Department of Pediatric Plastic Surgery, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, the Netherlands.
Seattle Children's Craniofacial Center, Department of Pediatrics, University of Washington, Seattle.
JAMA Pediatr. 2016 Sep 1;170(9):894-902. doi: 10.1001/jamapediatrics.2016.0796.
Robin sequence (RS) is a congenital condition characterized by micrognathia, glossoptosis, and upper airway obstruction. Currently, no consensus exists regarding the diagnosis and evaluation of children with RS. An international, multidisciplinary consensus group was formed to begin to overcome this limitation.
To report a consensus-derived set of best practices for the diagnosis and evaluation of infants with RS as a starting point for defining standards and management.
Based on a literature review and expert opinion, a clinical consensus report was generated.
Because RS can occur as an isolated condition or as part of a syndrome or multiple-anomaly disorder, the diagnostic process for each newborn may differ. Micrognathia is hypothesized as the initiating event, but the diagnosis of micrognathia is subjective. Glossoptosis and upper airway compromise complete the primary characteristics of RS. It can be difficult to judge the severity of tongue base airway obstruction, and the possibility of multilevel obstruction exists. The initial assessment of the clinical features and severity of respiratory distress is important and has practical implications. Signs of upper airway obstruction can be intermittent and are more likely to be present when the infant is asleep. Therefore, sleep studies are recommended. Feeding problems are common and may be exacerbated by the presence of a cleft palate. The clinical features and their severity can vary widely and ultimately dictate the required investigations and treatments.
Agreed-on recommendations for the initial evaluation of RS and clinical descriptors are provided in this consensus report. Researchers and clinicians will ideally use uniform definitions and comparable assessments. Prospective studies and the standard application of validated assessments are needed to build an evidence base guiding standards of care for infants and children with RS.
Robin 序列(RS)是一种先天性疾病,其特征为小下颌、悬雍垂后坠和上呼吸道阻塞。目前,对于 RS 患儿的诊断和评估尚无共识。为此,成立了一个国际性的多学科共识小组,以克服这一局限性。
报告一组基于共识的最佳实践,用于诊断和评估患有 RS 的婴儿,作为定义标准和管理的起点。
基于文献回顾和专家意见,生成了一份临床共识报告。
由于 RS 可作为孤立疾病发生,也可作为综合征或多种畸形障碍的一部分,因此每个新生儿的诊断过程可能不同。小下颌被假设为起始事件,但小下颌的诊断是主观的。悬雍垂后坠和上呼吸道阻塞完成了 RS 的主要特征。舌骨后气道阻塞的严重程度很难判断,而且可能存在多水平阻塞。评估临床特征和呼吸窘迫的严重程度很重要,具有实际意义。上呼吸道阻塞的迹象可能是间歇性的,并且在婴儿睡觉时更有可能出现。因此,建议进行睡眠研究。喂养问题很常见,腭裂的存在可能会使问题恶化。临床特征及其严重程度差异很大,最终决定了所需的检查和治疗。
本共识报告提供了 RS 初始评估和临床描述的既定建议。研究人员和临床医生最好使用统一的定义和可比较的评估方法。需要前瞻性研究和对经过验证的评估的标准应用,以建立指导 RS 婴儿和儿童护理标准的循证基础。