Razavi Reza S, Sharland Gurleen K, Simpson John M
Fetal Cardiology Unit, Department of Congenital Heart Disease, Guy's Hospital, London, United Kingdom.
Am J Cardiol. 2003 Feb 15;91(4):429-32. doi: 10.1016/s0002-9149(02)03238-1.
We reported echocardiographic findings and outcomes of fetuses with absent pulmonary valve syndrome diagnosed during fetal life. Cases were identified from a prospectively acquired computerized database of 18,308 pregnancies referred to a fetal cardiology center between January 1988 and July 2000. Twenty fetuses were identified with a median gestation of 23 weeks (range 18 to 36) at presentation. In 18 cases (90%), there was an associated ventricular septal defect. Eighteen cases (90%) had branch pulmonary artery diameters above the normal range. In four cases (20%), an arterial duct was present. A chromosome 22q11 deletion was identified in 2 of 9 cases (22%) in which this deletion was sought. There were 6 terminations of pregnancy (30%), 3 intrauterine deaths (15%), 5 neonatal deaths (25%), 3 infant deaths (15%), and 3 patients who did not die (15%). Ten of the 11 "liveborn" infants required early ventilation. The outcome of absent pulmonary valve syndrome diagnosed prenatally appears poor. The high morbidity and mortality is due to both cardiac disease and associated bronchomalacia.
我们报告了胎儿期诊断为肺动脉瓣缺如综合征的胎儿的超声心动图检查结果及预后情况。病例来自于一个前瞻性获取的计算机数据库,该数据库涵盖了1988年1月至2000年7月间转诊至胎儿心脏病中心的18308例妊娠。共识别出20例胎儿,就诊时的中位孕周为23周(范围18至36周)。18例(90%)伴有室间隔缺损。18例(90%)的分支肺动脉直径超出正常范围。4例(20%)存在动脉导管未闭。在9例进行了该缺失检测的病例中,2例(22%)检测到22号染色体q11缺失。6例(30%)终止妊娠,3例(15%)宫内死亡,5例(25%)新生儿死亡,3例(15%)婴儿死亡,3例(15%)患者存活。11例“活产”婴儿中有10例需要早期通气。产前诊断的肺动脉瓣缺如综合征预后似乎较差。高发病率和死亡率归因于心脏病及相关的支气管软化。