AlGhamdi Mohammed, Saiydoun Gabriel, Lebreton Guillaume, Mazzucotelli Jean-Philippe
Cardiac Surgery Division, King Abdulaziz University, Jeddah, Saudi Arabia.
Cardiac Surgery Division, Pitié-Salpêtrière Hospital, Sorbonne University, Paris, France.
Am Heart J Plus. 2025 Apr 9;54:100542. doi: 10.1016/j.ahjo.2025.100542. eCollection 2025 Jun.
This study systematically reviewed the safety and efficacy of atrial septostomy as a left ventricular (LV) unloading intervention in paediatric and adult patients undergoing peripheral venoarterial extracorporeal membrane oxygenation (VA-ECMO).
The PubMed, Cochrane, and Google Scholar online databases were searched, and studies describing patients who received VA-ECMO for refractory cardiogenic shock and underwent atrial septostomy for LV unloading were included. Laboratory experiments, animal studies, and patients who received ECMO with a method other than atrial septostomy for LV unloading were excluded.
From the 12 studies analysed, data were collected on 197 patients, including 97 (49 %) males and 75 (38 %) females (data unavailable for 25 patients) with ages ranging from 3.65 days to 70 years. VA-ECMO duration was 1.71 to 40 days ( < 0.001). Weaning from VA-ECMO with LV discharge was achieved successfully in 126 (64 %) patients, with 60 (30.5 %) in recovery ( = 0.006) and 66 (33.5 %) converted to a ventricular assistant device or transplantation. Additionally, 54 (27.4 %) patients experienced unsuccessful weaning. During atrial septostomy for LV unloading, 14 (7.1 %) patients experienced complications, whereas 180 (91.4 %) did not ( = 0.250). After LV unloading in patients receiving VA-ECMO, 60 (30.5 %) experienced early mortality ( = 0.286).
VA-ECMO-assisted percutaneous atrial septostomy is a viable, safe, and successful alternative for LV unloading in both children and adults with refractory cardiogenic shock. However, further studies with larger sample sizes are required to comprehensively assess the morbidity and mortality associated with this approach.
本研究系统回顾了房间隔造口术作为左心室(LV)卸载干预措施,在接受外周静脉 - 动脉体外膜肺氧合(VA - ECMO)的儿科和成人患者中的安全性和有效性。
检索了PubMed、Cochrane和谷歌学术在线数据库,纳入了描述因难治性心源性休克接受VA - ECMO并为左心室卸载而进行房间隔造口术的患者的研究。排除实验室实验、动物研究以及接受除房间隔造口术以外方法进行左心室卸载的ECMO患者。
在分析的12项研究中,收集了197例患者的数据,其中男性97例(49%),女性75例(38%)(25例患者数据缺失),年龄范围为3.65天至70岁。VA - ECMO持续时间为1.71至40天(P < 0.001)。126例(64%)患者成功从VA - ECMO撤机并左心室射血,60例(30.5%)康复(P = 0.006),66例(33.5%)转为心室辅助装置或接受移植。此外,54例(27.4%)患者撤机失败。在进行房间隔造口术以实现左心室卸载期间,14例(7.1%)患者出现并发症,180例(91.4%)未出现并发症(P = 0.250)。接受VA - ECMO的患者在左心室卸载后,60例(30.5%)出现早期死亡(P = 0.286)。
VA - ECMO辅助的经皮房间隔造口术是难治性心源性休克儿童和成人左心室卸载的一种可行、安全且成功的替代方法。然而,需要更大样本量的进一步研究来全面评估这种方法相关的发病率和死亡率。