首页> 外文期刊>Journal of cardiac failure >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
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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

机译:托伐普坦单药治疗与呋塞米,托伐普坦和呋塞米联合治疗心力衰竭和收缩功能障碍的多中心,随机,双盲,安慰剂对照研究

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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 HF (New York Heart Association Class II-III), 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 furosemide 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 β-blockers.
机译:背景:患有慢性心力衰竭(HF)的患者体内加压素水平可能升高,并通过对加压素V2受体的影响而有助于病理生理。背景利尿剂治疗的存在可能会混淆血管加压素受体拮抗剂(VRA)的评估。方法和结果:符合条件的患者患有HF(纽约心脏协会II-III级),收缩功能障碍(左心室射血分数≤0.40)和充血迹象(例如水肿、,音)。筛查时,将患者从基线利尿剂治疗中撤出,并接受低钠饮食(2 g /天)。在为期2天的磨合期后,将83例患者随机分为安慰剂组(n = 21),血管加压素V2受体拮抗剂托伐普坦(TLV)30 mg(n = 20)单药治疗,呋塞米80 mg(FURO,n = 22)或TLV 30 mg和FURO 80 mg(n = 20)每天一次,共7天。患者接受标准的背景治疗,并且在整个研究过程中均没有液体限制。在第8天,相对于基线,TLV,FURO和TLV + FURO的体重分别降低了-1.37±1.61 、、-0.54±1.59和-1.13±1.49 kg。在同一时间,安慰剂组结果显示,与基线相比,体重增加了+0.72±2.42 kg(TLV与安慰剂相比,P = .0006)。单独使用TLV(2646±1503 mL / 24小时)的尿液相对于基线的增加量大于FURO(894±853 mL / 24小时,P <.001)或PLC(423±786 mL / 24小时,P <.001),类似于TLV + FURO(2585±2119 mL / 24小时)。在TLV治疗的患者中也观察到血清钠含量在正常范围内增加(与安慰剂相比,P <.02;与FURO相比,P <.01)。没有观察到血清钾,其他实验室值或血压的变化。 TLV治疗耐受性良好。结论:对于有HF且有容量超负荷迹象的TLV单一疗法(无伴随利尿剂治疗),与安慰剂相比,在无钠电解质的情况下,在钠限制饮食期间和使用背景药物(包括血管紧张素转换酶抑制剂和β)时,体重减轻阻滞剂。

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