論文

2017年4月25日

Tolvaptan Reduces the Risk of Worsening Renal Function in Patients With Acute Decompensated Heart Failure and Preserved Left Ventricular Ejection Fraction - Prospective Randomized Controlled Study.

Circulation journal : official journal of the Japanese Circulation Society
  • Shunsuke Tamaki
  • Yoshihiro Sato
  • Takahisa Yamada
  • Takashi Morita
  • Yoshio Furukawa
  • Yusuke Iwasaki
  • Masato Kawasaki
  • Atsushi Kikuchi
  • Takumi Kondo
  • Tatsuhisa Ozaki
  • Masahiro Seo
  • Iyo Ikeda
  • Eiji Fukuhara
  • Makoto Abe
  • Jun Nakamura
  • Masatake Fukunami
  • 全て表示

81
5
開始ページ
740
終了ページ
747
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1253/circj.CJ-16-1122

BACKGROUND: Although the mainstay of treatment for acute decompensated heart failure (ADHF) is decongestion by diuretic therapy, it is often associated with worsening renal function (WRF). The effect of tolvaptan, a selective V2 receptor antagonist, on WRF in ADHF patients with preserved left ventricular ejection fraction (LVEF) is unknown.Methods and Results:We enrolled 50 consecutive ADHF patients whose LVEF on admission was ≥45%. Patients were randomly assigned to either tolvaptan add-on (n=26) or conventional diuretic therapy (n=24). The primary endpoint was the incidence of WRF, defined as an increase in serum creatinine (Cr) ≥0.3 mg/dL or 50% above baseline within 48 h of randomization. There was no significant difference between the 2 groups in the change in body weight or the total urine volume during 48 h. However, the change in Cr (∆Cr) at 24 and 48 h after randomization and the incidence of WRF (12% vs. 42%, P=0.0236) were significantly lower, and the fractional excretion of urea (FEUN) at 24 and 48 h after randomization was significantly higher in the tolvaptan group. There was an inverse correlation between ∆Cr and FEUN at 48 h after randomization. CONCLUSIONS: Tolvaptan can alleviate congestion with a significantly lower risk of WRF in ADHF patients with preserved LVEF, presumably through maintenance of renal perfusion.

リンク情報
DOI
https://doi.org/10.1253/circj.CJ-16-1122
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28202885
ID情報
  • DOI : 10.1253/circj.CJ-16-1122
  • PubMed ID : 28202885

エクスポート
BibTeX RIS