Cotter Gad, Davison Beth, Janiak Philip, Edwards Christopher, Novosadova Maria, Takagi Koji, Ozoux Marie-Laure, Lawson Francesca, Hayrapetyan Hamlet, Sisakian Hamayak, Ter-Grigoryan Victor R, Peoc'h Katell, Raynor Alexandre, Bruzeau Paul, Nguyen Alexis, Mebazaa Alexandre
Université Paris Cité, INSERM UMR-S 942 (MASCOT), Paris, France.
Momentum Research Inc, Durham, NC, USA.
Eur J Heart Fail. 2025 Feb;27(2):325-336. doi: 10.1002/ejhf.3555. Epub 2024 Dec 18.
We sought to characterize the clinical course of patients following worsening heart failure (WHF) treated in an outpatient setting and to identify factors associated with a poor response to standard of care with loop diuretics.
Between September 2022 and March 2023, 44 eligible patients (mean age 66.3 years, 84% male) with ejection fraction <50% and with WHF symptoms in the preceding week treated in an outpatient setting were enrolled. Patients were assessed weekly over 4 weeks following the WHF episode. At week 4, responses to fluid expansion and furosemide administration were assessed in 39 patients to unmask persistent subclinical congestion. Patients were on stable doses of guideline-directed medical therapy (GDMT) with a mean daily furosemide dose of 47.4 mg. Patient-reported and physician-assessed symptoms and quality of life improved over the 4 weeks. At 1 h following 1 L Ringer solution infused over 2 h, the median (interquartile range) urine volume and urine sodium excreted over 3 h were 300 (200.0-500.0) ml and 39.6 (12.4-63.0) mEq, respectively. Receiver-operating characteristic curves suggest that cystatin C >1.2 ng/ml, N-terminal pro-B-type natriuretic peptide (NT-proBNP) >1500 pg/ml, and high-sensitivity troponin T >20 pg/ml represent good predictors of non-response to a fluid challenge (diuresis, natriuresis, and rales) following an outpatient WHF, with having all three markers associated with the worst response.
Patients with high levels of troponin, or NT-proBNP, or cystatin C who develop WHF despite being treated with a loop diuretic, need novel therapies for WHF.
我们试图描述门诊治疗的心力衰竭恶化(WHF)患者的临床病程,并确定与对袢利尿剂标准治疗反应不佳相关的因素。
在2022年9月至2023年3月期间,纳入了44例符合条件的患者(平均年龄66.3岁,84%为男性),这些患者射血分数<50%,且在前一周有WHF症状,在门诊接受治疗。在WHF发作后的4周内每周对患者进行评估。在第4周时,对39例患者评估了液体扩容和呋塞米给药后的反应,以揭示持续的亚临床充血情况。患者接受稳定剂量的指南指导药物治疗(GDMT),平均每日呋塞米剂量为47.4毫克。患者报告的症状、医生评估的症状和生活质量在4周内有所改善。在2小时内输注1升林格溶液后1小时,3小时内的中位数(四分位间距)尿量和尿钠排泄量分别为300(200.0 - 500.0)毫升和 39.6(12.4 - 63.0)毫当量。受试者工作特征曲线表明,胱抑素C>1.2纳克/毫升、N末端B型利钠肽原(NT-proBNP)>1500皮克/毫升和高敏肌钙蛋白T>20皮克/毫升是门诊WHF后对液体激发试验(利尿、利钠和啰音)无反应的良好预测指标,同时具备这三个标志物与最差反应相关。
尽管接受了袢利尿剂治疗仍发生WHF的肌钙蛋白、NT-proBNP或胱抑素C水平高的患者,需要针对WHF的新疗法。