Center for Cardiovascular Innovation, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Eur J Heart Fail. 2013 Dec;15(12):1401-11. doi: 10.1093/eurjhf/hft110. Epub 2013 Jul 11.
Haemoconcentration has been studied as a marker of decongestion in patients with hospitalization for heart failure (HHF). We describe the relationship between haemoconcentration, worsening renal function, post-discharge outcomes, and clinical and laboratory markers of congestion in a large multinational cohort of patients with HHF.
In 1684 patients with HHF with ejection fraction (EF) ≤40% assigned to the placebo arm of the Efficacy of Vasopressin Antagonism in Heart Failure Outcome Study with Tolvaptan (EVEREST) trial, absolute in-hospital haematocrit change was calculated as the change between baseline and discharge or day 7 (whichever occurred first). Patient characteristics, changes in renal function, and outcomes over a median follow-up of 9.9 months were compared by in-hospital haematocrit change. Overall, 26% of patients had evidence of haemoconcentration (i.e., ≥3% absolute increase in haematocrit). Patients with greater increases in haematocrit tended to have better baseline renal function. Haemoconcentration correlated with greater risk of in-hospital worsening renal function, but renal parameters generally returned to baseline within 4 weeks post-discharge. Patients with haemoconcentration were less likely to have clinical congestion at discharge, and experienced greater in-hospital decreases in body weight and natriuretic peptide levels. After adjustment for baseline clinical risk factors, every 5% increase of in-hospital haematocrit change was associated with a decreased risk of all-cause death [hazard ratio (HR) 0.81, 95% confidence interval (CI) 0.70-0.95]. Haematocrit change was also associated with decreased cardiovascular mortality or heart failure (HF) hospitalization at ≤100 days post-randomization (HR 0.73, 95% CI 0.71-0.76).
In this large cohort of patients with HHF with reduced EF, haemoconcentration was associated with greater improvements in congestion and decreased mortality and HF re-hospitalization despite an increased risk of in-hospital worsening renal function.
血红细胞比容已被研究作为心力衰竭住院患者(HHF)去充血的标志物。我们描述了在一个大型的多国 HHF 患者队列中,血红细胞比容、肾功能恶化、出院后结局以及充血的临床和实验室标志物之间的关系。
在 EVEREST 试验(即托伐普坦治疗心衰利尿剂反应试验)的安慰剂组中,有 1684 名射血分数(EF)≤40%的 HHF 患者,计算了住院期间绝对血红细胞比容变化,即从基线到出院或第 7 天(以先发生者为准)的变化。根据住院期间血红细胞比容变化,比较了患者特征、肾功能变化和中位随访 9.9 个月的结局。总体而言,26%的患者存在血红细胞比容升高(即血红细胞比容绝对增加≥3%)。血红细胞比容增加较多的患者,其基线肾功能较好。血红细胞比容与住院期间肾功能恶化的风险增加相关,但肾功能参数通常在出院后 4 周内恢复到基线。血红细胞比容升高的患者在出院时发生临床充血的可能性较低,住院期间体重和利钠肽水平下降幅度较大。在校正了基线临床危险因素后,住院期间血红细胞比容变化每增加 5%,全因死亡风险降低[风险比(HR)0.81,95%置信区间(CI)0.70-0.95]。血红细胞比容变化也与≤100 天随机分组后心血管死亡率或心力衰竭(HF)住院率降低相关(HR 0.73,95%CI 0.71-0.76)。
在这个 EF 值降低的大型 HHF 患者队列中,尽管存在住院期间肾功能恶化风险增加,血红细胞比容升高与充血改善、死亡率和 HF 再住院率降低相关。