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Continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction

AIMS: There is paucity of clinical data comparing continuous infusion (CI) with bolus injection (BI) of intravenous loop diuretics in patients with acute decompensated heart failure (ADHF) and chronic renal dysfunction. This study aimed to compare the efficacy and safety of CI versus BI intravenous...

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Autores principales: Zheng, Zhigui, Jiang, Xinxin, Chen, Jianguo, He, Dongyuan, Xie, Xiaohui, Lu, Yunan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120396/
https://www.ncbi.nlm.nih.gov/pubmed/33689236
http://dx.doi.org/10.1002/ehf2.13286
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author Zheng, Zhigui
Jiang, Xinxin
Chen, Jianguo
He, Dongyuan
Xie, Xiaohui
Lu, Yunan
author_facet Zheng, Zhigui
Jiang, Xinxin
Chen, Jianguo
He, Dongyuan
Xie, Xiaohui
Lu, Yunan
author_sort Zheng, Zhigui
collection PubMed
description AIMS: There is paucity of clinical data comparing continuous infusion (CI) with bolus injection (BI) of intravenous loop diuretics in patients with acute decompensated heart failure (ADHF) and chronic renal dysfunction. This study aimed to compare the efficacy and safety of CI versus BI intravenous furosemide administration in patients with ADHF and moderate chronic renal insufficiency. METHODS AND RESULTS: Acute decompensated heart failure and moderate chronic renal insufficiency [with estimated glomerular filtration rate (eGFR) 15.0–44.9 mL/min/1.73 m(2)] were randomized to start intravenous furosemide by BI or by a 6 h CI. End points included freedom from congestion at 72 h, the degree of dyspnoea assessed using the 0–10 Borg's category ratio scale, net daily urine output, weight loss during the study, length of hospital stay, total urinary sodium excretion, and development of acute kidney injury or electrolyte disturbance. After 72 h of treatment, the rate of the primary endpoint of freedom from congestion in the CI group was significantly higher than that in the BI group (69.05% vs. 43.59%, P = 0.02). The modified Borg scale indicated patients in the CI group had lower dyspnoea score than those in the BI group at 48 h (4.29 ± 1.23 vs. 5.97 ± 1.56; P = 0.02) and 72 h (1.15 ± 0.35 vs. 2.66 ± 0.83; P = 0.003). There were other significant differences favouring the CI group with regard to net urine output at 72 h (5145.98 ± 621.37 mL vs. 3755.95 ± 456.93 mL; P = 0.007), the mean body weight loss (4.72 ± 1.01 kg vs. 3.53 ± 0.73 kg; P = 0.02) and the total urinary sodium excretion (385.05 ± 38.15 vs. 320.33 ± 37.67; P = 0.02). The length of hospitalization in the CI group was significantly shorter than that in the BI group (10.36 ± 4.20 days vs. 15.68 ± 6.15 days; P = 0.02). No significant differences were observed between groups in the frequency of acute kidney injury, tinnitus, electrolyte disturbance or mortality. CONCLUSIONS: Continuous intravenous infusion of furosemide resulted in significantly greater diuresis than bolus administration of an equal dose in patients with moderate chronic renal insufficiency and ADHF, while no differences emerged in terms of side effects or mortality.
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spelling pubmed-81203962021-05-21 Continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction Zheng, Zhigui Jiang, Xinxin Chen, Jianguo He, Dongyuan Xie, Xiaohui Lu, Yunan ESC Heart Fail Original Research Articles AIMS: There is paucity of clinical data comparing continuous infusion (CI) with bolus injection (BI) of intravenous loop diuretics in patients with acute decompensated heart failure (ADHF) and chronic renal dysfunction. This study aimed to compare the efficacy and safety of CI versus BI intravenous furosemide administration in patients with ADHF and moderate chronic renal insufficiency. METHODS AND RESULTS: Acute decompensated heart failure and moderate chronic renal insufficiency [with estimated glomerular filtration rate (eGFR) 15.0–44.9 mL/min/1.73 m(2)] were randomized to start intravenous furosemide by BI or by a 6 h CI. End points included freedom from congestion at 72 h, the degree of dyspnoea assessed using the 0–10 Borg's category ratio scale, net daily urine output, weight loss during the study, length of hospital stay, total urinary sodium excretion, and development of acute kidney injury or electrolyte disturbance. After 72 h of treatment, the rate of the primary endpoint of freedom from congestion in the CI group was significantly higher than that in the BI group (69.05% vs. 43.59%, P = 0.02). The modified Borg scale indicated patients in the CI group had lower dyspnoea score than those in the BI group at 48 h (4.29 ± 1.23 vs. 5.97 ± 1.56; P = 0.02) and 72 h (1.15 ± 0.35 vs. 2.66 ± 0.83; P = 0.003). There were other significant differences favouring the CI group with regard to net urine output at 72 h (5145.98 ± 621.37 mL vs. 3755.95 ± 456.93 mL; P = 0.007), the mean body weight loss (4.72 ± 1.01 kg vs. 3.53 ± 0.73 kg; P = 0.02) and the total urinary sodium excretion (385.05 ± 38.15 vs. 320.33 ± 37.67; P = 0.02). The length of hospitalization in the CI group was significantly shorter than that in the BI group (10.36 ± 4.20 days vs. 15.68 ± 6.15 days; P = 0.02). No significant differences were observed between groups in the frequency of acute kidney injury, tinnitus, electrolyte disturbance or mortality. CONCLUSIONS: Continuous intravenous infusion of furosemide resulted in significantly greater diuresis than bolus administration of an equal dose in patients with moderate chronic renal insufficiency and ADHF, while no differences emerged in terms of side effects or mortality. John Wiley and Sons Inc. 2021-03-10 /pmc/articles/PMC8120396/ /pubmed/33689236 http://dx.doi.org/10.1002/ehf2.13286 Text en © 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research Articles
Zheng, Zhigui
Jiang, Xinxin
Chen, Jianguo
He, Dongyuan
Xie, Xiaohui
Lu, Yunan
Continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction
title Continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction
title_full Continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction
title_fullStr Continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction
title_full_unstemmed Continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction
title_short Continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction
title_sort continuous versus intermittent use of furosemide in patients with heart failure and moderate chronic renal dysfunction
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120396/
https://www.ncbi.nlm.nih.gov/pubmed/33689236
http://dx.doi.org/10.1002/ehf2.13286
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