Glynn F, Fitzgerald D, Earley M J, Rowley H
Department of Otorhinolaryngology, Children's University Hospital Temple Street, Dublin 2, Ireland.
Int J Pediatr Otorhinolaryngol. 2011 Sep;75(9):1152-5. doi: 10.1016/j.ijporl.2011.06.009. Epub 2011 Jul 18.
To evaluate the course and prognosis of airway obstruction, feeding difficulties and hearing abnormalities in patients with Pierre Robin sequence (PRS).
A retrospective review was conducted, of 69 patients with PRS, attending between 1991 and 2010 at the Children's University Hospital in Dublin. Data regarding airway management, nutritional status and hearing difficulties was collected prospectively.
Airway obstruction requiring intervention other than positional therapy was seen in 39% (27) patients. Fifty nine percent (16/27) of these patients, who failed positional therapy, were successfully managed with a nasopharyngeal airway. Following failed intervention with nasopharyngeal airways, two patients had airway maintenance achieved with a successful glossopexy procedure. One patient had an adequate airway achieved with nasal continuous positive airway pressure. Eight patients (12%) required a surgical tracheostomy. Of those who required a tracheostomy, six patients had isolated PRS, one patient had PRS in association with Stickler syndrome and one patient had Nager acro-facial dystosis. Duration of tracheostomy tube ranged from 10 to 19 months, mean 13 months. Seventy percent (48 patients) required supplementary feeding in the form of nasogastric (NG) or gastrostomy tube. Forty-four patients were successfully managed with a temporary NG tube. One patient required a prolonged NG tube, and three required a gastrostomy tube. Twenty-one (30%) patients were successfully managed with a specialised Haberman bottle. Twenty-four patients (35%) who had their airway managed successfully by positional therapy, still required supplemental feeding. Thirty-one patients (45%) demonstrated a conductive hearing loss at some stage, which affected their speech and language development. Twenty-four patients (35%) required tympanostomy tube insertion once, while 7 (10%) of patients required ventilation tube insertion twice or more.
Airway management in the majority of PRS can be successfully achieved by conservative methods. Even in the presence of an adequate airway, many patients will require supplemental feeding. Early audiological assessment is necessary as many patients will need tympanostomy tube placement to ensure adequate speech and language development.
评估皮埃尔·罗宾序列征(PRS)患者气道阻塞、喂养困难及听力异常的病程及预后。
对1991年至2010年间在都柏林儿童医院就诊的69例PRS患者进行回顾性研究。前瞻性收集有关气道管理、营养状况及听力困难的数据。
39%(27例)患者出现需要体位治疗以外干预措施的气道阻塞。这些体位治疗失败的患者中,59%(16/27)通过鼻咽气道成功处理。鼻咽气道干预失败后,2例患者通过成功的舌固定术实现气道维持。1例患者通过鼻持续气道正压通气获得足够气道。8例患者(12%)需要手术气管切开术。在需要气管切开术的患者中,6例为孤立性PRS,1例PRS合并斯蒂克勒综合征,1例为纳杰尔肢端面部发育不全。气管切开管留置时间为10至19个月,平均13个月。70%(48例)患者需要鼻胃管(NG)或胃造瘘管形式的补充喂养。44例患者通过临时NG管成功处理。1例患者需要长期NG管,3例需要胃造瘘管。21例(30%)患者通过特制的哈伯曼奶瓶成功处理。24例(35%)通过体位治疗成功管理气道的患者仍需要补充喂养。31例患者(45%)在某个阶段出现传导性听力损失,影响其言语和语言发育。24例患者(35%)需要鼓膜置管一次,7例(10%)患者需要两次或更多次通气管置入。
多数PRS患者的气道管理可通过保守方法成功实现。即使气道足够,许多患者仍需要补充喂养。由于许多患者需要鼓膜置管以确保足够的言语和语言发育,早期听力评估很有必要。