, the mission of DystoniaNet Europe is to improve care and quality of life for people with dystonia by, among other endeavors, facilitating access to specialized care, overcoming the disparity in education of medical professionals, and serving as a solid platform to foster international clinical and research collaborations. In this review, both professionals within the dystonia field and patients and caregivers representing Dystonia Europe highlight important unsolved issues and promising new strategies and the role that a European network can play in activating them.
改善肌张力障碍患者的护理面临诸多挑战。在如何优化诊断流程、如何将病理生理学的发现转化为生物标志物以及如何为现有和新型治疗方法建立证据基础等方面,存在重大知识空白。肌张力障碍患者所面临的症状和困难范围广泛,远不止运动症状,这使得这些挑战更加严峻。临床医生、科学家和患者组成的网络可以提供资源,促进不同层面的信息交流,分享共同经验,并支持彼此的创新项目。过去已经发起了一些合作倡议,包括[具体倡议名称1]、[具体倡议名称2](然而该倡议仅存在了有限的时间)以及荷兰的[具体项目名称]项目。欧洲罕见神经系统疾病参考网络在一个专门的类别中将肌张力障碍列为影响中枢神经系统的其他罕见病症之一。目前,我们的目标是通过与ERN - RND密切合作,进一步扩大肌张力障碍网络(DystoniaNet),将这些倡议的范围扩大到全面的欧洲层面。与ERN - RND一致,欧洲肌张力障碍网络(DystoniaNet Europe)的使命是通过促进获得专科护理、克服医学专业人员教育方面的差距以及作为促进国际临床和研究合作的坚实平台等多种努力,改善肌张力障碍患者的护理和生活质量。在这篇综述中,肌张力障碍领域的专业人员以及代表欧洲肌张力障碍协会的患者和护理人员强调了重要的未解决问题、有前景的新策略以及欧洲网络在激活这些方面可以发挥的作用。