Management advances for congenital diaphragmatic hernia: integrating prenatal and postnatal perspectives.

IF 1.5 4区 医学 Q2 PEDIATRICS Translational pediatrics Pub Date : 2024-04-30 Epub Date: 2024-04-18 DOI:10.21037/tp-23-602
Ahmet A Baschat, Suneetha Desiraju, Meghan L Bernier, Shaun M Kunisaki, Jena L Miller
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Abstract

In congenital diaphragmatic hernia (CDH), abdominal organs are displaced into the chest, compress the lungs, and cause mediastinal shift. This contributes to development of pulmonary hypoplasia and hypertension, which is the primary determinant of morbidity and mortality for affected newborns. The severity is determined using prenatal imaging as early as the first trimester and is related to the laterality of the defect, extent of lung compression, and degree of liver herniation. Comprehensive evaluation of fetal CDH includes imaging-based severity assessment, severity assessment, and evaluation for structural or genetic abnormalities to differentiate isolated from complex cases. Prenatal management involves multispecialty counseling, consideration for fetal therapy with fetoscopic endoluminal tracheal occlusion (FETO) for severe cases, monitoring and intervention for associated polyhydramnios or signs of preterm labor if indicated, administration of antenatal corticosteroids in the appropriate setting, and planned delivery to optimize the fetal condition at birth. Integrated programs that provide a smooth transition from prenatal to postnatal care produce better outcomes. Neonatal care involves gentle ventilation to avoid hyperinflation and must account for transitional physiology to avoid exacerbating cardiac dysfunction and decompensation. Infants who have undergone and responded to FETO have greater pulmonary capacity than expected, but cardiac dysfunction seems unaffected. In about 25-30% of CDH neonates extracorporeal life support is utilized, and this provides a survival benefit for patients with the highest predicted mortality, including those who underwent FETO. Surgical repair after initial medical management for the first 24-48 hours of life is preferred since later repair is associated with delayed oral feeding, increased need for tube feeds, and increased post-repair ventilation requirement and supplemental oxygen at discharge. With overall survival rates >70%, contemporary care involves management of chronic morbidities in the context of a multidisciplinary clinic setting.

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先天性膈疝的管理进展:综合产前和产后的观点。
在先天性膈疝(CDH)中,腹部器官移位到胸部,压迫肺部并导致纵隔移位。这会导致肺发育不全和高血压,而这是受影响新生儿发病率和死亡率的主要决定因素。严重程度早在妊娠头三个月就可通过产前影像学检查确定,并与缺陷的侧位、肺受压程度和肝疝程度有关。胎儿 CDH 的综合评估包括基于影像学的严重程度评估、严重程度评估以及结构或遗传异常评估,以区分孤立和复杂病例。产前管理包括多专科咨询、对严重病例考虑使用胎儿镜下腔内气管闭塞术(FETO)进行胎儿治疗、监测和干预相关的多羊水或早产征象(如有指征)、在适当的环境下使用产前皮质类固醇激素,以及计划分娩以优化出生时的胎儿状况。从产前护理顺利过渡到产后护理的综合方案能产生更好的结果。新生儿护理包括轻柔通气,以避免过度充气,并必须考虑到过渡生理,以避免加重心脏功能障碍和失代偿。接受过 FETO 并对其有反应的婴儿的肺活量比预期的要大,但心脏功能障碍似乎不受影响。约有 25%-30% 的 CDH 新生儿需要使用体外生命支持,这为预测死亡率最高的患者(包括接受过 FETO 的患者)带来了生存益处。在新生儿出生后 24-48 小时内进行初步药物治疗后再进行手术修复更可取,因为较晚进行手术修复会导致口服喂养延迟、管饲需求增加、修复后通气需求增加以及出院时需要补充氧气。由于总体存活率大于 70%,现代护理包括在多学科诊所环境下对慢性病进行管理。
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来源期刊
Translational pediatrics
Translational pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
4.50
自引率
5.00%
发文量
108
期刊介绍: Information not localized
期刊最新文献
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