Venugopal Vinod, Spiro Jon, Zaphiriou Alex, Khan Sohail, Townend Jonathan N, Ludman Peter F, Doshi Sagar N
Queen Elizabeth Hospital, Mindelsohn Way, Edgbaston, Birmingham, B15 2TH, UK,
Cardiol Ther. 2015 Jun;4(1):47-58. doi: 10.1007/s40119-014-0033-8. Epub 2014 Dec 17.
The Impella is a percutaneous ventricular assist device. The majority of published data describes the 2.5L and 5.0L devices, and little data is available for the newer 3.8L device. We examined the indications and outcomes from our single-centre "real-world" registry at The Queen Elizabeth Hospital, Birmingham, UK, using all three pump sizes.
Records from all patients who underwent attempted Impella-assisted procedures at our centre were examined retrospectively. Impella implantation was attempted in 49 patients (mean age 72 ± 13 years; 80% male) and was successful in 48 (98%). 45 patients underwent high-risk percutaneous coronary intervention (PCI), one patient underwent balloon aortic valvuloplasty and 3 patients had Impella as a bridge to cardiac transplantation. The 2.5L and 3.8L devices were used in 36 (75%) and 11 (23%) patients, respectively, while one patient (2%) had the 5L device. Vascular complications occurred in only one patient (2%) and stroke and peri-procedural myocardial infarction occurred in one patient (2%), while in-hospital mortality was 20% (10/49).
In this large real-world registry, we have demonstrated the safety and feasibility of the Impella device for a wide range of indications. This includes the first series of the 3.8L device which provides superior support with no increase in vascular complications.
Impella是一种经皮心室辅助装置。大多数已发表的数据描述的是2.5L和5.0L的装置,而关于新型3.8L装置的数据很少。我们使用这三种泵的规格,对英国伯明翰伊丽莎白女王医院单中心“真实世界”登记处的适应症和结果进行了研究。
对在我们中心接受过Impella辅助手术尝试的所有患者的记录进行回顾性检查。49例患者(平均年龄72±13岁;80%为男性)尝试植入Impella,48例(98%)成功。45例患者接受了高危经皮冠状动脉介入治疗(PCI),1例患者接受了球囊主动脉瓣成形术,3例患者使用Impella作为心脏移植的桥梁。分别有36例(75%)和11例(23%)患者使用了2.5L和3.8L的装置,1例患者(2%)使用了5L的装置。仅1例患者(2%)发生血管并发症,1例患者(2%)发生中风和围手术期心肌梗死,住院死亡率为20%(10/49)。
在这个大型真实世界登记处中,我们证明了Impella装置在广泛适应症中的安全性和可行性。这包括首次使用3.8L装置的系列研究,该装置提供了更好的支持且未增加血管并发症。