Didier R A, Oliver E R, Rungsiprakarn P, Debari S E, Adams S E, Hedrick H L, Adzick N S, Khalek N, Howell L J, Coleman B G
Department of Radiology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Center for Fetal Diagnosis and Treatment, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Ultrasound Obstet Gynecol. 2021 Nov;58(5):744-749. doi: 10.1002/uog.23630.
To evaluate the influence of stomach position on postnatal outcome in cases of left congenital diaphragmatic hernia (CDH) without liver herniation, diagnosed and characterized on prenatal ultrasound (US), by comparing those with ('stomach-up' CDH) to those without ('stomach-down' CDH) intrathoracic stomach herniation.
Infants with left CDH who underwent prenatal US and postnatal repair at our institution between January 2008 and March 2017 were eligible for inclusion in this retrospective study. Detailed prenatal US examinations, fetal magnetic resonance imaging (MRI) studies, operative reports and medical records of infants enrolled in the pulmonary hypoplasia program at our institution were reviewed. Cases with liver herniation and those with an additional anomaly were excluded. Cases in which bowel loops were identified within the fetal chest on US while the stomach was intra-abdominal were categorized as having stomach-down CDH. Cases in which bowel loops and the stomach were visualized within the fetal chest on US were categorized as having stomach-up CDH. Prenatal imaging findings and postnatal outcomes were compared between the two groups.
In total, 152 patients with left CDH were initially eligible for inclusion. Seventy-eight patients had surgically confirmed liver herniation and were excluded. Of the 74 included CDH cases without liver herniation, 28 (37.8%) had stomach-down CDH and 46 (62.2%) had stomach-up CDH. Of the 28 stomach-down CDH cases, 10 (35.7%) were referred for a suspected lung lesion. Sixty-eight (91.9%) cases had postnatal outcome data available for analysis. There was no significant difference in median observed-to-expected (o/e) lung-area-to-head-circumference ratio (LHR) between cases with stomach-down CDH and those with stomach-up CDH (41.5% vs 38.4%; P = 0.41). Furthermore, there was no difference in median MRI o/e total lung volume (TLV) between the two groups (49.5% vs 44.0%; P = 0.22). Compared with stomach-up CDH patients, stomach-down CDH patients demonstrated lower median duration of intubation (18 days vs 9.5 days; P < 0.01), median duration of extracorporeal membrane oxygenation (495 h vs 223.5 h; P < 0.05), rate of supplemental oxygen requirement at 30 days of age (20/42 (47.6%) vs 3/26 (11.5%); P < 0.01) and rate of pulmonary hypertension at initial postnatal echocardiography (28/42 (66.7%) vs 9/26 (34.6%); P = 0.01). No neonatal death occurred in stomach-down CDH patients and one neonatal death was seen in a patient with intrathoracic stomach herniation.
In infants with left CDH without liver herniation, despite similar o/e-LHR and o/e-TLV, those with stomach-down CDH have decreased neonatal morbidity compared to those with stomach herniation. Progressive or variable physiological distension of the stomach over the course of gestation may explain these findings. Stomach-down left CDH is mistaken for a lung mass in a substantial proportion of cases. Accurate prenatal US characterization of CDH is crucial for appropriate prenatal counseling and patient management. © 2021 International Society of Ultrasound in Obstetrics and Gynecology.
通过比较胸腔内胃疝入(“胃上移”型先天性膈疝,CDH)与未疝入(“胃下移”型CDH)的左先天性膈疝(无肝脏疝入)病例,评估胃位置对产前超声(US)诊断并特征化的此类病例产后结局的影响。
2008年1月至2017年3月在我院接受产前超声检查及产后修复手术的左CDH婴儿符合纳入本回顾性研究的条件。回顾了我院肺发育不全项目中纳入婴儿的详细产前超声检查、胎儿磁共振成像(MRI)研究、手术报告及病历。排除有肝脏疝入及合并其他异常的病例。超声检查发现胎儿胸部有肠袢而胃位于腹腔内的病例归类为“胃下移”型CDH。超声检查发现胎儿胸部有肠袢及胃的病例归类为“胃上移”型CDH。比较两组的产前影像学表现及产后结局。
共有152例左CDH患者最初符合纳入条件。78例经手术证实有肝脏疝入,予以排除。在纳入的74例无肝脏疝入的CDH病例中,28例(37.8%)为 “胃下移” 型CDH,46例(62.2%)为 “胃上移” 型CDH。在28例“胃下移”型CDH病例中,10例(35.7%)因疑似肺部病变转诊。68例(91.9%)有产后结局数据可供分析。“胃下移”型CDH病例与“胃上移”型CDH病例的中位观察与预期(o/e)肺面积与头围比值(LHR)无显著差异(41.5% 对38.4%;P = 0.41)。此外,两组的中位MRI o/e总肺容积(TLV)无差异(49.5% 对44.0%;P = 0.22)。与“胃上移”型CDH患者相比,“胃下移”型CDH患者的中位插管持续时间较短(18天对9.5天;P < 0.01),中位体外膜肺氧合持续时间较短(495小时对223.5小时;P < 0.05),30日龄时补充氧气需求率较低(20/42(47.6%)对3/26(11.5%);P < 0.01),产后首次超声心动图检查时肺动脉高压发生率较低(28/42(66.7%)对9/26(34.6%);P = 0.01)。“胃下移”型CDH患者无新生儿死亡,1例胸腔内胃疝入患者出现1例新生儿死亡。
在无肝脏疝入的左CDH婴儿中,尽管o/e-LHR和o/e-TLV相似,但“胃下移”型CDH患者的新生儿发病率低于胃疝入患者。孕期胃的渐进性或可变生理性扩张可能解释这些发现。相当一部分“胃下移”型左CDH病例被误诊为肺部肿块。准确的产前超声对CDH进行特征化对于适当的产前咨询和患者管理至关重要。© 2021国际妇产科超声学会。