Kay-Rivest Emily, Khendek Léticia, Bernard Geneviève, Daniel Sam J
Department of Pediatric Otolaryngology - Head and Neck Surgery, Montreal Children's Hospital, McGill University Health Center, Montreal, Quebec, Canada.
Departments of Neurology and Neurosurgery, and Pediatrics, McGill University, Montreal, Canada; Department of Medical Genetics, Montreal Children's Hospital, McGill University Health Center, Montreal, Canada; Child Health and Human Development Program, Research Institute of the McGill University Health Center, Montreal, Canada.
Int J Pediatr Otorhinolaryngol. 2017 Oct;101:141-144. doi: 10.1016/j.ijporl.2017.07.039. Epub 2017 Jul 27.
Leukodystrophies consist of degenerative neurogenetic diseases often associated with comorbidities that extend beyond the neurological system. Despite their impacts on patients' quality of life and risks of complications, head and neck symptomology is poorly reported in the literature. The objective of this study was to identify and quantify the main head and neck complaints among a cohort of patients diagnosed with leukodystrophies and define the role of the otolaryngologist as part of a multidisciplinary team for treating these patients.
During the First Canadian National Conference on Leukodystrophies held at the Montreal's Children Hospital, a cohort of 12 patients diagnosed with leukodystrophies were recruited and evaluated by a multidisciplinary team. An otolaryngology-focused assessment was done through history and physical examination, and included a screening questionnaire for 23 common otolaryngology issues. If families reported a history of sialorrhea, a validated questionnaire (Drool Quality of Life Assessment Questionnaire (DroolQoL)) was subsequently distributed. Results from the questionnaires were then compiled and analyzed.
Of the 12 recruited patients, 83% (10/12) were known to an otolaryngologist. Drooling affected 67% (8/12) of patients although only 37.5% (3/8) of patients had undergone medical or surgical therapies for this issue. Four patients experienced at least one aspiration pneumonia. 58% (7/12) of the patients had dysphagia, of whom 43% (3/12) were fed exclusively via gastrostomy tube and 28% (2/7) required thickening of feeds. Two patients, despite suspicion of dysphagia and aspiration, had never undergone evaluation. As for otologic issues, it was noted that 25% (3/12) of patients had a history of pressure equalizing tubes (PETs) and one patient had a history of hearing loss.
Head and neck comorbidities affect children with leukodystrophies. Therefore, the otolaryngologist should be part of the multidisciplinary team, specifically for the management of dysphagia and sialorrhea.
脑白质营养不良是一类退行性神经遗传性疾病,常伴有神经系统以外的合并症。尽管这些疾病会影响患者的生活质量并带来并发症风险,但文献中对头颈部症状的报道较少。本研究的目的是识别和量化一组被诊断为脑白质营养不良的患者的主要头颈部症状,并确定耳鼻喉科医生作为多学科团队一部分在治疗这些患者中的作用。
在蒙特利尔儿童医院举行的第一届加拿大全国脑白质营养不良会议期间,招募了一组12名被诊断为脑白质营养不良的患者,并由一个多学科团队进行评估。通过病史和体格检查进行了以耳鼻喉科为重点的评估,包括一份针对23个常见耳鼻喉科问题的筛查问卷。如果家属报告有流涎病史,则随后发放一份经过验证的问卷(流涎生活质量评估问卷(DroolQoL))。然后对问卷结果进行汇总和分析。
在招募的12名患者中,83%(10/12)曾看过耳鼻喉科医生。流涎影响了67%(8/12)的患者,尽管只有37.5%(3/8)的患者针对这个问题接受过药物或手术治疗。4名患者经历过至少一次吸入性肺炎。58%(7/12)的患者有吞咽困难,其中43%(3/12)仅通过胃造瘘管进食,28%(2/7)需要增稠食物。两名患者尽管怀疑有吞咽困难和误吸,但从未接受过评估。至于耳部问题,注意到25%(3/12)的患者有鼓膜置管史,一名患者有听力损失史。
头颈部合并症会影响脑白质营养不良患儿。因此,耳鼻喉科医生应成为多学科团队的一部分,特别是在吞咽困难和流涎的管理方面。