The association between ivabradine and adverse cardiovascular events in acute decompensated HFrEF patients

Abstract Aims Ivabradine has been used in patients who have chronic heart failure (HF) with reduced ejection fraction (HFrEF) and concomitant sinus heart rate ≥70 bpm. This administration for acute HFrEF remains a concern. This study used a real‐world multicentre database to investigate the effects...

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Main Authors: Chia‐Te Liao, Jin‐Long Huang, Huai‐Wen Liang, Fa‐Po Chung, Ying‐Hsiang Lee, Po‐Lin Lin, Wei‐Ru Chiou, Wen‐Yu Lin, Chien‐Yi Hsu, Hung‐Yu Chang
Format: Article
Language:English
Published: Wiley 2021-10-01
Series:ESC Heart Failure
Subjects:
Online Access:https://doi.org/10.1002/ehf2.13536
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author Chia‐Te Liao
Jin‐Long Huang
Huai‐Wen Liang
Fa‐Po Chung
Ying‐Hsiang Lee
Po‐Lin Lin
Wei‐Ru Chiou
Wen‐Yu Lin
Chien‐Yi Hsu
Hung‐Yu Chang
author_facet Chia‐Te Liao
Jin‐Long Huang
Huai‐Wen Liang
Fa‐Po Chung
Ying‐Hsiang Lee
Po‐Lin Lin
Wei‐Ru Chiou
Wen‐Yu Lin
Chien‐Yi Hsu
Hung‐Yu Chang
author_sort Chia‐Te Liao
collection DOAJ
description Abstract Aims Ivabradine has been used in patients who have chronic heart failure (HF) with reduced ejection fraction (HFrEF) and concomitant sinus heart rate ≥70 bpm. This administration for acute HFrEF remains a concern. This study used a real‐world multicentre database to investigate the effects of ivabradine among patients with acute decompensated HFrEF before discharge. Methods and results This study retrospectively identified patients with acute decompensated HFrEF who were administered ivabradine at discharge from two multicentre HF databases. Propensity score matching was performed to adjust for confounders. Cardiovascular mortality, all‐cause mortality, and recurrent HF rehospitalization risks were then compared between those with and without ivabradine treatment. After 1:2 propensity score matching, 876 patients (age, 60.7 ± 14.6 years; female, 23.2%; left ventricular ejection fraction, 28.2% ± 7.8%; and heart rate at discharge, 84.3 ± 13.8 bpm) were included in the final analysis, including 292 and 584 patients with and without ivabradine treatment at discharge, respectively. No significant differences were observed in baseline characteristics between the two groups. At 1 year follow‐up, patients in the ivabradine group had significantly lower heart rates (77.6 ± 14.7 vs. 81.1 ± 16.3 bpm; P = 0.005) and lower HF severity symptoms (New York Heart Association Functional class, 2.1 ± 0.7 vs. 2.3 ± 0.9; P < 0.001) than those from the non‐ivabradine group. Ivabradine users had significantly lower risks of 1 year cardiovascular mortality (5.8 vs. 12.2 per 100‐person year; P = 0.003), all‐cause mortality (7.2 vs. 14.0 per 100‐person year; P = 0.003), and total HF rehospitalization (42.3 vs. 72.6 per 100‐person year; P < 0.001) than non‐ivabradine users. Following multivariate analysis, the predischarge prescription of ivabradine remained independently associated with lower 1 year all‐cause mortality (hazard ratio, 0.45; 95% confidence interval, 0.28–0.74; P = 0.002) and cardiovascular mortality (hazard ratio, 0.41; 95% confidence interval, 0.24–0.72; P = 0.002). Conclusions The current study findings suggest that ivabradine treatment is associated with reduced risks of cardiovascular mortality, all‐cause mortality, and HF rehospitalization within 1 year among patients with acute decompensated HFrEF in real‐world populations.
