Long-term assist device patients admitted to ICU: Tips and pitfalls

Michiel Morshuis, Hendrik Fox, Volker Lauenroth, Rene Schramm
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引用次数: 1

Abstract

Left ventricular assist device (LVAD) therapy is well-established in the treatment of end-stage cardiac failure. Indications are bridge to transplant (BTT), bridge to candidacy (BTC), bridge to recovery (BTR), and destination therapy (DT). The durability and adverse event (AE) rate of LVADs have improved over the years. However, due to donor shortage, the duration of support in the BTT population has increased tremendously; similarly, DT patients are on the device for a long time. Consequently, the number of readmissions of long-term LVAD patients has increased. In cases of severe AEs, intensive care unit (ICU) treatment can be necessary. Infectious complications are the most common AE. Furthermore, embolic or hemorrhagic strokes can occur due to foreign surfaces, acquired von Willebrand syndrome, and anticoagulation treatment. Another consequence of the coagulative status, in combination with the continuous flow, are gastrointestinal bleeding events. Moreover, in most patients, an isolated LVAD is implanted, and this involves the risk of late right heart failure. Adjustment of pump speed and optimization of the volume status can help solve this issue. Malignant arrhythmias, pre-existing or de novo after LVAD implantation, can be a life-threatening AE. Antiarrhythmic medical therapy or ablation are potential treatment options. As for specific LVADs, the Medtronic HeartWare™ ventricular assist device (HVAD) is not manufactured and distributed currently; however, 4000 patients are still on the device. Pump thrombosis can occur, wherein thrombolytic therapy is the first-line treatment option. Additionally, the HVAD can fail to restart after controller exchange due to technical issues, and precautions must be taken. The Momentum 3 trial showed superior survival without pump exchange or disabling stroke in patients treated with the HeartMate 3 (HM3; Abbott, Abbott Park, IL, USA) device in comparison to the HeartMate II (HMII). However, in a few cases, a twisted graft or bio debris formation between the outflow graft and bend relief could be observed, causing outflow graft obstruction. Patients on LVADs are still heart failure patients, in many cases with comorbidities. Therefore, many situations can occur requiring ICU treatment. Ethical aspects should always be the focus when taking care of these patients.

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入住ICU的长期辅助设备患者:提示和陷阱
左心室辅助装置(LVAD)治疗在治疗终末期心力衰竭方面已得到广泛认可。适应症包括移植桥(BTT)、候选桥(BTC)、康复桥(BTR)和目的地治疗(DT)。LVAD的耐久性和不良事件(AE)发生率多年来有所提高。然而,由于捐助者短缺,BTT人群的支持时间大幅增加;类似地,DT患者使用该设备的时间很长。因此,长期LVAD患者的再次入院人数有所增加。在严重AE的情况下,重症监护室(ICU)治疗可能是必要的。感染性并发症是最常见的AE。此外,由于异物表面、获得性von Willebrand综合征和抗凝治疗,可能会发生栓塞或出血性中风。凝血状态的另一个后果,结合持续流动,是胃肠道出血事件。此外,在大多数患者中,植入了孤立的LVAD,这涉及晚期右心衰竭的风险。泵速的调整和容积状态的优化可以帮助解决这个问题。LVAD植入后预先存在或新发的恶性心律失常可能是危及生命的AE。抗心律失常药物治疗或消融是潜在的治疗选择。对于特定的LVAD,美敦力HeartWare™ 心室辅助装置(HVAD)目前尚未生产和分销;然而,仍有4000名患者使用该设备。泵血栓形成可能发生,其中溶栓治疗是一线治疗选择。此外,由于技术问题,HVAD在更换控制器后可能无法重新启动,必须采取预防措施。Momentum 3试验显示,与HeartMate II(HMII)相比,使用HeartMate 3Ⓡ(HM3;Abbott,Abbott Park,IL,USA)设备治疗的患者在没有泵交换或致残性中风的情况下存活率更高。然而,在少数情况下,可以观察到流出移植物和弯曲缓解之间形成扭曲的移植物或生物碎片,导致流出移植物阻塞。LVAD患者仍然是心力衰竭患者,在许多情况下伴有合并症。因此,可能会出现许多需要ICU治疗的情况。在照顾这些病人时,伦理方面应该始终是重点。
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来源期刊
Journal of intensive medicine
Journal of intensive medicine Critical Care and Intensive Care Medicine
CiteScore
1.90
自引率
0.00%
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0
审稿时长
58 days
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