Panos A, Kalangos A, Urban P
Département de chirurgie, Hôpitaux Universitaires de Genève.
Schweiz Med Wochenschr. 1999 Oct 23;129(42):1529-34.
The hemopump is a transvalvular, catheter-mounted, left ventricular assist device, intended for surgical placement via the femoral artery (hemopump 21 Fr. outer diameter). This device has demonstrated its ability to unload the left ventricle, leading to myocardial protection and haemodynamic stabilisation in patients with cardiogenic shock and those undergoing high-risk coronary angioplasty (PTCA). Since 1994, a new hemopump system (14 Fr. in external diameter, flow rates of 1.5-2.2 l/min) has been developed for percutaneous insertion. The aim of this study is to describe the immediate and mid-term results obtained during Hemopump 14 Fr. assisted high-risk PTCA.
Between September, 1993 and July, 1996, 8 males and 5 female patients (mean age 68.5 +/- 8.6 years) underwent Hemopump 14 Fr. supported high-risk PTCA.
Mean duration of hemopump assistance was 108 +/- 62 min. Hemopump support on maximum speed led to an increase of cardiac index from 2.0 +/- 0.3 to 2.2 +/- 0.5 l/min (p = 0.04) and a decrease of pulmonary wedge pressure from 17 +/- 8 to 14 +/- 8 mm Hg (p = 0.004). LDH increased (463 +/- 305 to 558 +/- 237 u/l-p = 0.05) and the platelet count remained stable (192,840 +/- 60,904 to 190,230 +/- 56,492/mm3). Successful balloon angioplasty was performed in all patients. There was no hospital mortality. Three patients (23%) required blood transfusion. During follow-up, 1 patient (7.7%) developed femoral artery occlusion necessitating surgical repair, and 3 patients (23%) died from cardiac causes 3, 9 and 14 months after the procedure.
The 14 Fr. Hemopump device may constitute a useful percutaneous mode of haemodynamic support for patients undergoing high-risk PTCA. The haemolysis it causes is mild and not clinically significant, but the hemopump is associated with a significant rate of local vascular complications. Recent improvements in interventional techniques and hardware have decreased the necessity for circulatory assistance during elective PTCA, even for very ill patients. Nevertheless, indications such as cardiogenic shock, the "bridge" period prior to heart transplantation and video-assisted minimally invasive cardiac surgery, or haemodynamic support of the right ventricle are the new applications of the hemopump.
血液泵是一种经瓣膜、安装在导管上的左心室辅助装置,旨在通过股动脉进行手术植入(血液泵外径21 Fr.)。该装置已证明其能够减轻左心室负荷,从而对心源性休克患者和接受高风险冠状动脉血管成形术(PTCA)的患者起到心肌保护和血流动力学稳定的作用。自1994年以来,已开发出一种新型血液泵系统(外径14 Fr.,流速为1.5 - 2.2升/分钟)用于经皮插入。本研究的目的是描述在14 Fr.血液泵辅助下进行高风险PTCA期间获得的即刻和中期结果。
在1993年9月至1996年7月期间,8名男性和5名女性患者(平均年龄68.5±8.6岁)接受了14 Fr.血液泵支持的高风险PTCA。
血液泵辅助的平均持续时间为108±62分钟。血液泵以最大速度支持导致心脏指数从2.0±0.3增加到2.2±0.5升/分钟(p = 0.04),肺楔压从17±8降低到14±8毫米汞柱(p = 0.004)。乳酸脱氢酶升高(从463±305升高到558±237 u/l - p = 0.05),血小板计数保持稳定(从192,840±60,904降至190,230±56,492/mm³)。所有患者均成功进行了球囊血管成形术。无医院死亡病例。3名患者(23%)需要输血。在随访期间,1名患者(7.7%)发生股动脉闭塞,需要进行手术修复,3名患者(23%)在术后3、9和14个月死于心脏原因。
14 Fr.血液泵装置可能是接受高风险PTCA患者有用的经皮血流动力学支持方式。它引起的溶血轻微且无临床意义,但血液泵与较高的局部血管并发症发生率相关。介入技术和硬件的最新改进已减少了择期PTCA期间循环辅助的必要性,即使对于病情非常严重的患者也是如此。然而,诸如心源性休克、心脏移植前的“过渡”期和电视辅助微创心脏手术,或右心室的血流动力学支持等适应症是血液泵的新应用。