Author:
Yoshioka Kenji,Maeda Daichi,Okumura Takahiro,Kida Keisuke,Oishi Shogo,Akiyama Eiichi,Suzuki Satoshi,Yamamoto Masayoshi,Mizukami Akira,Kuroda Shunsuke,Kagiyama Nobuyuki,Yamaguchi Tetsuo,Sasano Tetsuo,Matsumura Akihiko,Kitai Takeshi,Matsue Yuya
Abstract
AbstractAlthough intravenous diuretics is a cornerstone of acute heart failure treatment (AHF), its optimal initial dose is unclear. This is a post-hoc analysis of the REALITY-AHF, a prospective multicentre observational registry of AHF. The initial intravenous diuretic dose used in each patient was categorised into below, standard, or above the recommended dose groups according to guideline-recommended initial intravenous diuretic dose. The recommended dose was individualised based on the oral diuretic dose taken at admission. We compared the study endpoints, including 60-day mortality, diuretics response within six hours, and length of hospital stay (HS). Of 1093 patients, 429, 558, and 106 were assigned to the Below, Standard, and Above groups, respectively. The diuretics response and HS were significantly greater in the Below group than in the Standard group after adjusting for covariates. Kaplan–Meier analysis indicated a significantly higher incidence of 60-day mortality in the Above group than the Standard group. This difference was retained after adjusting for other prognostic factors. Treatment with a lower than guideline-recommended intravenous diuretic dose was associated with longer HS, whereas above the guideline-recommended dose was associated with a higher 60-day mortality rate. Our results reconfirm that the guideline-recommended initial intravenous diuretic dose is feasible for AHF.
Funder
The Cardiovascular Research Fund
Japan Society for the Promotion of Science
Publisher
Springer Science and Business Media LLC
Cited by
5 articles.
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