CRESSC, SSD Coordinamento Neurofisiologia Clinica and Neurosurgery Unit, Department of Neuroscience, University of Torino, Torino, Italy.
Neuroscience Dpt, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Presidio CTO, via Zuretti, 29, Torino, Italy.
Neurol Sci. 2022 Feb;43(2):1327-1342. doi: 10.1007/s10072-021-05347-3. Epub 2021 Jun 15.
Syringomyelia and Chiari malformation are classified as rare diseases on Orphanet, but international guidelines on diagnostic criteria and case definition are missing.
to reach a consensus among international experts on controversial issues in diagnosis and treatment of Chiari 1 malformation and syringomyelia in adults.
A multidisciplinary panel of the Chiari and Syringomyelia Consortium (4 neurosurgeons, 2 neurologists, 1 neuroradiologist, 1 pediatric neurologist) appointed an international Jury of experts to elaborate a consensus document. After an evidence-based review and further discussions, 63 draft statements grouped in 4 domains (definition and classification/planning/surgery/isolated syringomyelia) were formulated. A Jury of 32 experts in the field of diagnosis and treatment of Chiari and syringomyelia and patient representatives were invited to take part in a three-round Delphi process. The Jury received a structured questionnaire containing the 63 statements, each to be voted on a 4-point Likert-type scale and commented. Statements with agreement <75% were revised and entered round 2. Round 3 was face-to-face, during the Chiari Consensus Conference (Milan, November 2019).
Thirty-one out of 32 Jury members (6 neurologists, 4 neuroradiologists, 19 neurosurgeons, and 2 patient association representatives) participated in the consensus. After round 2, a consensus was reached on 57/63 statements (90.5%). The six difficult statements were revised and voted in round 3, and the whole set of statements was further discussed and approved.
The consensus document consists of 63 statements which benefited from expert discussion and fine-tuning, serving clinicians and researchers following adults with Chiari and syringomyelia.
脊髓空洞症和 Chiari 畸形在 Orphanet 上被归类为罕见疾病,但缺乏国际诊断标准和病例定义指南。
在诊断和治疗成人 Chiari 1 畸形和脊髓空洞症方面,就有争议的问题在国际专家中达成共识。
Chiari 和脊髓空洞症联合会(4 名神经外科医生、2 名神经科医生、1 名神经放射科医生、1 名儿科神经科医生)的一个多学科小组任命了一个国际专家陪审团来制定一份共识文件。在进行基于证据的审查和进一步讨论后,制定了 63 份草案声明,分为 4 个领域(定义和分类/计划/手术/孤立性脊髓空洞症)。邀请了 32 名在 Chiari 和脊髓空洞症的诊断和治疗领域的专家和患者代表参加三轮 Delphi 流程。陪审团收到了一份包含 63 份声明的结构化问卷,每个声明都要在 4 分李克特量表上进行投票和评论。同意率<75%的声明进行修订并进入第二轮。第三轮是面对面的,在 Chiari 共识会议(2019 年 11 月,米兰)上进行。
32 名陪审团成员中的 31 名(6 名神经科医生、4 名神经放射科医生、19 名神经外科医生和 2 名患者协会代表)参加了共识。第二轮后,有 57/63 份声明(90.5%)达成共识。对 6 个困难的声明进行了修订,并在第三轮进行了投票,对整个声明集进行了进一步讨论和批准。
共识文件由 63 份声明组成,这些声明受益于专家讨论和微调,为治疗 Chiari 和脊髓空洞症的成人的临床医生和研究人员提供了帮助。