Asou Toshihide, Kawataki Motoyoshi, Takeda Yuko, Asai Hidetsugu, Tachibana Tsuyoshi, Toyoshima Katsuaki, Kim Ki-Sung, Ueda Hideaki
Department of Cardiovascular Surgery, Kanagawa Children's Medical Center, Yokohama, Japan.
Department of Neonatology, Kanagawa Children's Medical Center, Yokohama, Japan.
Eur J Cardiothorac Surg. 2020 Nov 1;58(5):957-963. doi: 10.1093/ejcts/ezaa139.
The purpose of this study is to review the short- and long-term outcomes of high-risk neonates with Ebstein anomaly treated with a newly developed rapid 2-stage Starnes procedure, which is aimed at reducing the size of the enlarged right side of the heart.
Fifty-two foetuses with Ebstein anomaly were analysed in this study and divided into 2 groups. The control group comprised 25 foetuses, referred to us before 2008, and the study group was composed of 27 foetuses, referred to us after 2009. The right atrial area index was defined as high risk when it was >1.5. We applied our management approach to 6 high-risk neonates in the study group. This approach consisted of reducing the size of the right side of the heart through a 2-stage process: (i) right atrial plication without the use of a bypass and (ii) a Starnes procedure. Cox proportional hazards models were used to evaluate the effects of our management approach on the survival rates of the neonates.
The mean follow-up period was 7.5 ± 3.3 years. All 6 high-risk neonates in the study group survived. The overall hazard ratio was 0.12 (95% confidence interval of 0.03-0.43) in the study group as compared with the control group (P = 0.0007). A Fontan operation was completed in all but 1 case, with the remaining case awaiting a Fontan operation.
We suggest that a rapid 2-stage Starnes approach can be effective in the treatment of high-risk neonates with Ebstein anomaly.
本研究旨在回顾采用新开发的快速两阶段斯塔恩斯手术治疗埃布斯坦畸形高危新生儿的短期和长期预后,该手术旨在减小扩大的右心尺寸。
本研究分析了52例患有埃布斯坦畸形的胎儿,并将其分为两组。对照组包括25例于2008年前转诊至我们这里的胎儿,研究组由27例于2009年后转诊至我们这里的胎儿组成。当右心房面积指数>1.5时被定义为高危。我们对研究组中的6例高危新生儿采用了我们的治疗方法。该方法包括通过两阶段过程减小右心尺寸:(i)不使用体外循环的右心房折叠术和(ii)斯塔恩斯手术。采用Cox比例风险模型评估我们的治疗方法对新生儿存活率的影响。
平均随访期为7.5±3.3年。研究组的所有6例高危新生儿均存活。与对照组相比,研究组的总体风险比为0.12(95%置信区间为0.03 - 0.43)(P = 0.0007)。除1例病例外,所有病例均完成了Fontan手术,其余1例正在等待Fontan手术。
我们认为快速两阶段斯塔恩斯手术方法在治疗埃布斯坦畸形高危新生儿方面可能有效。