Division of Cardiology, Johns Hopkins University, Baltimore, Maryland, United States of America.
Division of Cardiology, Brooklyn New York-Presbyterian Hospital, Brooklyn, New York, United States of America.
PLoS One. 2021 Jun 25;16(6):e0253014. doi: 10.1371/journal.pone.0253014. eCollection 2021.
Hospitalization for acute decompensated heart failure (ADHF) remains a major source of morbidity and mortality. The current study aimed to investigate the feasibility, safety, and efficacy of outpatient furosemide intravenous (IV) infusion following hospitalization for ADHF.
In a single center, prospective, randomized, double-blind study, 100 patients were randomized to receive standard of care (Group 1), IV placebo infusion (Group 2), or IV furosemide infusion (Group 3) over 3h, biweekly for a one-month period following ADHF hospitalization. Patients in Groups 2/3 also received a comprehensive HF-care protocol including bi-weekly clinic visits for dose-adjusted IV-diuretics, medication adjustment and education. Echocardiography, quality of life and depression questionnaires were performed at baseline and 30-day follow-up. The primary outcome was 30-day re-hospitalization for ADHF.
Overall, a total of 94 patients were included in the study (mean age 64 years, 56% males, 69% African American). There were a total of 14 (15%) hospitalizations for ADHF at 30 days, 6 (17.1%) in Group 1, 7 (22.6%) in Group 2, and 1 (3.7%) in Group 3 (overall p = 0.11; p = 0.037 comparing Groups 2 and 3). Patients receiving IV furosemide infusion experienced significantly greater urine output and weight loss compared to those receiving placebo without any significant increase creatinine and no significant between group differences in echocardiography parameters, KCCQ or depression scores.
The use of a standardized protocol of outpatient IV furosemide infusion for a one-month period following hospitalization for ADHF was found to be safe and efficacious in reducing 30-day re-hospitalization.
急性失代偿性心力衰竭(ADHF)住院仍然是发病率和死亡率的主要来源。本研究旨在探讨 ADHF 住院后门诊呋塞米静脉(IV)输注的可行性、安全性和疗效。
在单中心、前瞻性、随机、双盲研究中,100 名患者被随机分为接受标准治疗(第 1 组)、IV 安慰剂输注(第 2 组)或 IV 呋塞米输注(第 3 组),在 ADHF 住院后 3 小时内,每两周一次,持续一个月。第 2/3 组患者还接受了综合 HF 护理方案,包括每两周进行一次诊所就诊,以调整 IV 利尿剂的剂量、调整药物和进行教育。在基线和 30 天随访时进行超声心动图、生活质量和抑郁问卷评估。主要结局是 30 天内因 ADHF 再次住院。
共有 94 名患者入组(平均年龄 64 岁,56%为男性,69%为非裔美国人)。在 30 天时有 14 例(15%)因 ADHF 住院,第 1 组 6 例(17.1%),第 2 组 7 例(22.6%),第 3 组 1 例(3.7%)(总体 p = 0.11;第 2 组和第 3 组之间 p = 0.037)。与接受安慰剂的患者相比,接受 IV 呋塞米输注的患者的尿量和体重减轻明显更多,而肌酐没有明显增加,超声心动图参数、KCCQ 或抑郁评分在组间没有明显差异。
在 ADHF 住院后一个月内使用标准化方案门诊 IV 呋塞米输注被发现是安全有效的,可以降低 30 天内再住院率。