Frawley Geoff, Espenell Ainsley, Howe Peter, Shand Jocelyn, Heggie Andrew
Department of Paediatric Anaesthesia and Pain Management, Royal Children's Hospital, Melbourne, Vic., Australia.
Paediatr Anaesth. 2013 Apr;23(4):342-8. doi: 10.1111/pan.12049. Epub 2012 Oct 9.
To document the incidence of difficult intubation following mandibular distraction osteogenesis (MDO) in children with severe mandibular hypoplasia.
Syndromes associated with significant mandibular hypoplasia, especially Pierre Robin sequence, provide a challenge in airway management both in and out of the operating room. Mandibular advancement using mandibular distraction osteogenesis devices has been used in infants in an attempt to reduce the incidence of acute life-threatening airway obstruction. Whether MDO also reduces the incidence of difficult intubation has not been adequately described.
A retrospective chart review of 51 infants with upper airway obstruction secondary to mandibular hypoplasia who required MDO between January 2002 and 2012. The primary outcome was the incidence of difficult or failed intubation. Secondary outcomes were the relationship between syndrome type and the incidence of difficult intubation.
Fifty-one PRS infants were identified. Twenty-eight patients had isolated PRS, six had syndromic PRS, seven had Treacher Collins syndrome, and 10 had another coexisting syndrome. Prior to mandibular distraction osteogenesis (MDO), the incidence of difficult intubation was 71%, with the highest incidence in patients with Treacher Collins syndrome (100%), sPRS syndrome (100%), and PRS (65%). Following MDO, the incidence of difficult intubation was 8.3%. The difference was statistically significant for all patients (Kruskal-Wallis rank test P = 0.0001) those with isolated PRS (P = 0.0001), syndromic PRS (P = 0.0023), and other syndromes (P = 0.0002), but not for Treacher Collins syndrome (P = 0.21). Three patients had pre existing tracheostomies.
In a select group of infants with severe upper airway obstruction who have failed nonsurgical airway interventions, mandibular distraction osteogenesis reduces the incidence of difficult mask ventilation and difficult intubation. We were not able to compare the improvement in airway management to a comparable group of PRS infants who did not undergo surgical intervention. The improvement in laryngeal view was most marked for infants with isolated PRS but no significant benefit was demonstrated in infants with TCS.
记录严重下颌发育不全儿童行下颌骨牵张成骨术(MDO)后困难插管的发生率。
与显著下颌发育不全相关的综合征,尤其是皮埃尔·罗宾序列征,在手术室内外的气道管理中都构成挑战。使用下颌骨牵张成骨装置进行下颌前移已用于婴儿,以试图降低急性危及生命的气道阻塞的发生率。MDO是否也能降低困难插管的发生率尚未得到充分描述。
对2002年1月至2012年间51例因下颌发育不全导致上气道阻塞而需要MDO的婴儿进行回顾性病历审查。主要结局是困难或失败插管的发生率。次要结局是综合征类型与困难插管发生率之间的关系。
确定了51例皮埃尔·罗宾序列征婴儿。28例患者为孤立性皮埃尔·罗宾序列征,6例为综合征性皮埃尔·罗宾序列征,7例为特雷彻·柯林斯综合征,10例有另一种并存综合征。在下颌骨牵张成骨术(MDO)之前,困难插管的发生率为71%,在患有特雷彻·柯林斯综合征(100%)、综合征性皮埃尔·罗宾序列征(100%)和皮埃尔·罗宾序列征(65%)的患者中发生率最高。MDO后,困难插管的发生率为8.3%。所有患者(Kruskal-Wallis秩和检验P = 0.0001)以及孤立性皮埃尔·罗宾序列征患者(P = 0.0001)、综合征性皮埃尔·罗宾序列征患者(P = 0.0023)和其他综合征患者(P = 0.0002)的差异具有统计学意义,但特雷彻·柯林斯综合征患者(P = 0.21)无差异。3例患者术前已行气管切开术。
在一组非手术气道干预失败的严重上气道阻塞婴儿中,下颌骨牵张成骨术可降低困难面罩通气和困难插管的发生率。我们无法将气道管理的改善情况与一组未接受手术干预的类似皮埃尔·罗宾序列征婴儿进行比较。对于孤立性皮埃尔·罗宾序列征婴儿,喉镜视野的改善最为明显,但对于特雷彻·柯林斯综合征婴儿未显示出显著益处。