Hemorrhagic and thromboembolic complications in patients with implanted left ventricular assist devices in early postoperative period

O. Mazurenko, P. Nadzyakevich, O. Loskutov, L. Zgrzeblovska
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Abstract

The work is devoted to study hemorrhagic and thromboembolic complications in early postoperative period after implantation of left ventricular assist devices (LVAD). We performed retrospective analysis of 10 patients, males aged 55±13.5 years, with a BMI of 30.8±8.3, with a left ventricular ejection fraction ranging from 9% to 28%, which in the period from 11.03.2016 to 22.11.2017 year, in the Silesian center of the Heart Disease (Poland), in conditions of artificial blood circulation, LVAD was implanted. In the early postoperative period, patients received daily anticoagulant target therapy (ACCT), consisting of the following drugs: heparin (6-11 U/kg/h), aspirin (75-150 mg), Clopidogrel (75-150 mg), warfarin (1.5-7 mg), Nadroparinum Ca (0.3-0.6 ml/twice on day), Fondaparinux Na (2.5-5 mg/twice on day). Two patients received mono-heparin therapy, one patient received monotherapy with warfarin for 14 days. Other patients during the same period received combined heparin therapy in the first three days with a subsequent transition to warfarin, aspirin, Clopidogrel, Fraxiparin, or thrombin blocker. The mechanical support of the left ventricle was carried out essentially by two different implantable systems, performing one function of support of the left ventricle: POLVAD – programmed controlled pneumatic membrane mechanical circulation of blood to two patients, and LVAD program-controlled electro-centrifugal circulation for eight patients. The duration of support by POLVAD system was from 102 to 156 days. Length of support – LVAD ranged from 20 to 78 days. A comparison of the analyzed results led to the conclusion that anticoagulant mono-therapy with heparin or warfarin leads to an increase in the percentage of complications and mortality compared with the alternative combination anticoagulant targeted therapy consisting of the following drugs: heparin (6-11 U/kg/h), aspirin 75-150 mg), Clopidogrel (75-150 mg), warfarin (1.5-7 mg), Nadroparinum Ca (0.3-0.6 ml/ twice on day), Fondaparinux Na (2.5-5 mg/ twice on day), Where survival rates were significantly higher by 60%.
术后早期植入左心室辅助装置患者的出血和血栓栓塞并发症
本研究旨在探讨左心室辅助装置(LVAD)植入术后早期出血及血栓栓塞并发症。回顾性分析2016年3月11日至2017年11月22日在波兰西里西亚心脏病中心人工血液循环条件下植入LVAD的10例患者,男性,年龄55±13.5岁,BMI为30.8±8.3,左心室射血分数为9% ~ 28%。术后早期患者每日给予抗凝靶向治疗(ACCT),包括肝素(6-11 U/kg/h)、阿司匹林(75-150 mg)、氯吡格雷(75-150 mg)、华法林(1.5-7 mg)、Nadroparinum Ca (0.3-0.6 ml/ 2次/ d)、Fondaparinux Na (2.5-5 mg/ 2次/ d)。2例患者接受单肝素治疗,1例患者接受华法林单药治疗,疗程14天。同一时期的其他患者在前三天接受联合肝素治疗,随后改用华法林、阿司匹林、氯吡格雷、弗拉西帕林或凝血酶阻滞剂。左心室的机械支持主要由两个不同的植入式系统进行,执行一个左心室的支持功能:POLVAD -程序化控制的气动膜机械血液循环2例,LVAD -程序化控制的电离心循环8例。POLVAD系统支持时间为102 ~ 156天。LVAD支持时间从20天到78天不等。通过对分析结果的比较,得出结论:与由以下药物组成的抗凝药物联合靶向治疗相比,肝素或华法林单药抗凝治疗导致并发症和死亡率的百分比增加:肝素(6-11 U/kg/h)、阿司匹林75-150 mg)、氯吡格雷(75-150 mg)、华法林(1.5-7 mg)、Nadroparinum Ca (0.3-0.6 ml/ 2次/ d)、Fondaparinux Na (2.5-5 mg/ 2次/ d),存活率显著提高60%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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