Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
Department of Neonatology, Royal Hospital for Children, Glasgow, United Kingdom.
Am J Perinatol. 2024 May;41(S 01):e1709-e1716. doi: 10.1055/a-2067-7925. Epub 2023 Apr 3.
Despite advances in caring for neonates with congenital diaphragmatic hernia (CDH), mortality and morbidity continues to be high. Additionally, the pathophysiology of cardiac dysfunction in this condition is poorly understood. Postnatal cardiac dysfunction in neonates with CDH may be multifactorial with origins in fetal life. Mechanical obstruction, competition from herniated abdominal organs into thoracic cavity combined with redirection of ductus venosus flow away from patent foramen ovale leading to smaller left-sided structures may be a contributing factor. This shunting decreases left atrial and left ventricular blood volume, which may result in altered micro- and macrovascular aberrations affecting cardiac development in the prenatal period. Direct mass effect from herniated intra-abdominal contents restricting cardiac growth and/or reduced left ventricular preload may contribute independently to left ventricular dysfunction in the absence of right ventricular dysfunction and or pulmonary hypertension. With variable clinical phenotypes of cardiac dysfunction, pulmonary hypertension, and respiratory failure in patients with CDH, there is increased need for individualized diagnosis and tailored therapy. Routine use of therapy such as inhaled nitric oxide and sildenafil that induces significant pulmonary vasodilation may be detrimental in left ventricle dysfunction, whereas in a patient with pure right ventricle dysfunction, they may be beneficial. Targeted functional echocardiography serves as a real-time tool for defining the pathophysiology and aids optimization of vasoactive therapy in affected neonates. KEY POINTS: · Cardiac dysfunction in neonates with CDH is multifactorial.. · Postnatal cardiac dysfunction in patients with CDH has its origins in fetal life.. · Right ventricular dysfunction contributes to systemic hypotension.. · Left ventricular dysfunction contributes to systemic hypotension.. · Supportive therapy should be tailored to clinical phenotype..
尽管在治疗先天性膈疝 (CDH) 新生儿方面取得了进展,但死亡率和发病率仍然很高。此外,这种情况下心脏功能障碍的病理生理学仍知之甚少。CDH 新生儿的产后心脏功能障碍可能是多因素的,起源于胎儿期。机械性梗阻、疝入胸腔的腹部器官与静脉窦血流从未闭卵圆孔转向的竞争,导致左侧结构较小,可能是一个促成因素。这种分流减少了左心房和左心室的血量,这可能导致在产前时期影响心脏发育的微血管和大血管异常。疝入的腹腔内容物的直接质量效应限制了心脏生长和/或减少左心室前负荷可能独立导致左心室功能障碍,而在没有右心室功能障碍和/或肺动脉高压的情况下。由于 CDH 患者存在不同的心脏功能障碍、肺动脉高压和呼吸衰竭的临床表现,因此需要个体化诊断和量身定制治疗。常规使用吸入性一氧化氮和西地那非等可引起显著肺血管扩张的治疗方法可能对左心室功能障碍有害,而对单纯右心室功能障碍的患者可能有益。靶向功能超声心动图是一种实时工具,可用于定义病理生理学,并有助于优化受影响新生儿的血管活性治疗。关键点:· CDH 新生儿的心脏功能障碍是多因素的。· CDH 患者的产后心脏功能障碍起源于胎儿期。· 右心室功能障碍导致全身低血压。· 左心室功能障碍导致全身低血压。· 支持性治疗应根据临床表型量身定制。