It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Aims
Furosemide, a short‐acting loop diuretic (SD), is the dominant agent prescribed for heart failure (HF) in clinical practice. However, accumulating data suggests that long‐acting loop diuretics (LD), such as torsemide or azosemide, might have more favourable pharmacological profiles. This study aimed to investigate the relationship between the type of loop diuretics and long‐term outcomes among patients hospitalized for acute HF enrolled in a contemporary multicentre registry.
Methods and results
Within the West Tokyo Heart Failure Registry from 2006 to 2017, a total of 2680 patients (60.1% men with a median age of 77 years) were analysed. The patients were characterized by the type of diuretics used at the time of discharge; 2073 (77.4%) used SD, and 607 (22.6%) used LD. The primary endpoint was composite of all‐cause death or HF re‐admission after discharge, and the secondary endpoints were all‐cause death and HF re‐admission, respectively. During the median follow‐up period of 2.1 years, 639 patients died [n = 519 (25.0%) in the SD group; n = 120 (19.8%) in the LD group], and 868 patients were readmitted for HF [n = 697 (33.6%) in the SD group; n = 171 (28.2%) in the LD group]. After multivariable adjustment, the LD group had lower risk for the composite outcome [hazard ratio (HR), 0.80; 95% confidence interval (CI), 0.66–0.96; P = 0.017], including all‐cause death (HR; 0.73; 95% CI; 0.54–0.99; P = 0.044) and HF re‐admission (HR, 0.81; 95% CI, 0.66–0.99; P = 0.038), than the SD group. Propensity score matching yielded estimates that were consistent with those of the multivariable analyses, with sub‐group analyses demonstrating that use of LD was associated with favourable outcomes predominantly in younger patients with reduced ejection fraction.
Conclusions
LD was associated with lower risk of long‐term outcomes in patients with HF and a recent episode of acute decompensation.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
; Shiraishi, Yasuyuki 1 ; Kohsaka, Shun 1 ; Niimi, Nozomi 1 ; Goda, Ayumi 2 ; Nagatomo, Yuji 3 ; Takei, Makoto 4 ; Saji, Mike 5 ; Nakano, Shintaro 6 ; Kohno, Takashi 2 ; Fukuda, Keiichi 1 ; Yoshikawa, Tsutomu 5 1 Department of Cardiology, Keio University School of Medicine, Tokyo, Japan
2 Department of Cardiovascular Medicine, Kyorin University Fuculty of Medicine, Tokyo, Japan
3 Department of Cardiology, National Defense Medical College Hospital, Tokorozawa, Japan
4 Department of Cardiology, Saiseikai Central Hospital, Tokyo, Japan
5 Department of Cardiology, Sakakibara Heart Institute, Tokyo, Japan
6 Department of Cardiology, Saitama Medical University International Medical Center, Saitama, Japan





