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胎儿心肺循环持续存在:新生儿暂时性呼吸急促的一种表现。

Persistence of fetal cardiopulmonary circulation: one manifestation of transient tachypnea of the newborn.

作者信息

Bucciarelli R L, Egan E A, Gessner I H, Eitzman D V

出版信息

Pediatrics. 1976 Aug;58(2):192-7.

PMID:951133
Abstract

Five cyanotic newborn infants underwent cardiac catheterization between 8 and 36 hours of age with a tentative diagnosis of cyanotic congenital heart disease. All had normal cardiovascular anatomy. Cyanosis was the result of persistence of fetal cardiopulmonary circulation with right-to-left shunting across the ductus arteriosus. In all infants, cyanosis resolved spontaneously and the infants survived without sequelae. Admission chest roentgenograms of all infants showed marked hyperinflation of the lungs. Except for severe hypoxemia, the clinical presentation, chest films, and course of illness of these infants were consistent with transient tachypnea of the newborn. It is proposed that an increase in pulmonary vascular resistance, due to hyperinflation of the lungs, was the mechanism which reopened the fetal cardiopulmonary circulatory channels and produced hypoxemia, and that these infants suffered from a rare manifestation of a usually benign newborn respiratory condition. Further, given these pathophysiologic mechanisms, the use of continuous transpulmonary pressure gradients in the management of such infants would be contraindicated.

摘要

五名发绀型新生儿在出生8至36小时之间接受了心导管检查,初步诊断为发绀型先天性心脏病。所有患儿心血管解剖结构均正常。发绀是由于胎儿心肺循环持续存在,经动脉导管发生右向左分流所致。所有患儿发绀均自行消退,且存活下来无后遗症。所有患儿入院时的胸部X线片均显示肺部明显过度充气。除严重低氧血症外,这些患儿的临床表现、胸片及病程均与新生儿短暂性呼吸急促相符。有人提出,肺部过度充气导致肺血管阻力增加,这是重新开启胎儿心肺循环通道并导致低氧血症的机制,且这些患儿患的是一种通常为良性的新生儿呼吸系统疾病的罕见表现形式。此外,鉴于这些病理生理机制,在这类患儿的治疗中使用连续跨肺压力梯度是禁忌的。

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