Cardiology Department, Hospital del Mar, Barcelona, Spain.
Cardiology Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
ESC Heart Fail. 2022 Feb;9(1):656-666. doi: 10.1002/ehf2.13696. Epub 2021 Nov 11.
The outpatient diuretic dose is a marker of diuretic resistance and prognosis in chronic heart failure (HF). Still, the impact of the preadmission dose on diuretic efficiency (DE) and prognosis in acute HF is not fully known.
We conducted an observational and prospective study. All patients admitted for acute HF treated with intravenous diuretic and at least one criterion of congestion on admission were evaluated. Decongestion [physical examination, hemoconcentration, N-terminal pro-brain natriuretic peptide (NT-proBNP) change, and lung ultrasound], DE (weight loss and urine output per unit of 40 mg furosemide), and urinary sodium were monitored on the fifth day of admission. DE was dichotomized into high-low based on the median value. A multivariate Cox regression analysis was conducted to find predictors of HF readmission or mortality. A total of 105 patients were included between July 2017 and July 2019. Mean age was 74.5 ± 12.0 years, 64.8% were male, 33.3% had de novo HF, and mean left ventricular ejection fraction was 46 ± 17%. Median follow-up was 26 [15-35] months. Low DE based on weight loss was associated with a higher previous dose of furosemide (odds ratio [OR] 1.01 [1.00-1.02]), thiazide treatment before admission (OR 9.37 [2.19-40.14]), and lower diastolic blood pressure (OR 0.95 [0.91-0.98]) in the multivariate regression model. Only previous dose of furosemide (OR 1.01 [1.00-1.02]) and haemoglobin at admission (OR 0.76 [0.58-0.99]) were associated with low DE based on urine output in the multivariate analysis. The correlation between the previous dose of furosemide and DE based on weight loss was poor (r = -0.12; P = 0.209) and with DE based on urine output was weak to moderate (r = -0.33; P < 0.001). Low DE based on weight loss and urine output was associated with lesser decongestion measured by NT-proBNP (P = 0.011; P = 0.007), hemoconcentration (P = 0.006; P = 0.044), and lung ultrasound (P = 0.034; P = 0.029), but not by physical examination (P = 0.506; P = 0.560). Survival and event-free survival in acute decompensated HF (ADHF) were lower than in de novo HF; a preadmission dose of furosemide > 80 mg in ADHF identified patients with particularly poor prognosis (log-rank < 0.001). In ADHF, the preadmission dose of furosemide (hazard ratio [HR] 1.34 [1.08-1.67] per 40 mg) and NT-proBNP at admission (HR 1.03 [1.01-1.06] per 1000 pg/mL) were independently associated with mortality or HF readmission in the multivariate Cox regression analysis.
The outpatient dose of furosemide before acute HF admission predicts DE and must be taken into account when deciding on the initial diuretic dose. In ADHF, the outpatient dose of furosemide can predict long-term prognosis better than DE during hospitalization.
门诊利尿剂剂量是慢性心力衰竭(HF)中利尿剂抵抗和预后的标志物。然而,入院前剂量对急性 HF 中利尿剂效率(DE)和预后的影响尚不完全清楚。
我们进行了一项观察性和前瞻性研究。所有因急性 HF 入院并在入院时至少有一项充血标准的患者均接受评估。入院第 5 天监测充血情况[体格检查、血液浓缩、N 末端脑利钠肽前体(NT-proBNP)变化和肺部超声]、DE(体重减轻和每单位 40mg 呋塞米的尿量)和尿钠。根据中位数将 DE 分为高低两组。使用多变量 Cox 回归分析来寻找 HF 再入院或死亡的预测因素。2017 年 7 月至 2019 年 7 月期间共纳入 105 例患者。平均年龄为 74.5±12.0 岁,64.8%为男性,33.3%为新发 HF,平均左心室射血分数为 46±17%。中位随访时间为 26[15-35]个月。基于体重减轻的低 DE 与呋塞米的先前剂量更高(比值比[OR]1.01[1.00-1.02])、入院前噻嗪类药物治疗(OR 9.37[2.19-40.14])和舒张压较低(OR 0.95[0.91-0.98])有关,在多变量回归模型中。只有呋塞米的先前剂量(OR 1.01[1.00-1.02])和入院时的血红蛋白(OR 0.76[0.58-0.99])与基于尿量的低 DE 相关,在多变量分析中。呋塞米的先前剂量与基于体重减轻的 DE 之间的相关性较差(r=-0.12;P=0.209),与基于尿量的 DE 的相关性较弱到中度(r=-0.33;P<0.001)。基于体重减轻和尿量的低 DE 与 NT-proBNP 测量的充血减轻相关(P=0.011;P=0.007)、血液浓缩(P=0.006;P=0.044)和肺部超声(P=0.034;P=0.029),但与体格检查无关(P=0.506;P=0.560)。急性失代偿性 HF(ADHF)中的生存和无事件生存低于新发 HF;ADHF 中呋塞米的入院前剂量>80mg 可识别出预后特别差的患者(对数秩检验<0.001)。在 ADHF 中,呋塞米的入院前剂量(HR 1.34[1.08-1.67]每 40mg)和入院时的 NT-proBNP(HR 1.03[1.01-1.06]每 1000pg/mL)与多变量 Cox 回归分析中的死亡率或 HF 再入院独立相关。
急性 HF 入院前的门诊呋塞米剂量可预测 DE,在决定初始利尿剂剂量时必须考虑这一点。在 ADHF 中,入院前的呋塞米剂量可以比住院期间的 DE 更好地预测长期预后。