新生儿先天性膈疝体外膜氧合:初步经验

Taehoon Kim, M. Cho, Jeong-Jun Park, D. Kim, S. Kim, I. Kim
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引用次数: 2

摘要

【体外膜氧合(ECMO)已被应用于先天性膈疝(CDH)患者严重呼吸衰竭,对常规药物治疗无反应。】我们回顾性回顾了2008年4月至2011年2月在我中心接受ECMO治疗的12例CDH患者。分析ECMO前和ECMO后的变量包括胎龄、性别、出生体重、插管时的年龄、动脉血气分析结果、CDH位置、CDH修复手术时机、并发症和生存率。有9个男孩和3个女孩。所有患者均进行了产前诊断。平均胎龄为38.8美元1.7美元周,平均出生体重为3031美元499美元克。ECMO插管时的平均年龄为$29.9{\pm}28.9$小时。有4名患者存活。幸存者的5分钟Apgar评分较高(8.25{\pm}0.96美元比7.00{\pm}1.20美元,p=0.109), ECMO前平均pH较高(7.258 {\pm}0.830美元比7.159{\pm}0.986美元,p=0.073), ECMO前PaCO_2$较低(48.2{\pm}7.9美元比64.8{\pm}16.1美元,p=0.109),但无统计学意义。疝位于左侧10例,右侧2例。早期5例置入ECMO至手术修复时间间隔约3~4天,其余病例约24天。术后出血需再次手术3例,腹膜间室综合征需腹筋膜重新开放2例。4例需要重新定位ECMO导管。发现动脉或静脉血栓形成3例,经随访改善。我们的数据表明,ECMO治疗可以挽救一些不能维持其他治疗方式的CDH新生儿的生命。方案化的管理和病例经验的积累可能对改善ECMO治疗新生儿CDH的预后有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extracorporeal Membrane Oxygenation in Neonates with Congenital Diaphragmatic Hernia: a Preliminary Experience
【Extracorporeal membrane oxygenation (ECMO) has been utilized in congenital diaphragmatic hernia (CDH) patients with severe respiratory failure unresponsive to conventional medical treatment. We retrospectively reviewed 12 CDH patients who were treated using ECMO in our center between April 2008 and February 2011. The pre ECMO and on ECMO variables analyzed included gestational age, sex, birth weight, age at the time of ECMO cannulation, arterial blood gas analysis results, CDH location, timing of CDH repair operation, complications and survival. There were 9 boys and 3 girls. All patients were prenatally diagnosed. Mean gestational age was $38.8{\pm}1.7$ weeks and mean birth weight was $3031{\pm}499$ gram. Mean age at the time of ECMO cannulation was $29.9{\pm}28.9$ hours. There were 4 patients who survived. Survivors showed higher 5 min Apgar scores ( $8.25{\pm}0.96$ vs. $7.00{\pm}1.20$ , p=0.109), higher pre ECMO mean pH ( $7.258 {\pm}0.830$ vs. $7.159{\pm}0.986$ , p=0.073) and lower pre ECMO $PaCO_2$ ( $48.2{\pm}7.9$ vs. $64.8{\pm}16.1$ , p=0.109) without statistical significance. The hernia was located on the left side in 10 patients and the right side in 2 patients. The time interval from ECMO placement to operative repair was about 3~4 days in 5 early cases and around 24 in the remaining cases. There were 3 cases of post operative bleeding requiring re operation and 2 cases of abdominal compartment syndrome requiring abdominal fascia reopening. ECMO catheter reposition was required in 4 cases. Three cases of arterial or venous thrombosis were detected and improved with follow up. Our data suggests that ECMO therapy could save the lives of some neonates with CDH who can not be maintained on other treatment modalities. Protocolized management and accumulation of case experience might be valuable in improving outcomes for neonates with CDH treated with ECMO.】
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