长期肌力疗法治疗晚期心脏淀粉样变性的经验

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.2024.10.020
Ashwin Pillai , Kerry Singh , Seth Fakess , Ina Lico , Abhishek Jaiswal
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引用次数: 0

摘要

背景:症状性心脏淀粉样变性(CA)患者的治疗选择有限,许多患者不适合使用左心室辅助装置或心脏移植。他法非底斯在逆转晚期难治性CA方面的疗效有限。虽然长期持续静脉肌力输注治疗(LTInoT)可能改善晚期心力衰竭患者的生活质量,但其在由心脏淀粉样变性引起的症状性难治性心力衰竭中的应用尚不清楚。我们描述了我们在患有心脏淀粉样变性和难治性心力衰竭的患者中使用LTInoT的经验。方法:我们对2019-2023年连续入组的LTInoT心脏淀粉样变性患者进行了回顾性研究,累计随访9031人日(~ 301人月)。结果纳入17例患者,其中男性12例。参与者主要为白人(n=11),平均年龄为79±8岁。10名参与者患有HFrEF, 13名患有ATTR。慢性肾病、高脂血症和房颤分别在13例(76%)、12例(71%)和12例(71%)患者中合并症。平均左室EF为32±14%。LTInoT由米立酮(n=10)和多巴酚丁胺(n=7)组成。同时服用的药物包括矿皮质激素受体拮抗剂(n=11, 65%)、他法米底斯(n=9, 53%)和钠-葡萄糖共转运蛋白抑制剂(n=7, 41%)。与一年前相比,接受LTInoT治疗的心血管住院率(中位数[四分位数1-3])下降(2[1-3]vs 3[2-4], p=0.03)。全因住院情况相似(3[2-4])。6例(35%)患者在LInoT治疗一年内死亡(表)。死亡发生后的中位持续时间为6个月(Q1-Q3: 3-16个月)。结论ltinot具有降低心肌淀粉样变性晚期心力衰竭患者心血管住院率的潜力。需要进一步的研究来确定合适的LInoT候选者。
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Experience With Long-term Inotrope Therapy In Advanced Cardiac Amyloidosis Management

Background

Patients with symptomatic cardiac amyloidosis (CA) have limited therapeutic options with many being ineligible for left ventricular assist devices or heart transplants. Tafamidis has limited efficacy in reversing advanced refractory CA. While long term continuous intravenous inotrope infusion therapy (LTInoT) might improve quality of life in individuals with advanced heart failure, its utility in symptomatic, refractory heart failure due to cardiac amyloidosis remains unknown. We describe our experience with LTInoT in patients with cardiac amyloidosis and refractory heart failure.

Methods

We conducted a retrospective review of consecutively enrolled patients with cardiac amyloidosis on LTInoT from 2019-2023, cumulatively for 9031 person-days of follow-up (∼301 person-months).

Results

17 patients (12 male) were included. Participants were predominantly White (n=11) with a mean age of 79±8 years. 10 participants had HFrEF and 13 had ATTR. Chronic kidney disease, hyperlipidemia, and atrial fibrillation were comorbid in 13(76%), 12(71%), and 12(71%) patients, respectively. The mean left ventricular EF was 32±14%. LTInoT comprised milrinone (n=10) and dobutamine (n=7). Concurrent medications included a mineralocorticoid receptor antagonist (n=11, 65%), Tafamidis (n=9, 53%), and sodium-glucose co-transporter inhibitor (n=7, 41%). Cardiovascular hospitalizations (Median [quartile 1-3]) decreased while receiving LTInoT relative to a year prior (2[1-3] vs 3[2-4], p=0.03). All-cause hospitalizations were similar (3[2-4]). 6 (35%) patients died within a year of LInoT (Table). The median duration after which mortality occurred was 6 months (Q1-Q3: 3-16 months).

Conclusion

LTInoT has potential to reduce cardiovascular hospitalizations in advanced heart failure due to cardiac amyloidosis. Further investigation is needed to identify suitable candidates for LInoT.
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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.
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