TY - JOUR
T1 - Association between class of foundational medication for heart failure and prognosis in heart failure with reduced/mildly reduced ejection fraction
AU - Ito, Miyuki
AU - Maeda, Daichi
AU - Matsue, Yuya
AU - Shiraishi, Yasuyuki
AU - Dotare, Taishi
AU - Sunayama, Tsutomu
AU - Nogi, Kazutaka
AU - Takei, Makoto
AU - Ueda, Tomoya
AU - Nogi, Maki
AU - Ishihara, Satomi
AU - Nakada, Yasuki
AU - Kawakami, Rika
AU - Kagiyama, Nobuyuki
AU - Kitai, Takeshi
AU - Oishi, Shogo
AU - Akiyama, Eiichi
AU - Suzuki, Satoshi
AU - Yamamoto, Masayoshi
AU - Kida, Keisuke
AU - Okumura, Takahiro
AU - Nagatomo, Yuji
AU - Kohno, Takashi
AU - Nakano, Shintaro
AU - Kohsaka, Shun
AU - Yoshikawa, Tsutomu
AU - Saito, Yoshihiko
AU - Minamino, Tohru
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - We clarified the association between changes in the number of foundational medications for heart failure (FMHF) during hospitalization for worsening heart failure (HF) and post-discharge prognosis. We retrospectively analyzed a combined dataset from three large-scale registries of hospitalized patients with HF in Japan (NARA-HF, WET-HF, and REALITY-AHF) and patients diagnosed with HF with reduced or mildly reduced left ventricular ejection fraction (HFr/mrEF) before admission. Patients were stratified by changes in the number of prescribed FMHF classes from admission to discharge: angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, beta-blockers, and mineralocorticoid receptor blockers. Primary endpoint was the combined endpoint of HF rehospitalization and all-cause death within 1 year of discharge. The cohort comprised 1113 patients, and 482 combined endpoints were observed. Overall, FMHF prescriptions increased in 413 (37.1%) patients (increased group), remained unchanged in 607 (54.5%) (unchanged group), and decreased in 93 (8.4%) (decreased group) at discharge compared with that during admission. In the multivariable analysis, the increased group had a significantly lower incidence of the primary endpoint than the unchanged group (hazard ratio 0.56, 95% confidence interval 0.45–0.60; P < 0.001). In conclusion, increase in FMHF classes during HF hospitalization is associated with a better prognosis in patients with HFr/mrEF.
AB - We clarified the association between changes in the number of foundational medications for heart failure (FMHF) during hospitalization for worsening heart failure (HF) and post-discharge prognosis. We retrospectively analyzed a combined dataset from three large-scale registries of hospitalized patients with HF in Japan (NARA-HF, WET-HF, and REALITY-AHF) and patients diagnosed with HF with reduced or mildly reduced left ventricular ejection fraction (HFr/mrEF) before admission. Patients were stratified by changes in the number of prescribed FMHF classes from admission to discharge: angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, beta-blockers, and mineralocorticoid receptor blockers. Primary endpoint was the combined endpoint of HF rehospitalization and all-cause death within 1 year of discharge. The cohort comprised 1113 patients, and 482 combined endpoints were observed. Overall, FMHF prescriptions increased in 413 (37.1%) patients (increased group), remained unchanged in 607 (54.5%) (unchanged group), and decreased in 93 (8.4%) (decreased group) at discharge compared with that during admission. In the multivariable analysis, the increased group had a significantly lower incidence of the primary endpoint than the unchanged group (hazard ratio 0.56, 95% confidence interval 0.45–0.60; P < 0.001). In conclusion, increase in FMHF classes during HF hospitalization is associated with a better prognosis in patients with HFr/mrEF.
UR - https://www.scopus.com/pages/publications/85139294850
UR - https://www.scopus.com/pages/publications/85139294850#tab=citedBy
U2 - 10.1038/s41598-022-20892-3
DO - 10.1038/s41598-022-20892-3
M3 - Article
C2 - 36198895
AN - SCOPUS:85139294850
SN - 2045-2322
VL - 12
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 16611
ER -