Cohen Stephanie M, Greathouse S Travis, Rabbani Cyrus C, O'Neil Joseph, Kardatzke Matthew A, Hall Tasha E, Bennett William E, Daftary Ameet S, Matt Bruce H, Tholpady Sunil S
Division of Plastic and Reconstructive Surgery, Indiana University School of Medicine, Indianapolis.
Reid Health, Richmond.
J Multidiscip Healthc. 2017 Mar 27;10:121-132. doi: 10.2147/JMDH.S98967. eCollection 2017.
Robin sequence (RS) is a commonly encountered triad of micrognathia, glossoptosis, and airway obstruction, with or without a cleft palate. The management of airway obstruction is of paramount importance, and multiple reviews and retrospective series outline the diagnosis and treatment of RS. This article focuses on the multidisciplinary nature of RS and the specialists' contributions and thought processes regarding the management of the RS child from birth to skeletal maturity. This review demonstrates that the care of these children extends far beyond the acute airway obstruction and that thorough monitoring and appropriate intervention are required to help them achieve optimal outcomes.
罗宾序列征(RS)是一种常见的三联征,包括小颌畸形、舌后坠和气道阻塞,可伴有或不伴有腭裂。气道阻塞的处理至关重要,多项综述和回顾性系列研究概述了RS的诊断和治疗。本文重点关注RS的多学科性质以及专家们对于从出生到骨骼成熟阶段RS患儿管理的贡献和思维过程。本综述表明,这些患儿的护理远不止于急性气道阻塞,需要进行全面监测和适当干预,以帮助他们获得最佳预后。