Wolter Nikolaus E, Dell Sharon D, James Adrian L, Campisi Paolo
University of Toronto, Department of Otolaryngology-Head and Neck Surgery, Hospital for Sick Children, Toronto, Ontario, Canada.
Int J Pediatr Otorhinolaryngol. 2012 Nov;76(11):1565-8. doi: 10.1016/j.ijporl.2012.07.011. Epub 2012 Aug 9.
Otitis media with effusion (OME) in children with primary ciliary dyskinesia (PCD) is recurrent and persistent and presents a complex clinical problem for otolaryngologists. We sought to review the otological presentation of children with PCD treated medically and surgically and to compare audiological outcomes and complications of surgical and medical management in children with PCD and correlate these findings with known PCD ultrastructural ciliary phenotype.
A retrospective review was performed of all patients with PCD and OME presenting from 1991 to 2009. Patients were grouped into "medical management" and "ventilation tube (VT) insertion" groups to observe changes in hearing and post-operative complications.
Of 31 patients with PCD and OME, 20 received VTs and 11 were treated by medical management strategies. A median of one set of VTs (range 1-5) were inserted per patient. Hearing thresholds improved to normal (<25 dB HL) in 80% ears with VTs (mean improvement from 27.1 dB to 22.1 dB (p=0.034)), whereas patients managed medically had stable thresholds (22.7-23.6 dB (p=0.397) over the study period. At least one episode of post-operative otorrhea occurred in eight (42.1%) VT insertion patients during the study period, and four had multiple episodes. We could not demonstrate any differences in post-surgical outcomes between patient groups based on ultrastructural ciliary phenotype. Otorrhea was well controlled with medical therapy with only one requiring tube removal. Bilateral cholesteatoma was found in two patients.
Our data support the use of VT insertion as an option for patients with PCD and OME with mild to moderate hearing loss. Patients should be counseled on the possibility of multiple insertions and the likelihood of post-operative otorrhea, although this was not very troublesome in our group. Ultrastructural ciliary phenotype did not appear to alter the likelihood of post-operative otorrhea in our series. Cholesteatoma should be considered as a potential cause of otorrhea in PCD.
原发性纤毛运动障碍(PCD)患儿的中耳积液(OME)反复发作且持续存在,给耳鼻喉科医生带来了复杂的临床问题。我们旨在回顾接受药物和手术治疗的PCD患儿的耳科表现,比较PCD患儿手术和药物治疗的听力结果及并发症,并将这些结果与已知的PCD超微结构纤毛表型相关联。
对1991年至2009年期间所有患有PCD和OME的患者进行回顾性研究。将患者分为“药物治疗组”和“置管(VT)组”,以观察听力变化和术后并发症。
在31例患有PCD和OME的患者中,20例接受了VT治疗,11例采用药物治疗策略。每位患者平均置入一组VT(范围1 - 5组)。接受VT治疗的耳朵中,80%的听力阈值改善至正常(<25 dB HL)(平均从27.1 dB改善至22.1 dB(p = 0.034)),而接受药物治疗的患者在研究期间听力阈值稳定(22.7 - 23.6 dB(p = 0.397))。在研究期间,8例(42.1%)置管患者至少发生一次术后耳漏,4例有多次耳漏发作。我们未能证明基于超微结构纤毛表型的患者组之间手术结果存在差异。耳漏通过药物治疗得到良好控制,仅1例需要拔管。2例患者发现双侧胆脂瘤。
我们的数据支持将置管作为患有PCD和OME且伴有轻度至中度听力损失患者的一种选择。应告知患者可能需要多次置管以及术后耳漏的可能性,尽管在我们的研究组中这并不是很麻烦。在我们的系列研究中,超微结构纤毛表型似乎并未改变术后耳漏的可能性。胆脂瘤应被视为PCD中耳漏的潜在原因。