使用 Impella 5.5 支持系统的患者出现不良预后是否存在特定病因的风险因素?

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引用次数: 0

摘要

目的确定缺血性(ICM)和非缺血性心肌病(NICM)患者在接受 Impella 5.5 支持期间发生主要不良事件的术前风险因素可能存在的病因特异性差异。方法从 2019 年 10 月到 2023 年 1 月,我院共植入了 228 台 Impella 5.5 装置。患者被分为 ICM 组(124 人)和 NICM 组(104 人)。主要结果是在积极接受Impella 5.5支持期间死亡/中风/新发透析的复合结果。随机森林分别确定了每个队列中预测主要结局的术前因素,并按变量重要性进行了排序。结果42(34%)名 ICM 患者和 35(34%)名 NICM 患者出现了主要结局。21 名 ICM 患者(17%)和 21 名 NICM 患者(20%)在接受 Impella 5.5 支持期间死亡;12 名 ICM 患者(9.7%)和 3 名 NICM 患者(2.9%)发生中风;23 名 ICM 患者(19%)和 24 名 NICM 患者(23%)在积极接受 Impella 5.5 支持期间开始新发透析。反映全身和心肌细胞损伤、内脏器官和心肺功能衰竭、右心室功能障碍和左心室尺寸较小的风险因素最能预测这两组患者的不良预后。结论与术前稳定性、右心室功能障碍和左心室尺寸相关的风险因素比适应症或设备策略更能预测积极接受Impella 5.5支持时的不良预后。这些因素有助于识别高风险患者,这些患者可能受益于额外的定制化管理,以降低他们在接受Impella 5.5支持时出现这些有影响的不良后果的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Are there etiology-specific risk factors for adverse outcomes in patients on Impella 5.5 support?

Objectives

To identify possible etiology-specific differences in preoperative risk factors for major adverse events during Impella 5.5 support in patients with ischemic (ICM) and nonischemic cardiomyopathy (NICM).

Methods

From October 2019 to January 2023, 228 Impella 5.5 devices were inserted at our institution. Patients were stratified into ICM (n = 124) and NICM (n = 104) cohorts. The primary outcome was a composite of death/stroke/new-onset dialysis while actively receiving Impella 5.5 support. Random forests identified preoperative factors predictive of the primary outcome separately for each cohort, with ranking by variable importance.

Results

The primary outcome occurred in 42 (34%) patients with ICM and 35 (34%) patients with NICM. Twenty-one (17%) patients with ICM and 21 (20%) patients with NICM died on Impella 5.5; stroke occurred in 12 (9.7%) patients with ICM and 3 (2.9%) patients with NICM, and new-onset dialysis was initiated in 23 (19%) patients with ICM and 24 (23%) patients with NICM while actively receiving Impella 5.5 support. Risk factors reflecting systemic and myocardial cellular injury, end-organ and cardiopulmonary failure, right ventricular dysfunction, and smaller left ventricular dimensions were most predictive of adverse outcomes in both cohorts. Indications for Impella 5.5 and device strategy (bridge to recovery, advanced therapies, or decision) were not top risk factors in either cohort.

Conclusions

Risk factors related to preoperative stability, right ventricular dysfunction, and left ventricular size were more predictive of adverse outcomes while actively receiving Impella 5.5 support than indication or device strategy. These factors could help identify high-risk patients who may benefit from additional tailored management to reduce their risk for these impactful adverse outcomes while on Impella 5.5 support.
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