Intravenous diuretics are the cornerstone of management for patients hospitalized for heart failure. Physiologic data suggest that intermittent high-dose furosemide promotes neurohormonal activation, which a slow continuous infusion might remediate. However, the limited clinical data comparing dosing schemes are confounded. This study was a randomized, open-label, single-center trial of twice-daily bolus injection versus continuous infusion furosemide in patients hospitalized with heart failure and volume overload. The primary outcome was change in creatinine from admission to hospital day 3 or discharge. Twenty-one patients were randomized to bolus injection and 20 patients to continuous infusion. Baseline characteristics were balanced between study arms except for gender, with a mean age of 60 ± 15 years, a mean ejection fraction of 35 ± 19%, and a mean creatinine level of 1.9 ± 1.2 mg/dl. The mean doses of furosemide were similar between arms over the first 48 hours (162 ± 48 and 162 ± 52 mg/24 hours). None of the outcomes differed significantly between bolus and continuous dosing from admission to hospital day 3 or discharge (mean change in creatinine −0.02 vs 0.13 mg/dl, p = 0.18; urine output 5,113 vs 4,894 ml, p = 0.78; length of stay 8.8 vs 9.9 days, p = 0.69). All patients survived to discharge. In conclusion, there were no substantial differences between bolus injection and continuous infusion of equal doses of furosemide for the treatment of patients hospitalized with heart failure. Given the high prevalence of heart failure hospitalization and the disparate results of small studies regarding optimal dosing of loop diuretics to treat these patients, larger multicenter blinded studies are needed.
Given the high prevalence of the use of intravenous loop diuretics for patients hospitalized with acute decompensated heart failure (HF) and the paucity of data guiding best practices for administration, we carried out a randomized pilot study of furosemide by continuous infusion versus twice-daily bolus injection for the treatment of such patients. Our primary hypothesis was that continuous dosing of intravenous furosemide provides gradual diuresis with less neurohormonal activation, which would manifest as less renal dysfunction, compared to bolus dosing in the treatment of acute decompensated HF with volume overload.
Methods
This study was a prospective, open-label, single-center, randomized trial of bolus injection versus continuous infusion of furosemide after hospital admission for HF. Patients were enrolled from Duke University Medical Center from 1999 to 2005. Patients were eligible if they were admitted with a primary diagnosis of acute decompensated HF, could be randomized <24 hours from hospital presentation, and had evidence of volume overload (pulmonary congestion on chest x-ray or pro–B-type natriuretic peptide greater than the upper limit of normal for age). Patients were excluded if they had end-stage renal disease or anticipated need for renal replacement therapy, were not expected to survive hospitalization, or were pregnant. All patients signed informed consent. The study was approved by the Duke institutional review board.
Once enrolled, the dose of intravenous furosemide to be given per 24 hours was decided upon by the attending physician. Patients were then randomized in a 1:1 ratio using a computer-generated scheme to receive the decided upon furosemide dose divided into twice-daily bolus injection or continuous infusion (mixed as a 1:1 ratio in 5% dextrose in water) for ≥48 hours. Subsequent titration of furosemide dose was at the discretion of the attending physician but was guided by a dose-escalation algorithm.
Data were collected at the time of enrollment and then daily through review of the medical record, an interview with the patient, and a physical examination. During the study, patients received daily blood work as part of routine care, including a daily basic metabolic panel as standard care for patients receiving intravenous diuretic therapy. The protocol also recommended the maintenance of serum potassium >4.0 mEq/L and serum magnesium >2.0 mEq/L. Electrolyte repletion was left to the discretion of the physician of record.
The primary outcome measure was change in serum creatinine from admission (hospital day 0) to hospital day 3 or hospital discharge, whichever came first. Creatinine was chosen on the basis of its ease of measurement and strong association with other clinical end points. Secondary outcome measures included cumulative urine output and other electrolyte changes from admission to hospital day 3 (or hospital discharge), as well as hospital length of stay. Observed survival was assessed through a search of the Duke electronic medical record and the Social Security Death Index. An estimated 42 patients were required to detect a clinically significant difference in the primary outcome of 0.3 mg/dl with power of 80%, assuming a standard deviation of 0.33 mg/dl and a 2-sided p value of 0.05.
Estimated glomerular filtration rate was calculated using the Modification of Diet in Renal Disease (MDRD) equation. Torsemide was converted to furosemide equivalents (torsemide 1 mg = furosemide 2 mg). Analysis for all end points was performed on an intention-to-treat basis. Comparisons of changes in outcomes from admission (hospital day 0) to hospital day 3 (or discharge, whichever came first) between the bolus and continuous arms were performed using Wilcoxon’s rank-sum test for continuous variables and the chi-square test for categorical variables. A 2-tailed p value of 0.05 was used to determine significance. Analyses were conducted with SAS version 9.1 (SAS Institute Inc., Cary, North Carolina).
