Elsevier

International Journal of Cardiology

Volume 205, 15 February 2016, Pages 37-42
International Journal of Cardiology

Efficacy and safety of tolvaptan for pediatric patients with congestive heart failure. Multicenter survey in the working group of the Japanese Society of PEdiatric Circulation and Hemodynamics (J-SPECH)

https://doi.org/10.1016/j.ijcard.2015.12.003Get rights and content

Abstract

Background

Tolvaptan, a vasopressin V2-receptor antagonist, has been reported to improve congestion in adult patients with heart failure. However, it has not been fully clarified whether tolvaptan is also effective and safe for pediatric patients as well as adult.

Methods

This trial was a multicenter, retrospective, observational study, and was led by the Japanese Society of PEdiatric Circulation and Hemodynamics (J-SPECH). Thirty-four pediatric patients who received tolvaptan to treat congestive heart failure were enrolled in this study.

Results

An increment in the urinary volume and decrease in the body weight from baseline were significant at day 1 (+ 106.7 ± 241.5%, p = 0.008 and − 2.30 ± 4.17%, p = 0.01), day 3 (+ 113.5 ± 261.9%, p = 0.02 and − 2.30 ± 4.17%, p = 0.01), week 1 (+ 56.3 ± 163.5%, p = 0.01 and − 1.55 ± 4.09%, p = 0.03) and month 1 (+ 91.1 ± 171.6%, p = 0.01 and − 2.95 ± 5.98, p = 0.03). The significant predictive factors in responders, who was defined as patients who achieved an increase in the urinary volume at day 1, were older age (p = 0.03), larger body weight before exacerbation (p = 0.04), higher weight at one day before the first administration of tolvaptan (p = 0.03), higher aspartate aminotransferase levels (p = 0.03) and higher urinary osmolality levels (p = 0.03). A logistic regression analysis showed that the urinary osmolality was the only significant predictive factor for responders to tolvaptan. Adverse drug reactions were observed in 7 patients (20.6%). Six patients had thirst and a dry month, and 1 had a mild increase in the alanine aminotransferase and aspartate aminotransferase.

Conclusion

Tolvaptan can be effectively and safely administered in pediatric patients. Because the kidneys in neonates and infants are resistant to arginine vasopressin, the efficacy of tolvaptan may be less effective compared to older children.

Introduction

Tolvaptan, a competitive oral vasopressin V2-receptor antagonist, has recently become available for patients with heart failure and symptomatic congestion [1], [2], [3]. Recent clinical studies in adult patients with congestive heart failure have demonstrated that short-term tolvaptan treatment increases the urinary volume, decreases the body weight, and improves the signs of a fluid overload [4], [5], [6]. Moreover, the current guidelines concerning the management of acute heart failure in Japan (that were updated in 2013) recommend using tolvaptan for patients with a volume overload and symptoms of right and left heart failure [7]. However, there is a little data concerning the efficacy of tolvaptan in pediatric patients with congestive heart failure [8], [9]. Therefore, we conducted this trial to clarify the efficacy and safety of tolvaptan therapy in pediatric patients with congestive heart failure.

Section snippets

Study population

This trial was a multicenter, retrospective, observational study. Seven pediatric cardiology institutes, which were registered in the Japanese Society of PEdiatric Circulation and Hemodynamics (J-SPECH) trial participated in this study (Chiba Children's Hospital, Fukuoka Children's Hospital, Kyoto Prefectural University, National Cerebral and Cardiovascular Center, Kitasato University, Saitama Medical University, and Hokkaido University). Thirty-four pediatric patients with congestive heart

Patient characteristics

The background and demographic data of the 34 patients who were enrolled in this study are shown in Table 1. The mean age was 49.1 ± 60.8 months (range 2–202 months) and 24 patients (70.6%) were under 48 months. The prevalence of classes III and IV heart failure according to the NYHA classification was 79.4%. Concerning basic disorders, 28 patients (82.4%) had congenital heart disease and the remaining 6 (17.6%) suffered from cardiomyopathy (Table 1). The reasons for starting tolvaptan were

Discussion

Regan and colleagues previously demonstrated that tolvaptan increased the urine volume and elevated the serum sodium concentration in pediatric patients with heart failure for 3 days [8]. In the present study, we also showed that the tolvaptan increased the urinary volume, reduced the body weight, and normalized the serum sodium concentration in most pediatric patients with congestive heart failure not only for 3 days, but also for 1 month. The decreased urinary osmolality means that the tolvaptan

Grant support

None.

Conflicts of interest

None.

References (14)

  • G. Decaux et al.

    Non-peptide arginine-vasopressin antagonists: the vaptans

    Lancet

    (2008)
  • K. Watanabe et al.

    Short-term effects of low-dose tolvaptan on hemodynamic parameters in patients with chronic heart failure

    J. Cardiol.

    (2012)
  • T. Miyazaki et al.

    Tolvaptan, an orally active vasopressin V(2)-receptor antagonist — pharmacology and clinical trials

    Cardiovasc. Drug Rev.

    (2007)
  • M. Gheorghiade et al.

    Short-term clinical effects of tolvaptan, an oral vasopressin antagonist, in patients hospitalized for heart failure: the EVEREST clinical status trials

    JAMA

    (2007)
  • T. Inomata et al.

    Phase III clinical pharmacology study of tolvaptan

    Cardiovasc. Drugs Ther.

    (2011)
  • K. Kinugawa et al.

    Efficacy and safety of tolvaptan in heart failure patients with volume overload

    Circ. J.

    (2014)
  • JCS Joint Working Group

    Guidelines for treatment of acute heart failure (JCS 2011): digest version

    Circ. J.

    (2013)
There are more references available in the full text version of this article.

Cited by (0)

These authors take responsibility for all aspects of the reliability and freedom from bias of the data presented and their discussed interpretation.

View full text