Skip Navigation

European Journal of Heart Failure 2000 2(3):305-313; doi:10.1016/S1388-9842(00)00094-5
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (20)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Paterna, S.
Right arrow Articles by Licata, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Paterna, S.
Right arrow Articles by Licata, G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2000 European Society of Cardiology

Effects of high-dose furosemide and small-volume hypertonic saline solution infusion in comparison with a high dose of furosemide as a bolus, in refractory congestive heart failure

Salvatore Paternaa, Pietro Di Pasqualeb,*, Gaspare Parrinelloa, Piera Amatoa, Antonella Cardinalea, Giuseppe Follonea, Alfonso Giubilatob and Giuseppe Licataa

a Department of Internal Medicine, University of Palermo Palermo, Italy
b Division of Cardiology, ‘Paolo Borsellino’, G. F. Ingrassia Hospital Palermo, Italy

* Corresponding author. Chief Division of Cardiology, ‘Paolo Borsellino’, Via Val Platani 3, 90144, Palermo, Italy. Tel. : +39-091-524181; fax: +39-091-7033742


   Abstract

Background: Diuretics, have been accepted as first-line treatment in refractory heart failure, but a lack of response is a frequent event. A randomised single blind study was performed to evaluate the effects of the combination of high-dose furosemide and small-volume hypertonic saline solution (HSS) infusion in the treatment of refractory NYHA class IV congestive heart failure (CHF).

Materials and methods: Sixty patients (21 F/39 M) with refractory CHF (NYHA class IV) of different etiologies, unresponsive to high oral doses of furosemide, ACE-inhibitors, digitalis, and nitrates, aged 65–90 years, were enrolled. They had to have an ejection fraction (EF) < 35%, serum creatinine < 2 mg/dl, BUN ≤60 mg/dl, a reduced urinary volume and a low natriuresis. The patients were randomised in two groups (single blind): group 1 (11 F/19 M) received an i.v. infusion of furosemide (500–1000 mg) plus HSS (150 ml of 1.4–4.6% NaCl) b.i.d. in 30 min. Group 2 (10 F/20 M) received an i.v. bolus of furosemide (500–1000 mg) b.i.d., without HSS, during a period lasting 6–12 days. Both groups received KCl (20–40 mEq.) i.v. to prevent hypokalemia. All patients underwent at entry a physical examination, measurement of body weight (BW), blood pressure (BP), heart rate (HR), evaluation of signs of CHF, and controls of serum Na, K, Cl, bicarbonate, albumin, uric acid, creatinine, urea and glycemia and daily during hospitalization, as well as the daily output of urine for, Na, K and Cl measurements. Chest X-ray, ECG and echocardiogram were obtained at entry during and at the discharge. During the treatment and after discharge the daily dietary Na intake was 120 mmol with a drink fluid intake of 1000 ml daily. An assessment of BW and 24-h urinary volume, serum and urinary laboratory parameters, until reaching a compensated state, were performed daily, when i.v. furosemide was replaced with oral administration (250–500 mg/day). After discharge, patients were followed as outpatients weekly for the first 3 months and subsequently once per month.

Results: The groups were similar for age, sex, EF, risk factors, treatment and etiology of CHF. All patients showed a clinical improvement. Six patients in both groups had hyponatremia (from 120 to 128 mEq./l) at entry. A significant increase in daily diuresis in both groups was observed (from 390±155 to 2100±626, and from 433±141 to 1650±537 ml/24 h, P < 0.05). Natriuresis (from 49±15 to 198±28 mEq./24 h) was higher in group 1 vs. group 2 (from 53.83±12 to 129±39 mEq./24 h, P < 0.05). Serum Na (from 135.9±6.8 to 142.2±3.8 mEq./l, P < 0.05) increased in the group 1 and decreased in the group 2 (from 134.7±7.9 to 130.1±4.3 mEq./l). Serum K was decreased (from 4.4±0.6 to 3.9±0.6, and 4.6±9 to 3.6±0.5 mEq./l, P < 0. 05) in both groups. BW was reduced (from 73.8±9.1 to 63.8±8.8, and from 72.9±10.2 to 64.5±7.5 kg, P < 0.05) in both groups. Group 2 showed more patients in NYHA class III than group 1 (18 vs. 2 patients, P < 0.05). Group 2 showed an increase of serum creatinine. Serum uric acid increased in both groups. BP values decreased, and HR was corrected to normal values in both groups. Group 2 showed a longer hospitalization time than group receiving HHS infusion (11.67±1.8 vs. 8.57±2.3 days, P < 0.001). In the follow-up (6–12 months), none of the patients from group 1 were readmitted to the hospital and they maintained the NYHA class achieved at the discharge. Group 2 showed 12 patients readmitted to hospital and a higher class than at discharge.

Conclusion: Our data suggest that the combination of furosemide with HSS is feasible and it appears that this combination produces an improvement of hemodynamic and clinical parameters, reduces the hospitalization time and maintains the obtained results over time in comparison with those receiving high-dose furosemide as bolus.

Key Words: Furosemide • Hypertonic saline solution • Refractory congestive heart failure

Received February 20, 2000; Revised April 24, 2000; Accepted May 23, 2000


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Eur J Heart FailHome page
M. J. Johnson, S. G. Oxberry, J. G.F. Cleland, and A. L. Clark
Measurement of breathlessness in clinical trials in patients with chronic heart failure: the need for a standardized approach: a systematic review
Eur J Heart Fail, February 1, 2010; 12(2): 137 - 147.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
J. E. Udelson, C. Orlandi, J. Ouyang, H. Krasa, C. A. Zimmer, G. Frivold, W. H. Haught, S. Meymandi, C. Macarie, D. Raef, et al.
Acute Hemodynamic Effects of Tolvaptan, a Vasopressin V2 Receptor Blocker, in Patients With Symptomatic Heart Failure and Systolic Dysfunction: An International, Multicenter, Randomized, Placebo-Controlled Trial
J. Am. Coll. Cardiol., November 4, 2008; 52(19): 1540 - 1545.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
M. Damgaard, P. Norsk, F. Gustafsson, J. K. Kanters, N. J. Christensen, P. Bie, L. Friberg, and N. Gadsboll
Hemodynamic and neuroendocrine responses to changes in sodium intake in compensated heart failure
Am J Physiol Regulatory Integrative Comp Physiol, May 1, 2006; 290(5): R1294 - R1301.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
S. Paterna, P. Di Pasquale, G. Parrinello, E. Fornaciari, F. Di Gaudio, S. Fasullo, M. Giammanco, F. M. Sarullo, and G. Licata
Changes in Brain Natriuretic Peptide Levels and Bioelectrical Impedance Measurements After Treatment With High-Dose Furosemide and Hypertonic Saline Solution Versus High-Dose Furosemide Alone in Refractory Congestive Heart Failure: A Double-Blind Study
J. Am. Coll. Cardiol., June 21, 2005; 45(12): 1997 - 2003.
[Abstract] [Full Text] [PDF]


Home page
Eur J Heart FailHome page
A. J. Reyes
The increase in serum uric acid concentration caused by diuretics might be beneficial in heart failure
Eur J Heart Fail, June 1, 2005; 7(4): 461 - 467.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.