Literature DB >> 33527152

Clinical effectiveness and adverse events associated with tolvaptan in patients above 90 years of age with acute decompensated heart failure.

Yusuke Morita1, Akihiro Endo2, Yuzo Kagawa2, Kazuto Yamaguchi2, Hirotomo Sato2, Takeshi Ouchi2, Nobuhide Watanabe2, Kazuaki Tanabe2.   

Abstract

With the aging society, the number of very-elderly (VE) patients with acute decompensated heart failure (ADHF) is increasing. Although tolvaptan is recommended for patients with ADHF in whom conventional diuretic therapy is ineffective, few reports exist on VE patients over 90 years of age. Therefore, we aimed to evaluate the clinical effectiveness and adverse events associated with tolvaptan in VE patients with ADHF. From January 2011 to December 2018, we retrospectively studied 180 patients with ADHF who were first administered tolvaptan during hospitalization. Patients were divided into two groups, namely, VE patients who were ≥ 90 years of age (n = 32) and not-VE patients (NVE) who were < 90 years of age (n = 148). The primary effective endpoints were the total urine volume and change in body weight. The safety endpoints evaluated were the incidence of hypernatremia (≥ 150 mEq/L) and worsening renal function (WRF) at any time during hospitalization. The median [interquartile range] patient age was 93 [91-94] years in the VE group and 80 [69-85] years in the NVE group. The mean dose of tolvaptan for the first week of administration was similar between groups (7.9 ± 5.0 mg, VE group; 7.3 ± 3.7 mg, NVE group; p = 0.52). There were no significant differences between the two groups in the total urine volume at 24 h (1901 ± 666 mL, VE group; 2101 ± 1167 mL, NVE group; p = 0.33) and that at 48 h (3707 ± 1274 mL, VE group; 4195 ± 1990 mL, NVE group; p = 0.19) and in the mean change in body weight (- 2.5 ± 2.0 kg, VE group; -2.7 ± 2.4 kg, NVE group; p = 0.70). The median duration of hospitalization was 24 [20-9] and 31 [20-42] days in the VE and NVE groups, respectively (p = 0.67). The incidence of hypernatremia (6.3% (2/32), VE group; 3.4% (5/148), NVE group; p = 0.61) and WRF (25.0% (8/32) VE group; 19.6% (29/148), NVE group; p = 0.31) was similar between the groups. In conclusion, tolvaptan has similar clinical effectiveness in increasing urine volume and decreasing body weight, without increased adverse events, in VE patients with ADHF who were ≥ 90 years of age compared to NVE patients with ADHF.

Entities:  

Keywords:  Acute decompensated heart failure; Adverse event; Effectiveness; Elderly patient; Tolvaptan

Year:  2021        PMID: 33527152     DOI: 10.1007/s00380-020-01753-3

Source DB:  PubMed          Journal:  Heart Vessels        ISSN: 0910-8327            Impact factor:   2.037


  1 in total

1.  Clinical utility of early use of tolvaptan in very elderly patients with acute decompensated heart failure.

Authors:  Hiroki Niikura; Raisuke Iijima; Hitoshi Anzai; Norihiro Kogame; Ryo Fukui; Hiroki Takenaka; Nobuyuki Kobayashi
Journal:  Anatol J Cardiol       Date:  2017-08-02       Impact factor: 1.596

  1 in total
  1 in total

1.  Clinical features and long-term prognosis of patients with congestive heart failure taking tolvaptan: a comparison of patients with preserved and reduced left ventricular ejection fraction.

Authors:  Toshiki Seki; Yoshiaki Kubota; Junya Matsuda; Yukichi Tokita; Yu-Ki Iwasaki; Wataru Shimizu
Journal:  Heart Vessels       Date:  2021-10-14       Impact factor: 2.037

  1 in total

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