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在一个新兴国家成功建立左心室辅助装置项目:一年经验

Successful establishment of a left ventricular assist device program in an emerging country: one year experience.

作者信息

Nestorovic Emilija, Schmitto Jan D, Kushwaha Sudhir S, Putnik Svetozar, Terzic Dusko, Milic Natasa, Mikic Aleksandar, Markovic Dejan, Trifunovic Danijela, Ristic Arsen, Ristic Miljko

机构信息

Department for Heart Transplant, LVAD and ECMO, Hospital for Cardiac Surgery, Clinical Center of Serbia, Belgrade, Serbia.

Department of Cardiothoracic, Transplantation and Vascular Surgery, Hannover Medical School, Hannover, Germany.

出版信息

J Thorac Dis. 2018 Jun;10(Suppl 15):S1743-S1750. doi: 10.21037/jtd.2018.04.147.

Abstract

BACKGROUND

The primary goal of this study was to evaluate the outcomes of patients with end-stage heart failure (HF) who underwent continuous flow left ventricular assist device (CF-LVAD) in a developing country and to compare to those reported by more developed countries. The secondary goal was on determining factors that may be connected to improved survival.

METHODS

We prospectively analyzed 47 consecutive patients who underwent CF-LVAD at our institution. After one year the survival and adverse event profiles of patients were evaluated. At 3, 6 and 12 months, the cardiac, renal and liver function outcomes were assessed.

RESULTS

The 30-day, 6-month and 1-year survival rates were 89%, 85% and 80%, respectively. A significant improvement in dimensions and ejection fraction of left ventricle, BNP, functional capacity, blood urea nitrogen (BUN) and total bilirubin (P<0.05 for all) were noticed 3 months post-CF-LVAD implantation, and patients were stable throughout the entire first year follow up. In the group of patients with baseline renal dysfunction (RD) there were significant improvements of renal function (P=0.004), with no changes on follow up. 57% of patients exhibited some kind of adverse event, commonly in the form of bleeding. In multivariate Cox regression analysis renal failure was found to be as an independent risk factor for the overall survival (HR =13.1, P<0.001).

CONCLUSIONS

In conclusion, our data extends previous findings from centers of developed countries, that CF-LVAD is an adequate treatment option for patients suffering from end-stage HF, and encourages expansion of CF-LVAD implantation in developing countries with nascent HT program.

摘要

背景

本研究的主要目的是评估在一个发展中国家接受连续流左心室辅助装置(CF-LVAD)治疗的终末期心力衰竭(HF)患者的治疗效果,并与更发达国家报道的结果进行比较。次要目的是确定可能与生存率提高相关的因素。

方法

我们对在我院接受CF-LVAD治疗的47例连续患者进行了前瞻性分析。一年后评估患者的生存情况和不良事件。在3、6和12个月时,评估心脏、肾脏和肝脏功能结果。

结果

30天、6个月和1年生存率分别为89%、85%和80%。CF-LVAD植入后3个月,左心室尺寸和射血分数、脑钠肽、功能能力、血尿素氮(BUN)和总胆红素均有显著改善(所有P<0.05),并且在整个第一年随访期间患者情况稳定。在基线肾功能不全(RD)患者组中,肾功能有显著改善(P=0.004),随访期间无变化。57%的患者出现某种不良事件,常见形式为出血。在多变量Cox回归分析中,肾衰竭被发现是总体生存的独立危险因素(HR =13.1,P<0.001)。

结论

总之,我们的数据扩展了发达国家中心先前的研究结果,即CF-LVAD是终末期HF患者的一种合适治疗选择,并鼓励在有新兴心脏移植项目的发展中国家扩大CF-LVAD植入。

相似文献

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1
First Implantation of a Novel Left Ventricular Assist Device: The ReliantHeart aVAD.
Ann Thorac Surg. 2017 Oct;104(4):e311-e313. doi: 10.1016/j.athoracsur.2017.04.049.
2
First experiences with HeartMate 3 follow-up and adverse events.首份 HeartMate 3 随访和不良事件经验报告。
J Thorac Cardiovasc Surg. 2017 Jul;154(1):173-178. doi: 10.1016/j.jtcvs.2017.01.045. Epub 2017 Feb 9.
9
Minimally-invasive LVAD Implantation: State of the Art.微创左心室辅助装置植入术:当前技术水平
Curr Cardiol Rev. 2015;11(3):246-51. doi: 10.2174/1573403x1103150514151750.

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