Walker Ryan D, Irace Alexandria L, Kenna Margaret A, Urion David K, Rahbar Reza
Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts.
Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts2Department of Otolaryngology, Harvard Medical School, Boston, Massachusetts.
JAMA Otolaryngol Head Neck Surg. 2017 Jul 1;143(7):651-655. doi: 10.1001/jamaoto.2016.4735.
Referral to a neurologist and imaging play important roles in the management of laryngeal cleft. Swallowing involves a complex series of neuromuscular interactions, and aspiration can result from anatomical causes (eg, laryngeal cleft), neuromuscular disorders, or some combination thereof. To date, no protocols or guidelines exist to identify which patients with laryngeal cleft should undergo neuroimaging studies and/or consultation with a neurologist.
To establish guidelines for neurologic evaluation and imaging techniques to identify or rule out neuromuscular dysfunction in children with laryngeal cleft.
Retrospective review of the medical records of 242 patients who were diagnosed with laryngeal cleft at a tertiary children's hospital between March 1, 1998, and July 6, 2015. Based on this review, an algorithm to guide management of laryngeal cleft is proposed.
Data extracted from patient medical records included the type of laryngeal cleft, details of neurologic referral, results of neuroimaging studies, and objective swallow study outcomes.
Of the 242 patients, 142 were male and 100 were female. Mean age at the time of data analysis was 8.7 years (range, 10 months to 25 years), and there were 164 type I clefts, 64 type II, 13 type III, and 1 type IV. In all, 86 patients (35.5%) were referred to a neurologist; among these, 33 (38.4%) had examination findings indicative of neuromuscular dysfunction or dyscoordination (eg, hypotonia, spasticity, or weakness). Abnormal findings were identified in 32 of 50 patients (64.0%) who underwent brain imaging. Neurosurgical intervention was necessary in 3 patients diagnosed with Chiari malformation and in 1 patient with an intraventricular tumor detected on neuroimaging.
A substantial proportion of patients with laryngeal cleft have coexistent neuromuscular dysfunction as a likely contributing factor to dysphagia and aspiration. Collaboration with a neurologist and appropriate neuroimaging may provide diagnostic and prognostic information in this subset of patients. At times, imaging will identify critical congenital malformations that require surgical treatment.
转诊至神经科医生处并进行影像学检查在喉裂的管理中发挥着重要作用。吞咽涉及一系列复杂的神经肌肉相互作用,误吸可能由解剖学原因(如喉裂)、神经肌肉疾病或两者的某种组合导致。迄今为止,尚无协议或指南来确定哪些喉裂患者应接受神经影像学检查和/或咨询神经科医生。
制定神经学评估和影像学检查技术的指南,以识别或排除喉裂患儿的神经肌肉功能障碍。
对1998年3月1日至2015年7月6日期间在一家三级儿童医院被诊断为喉裂的242例患者的病历进行回顾性研究。基于该回顾,提出了一种指导喉裂管理的算法。
从患者病历中提取的数据包括喉裂类型、神经科转诊细节、神经影像学检查结果以及客观吞咽研究结果。
242例患者中,142例为男性,100例为女性。数据分析时的平均年龄为8.7岁(范围为10个月至25岁),I型裂164例,II型64例,III型13例,IV型1例。共有86例患者(35.5%)被转诊至神经科医生处;其中,33例(38.4%)有提示神经肌肉功能障碍或不协调的检查结果(如肌张力减退、痉挛或无力)。在接受脑部成像的50例患者中,32例(64.0%)发现异常结果。3例被诊断为Chiari畸形的患者和1例在神经影像学检查中发现脑室内肿瘤的患者需要进行神经外科干预。
相当一部分喉裂患者存在并存的神经肌肉功能障碍,这可能是吞咽困难和误吸的一个促成因素。与神经科医生合作并进行适当的神经影像学检查可能为这部分患者提供诊断和预后信息。有时,影像学检查会发现需要手术治疗的严重先天性畸形。