Kido Takashi, Nishigaki Kyoichi, Kawahira Yoichi, Kagisaki Koji, Tanimoto Kazuki, Ehara Eiji, Murakami Yosuke
Department of Pediatric Cardiovascular Surgery, Osaka City General Hospital, Osaka, Japan.
Department of Pediatric Cardiology, Osaka City General Hospital, Osaka, Japan.
Interact Cardiovasc Thorac Surg. 2018 May 1;26(5):840-844. doi: 10.1093/icvts/ivx417.
This study aimed to review the clinical outcomes of staged cardiac surgery in extremely low-birthweight infants with congenital heart disease and pulmonary overcirculation.
Six extremely low-birthweight infants with congenital heart disease and pulmonary overcirculation underwent staged cardiac surgery between 2005 and 2017. The median birthweight was 895 g (range 620-990 g), and the median gestational age was 28 weeks (range 23-31 weeks). Clinical outcomes were evaluated, and we focused on pulmonary haemodynamics.
Pulmonary artery banding or bilateral pulmonary artery banding was performed as the initial palliation at a median age of 23 days with a median body weight of 880 g. Corrective surgery was performed at a median age of 187 days with a median body weight of 3.9 kg. All of the patients successfully underwent corrective surgery and survived to date. Pulmonary hypertension regressed after corrective surgery in all of the patients, except for 1 patient with severe bronchopulmonary dysplasia.
Acceptable outcomes can be obtained by staged cardiac surgery in extremely low-birthweight infants with congenital heart disease and pulmonary overcirculation. While early pulmonary artery banding can lead to regression of pulmonary hypertension after corrective surgery, close follow-up is required.
本研究旨在回顾患有先天性心脏病和肺循环过度的极低出生体重儿分期心脏手术的临床结果。
2005年至2017年间,6例患有先天性心脏病和肺循环过度的极低出生体重儿接受了分期心脏手术。中位出生体重为895克(范围620 - 990克),中位胎龄为28周(范围23 - 31周)。评估了临床结果,我们重点关注肺血流动力学。
肺动脉环扎术或双侧肺动脉环扎术作为初始姑息治疗,中位年龄为23天,中位体重为880克。矫正手术在中位年龄187天、中位体重3.9千克时进行。所有患者均成功接受矫正手术并存活至今。除1例患有严重支气管肺发育不良的患者外,所有患者矫正手术后肺动脉高压均有所消退。
对于患有先天性心脏病和肺循环过度的极低出生体重儿,分期心脏手术可获得可接受的结果。虽然早期肺动脉环扎术可导致矫正手术后肺动脉高压消退,但仍需要密切随访。