Literature DB >> 22673023

Efficacy of oral tolvaptan in acute heart failure patients with hypotension and renal impairment.

Muthiah Vaduganathan1, Mihai Gheorghiade, Peter S Pang, Marvin A Konstam, Faiez Zannad, Karl Swedberg, Liliana Grinfeld, John C Burnett, Holly B Krasa, Christopher Zimmer, John Blair, John Ouyang, Aldo P Maggioni.   

Abstract

AIMS: Although congestion is the main reason for admission in patients with worsening acute heart failure syndromes, patients presenting with low SBP and renal impairment often do not respond adequately to and may not tolerate traditional diuretic therapy. We sought to determine the short-term hemodynamic effects of tolvaptan in this high-risk population.
METHODS: In a subset analysis of the Efficacy of Vasopressin Antagonism in Heart Failure Outcome Study with Tolvaptan trial, 759 patients (18% of total) had elevated blood urea nitrogen (BUN) (> 20  mg/dl) and low SBP (<105  mmHg) at admission. Of these, 386 were randomized to tolvaptan and 373 to placebo.
RESULTS: Demographics and baseline characteristics were similar in both groups. Greater reductions from baseline in body weight were observed for tolvaptan (1.63 ±  2.00 vs. 0.76  ±  1.75  kg, P  <  0.0001 at day 1 and 3.23  ±  3.36 vs. 2.10  ±  3.47  kg, P  <  0.0001 at day 7 or discharge). Greater increases in serum sodium concentration were also observed in the tolvaptan group as early as day 1 (4.41  ±  3.67 vs. 1.32  ±  3.93  mEq/l, P  <  0.0001) and persisted through day 7 or discharge (4.79  ±  4.89 vs. 1.25  ±  5.00  mEq/l, P  <  0.0001). Similarly, improvements in patient-reported dyspnea and investigator-assessed orthopnea were significantly greater in the tolvaptan group as early as day 1 of treatment. These changes were not associated with significant differences in heart rate, SBP, DBP or serum creatinine between patients in the two treatment groups during hospitalization. In-hospital mortality rates (total and cause-specific) were comparable to patients who had presented with SBP more than 105  mmHg and BUN less than 20  mg/dl.
CONCLUSION: In this subgroup analysis of patients with hypotension and renal impairment, tolvaptan improved symptoms, reduced body weight and increased serum sodium as early as inpatient day 1 without adversely affecting blood pressure or renal function.

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Year:  2012        PMID: 22673023     DOI: 10.2459/JCM.0b013e328355a740

Source DB:  PubMed          Journal:  J Cardiovasc Med (Hagerstown)        ISSN: 1558-2027            Impact factor:   2.160


  8 in total

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Review 2.  Interventions for chronic non-hypovolaemic hypotonic hyponatraemia.

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4.  First experience with Tolvaptan for the treatment of neonates and infants with capillary leak syndrome after cardiac surgery.

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5.  Tolvaptan in reversing worsening acute heart failure: A systematic review and meta-analysis.

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6.  The effects of tolvaptan on patients with severe chronic kidney disease complicated by congestive heart failure.

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7.  Short term efficacy and safety of low dose tolvaptan in patients with acute decompensated heart failure with hyponatremia: a prospective observational pilot study from a single center in South India.

Authors:  Soumya Patra; Basant Kumar; Kaushal K Harlalka; Apoorva Jain; H M Bhanuprakash; K S Sadananda; Harsha Basappa; K Santhosh; K S Rajith; K S Bharathi; C N Manjunath
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8.  Pharmacological approaches to cardio-renal syndrome: a role for the inodilator levosimendan.

Authors:  Francesco Fedele; Kristjan Karason; Simon Matskeplishvili
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  8 in total

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