EA 3450 DevAH - Development, Adaptation and Handicap, Faculty of Medicine, University of Lorraine, Nancy, France
Paediatric Neurosurgery, CHRU de Nancy, Nancy, France.
BMJ Open. 2022 May 12;12(5):e056647. doi: 10.1136/bmjopen-2021-056647.
Chiari I malformation (CM1) is an anatomical abnormality characterised by the cerebellar tonsils descending at least 5 mm below the foramen magnum. CM1 causes obstruction of cerebrospinal fluid (CSF) circulation as well as direct compression on the brainstem, thus causing typical consequences (syringomyelia), and typical clinical features (characteristic headaches and neurological impairment). Surgery is the only available treatment, indicated when symptomatology is present. However, sometimes patients have atypical complaints, which are often suggestive of otolaryngological (ears, nose and throat, ENT) involvement. This may be difficult for a neurosurgeon to explain. Our study aims to investigate the relationship between one of these atypical symptoms, for example, postural instability, in a paediatric population using a Computerised Dynamic Posturography (Equitest, NeuroCom, Clackamas, OR). To our knowledge, there are no previously published studies carried out on children with CM1, using dynamic posturography.
Forty-five children aged 6-18 years old presenting with radiologically confirmed CM1 and presenting ENT clinical complaints will be included in the study for a duration of 3 years. As primary endpoint, posturographic results will be described in the population study. Second, posturographic results will be compared between patients with and without indication for surgery. Finally, preoperative and postoperative posturographic results, as well as CSF circulation quality at foramen magnum level, syringomyelia, sleep apnoea syndrome, scoliosis and behaviour will be compared in the operated patient group.
This protocol received ethical approval from the Clinical Research Delegation of Nancy University Hospital, in accordance with the National Commission on Informatics and Liberties (Commission Nationale de l'Informatique et des Libertés) (protocol number 2019PI256-107). Our data treatment was in accordance with the Methodology of reference Methodology Reference-004 specification for data policy. The study findings will be disseminated via peer-reviewed publications and conference presentations, especially to the Neurosphynx's rare disease healthcare network.
NCT04679792; Pre-results.
Chiari I 畸形(CM1)是一种解剖学异常,其特征是小脑扁桃体至少向下延伸 5 毫米至枕骨大孔以下。CM1 导致脑脊液(CSF)循环受阻,以及对脑干的直接压迫,从而导致典型的后果(脊髓空洞症)和典型的临床特征(特征性头痛和神经功能障碍)。手术是唯一可行的治疗方法,当出现症状时才需要进行手术。然而,有时患者会出现非典型症状,这些症状通常提示耳鼻喉科(耳朵、鼻子和喉咙,ENT)受累。这可能让神经外科医生难以解释。我们的研究旨在使用计算机动态姿势描记法(Equitest,NeuroCom,Clackamas,OR)调查儿科人群中一种非典型症状(例如姿势不稳)与 Chiari I 畸形之间的关系。据我们所知,目前还没有针对 Chiari I 畸形儿童使用动态姿势描记法进行的研究。
将在 3 年内纳入 45 名年龄在 6-18 岁之间的经放射学证实患有 Chiari I 畸形并伴有 ENT 临床症状的儿童进行研究。作为主要终点,将在人群研究中描述姿势描记结果。其次,将比较有手术指征和无手术指征的患者之间的姿势描记结果。最后,在接受手术的患者组中,将比较术前和术后的姿势描记结果以及枕骨大孔水平的 CSF 循环质量、脊髓空洞症、睡眠呼吸暂停综合征、脊柱侧凸和行为。
本方案获得了南锡大学医院临床研究代表的伦理批准,符合国家信息学和自由委员会(Commission Nationale de l'Informatique et des Libertés)(方案编号 2019PI256-107)。我们的数据处理符合数据政策参考方法参考-004 规范。研究结果将通过同行评审的出版物和会议报告进行传播,特别是向 Neurosphynx 的罕见病医疗保健网络传播。
NCT04679792;预结果。