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spelling doaj.art-1a4b0041385f427cb641ad8366560ce52022-12-21T23:14:23ZengWileyESC Heart Failure2055-58222021-10-01854199421010.1002/ehf2.13536The association between ivabradine and adverse cardiovascular events in acute decompensated HFrEF patientsChia‐Te Liao0Jin‐Long Huang1Huai‐Wen Liang2Fa‐Po Chung3Ying‐Hsiang Lee4Po‐Lin Lin5Wei‐Ru Chiou6Wen‐Yu Lin7Chien‐Yi Hsu8Hung‐Yu Chang9Division of Cardiology Chi‐Mei Medical Center Tainan TaiwanCardiovascular Center Taichung Veterans General Hospital Taichung TaiwanDivision of Cardiology, Department of Internal Medicine, E‐Da hospital I‐Shou University Kaohsiung TaiwanFaculty of Medicine, School of Medicine National Yang Ming Chiao Tung University Taipei TaiwanDepartment of Medicine Mackay Medical College New Taipei TaiwanDepartment of Medicine Mackay Medical College New Taipei TaiwanDepartment of Medicine Mackay Medical College New Taipei TaiwanDivision of Cardiology, Department of Medicine, Tri‐Service General Hospital National Defense Medical Center Taipei TaiwanFaculty of Medicine, School of Medicine National Yang Ming Chiao Tung University Taipei TaiwanFaculty of Medicine, School of Medicine National Yang Ming Chiao Tung University Taipei TaiwanAbstract Aims Ivabradine has been used in patients who have chronic heart failure (HF) with reduced ejection fraction (HFrEF) and concomitant sinus heart rate ≥70 bpm. This administration for acute HFrEF remains a concern. This study used a real‐world multicentre database to investigate the effects of ivabradine among patients with acute decompensated HFrEF before discharge. Methods and results This study retrospectively identified patients with acute decompensated HFrEF who were administered ivabradine at discharge from two multicentre HF databases. Propensity score matching was performed to adjust for confounders. Cardiovascular mortality, all‐cause mortality, and recurrent HF rehospitalization risks were then compared between those with and without ivabradine treatment. After 1:2 propensity score matching, 876 patients (age, 60.7 ± 14.6 years; female, 23.2%; left ventricular ejection fraction, 28.2% ± 7.8%; and heart rate at discharge, 84.3 ± 13.8 bpm) were included in the final analysis, including 292 and 584 patients with and without ivabradine treatment at discharge, respectively. No significant differences were observed in baseline characteristics between the two groups. At 1 year follow‐up, patients in the ivabradine group had significantly lower heart rates (77.6 ± 14.7 vs. 81.1 ± 16.3 bpm; P = 0.005) and lower HF severity symptoms (New York Heart Association Functional class, 2.1 ± 0.7 vs. 2.3 ± 0.9; P < 0.001) than those from the non‐ivabradine group. Ivabradine users had significantly lower risks of 1 year cardiovascular mortality (5.8 vs. 12.2 per 100‐person year; P = 0.003), all‐cause mortality (7.2 vs. 14.0 per 100‐person year; P = 0.003), and total HF rehospitalization (42.3 vs. 72.6 per 100‐person year; P < 0.001) than non‐ivabradine users. Following multivariate analysis, the predischarge prescription of ivabradine remained independently associated with lower 1 year all‐cause mortality (hazard ratio, 0.45; 95% confidence interval, 0.28–0.74; P = 0.002) and cardiovascular mortality (hazard ratio, 0.41; 95% confidence interval, 0.24–0.72; P = 0.002). Conclusions The current study findings suggest that ivabradine treatment is associated with reduced risks of cardiovascular mortality, all‐cause mortality, and HF rehospitalization within 1 year among patients with acute decompensated HFrEF in real‐world populations.https://doi.org/10.1002/ehf2.13536Heart failureHospitalizationIvabradineMortalityReal‐world
spellingShingle Chia‐Te Liao
Jin‐Long Huang
Huai‐Wen Liang
Fa‐Po Chung
Ying‐Hsiang Lee
Po‐Lin Lin
Wei‐Ru Chiou
Wen‐Yu Lin
Chien‐Yi Hsu
Hung‐Yu Chang
The association between ivabradine and adverse cardiovascular events in acute decompensated HFrEF patients
ESC Heart Failure
Heart failure
Hospitalization
Ivabradine
Mortality
Real‐world
title The association between ivabradine and adverse cardiovascular events in acute decompensated HFrEF patients
title_full The association between ivabradine and adverse cardiovascular events in acute decompensated HFrEF patients
title_fullStr The association between ivabradine and adverse cardiovascular events in acute decompensated HFrEF patients
title_full_unstemmed The association between ivabradine and adverse cardiovascular events in acute decompensated HFrEF patients
title_short The association between ivabradine and adverse cardiovascular events in acute decompensated HFrEF patients
title_sort association between ivabradine and adverse cardiovascular events in acute decompensated hfref patients
topic Heart failure
Hospitalization
Ivabradine
Mortality
Real‐world
url https://doi.org/10.1002/ehf2.13536
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