Optimal Therapeutic Strategy for Ventricular Septal Defect Closure in Extremely Preterm Infants with Chronic Lung Disease and Severe Pulmonary Hypertension.

IF 1.3 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Akari Sato, Mai Sekine, Hidenori Kawasaki, Masayo Kanai, Hirotaka Ishido, Yoichi Iwamoto, Hideaki Senzaki, Ayumu Masuoka, Fujito Numano, Jun Muneuchi, Norie Mitsushita, Satoshi Masutani
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Abstract

In preterm infants with large ventricular septal defects (VSD), severe chronic lung disease (CLD), and pulmonary hypertension (PH), hemodynamic instability may occur after open-heart surgery. The selection of first pulmonary artery banding or one stage VSD closure is a clinical issue. At present, no guidelines exist to support decision-making in this unique population. This study reports the case of a preterm infant with a gestational age of 23 weeks and 4 days, a birth weight of 540 g, and elevated immunoglobulin-M levels, who was successfully treated with pulmonary artery banding and subsequently VSD closure. Before pulmonary artery banding, the pulmonary-to-systemic blood flow ratio was 2.5 and pulmonary vascular resistance was 2.6 U·m2 under general anesthesia with FiO2 = 0.6. However, pulmonary artery banding preceded considering the severe CLD and the risk of PH crisis after cardiopulmonary bypass. In a review of the literature on preterm infants with VSD with CLD and PH, only five infants, including the one in this case, were found. One infant underwent pulmonary artery banding first and survived, and three infants underwent one-stage VSD closure, after which one died (trisomy 21) due to a postoperative PH crisis. Three of the five cases underwent tracheostomy. The selection of first pulmonary artery banding or one-stage VSD closure needs to be carefully considered on a case-by-case basis, taking into consideration the severity of the VSD with CLD and PH. A future registry study will be needed to review these cases and clarify the outcome of the two strategies.

慢性肺病合并重度肺动脉高压的极早产儿室间隔缺损闭合的最佳治疗策略。
对于有大室间隔缺损(VSD)、严重慢性肺病(CLD)和肺动脉高压(PH)的早产儿,心内直视手术后可能出现血流动力学不稳定。选择第一肺动脉束带或一期室间隔关闭是一个临床问题。目前,尚无指导方针支持这一独特人群的决策。本研究报告了一例胎龄23周零4天,出生体重540 g,免疫球蛋白m水平升高的早产儿,成功地接受了肺动脉束带和随后的室间隔关闭治疗。肺动脉束带前,全麻FiO2 = 0.6时肺-全身血流量比为2.5,肺血管阻力为2.6 U·m2。然而,考虑到严重的CLD和体外循环后PH危机的风险,首选肺动脉绑扎。在一篇关于室间隔缺损合并CLD和PH的早产儿的文献综述中,只发现了5例婴儿,包括本例中的一例。一名婴儿首先接受了肺动脉捆扎术并存活下来,三名婴儿接受了一期室间隔关闭术,其中一名婴儿因术后PH危机死亡(21三体)。5例中有3例行气管切开术。第一肺动脉捆扎术或一期室间隔封闭术的选择需要在个案的基础上仔细考虑,考虑到室间隔缺损合并CLD和ph的严重程度。未来的注册研究将需要回顾这些病例并澄清这两种策略的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International heart journal
International heart journal 医学-心血管系统
CiteScore
2.50
自引率
6.70%
发文量
148
审稿时长
6-12 weeks
期刊介绍: Authors of research articles should disclose at the time of submission any financial arrangement they may have with a company whose product figures prominently in the submitted manuscript or with a company making a competing product. Such information will be held in confidence while the paper is under review and will not influence the editorial decision, but if the article is accepted for publication, the editors will usually discuss with the authors the manner in which such information is to be communicated to the reader.
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