TY - JOUR
T1 - Heart Failure With Midrange Ejection Fraction in Patients Admitted for Acute Decompensation
T2 - A Report from the Japanese Multicenter Registry
AU - Takei, Makoto
AU - Kohsaka, Shun
AU - Shiraishi, Yasuyuki
AU - Goda, A.
AU - Nagatomo, Yuji
AU - Mizuno, Atsushi
AU - Suzino, Yasumori
AU - Kohno, Takashi
AU - Fukuda, Keiichi
AU - Yoshikawa, Tsutomu
N1 - Funding Information:
Funding: This work was supported by the Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT) KAKENHI , grant number 26461088 ; a grant from the Japan Agency for Medical Research and Development (201439013C; S.K.); a Grant-in-Aid for Scientific Research (JPSS KAKENHI, 23591062, 26461088; T.Y.); a Grant-in-Aid for Young Scientists (JPSS KAKENHI, 18K15860 [Y.S.]); a Health Labour Sciences Research Grant (14528506; S.K.); and a Sakakibara Clinical Research Grant for Promotion of Sciences, 2012, 2013, 2014 (T.Y.); a Grant-in-Aid for Scientific Research (23591062, 26461088 [T.Y.] 17K09526 [T.K.]).
Funding Information:
This work was supported by the Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT) KAKENHI grant 26461088; a grant from the Japan Agency for Medical Research and Development (201439013C; S.K.); a Grant-in-Aid for Scientific Research (JPSS KAKENHI, 23591062, 26461088; T.Y.); a Grant-in-Aid for Young Scientists (JPSS KAKENHI, 18K15860 [Y.S.]); Health Labour Sciences Research Grant (14528506; S.K.); and a Sakakibara Clinical Research Grant for Promotion of Sciences, 2012, 2013, 2014 (T.Y.). Dr. Kohsaka received an unrestricted research grant for the Department of Cardiology, Keio University School of Medicine from Bayer Pharmaceutical and Daiichi Sankyo. The other authors have no conflicts of interest to disclose. There are no patents, products in development or marketed products to declare.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/8
Y1 - 2019/8
N2 - Background: Patients having heart failure with midrange ejection fraction (HFmrEF: 40% ≤ EF < 50%) are increasingly being considered a new subset of the population with heart failure. Despite recent advances in heart-failure treatment strategies, the prognosis of these patients has not improved substantially over time. In addition, the significance of this new phenotype in hospitalized patients with acute decompensated heart failure (ADHF), another population whose prognosis has not improved, also remains poorly understood. This study aimed to describe the clinical characteristics, prognosis and treatment responses of patients with HFmrEF hospitalized for ADHF. Methods: On the basis of consecutive inpatient data from a multicenter ADHF registry, 651 of 3572 patients (17.1%) were classified as having HFmrEF. Prognostic factors predicting composite outcomes, defined as all-cause death and heart failure readmission, as well as all-cause death alone, were analyzed. Results: In the median follow-up duration of 724 days, both composite endpoints and all-cause death alone were comparable in those with heart failure with preserved ejection fraction, HFmrEF and heart failure with reduced ejection fraction. Age, anemia, hyponatremia, elevated blood urea nitrogen, chronic kidney disease, and elevated plasma brain natriuretic peptide levels were significant predictors of composite outcomes in HFmrEF. Conclusions: Roughly one-sixth of the patients with ADHF had HFmrEF. The long-term prognosis of patients with HFmrEF was not significantly different from that of patients with heart failure with preserved ejection fraction and heart failure with reduced ejection fraction in the population with ADHF. Risk factors for adverse outcomes in HFmrEF were also similar to those for heart failure with preserved ejection fraction and HFmrEF in the hospitalized population with ADHF.
AB - Background: Patients having heart failure with midrange ejection fraction (HFmrEF: 40% ≤ EF < 50%) are increasingly being considered a new subset of the population with heart failure. Despite recent advances in heart-failure treatment strategies, the prognosis of these patients has not improved substantially over time. In addition, the significance of this new phenotype in hospitalized patients with acute decompensated heart failure (ADHF), another population whose prognosis has not improved, also remains poorly understood. This study aimed to describe the clinical characteristics, prognosis and treatment responses of patients with HFmrEF hospitalized for ADHF. Methods: On the basis of consecutive inpatient data from a multicenter ADHF registry, 651 of 3572 patients (17.1%) were classified as having HFmrEF. Prognostic factors predicting composite outcomes, defined as all-cause death and heart failure readmission, as well as all-cause death alone, were analyzed. Results: In the median follow-up duration of 724 days, both composite endpoints and all-cause death alone were comparable in those with heart failure with preserved ejection fraction, HFmrEF and heart failure with reduced ejection fraction. Age, anemia, hyponatremia, elevated blood urea nitrogen, chronic kidney disease, and elevated plasma brain natriuretic peptide levels were significant predictors of composite outcomes in HFmrEF. Conclusions: Roughly one-sixth of the patients with ADHF had HFmrEF. The long-term prognosis of patients with HFmrEF was not significantly different from that of patients with heart failure with preserved ejection fraction and heart failure with reduced ejection fraction in the population with ADHF. Risk factors for adverse outcomes in HFmrEF were also similar to those for heart failure with preserved ejection fraction and HFmrEF in the hospitalized population with ADHF.
KW - East Asian
KW - Heart failure with midrange ejection fraction
KW - acute decompensated heart failure
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U2 - 10.1016/j.cardfail.2019.05.010
DO - 10.1016/j.cardfail.2019.05.010
M3 - Article
C2 - 31129270
AN - SCOPUS:85067249153
SN - 1071-9164
VL - 25
SP - 666
EP - 673
JO - Journal of Cardiac Failure
JF - Journal of Cardiac Failure
IS - 8
ER -