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Heart failure etiology and risk of right heart failure in adult left ventricular assist device support: the European Registry for Patients with Mechanical Circulatory Support (EUROMACS).
Scandinavian Cardiovascular Journal ( IF 1.2 ) Pub Date : 2020-06-18 , DOI: 10.1080/14017431.2020.1781239
Brian Bridal Løgstrup 1 , Petr Nemec 2 , Felix Schoenrath 3, 4 , Jan Gummert 5 , Yuri Pya 6 , Evgenij Potapov 3 , Ivan Netuka 7 , Faiz Ramjankhan 8 , Eric Thorlund Parner 9 , Theo De By 10 , Hans Eiskjaer 1
Affiliation  

Abstract

Objectives: Development of right ventricular failure (RVF) after left ventricular assist device (LVAD) implantation remains a leading cause of perioperative morbidity, end-organ dysfunction and mortality. The objective of this study was to investigate whether the etiology of HF (ischemic HF versus non-ischemic HF) affects the risk of RVF within admission for LVAD implantation and during long-term follow-up. Methods: Between January 2011 and June 27, 2018, 3536 patients were prospectively enrolled into EUROMACS registry. Adult patients (>18 years) who received a first time LVAD were included. When excluding patients with congenital, restrictive, hypertrophic, valvular cardiomyopathies, and myocarditis the total population consisted of 2404 patients. Results: The total cohort consists of 2404 patients. Mean age were 55 years and predominantly male sex [2024 (84.2%)]. At the time of LVAD implantation 1355 (56.4%) patients had ischemic HF and 1049 (43.6%) patients had non-ischemic HF. The incidence of RVF was significantly increased in the non-ischemic HF group in the adjusted model (p = .026). The relative risk difference for RVF in patients with non-ischemic HF was in the adjusted model increased by an absolute value of 5.1% (95% CI: 0.61–9.6). In the ischemic HF group 76 patients (13.4%) developed late RVF and 62 patients (14.8%) in the non-ischemic HF group (p = .56). No differences in occurrence of RVF between HF etiology was observed after 2 and 4 years of follow-up, respectively (crude: p = .25, adjusted (sex and age) p = .2 and crude: p = .59, adjusted (sex and age) p = .44). Conclusions: Patients with non-ischemic HF undergoing LVAD had an increased incidence of early RVF compared to patients with ischemic HF in a large European population. During follow-up after discharge 14% patients developed RVF. We recommend HF etiology to be considered in identifying patients who are at risk for postoperative RVF after LVAD implantation.



中文翻译:

成人左心室辅助设备支持中的心力衰竭病因学和右心衰竭风险:欧洲机械循环支持患者注册中心(EUROMACS)。

摘要

目的:植入左室辅助装置(LVAD)后发生右室衰竭(RVF)仍是围手术期发病率,终末器官功能障碍和死亡率的主要原因。这项研究的目的是调查HF的病因(缺血性HF与非缺血性HF)是否会影响LVAD植入入院时以及长期随访期间RVF的风险。方法: 2011年1月至2018年6月27日,前瞻性地将3536例患者纳入EUROMACS登记册。包括首次接受LVAD的成年患者(> 18岁)。当排除患有先天性,限制性,肥厚性,瓣膜型心肌病和心肌炎的患者时,总人口为2404名患者。结果:总队列包括2404名患者。平均年龄为55岁,主要为男性[2024(84.2%)]。LVAD植入时,有1355名患者(56.4%)有缺血性HF,有1049名患者(43.6%)有非缺血性HF。在调整后的模型中,非缺血性HF组的RVF发生率显着增加(p  = .026)。在调整后的模型中,非缺血性HF患者RVF的相对风险差异增加了5.1%的绝对值(95%CI:0.61-9.6)。在缺血性HF组中,有76例患者(占13.4%)发展为晚期RVF,在非缺血性HF组中有62例患者(占14.8%)(p  = 0.56)。分别在随访2年和4年后,在HF病因之间没有观察到RVF发生的差异(粗略:p = .25,调整后的(性别和年龄)p  = 0.2,而原油:p  = .59,调整后的(性别和年龄)p  = 0.44)。结论:与欧洲大量人群缺血性HF患者相比,接受LVAD的非缺血性HF患者的早期RVF发生率增加。在出院后的随访中,有14%的患者出现RVF。我们建议在确定LVAD植入后有术后RVF风险的患者时应考虑HF病因。

更新日期:2020-06-18
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