Sen Lu, Pin Wang, Xiao-Qin Zhang, Gang Feng, Hong-Li He, Yue Chen, Xiao-Bo Huang, Chun Pan, Jing-Chao Luo
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引用次数: 0
摘要
背景:静脉-动脉(V-A)和静脉-静脉(V-V)体外膜氧合(ECMO)是肺移植过程中至关重要的支持方式,但其比较效果尚不清楚。方法:我们对62例接受术中ECMO的肺移植患者(29 V-A, 33 V-V)进行了8年的回顾性分析。比较基线特征、手术参数和临床结果。为了解决潜在的选择偏差,我们采用了熵加权处理加权逆概率(IPTW-EW)。结果:iptww - ew调整后,V-A ECMO与优越的血流动力学和呼吸参数相关,包括较低的肺动脉收缩压(30对37 mmHg, p = 0.007),较高的动脉氧分压(119对78 mmHg, p = 0.002)和较轻的肺水肿(1级:50%对3%,2级:45%对38%,3级:5%对59%,p。与V-V ECMO相比,V-A ECMO在肺移植中提供了更好的肺循环卸载,并与改善的生存结果相关,建议在临床合适时优先使用V-V ECMO。
The superiority of veno-arterial over veno-venous extracorporeal membrane oxygenation for operative support of lung transplantation.
Background: Veno-arterial (V-A) and veno-venous (V-V) extracorporeal membrane oxygenation (ECMO) are crucial support modalities during lung transplantation, yet their comparative effectiveness remains unclear.
Methods: We conducted an 8-year retrospective analysis of 62 lung transplant recipients who received intraoperative ECMO (29 V-A, 33 V-V). Baseline characteristics, surgical parameters, and clinical outcomes were compared. To address potential selection bias, we employed entropy weighted inverse probability of treatment weighting (IPTW-EW).
Results: After IPTW-EW adjustment, V-A ECMO was associated with superior hemodynamic and respiratory parameters, including lower systolic pulmonary artery pressure (30 vs. 37 mmHg, p = 0.007), higher arterial oxygen partial pressure (119 vs. 78 mmHg, p = 0.002), and less severe pulmonary edema (Grade 1: 50% vs. 3%, Grade 2: 45% vs. 38%, Grade 3: 5% vs. 59%, p < 0.001). Notably, V-A ECMO demonstrated significantly lower 28-day (5% vs. 29%, p = 0.017) and hospital mortalities (21% vs. 69%, p = 0.035).
Conclusions: V-A ECMO provides superior pulmonary circulation unloading and is associated with improved survival outcomes compared to V-V ECMO in lung transplantation, suggesting its preferential use when clinically appropriate.
期刊介绍:
BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.