Key result
IV furosemide fails to improve central hemodynamics or LV filling pressures in anuric hemodialysis patients.
Why the study?
Previous studies showed conflicting findings regarding the vascular effects of furosemide in patients with end-stage renal disease, necessitating investigation of its effects on central cardiac haemodynamics in anuric ESRD patients.
Does intravenous furosemide improve central cardiac haemodynamics in anuric haemodialysis patients?
Does intravenous furosemide improve central cardiac haemodynamics in anuric haemodialysis patients?
p-value: p=ns
Intravenous furosemide does not acutely alter central cardiac hemodynamics in anuric hemodialysis patients, suggesting it may not be effective for acute pulmonary edema in this population.
No hemodynamic effect of IV furosemide seen in anuric HD; leaves open whether alternative agents improve acute decongestion and warrants randomized trials.
BACKGROUND: In patients with pulmonary oedema and preserved renal function, furosemide has not only a renal, but also a vascular effect, causing a rapid fall in left ventricular filling pressure accompanied by an increase in venous compliance. Previous studies have shown conflicting findings regarding the vascular effects of furosemide in patients with end-stage renal disease (ESRD). The objective of our study was to investigate whether furosemide induces changes in central cardiac haemodynamics in anuric ESRD patients, using conventional echocardiography and colour tissue Doppler velocity imaging (TVI), a new quantitative and sensitive method. METHODS: Repeated low doses (40 mg followed by an additional dose of 40 mg after 30 min) of i.v. furosemide were administered to 12 (61.6 +/- 16 years, 7 men) and a high dose (250 mg) of i.v. furosemide to 6 (64.1 +/- 3.6 years, 5 men) clinically stable anuric haemodialysis (HD) patients. Conventional two-dimensional echocardiography and colour TVI images were recorded immediately before (0 min) the furosemide infusion in both groups, and in the group receiving the repeated low-dose infusion (at 0 and 30 min), 10, 20, 30, 40, 50 and 70 min after the administration of the first infusion. In the group receiving the single high dose of furosemide the ultrasound investigation was repeated 10, 20, 30 and 40 min after the infusion. The myocardial tissue velocities (v; cm/s) for isovolumetric contraction (IVC), peak systole (PS), early (E') and late (A') myocardial diastolic filling velocities were measured in the left ventricle (LV) at six sites (infero-septal, antero-lateral, inferior, anterior, infero-lateral and antero-septal walls) at the basal region. IVC time (IVCT), IV relaxation time (IVRT), PS time (PSt), RR interval, mitral annulus motion (MAM), strain rate (SR), left ventricular filling pressure (E/E') and cardiac output were also measured. The average of the different walls was used to evaluate global function. Right ventricle (RV) dynamics was evaluated from measurements of IVC velocity (IVCv), peak systolic velocity (PSv), E' and A' from the RV free wall. RESULTS: No significant changes in cardiac output, IVCv, PSv, SR, MAM, E', A', E'/A', IVRT and LV filling pressure were observed, indicating that neither 40 mg (plus additional 40 mg after 30 min) nor 250 mg of furosemide had any measurable effects on LV filling pressure and LV and RV systolic and diastolic function. CONCLUSIONS: In anuric HD patients, low and high doses of furosemide had no significant effects on central cardiac haemodynamics. Therefore, the use of furosemide infusion in anuric ESRD patients with acute pulmonary oedema is not supported by the results of this study.
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Hayashi et al. (2007) studied Anuric end-stage renal disease on haemodialysis (n=18). Intravenous furosemide vs. Baseline (pre-infusion) was evaluated on Central cardiac haemodynamics (cardiac output, LV filling pressure, LV and RV systolic and diastolic function) (p=ns). Intravenous furosemide at low (80 mg total) or high (250 mg) doses had no significant effects on central cardiac haemodynamics or left ventricular filling pressure in anuric haemodialysis patients.
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