Reevaluating How We View Renal Dysfunction During Left Ventricular Assist Device Consideration

IF 8.2 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiac Failure Pub Date : 2025-01-01 Epub Date: 2025-01-14 DOI:10.1016/j.cardfail.2024.10.071
Martin Osorio Nader , Michael S. Debakey , Kristin Wittersheim , Mani Daneshmand , John David Vega , Divya Gupta
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Abstract

Introduction

Renal dysfunction is often seen in patients with advanced heart failure and is the cause of exclusion from LVAD implantation for many. As technology advances, such as with the continuous-flow design of the HeartMate3 (HM3), we must reevaluate how we view comorbidities like renal disease when considering patients for LVADs. We aimed to review patients implanted with an HM3 and examine their survival through the lens of their eGFR to determine if those with a lower eGFR (≤ 30) or on dialysis at the time of implantation had comparable outcomes to patients with higher eGFR.

Methods

This is a single-center retrospective review of patients at our institution implanted with an HM3 between 1/1/2021 and 7/1/2023. Patients were sorted into groups by eGFR at the time of implantation as follows: Group A (eGFR ≥ 60), Group B (60 > eGFR > 30), and Group C (eGFR ≤ 30 or on dialysis). We evaluated each group's survival at 6, 12, and 24 months and compared their development or redevelopment of a dialysis requirement post-implant with a chi-squared test. At respective survival calculations, we censored patients who were alive but had not reached or had a transplant before an endpoint.

Results

We reviewed a total of 177 patients. Group A consisted of 73 patients (mean age: 49.1, % male: 67.1), Group B of 64 patients (mean age: 56.1, % male: 79.7), and Group C of 40 patients (mean age: 56.5, % male: 77.5). Eleven Group C patients were on dialysis at the time of implantation (1 hemodialysis, 10 CRRT) with three remaining on dialysis indefinitely post-implant. The median length of dialysis requirement for these eleven patients after LVAD implantation was 33 days. Group C patients had a seemingly lower 6-month survival rate; however, they had a similar 12 and 24-month survival compared to higher eGFR groups (Figure, Table). The percentage of patients who developed or redeveloped a dialysis requirement in each group was 12.3%, 12.5%, and 18.9%, respectively (p=0.59).

Conclusion

This study demonstrated that an eGFR ≤ 30 or being on dialysis at implantation is likely insufficient to predict a poor outcome post-LVAD in those implanted with an HM3. Additional investigation is needed to improve how we evaluate patients with renal disease for LVADs to provide better access to lifesaving implantations in a population with a common comorbid condition.
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重新评估我们在考虑左心室辅助装置时如何看待肾功能不全
肾功能不全常见于晚期心力衰竭患者,是许多患者排除左室辅助装置植入的原因。随着技术的进步,例如HeartMate3 (HM3)的连续流设计,我们必须重新评估在考虑lvad患者时如何看待肾脏疾病等合并症。我们的目的是回顾植入HM3的患者,并通过他们的eGFR检查他们的生存,以确定植入时eGFR较低(≤30)或透析的患者是否与eGFR较高的患者具有相似的结果。方法:本研究为单中心回顾性研究,纳入我院2021年1月1日至2023年7月1日期间植入HM3的患者。根据植入时的eGFR将患者分为:A组(eGFR≥60),B组(60 >;表皮生长因子受体在C组(eGFR≤30或正在透析)。我们在6个月、12个月和24个月时评估了每组患者的生存,并通过卡方检验比较了他们植入后透析需求的发展或再发展。在各自的生存计算中,我们剔除了存活但未达到终点或未在终点前进行移植的患者。结果共纳入177例患者。A组73例,平均年龄49.1岁,男性占67.1岁;B组64例,平均年龄56.1岁,男性占79.7岁;C组40例,平均年龄56.5岁,男性占77.5岁。C组11例患者在植入时进行透析(1例血液透析,10例CRRT), 3例患者在植入后无限期透析。这11例患者在LVAD植入后所需透析时间的中位数为33天。C组患者的6个月生存率似乎较低;然而,与eGFR较高的组相比,他们的12个月和24个月生存率相似(图,表)。两组发生或再发生透析需求的患者比例分别为12.3%、12.5%和18.9% (p=0.59)。结论:本研究表明,eGFR≤30或在植入时进行透析可能不足以预测HM3植入者lvad后的不良预后。需要进一步的研究来改进我们如何评估肾脏疾病患者的lvad,以便在有常见合并症的人群中更好地获得挽救生命的植入。
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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来源期刊
Journal of Cardiac Failure
Journal of Cardiac Failure 医学-心血管系统
CiteScore
7.80
自引率
8.30%
发文量
653
审稿时长
21 days
期刊介绍: Journal of Cardiac Failure publishes original, peer-reviewed communications of scientific excellence and review articles on clinical research, basic human studies, animal studies, and bench research with potential clinical applications to heart failure - pathogenesis, etiology, epidemiology, pathophysiological mechanisms, assessment, prevention, and treatment.
期刊最新文献
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