Results
We enrolled and randomized 41 patients. For the overall cohort, the mean age was 60 ± 15 years, the mean ejection fraction was 35 ± 19%, and the mean estimated glomerular filtration rate was 54 ± 30 ml/min/1.73 m 2 . Mean oral home dose of furosemide equivalent before admission was 99 ± 108 mg/24 hours, with 29% (n = 12) of patients taking no loop diuretics before admission. Baseline characteristics were not statistically different between arms except for gender, which by random sampling produced fewer women in the continuous infusion arm (p = 0.005; Table 1 ).
| Variable | Twice Daily (n = 21) | Continuous (n = 20) |
|---|---|---|
| Age (years) | 58 ± 16 (46, 63, 68) | 61 ± 14 (49, 62, 72) |
| Black | 20 (48%) | 7 (35%) |
| Women | 12 (57%) | 3 (15%) |
| Diabetes mellitus | 15 (71%) | 9 (45%) |
| Hypertension | 18 (86%) | 14 (70%) |
| Atrial fibrillation | 7 (33%) | 9 (45%) |
| Coronary artery disease | 9 (43%) | 11 (55%) |
| Left ventricular ejection fraction (%) | 39 ± 20 (17, 35, 60) | 31 ± 18 (15, 30, 55) |
| Furosemide, home | 14 (67%) | 10 (50%) |
| Torsemide, home | 2 (10%) | 3 (15%) |
| Home oral furosemide equivalent (mg/24 h) | 110 ± 114 (0, 80, 160) | 87 ± 102 (0, 80, 120) |
| Thiazide or thiazide-type diuretic | 1 (5%) | 1 (5%) |
| Spironolactone | 7 (33%) | 8 (40%) |
| Angiotensin-converting enzyme inhibitor or angiotensin receptor blocker | 17 (81%) | 16 (80%) |
| β blocker | 14 (67%) | 17 (85%) |
| Systolic blood pressure (mm Hg) | 127 ± 22 (108, 124, 140) | 112 ± 20 (99, 105, 124) |
| Heart rate (beats/min) | 85 ± 17 (72, 84, 97) | 80 ± 17 (71, 78, 88) |
| Weight (kg) | 104 ± 34 (81, 102, 127) | 96 ± 23 (80, 96, 111) |
| Sodium (mEq) | 141 ± 31 (39, 142, 143) | 139 ± 51 (36, 139, 142) |
| Potassium (mEq) | 3.9 ± 0.5 (3.7, 3.8, 4.1) | 4.2 ± 0.6 (3.8, 4.2, 4.6) |
| Urea nitrogen (mg/dl) | 37 ± 31 (16, 24, 45) | 33 ± 19 (19, 26, 38) |
| Creatinine (mg/dl) | 2.1 ± 1.3 (1.1, 1.5, 2.8) | 1.8 ± 1.0 (1.1, 1.4, 1.9) |
| Glomerular filtration rate (ml/min/1.73 m 2 ) | 48 ± 27 (20, 46, 70) | 59 ± 33 (32, 52, 82) |
| Hemoglobin (g/dl) | 11.1 ± 2.5 (9.2, 11.4, 13.2) | 12.1 ± 2.2 (10.0, 12.2, 13.5) |
Follow-up was 100% at discharge. There were no protocol violations, with all patients receiving furosemide dosing as dictated by study assignment starting <24 hours after enrollment and continuing during the 48 hours after randomization. The mean doses of furosemide were similar between arms over the first 48 hours ( Table 2 ).
| Variable | Twice Daily (n = 21) | Continuous (n = 20) | p Value |
|---|---|---|---|
| Furosemide dose (mg/24 h) | 162 ± 48 | 162 ± 52 | 1.00 |
| 160 (140 to 200) | 160 (120 to 240) | ||
| Δ creatinine (mg/dl) | −0.02 ± 0.39 | 0.13 ± 0.34 | 0.18 |
| 0.1 (−0.1 to 0.2) | 0.05 (−0.05 to 0.35) | ||
| Urine output (ml) | 5,113 ± 2,258 | 4,894 ± 2,205 | 0.64 |
| 4,675 (3,230 to 6,250) | 4,448 (3,625 to 4,650) | ||
| Δ weight (kg) | −1.64 ± 2.34 | −2.66 ± 2.44 | 0.27 |
| −2.55 (−3.30 to 0.25) | −2.10 (−4.85 to −1.25) | ||
| Δ serum potassium (mEq/L) | −0.07 ± 0.57 | 0.22 ± 0.67 | 0.08 |
| −0.2 (−0.5 to 0.3) | 0.3 (−0.2 to 0.7) | ||
| Rates of hypokalemia (<3.5 mEq/L) | 5 (24%) | 2 (10%) | 0.44 |
| Δ serum sodium (mEq/L) | −2.19 ± 3.25 | −1.15 ± 3.12 | 0.30 |
| −2 (−5 to 0) | −1 (−4 to 1) | ||
| Δ systolic blood pressure (mm Hg) | −5.6 ± 21.2 | 2.9 ± 15.0 | 0.11 |
| −3 (−15 to 7) | 0 (−2 to 4) | ||
| Length of stay (days) | 8.86 ± 3.82 | 9.85 ± 11.72 | 0.69 |
| 7 (5.5 to 11) | 7 (4.5 to 9.5) |
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