Perkins J A, Sie K C, Milczuk H, Richardson M A
Medical Corps, Otolaryngology-Head and Neck Surgery Service, Madigan Army Medical Center, Tacoma, Washington, USA.
Cleft Palate Craniofac J. 1997 Mar;34(2):135-40. doi: 10.1597/1545-1569_1997_034_0135_amicwc_2.3.co_2.
Craniofacial anomalies (CFA) predispose children to airway obstruction. A retrospective study was conducted to describe airway intervention required to manage patients with craniofacial syndromes and diseases involving the midface and mandible (i.e., Pierre Robin, Apert, Treacher Collins, Saethre-Chotzen, CHARGE, Nager, Stickler, Goldenhar, and Pfeiffer). The type of airway intervention, duration of intervention, and associated physical and medical conditions were evaluated. One hundred nine patients had charts available for review and met inclusion criteria. Sixty-five of these patients required airway management, most commonly in the first month of life, ranging from positioning to tracheotomy. Nineteen patients required a tracheotomy. Associated medical conditions and feeding difficulties were associated with airway obstruction. This study evaluates factors that predispose children with CFA to have airway problems that need treatment, as well as the types of airway management that are necessary.
颅面畸形(CFA)使儿童易患气道阻塞。进行了一项回顾性研究,以描述治疗患有涉及中面部和下颌骨的颅面综合征及疾病(即皮埃尔·罗宾综合征、阿佩尔综合征、特雷彻·柯林斯综合征、塞特勒-乔岑综合征、CHARGE综合征、纳格尔综合征、斯蒂克勒综合征、戈尔登哈综合征和法伊弗综合征)的患者所需的气道干预措施。评估了气道干预的类型、干预持续时间以及相关的身体和医疗状况。109例患者有可供审查的病历并符合纳入标准。其中65例患者需要气道管理,最常见于出生后的第一个月,范围从体位调整到气管切开术。19例患者需要气管切开术。相关的医疗状况和喂养困难与气道阻塞有关。本研究评估了使患有CFA的儿童易出现需要治疗的气道问题的因素,以及必要的气道管理类型。