关于合并使用伏索利特和肢体手术的考虑因素的国际专家意见:改良德尔菲研究

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Silvio Boero, Julia Vodopiutz, Mohamad Maghnie, Josep M. de Bergua, Ignacio Ginebreda, Hiroshi Kitoh, Micha Langendörfer, Antonio Leiva-Gea, Jason Malone, Philip McClure, Gabriel T. Mindler, Dmitry Popkov, Robert Rodl, Pablo Rosselli, Fabio Verdoni, Viktor Vilenskii, Aaron J. Huser
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引用次数: 0

摘要

软骨发育不全症是一种最常见的骨骼疾病,患者身材矮小,不成比例。沃索利肽是第一种针对特定疾病的精准药物疗法,可提高软骨发育不全儿童的生长速度。肢体手术是增加身高和臂展、改善比例和功能以及矫正畸形的标准方法。这项研究的目的是了解专家对在患有软骨发育不全症的儿童和青少年中联合使用伏索利特和肢体手术的看法。我们召集了一个由 17 名临床医生和矫形外科医生组成的国际专家小组,并采用了改良的德尔菲程序。专家组审查了 120 项陈述的措辞,删除了不必要的陈述,并补充了他们认为缺失的陈述。有 26 项陈述被确定为事实,没有被纳入随后的投票中。共对 97 项陈述进行了十级评分,其中 1 分代表 "完全不同意",10 分代表 "完全同意"。≥7分为同意,≤4分为不同意。所有评分≤ 4 分的专家都被邀请发表意见。100%的专家同意以下几项声明,包括 "达到目标身高、臂展或上肢长度,以改善日常活动"(平均同意度[LoA]9.47,范围8-10)、"专科中心的多学科团队参与患者随访"(平均同意度9.67,范围 7-10)、"根据年龄和青春期阶段规划治疗策略"(平均 LoA 9.60,范围 8-10)和 "根据个体化治疗规划确定短期和长期目标"(平均 LoA 9.27,范围 7-10)等。主要由于缺乏可用数据,对综合方法的顺序和对体格的潜在影响存在分歧。从回答的范围可以清楚地看出,既然软骨发育不全的药物治疗方法已经问世,那么经过修改的德尔菲程序仅仅是新考虑的开始。在获得综合治疗方法的数据之前,分享专家意见是为临床社区提供支持和指导的重要方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
International expert opinion on the considerations for combining vosoritide and limb surgery: a modified delphi study
Achondroplasia is the most common form of skeletal disorder with disproportionate short stature. Vosoritide is the first disease-specific, precision pharmacotherapy to increase growth velocity in children with achondroplasia. Limb surgery is a standard approach to increase height and arm span, improve proportionality and functionality, as well as correcting deformities. The aim of this study was to gain expert opinion on the combined use of vosoritide and limb surgery in children and adolescents with achondroplasia. An international expert panel of 17 clinicians and orthopaedic surgeons was convened, and a modified Delphi process undertaken. The panel reviewed 120 statements for wording, removed any unnecessary statements, and added any that they felt were missing. There were 26 statements identified as facts that were not included in subsequent rounds of voting. A total of 97 statements were rated on a ten-point scale where 1 was ‘Completely disagree’ and 10 ‘Completely agree’. A score of ≥ 7 was identified as agreement, and ≤ 4 as disagreement. All experts who scored a statement ≤ 4 were invited to provide comments. There was 100% agreement with several statements including, “Achieve a target height, arm span or upper limb length to improve daily activities” (mean level of agreement [LoA] 9.47, range 8–10), the “Involvement of a multidisciplinary team in a specialist centre to follow up the patient” (mean LoA 9.67, range 7–10), “Planning a treatment strategy based on age and pubertal stage” (mean LoA 9.60, range 8–10), and “Identification of short- and long-term goals, based on individualised treatment planning” (mean LoA 9.27, range 7–10), among others. The sequence of a combined approach and potential impact on the physes caused disagreement, largely due to a lack of available data. It is clear from the range of responses that this modified Delphi process is only the beginning of new considerations, now that a medical therapy for achondroplasia is available. Until data on a combined treatment approach are available, sharing expert opinion is a vital way of providing support and guidance to the clinical community.
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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.
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