| Background Heart failure (HF) is a common clinical disease. It wasdiscovered that arginine vasopressin levels were elevated in patients withheart failure and the elevation was proportional to the severity of heartfailure.Aim Selective vasopressin Receptor Antagonists(V2-receptor) inducesfree water excretion without increasing urinary sodium, improvewater-sodium retention. To assess the efficacy and safety of tolvaptan forheart failure.Methods We included all RCTs in the databases including Pubmedã€Medlineã€Embaseã€Cochrane Libraryã€CNKI. Time limit to Dec1,2013.Results were assessed by Jadad score. We analyzed data with softwareRevMan5.2.Results10randomized controlled trials (RCTs) were identified. Bodyweight significantly decreased after a single dose of tolvaptan [WMD,-0.82Kg;95%CI,(-0.90,-0.73)Kg; P<0.00001] and continued to decreasein short-term [WMD,-1.11Kg;95%CI,(-1.47,-0.75)Kg; P<0.00001].Improvement in edema and rales resolution had no significantly difference [RR,1.33;95%CI,(0.95,1.87); P=0.09] and [RR,1.43;95%CI,(0.63,3.22);P=0.39]. Changes from baseline serum sodium level was significantlyincreased [WMD,3.44MEq/L;95%CI,(2.70,4.17); P<0.00001].Incidence of worsening heart failure a significantly decreased [RR,0.68;95%CI,(0.49,0.95); P=0.02], respectively. The incidence of urinefrequency was significantly increased [RR,4.60;95%CI,(2.75,7.71);P<0.00001], the incidence of dry mouth or thirst was significantlyincreased [RR,5.65;95%CI,(4.63,6.89); P<0.00001]. The overallmortality rate had no significantly difference [RR,0.97;95%CI,(0.88,1.07); P=0.55].Conclusions Tolvaptan is efficacy and safety in patients with heartfailure in short-term. |