Goergen Stacy, Christie James, Jackson Tracy, Smet Maria-Elisabeth, Robertson Simon, Malhotra Atul, Kroushev Annie, Lovell Mark
Monash Imaging, Monash Health, Melbourne, Australia.
School of Clinical Sciences, Monash University, Melbourne, Australia.
Prenat Diagn. 2024 Dec;44(13):1593-1602. doi: 10.1002/pd.6651. Epub 2024 Sep 24.
Neonatal airway compromise requiring intubation, due to micrognathia or a mass lesion obstructing the fetal airway, remains difficult but important to predict prenatally. We aimed to validate MR predictors of difficult neonatal airway (DNA) in a multicentre retrospective cohort of fetuses with micrognathia and oropharyngeal/neck masses.
The radiology databases of two large Australian maternal-fetal medicine centers were searched for subjects meeting inclusion criteria: Pregnancies of > 18 weeks' gestation evaluated with prenatal ultrasound and MRI between 2007 and 2022 where either fetal micrognathia or a fetal cervical, oral or oropharyngeal mass was identified on prenatal ultrasound and MRI, and details of delivery/postnatal course were available including: nature of delivery, need for the fetal airway to be secured at delivery, degree of difficulty in airway securement, survival > 24 h postnatally. Imaging predictors of a difficult neonatal airway (DNA) were assessed blinded to these neonatal outcomes.
Twenty-six fetuses met the inclusion criteria. Oropharyngeal and neck mass location with polyhydramnios was 100% sensitive and 82% specific for DNA. JI < 5th centile with polyhydramnios was 83% sensitive and 70% specific. JI < 5th centile with polyhydramnios was associated with DNA in 80% of cases delivered by ex utero intrapartum (EXIT) delivery and none with non-EXIT delivery mode.
A cervical or oropharyngeal mass with polyhydramnios predicted a difficult neonatal airway. Polyhydramnios with jaw index < 5th centile was less sensitive and less specific for a difficult neonatal airway.
由于小颌畸形或肿块病变阻塞胎儿气道而需要插管的新生儿气道受损,在产前预测仍然困难但很重要。我们旨在在一个多中心回顾性队列中验证小颌畸形和口咽/颈部肿块胎儿的新生儿气道困难(DNA)的磁共振成像预测指标。
检索澳大利亚两个大型母胎医学中心的放射学数据库,寻找符合纳入标准的受试者:2007年至2022年期间妊娠超过18周,接受产前超声和磁共振成像评估,产前超声和磁共振成像发现胎儿小颌畸形或胎儿颈部、口腔或口咽肿块,且有分娩/产后病程细节,包括:分娩方式、分娩时确保胎儿气道安全的必要性、气道安全保障的困难程度、出生后存活超过24小时。在对这些新生儿结局不知情的情况下评估新生儿气道困难(DNA)的影像学预测指标。
26例胎儿符合纳入标准。羊水过多时口咽和颈部肿块位置对DNA的敏感性为100%,特异性为82%。羊水过多时颌指数<第5百分位数的敏感性为83%,特异性为70%。羊水过多时颌指数<第5百分位数在80%的经产时子宫外产时处理(EXIT)分娩的病例中与DNA相关,而在非EXIT分娩方式中无一例相关。
伴有羊水过多的颈部或口咽肿块预示新生儿气道困难。羊水过多且颌指数<第5百分位数对新生儿气道困难的敏感性和特异性较低。