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避免使用皮下呋塞米治疗心力衰竭恶化:一项试点研究(AT HOME-HF)。

Avoiding Treatment in Hospital With Subcutaneous Furosemide for Worsening Heart Failure: A Pilot Study (AT HOME-HF).

机构信息

Tufts Medical Center, and Tufts University School of Medicine, Boston, Massachusetts, USA.

Boston University School of Public Health, Boston, Massachusetts, USA.

出版信息

JACC Heart Fail. 2024 Nov;12(11):1830-1841. doi: 10.1016/j.jchf.2024.07.015. Epub 2024 Sep 11.

Abstract

BACKGROUND

Therapies are needed to address worsening congestion, without hospitalization, in patients with chronic heart failure (HF).

OBJECTIVES

This pilot study assessed outcomes of a novel subcutaneous (SC) furosemide formulation compared to usual care in outpatients with worsening congestion.

METHODS

Participants with chronic HF and worsening congestion were randomized open-label 2:1 to SC furosemide compared to usual care (UC). Decongestion was estimated by tracking body weight. The primary endpoint was a win ratio of a 30-day hierarchical composite of cardiovascular death, HF events, and change in N-terminal pro-B-type natriuretic peptide. Secondary endpoints included dyspnea severity, functional capacity, and quality of life.

RESULTS

Thirty-four participants were randomized to SC furosemide and 17 to UC. SC furosemide caused greater reduction in body weight: between-group difference in least square mean change was -2.02 kg at day 3 (95% CI: -3.9 to -0.14; P = 0.035). SC furosemide-to-UC win ratio was 1.11 (95% CI: 0.48-2.50; P = 0.806). Significant between-group least square mean differences favoring SC furosemide occurred in 7-point dyspnea score (P = 0.017) and 6-minute walk test (P = 0.032), with trend in Kansas City Cardiomyopathy Questionnaire (KCCQ)-12 Overall Summary Score of 9.15 (95% CI: 1.95-20.3; P = 0.106). The most common related adverse event with SC furosemide was mild infusion site pain (11.8%).

CONCLUSIONS

SC furosemide augmented weight loss in patients with HF and worsening congestion. The composite primary endpoint was not statistically significant in this pilot investigation. However, findings of improved dyspnea scores and functional capacity, with favorable trend in KCCQ-12 score, warrant additional investigation to further document the clinical value of SC furosemide as an alternative to hospitalization (AT HOME-HF [Avoiding Treatment in the Hospital With Furoscix for the Management of Congestion in Heart Failure-A Pilot Study]; NCT04593823).

摘要

背景

需要治疗方法来解决慢性心力衰竭(HF)患者因充血而无需住院的问题。

目的

本研究评估了一种新型皮下(SC)呋塞米制剂与门诊充血恶化患者常规治疗相比的结局。

方法

将慢性 HF 且充血恶化的患者随机分为 2:1 的 SC 呋塞米组与常规治疗(UC)组。通过跟踪体重来评估去充血效果。主要终点是心血管死亡、HF 事件和 N 末端 pro-B 型利钠肽变化的 30 天分层复合终点的赢率。次要终点包括呼吸困难严重程度、功能能力和生活质量。

结果

34 名患者被随机分配至 SC 呋塞米组,17 名患者被分配至 UC 组。SC 呋塞米组体重减轻更明显:组间最小二乘均值变化差异为第 3 天-2.02kg(95%CI:-3.9 至-0.14;P=0.035)。SC 呋塞米与 UC 的赢率为 1.11(95%CI:0.48-2.50;P=0.806)。SC 呋塞米组显著优于 UC 组的最小二乘均值差异发生在 7 分呼吸困难评分(P=0.017)和 6 分钟步行试验(P=0.032),堪萨斯城心肌病问卷(KCCQ)-12 总体综合评分有 9.15 分的趋势(95%CI:1.95-20.3;P=0.106)。SC 呋塞米最常见的相关不良事件是轻度输注部位疼痛(11.8%)。

结论

SC 呋塞米可增加 HF 伴充血恶化患者的体重减轻。该主要复合终点在本研究中无统计学意义。然而,呼吸困难评分和功能能力的改善,以及 KCCQ-12 评分的有利趋势,值得进一步研究以进一步证明 SC 呋塞米作为住院替代治疗(HF 患者的住院治疗避免治疗(AT HOME-HF)[避免使用呋塞米治疗充血的心力衰竭管理研究];NCT04593823)的临床价值。

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