Hardwicke Joseph T, Richards Helen, Cafferky Louise, Underwood Imogen, Horst Britt Ter, Slator Rona
Birmingham, United Kingdom From the West Midlands Cleft Lip and Palate Service and Speech and Language Therapy, Birmingham Children's Hospital NHS Trust, and the School of Clinical and Experimental Medicine, University of Birmingham, The Medical School.
Plast Reconstr Surg. 2016 Mar;137(3):927-935. doi: 10.1097/01.prs.0000475829.32402.a8.
Pierre Robin sequence results from a cascade of events that occur during embryologic development and frequently presents with cleft palate. Some studies have shown speech outcomes to be worse in patients with Pierre Robin sequence after cleft palate repair.
A cohort of Pierre Robin sequence patients who all required an airway intervention and nasogastric feeding in the neonatal period were identified and speech outcomes assessed at 5 years of age. A cleft- and sex-matched non-Pierre Robin sequence, cleft palate-only comparison group was also identified from the same institution and study period.
A total of 24 patients with Pierre Robin sequence that required airway and nutritional support in the neonatal period were matched for age, sex, and cleft type to a group of 24 non-Pierre Robin sequence cleft patients. There was no significant difference in the incidence of oronasal fistula between the groups. Secondary surgery for velopharyngeal incompetence was significantly more (p = 0.017) in the Pierre Robin sequence group, who also had significantly greater nasality (p = 0.031) and cleft speech characteristic (p = 0.023) scores.
The authors hypothesize that other factors may exist in Pierre Robin sequence that may lead to poor speech outcomes. The authors would suggest counseling parents of children with Pierre Robin sequence that have required a neonatal airway intervention, that speech development may be poorer than in other children with cleft palate, and that these children will have a significantly higher incidence of secondary speech surgery.
CLINICAL QUESTION/LEVEL OF EVIDENCE: Risk, II.
皮埃尔·罗宾序列征是胚胎发育过程中一系列事件导致的结果,常伴有腭裂。一些研究表明,腭裂修复术后皮埃尔·罗宾序列征患者的语音结果较差。
确定一组在新生儿期均需要气道干预和鼻胃管喂养的皮埃尔·罗宾序列征患者,并在5岁时评估其语音结果。还从同一机构和研究期间确定了一个与腭裂类型和性别匹配的非皮埃尔·罗宾序列征、仅腭裂的对照组。
共有24例在新生儿期需要气道和营养支持的皮埃尔·罗宾序列征患者,在年龄、性别和腭裂类型方面与24例非皮埃尔·罗宾序列征腭裂患者进行匹配。两组间口鼻瘘的发生率无显著差异。皮埃尔·罗宾序列征组中因腭咽功能不全进行二次手术的比例显著更高(p = 0.017),该组患者的鼻音(p = 0.031)和腭裂语音特征(p = 0.023)评分也显著更高。
作者推测皮埃尔·罗宾序列征可能存在其他导致语音结果不佳的因素。作者建议为新生儿期需要气道干预的皮埃尔·罗宾序列征患儿的家长提供咨询,告知他们这些患儿的语音发育可能比其他腭裂患儿差,且二次语音手术的发生率会显著更高。
临床问题/证据水平:风险,II级。