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International Guidelines for the Treatment of Huntingtons Disease

机译:国际亨廷顿舞蹈病治疗指南

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摘要

The European Huntington's Disease Network (EHDN) commissioned an international task force to provide global evidence-based recommendations for everyday clinical practice for treatment of Huntington's disease (HD). The objectives of such guidelines are to standardize pharmacological, surgical and non-pharmacological treatment regimen and improve care and quality of life of patients. A formalized consensus method, adapted from the French Health Authority recommendations was used. First, national committees (French and English Experts) reviewed all studies published between 1965 and 2015 included dealing with HD symptoms classified in motor, cognitive, psychiatric, and somatic categories. Quality grades were attributed to these studies based on levels of scientific evidence. Provisional recommendations were formulated based on the strength and the accumulation of scientific evidence available. When evidence was not available, recommendations were framed based on professional agreement. A European Steering committee supervised the writing of the final recommendations through a consensus process involving two rounds of online questionnaire completion with international multidisciplinary HD health professionals. Patients' associations were invited to review the guidelines including the HD symptoms. Two hundred and nineteen statements were retained in the final guidelines. We suggest to use this adapted method associating evidence base–medicine and expert consensus to other rare diseases.
机译:欧洲亨廷顿氏病网络(EHDN)委托一个国际工作组,为亨廷顿氏病(HD)的日常临床实践提供基于全球证据的建议。此类指南的目标是标准化药理,手术和非药理治疗方案,并改善患者的护理和生活质量。使用了根据法国卫生局的建议改编的正式共识方法。首先,国家委员会(法语和英语专家)审查了1965年至2015年之间发表的所有研究,其中包括针对运动,认知,精神病和躯体类别中的高清症状的处理。根据科学证据的水平,将质量等级归因于这些研究。临时建议是根据现有科学证据的实力和积累而制定的。如果没有证据,则根据专业协议制定建议。欧洲指导委员会通过共识过程监督最终建议的撰写,该过程涉及与国际多学科高清卫生专业人员进行的两轮在线问卷调查。邀请患者协会审查包括HD症状在内的指南。最终指南保留了219条声明。我们建议使用这种改编的方法将基础医学和专家共识与其他罕见疾病相关联。

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