A Multicenter, Randomized, Double-blind, Placebo-controlled Study of Tolvaptan Monotherapy Compared to Furosemide and the Combination of Tolvaptan and Furosemide in Patients With Heart Failure and Systolic Dysfunction

被引:65
作者
Udelson, James E. [1 ,2 ]
Bilsker, Martin [3 ]
Hauptman, Paul J. [4 ]
Sequeira, Rafael [3 ]
Thomas, Ignatius [5 ]
O'Brien, Terrence [6 ]
Zimmer, Christopher [7 ]
Orlandi, Cesare [7 ]
Konstam, Marvin A. [1 ,2 ]
机构
[1] Tufts Med Ctr, Div Cardiol, Boston, MA 02111 USA
[2] Tufts Med Ctr, CardioVasc Ctr, Boston, MA 02111 USA
[3] Univ Miami, Jackson Mem Hosp, Div Cardiol, Miami, FL 33136 USA
[4] St Louis Univ, Sch Med, St Louis, MO USA
[5] Med Res Inst, Slidell, LA USA
[6] Ralph H Johnson Vet Adm Med Ctr, Charleston, SC USA
[7] Otsuka Maryland Res Inst, Rockville, MD USA
关键词
Heart failure; diuretics; vasopressin; LEFT-VENTRICULAR DYSFUNCTION; VASOPRESSIN ANTAGONIST; RENAL-FUNCTION; RECEPTOR ANTAGONIST; PROTEIN-SYNTHESIS; ACTIVATION; SODIUM; INCREASES;
D O I
10.1016/j.cardfail.2011.08.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Increased vasopressin levels may be present in patient with chronic heart failure (HF) and contribute to pathophysiology through effects on the vasopressin V2 receptor. The presence of background diuretic therapy may confound evaluations of vasopressin receptor antagonists (VRA). Methods and Results: Eligible patients had FIF (New York Heart Association Class 11411), systolic dysfunction (left ventricular ejection fraction <= 0.40) and signs of congestion (eg, edema, rales). At screening, patients were removed from baseline diuretic therapy and placed on a low-sodium diet (2 g/day). After a 2-day run-in period, 83 patients were randomized to placebo (n = 21), monotherapy with the vasopressin V2 receptor antagonist tolvaptan (TLV) 30 mg (n = 20), monotherapy with furosernide 80 mg (FURO, n = 22) or both TLV 30 mg and FURO 80 mg (n = 20) once daily for 7 days. Patients were on standard background therapy and not fluid-restricted throughout the study. A decrease in body weight of -1.37 +/- 1.61, -0.54 +/- 1.59, and -1.13 +/- 1.49 kg was observed versus baseline for TLV, FURO, and TLV+FURO, respectively, at day 8. At the same point, the placebo group showed a body weight increase of +0.72 +/- 2.42 kg versus baseline (P = .0006 for TLV versus placebo). Increases in urine volume from baseline were greater with TLV alone (2646 +/- 1503 mL/24 hours) than with FURO (894 +/- 853 mL/24 hours, P < .001), or PLC (423 +/- 786 mL/24 hours, P < .001), and similar to TLV+FURO (2585 2119 mL/24 hours). An increase in serum sodium within the normal range was also observed in TLV-treated patients (P < .02 versus placebo; P < .01 versus FURO). No changes in serum potassium, other laboratory values, or blood pressure were observed. TLV therapy was well tolerated. Conclusions: In patients with HF and signs of volume overload, TLV monotherapy without concomitant loop diuretic therapy reduced body weight when compared to placebo without adverse changes in serum electrolytes, during a sodium restricted diet while on background medications including angiotensin-converting enzyme inhibitors and beta-blockers. (J Cardiac Fail 2011;17:973-981)
引用
收藏
页码:973 / 981
页数:9
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