Kwinter Adam, Dworschak-Stokan Ann, Paradis Josee, Husein Murad
Department of Otolaryngology- Head and Neck Surgery, Children's Hospital, 800 Commissioners Rd E, London, ON, N6A 5A5, Canada.
Thames Valley Children's Center, 779 Base Line Rd E, London, ON, N6C 5Y6, Canada.
Int J Pediatr Otorhinolaryngol. 2018 Dec;115:77-81. doi: 10.1016/j.ijporl.2018.09.022. Epub 2018 Sep 22.
Submucous cleft palate (SMCP) is the most common congenital malformation of the posterior palate and characterized in part by palatal muscle diastasis. Patients with SMCP are considered symptomatic when suffering from velopharyngeal insufficiency which leads to hypernasality of speech and excess nasal air emission. SMCP results from defects in the muscles thought to be responsible for regulating the patency of the eustachian tube which can lead to a number of middle ear pathologies and ultimately hearing loss. Hearing loss, especially at a young age, can make speech acquisition a challenge. The purpose of this study was to review patients with symptomatic SMCP (SSMCP) who have presented to our center and report on the association between SSMCP and otologic disease.
This study was a retrospective review of all patients presenting to our center between 2004 and 2016. Patients with SSMCP were identified through a patient database maintained on site. Inclusion criteria were diagnosis of SMCP and documentation of the presence or absence of otologic disease. Once identified patient records were reviewed and various demographic and patient factors were recorded. Patients were then grouped into cohorts of those with and without otologic disease and those requiring tympanostomy tubes and not. T-tests were then used to compare various factors between cohorts.
A total of 73 patients were identified and 58 met inclusion criteria (mean age 5.8 years, male:female 36:22). 27.5% of patients were diagnosed with a genetic condition. 69% of patients had otologic disease and 47% required at least one set of bilateral tympanostomy myringotomy tubes. The cohort with ear disease tended to have worse scores on ACPA testing though this was not statistically significant. There were no significant demographic differences between the cohorts.
Patients with symptomatic SMCP suffer from a higher incidence of otologic disease and bilateral myringotomy tube placement than the general population. This is an important potential comorbidity in SSMCP patients as it can act as a further barrier to speech acquisition. Further research is needed to determine if otologic disease can be used for prognostication or treatment purposes.
黏膜下腭裂(SMCP)是腭后部最常见的先天性畸形,部分特征为腭肌分离。患有SMCP的患者在出现腭咽闭合不全时被认为有症状,这会导致语音鼻音过重和鼻腔过度漏气。SMCP是由被认为负责调节咽鼓管通畅性的肌肉缺陷引起的,这可能导致多种中耳病变并最终导致听力损失。听力损失,尤其是在年轻时,会使语言习得成为一项挑战。本研究的目的是回顾到我们中心就诊的有症状的黏膜下腭裂(SSMCP)患者,并报告SSMCP与耳科疾病之间的关联。
本研究是对2004年至2016年间到我们中心就诊的所有患者的回顾性研究。通过现场维护的患者数据库识别出患有SSMCP的患者。纳入标准为SMCP的诊断以及耳科疾病存在与否的记录。一旦识别出患者记录,就会进行审查并记录各种人口统计学和患者因素。然后将患者分为有耳科疾病和无耳科疾病以及需要鼓膜切开置管和不需要的队列。然后使用t检验比较队列之间的各种因素。
共识别出73例患者,58例符合纳入标准(平均年龄5.8岁,男:女为36:22)。27.5%的患者被诊断患有遗传疾病。69%的患者患有耳科疾病,47%的患者至少需要一组双侧鼓膜切开置管。患有耳部疾病的队列在ACPA测试中的得分往往较低,尽管这在统计学上并不显著。队列之间在人口统计学上没有显著差异。
有症状的黏膜下腭裂患者比一般人群患有耳科疾病和双侧鼓膜切开置管的发生率更高。这是SSMCP患者中一个重要的潜在合并症,因为它可能成为语言习得的进一步障碍。需要进一步研究以确定耳科疾病是否可用于预后或治疗目的。