TY - JOUR
T1 - Low blood pressure and guideline-directed medical therapy in patients with heart failure with reduced ejection fraction
AU - West Tokyo Heart Failure Registry Investigators
AU - Izumi, Keiichi
AU - Kohno, Takashi
AU - Goda, Ayumi
AU - Takeuchi, Shinsuke
AU - Shiraishi, Yasuyuki
AU - Saji, Mike
AU - Nagatomo, Yuji
AU - Tanaka, Toshikazu D.
AU - Takei, Makoto
AU - Nakano, Shintaro
AU - Soejima, Kyoko
AU - Kohsaka, Shun
AU - Yoshikawa, Tsutomu
N1 - Funding Information:
Dr. Shiraishi, who is affiliated with an endowed department that is supported by Nippon Shinyaku Co., Ltd., Medtronic Japan Co., Ltd., and BIOTRONIK JAPAN Inc., and received honorarium from Otsuka Pharmaceutical Co., Ltd. and Ono Pharmaceuticals Co., Ltd.. Dr. Kohsaka received unrestricted research grants from the Department of Cardiology, Keio University School of Medicine; Bayer Pharmaceutical Co., Ltd.; and Daiichi Sankyo Co., Ltd. The remaining authors have no conflicts of interest to disclose. There are no patents, products in development, or marketed products to declare.
Funding Information:
The West Tokyo Heart Failure Registry was supported by a grant from the Japan Agency for Medical Research and Development [S.K. 201439013C ], Grants-in-Aid for Scientific Research [T.Y. JPSS KAKENHI, 23591062 , 26461088, 18K08056, 21K08142 ; T.K. 17K09526 , 20K08408 ; A.G. 21K08087; S.K. 20H03915 ], a Grant-in-Aid for Young Scientists [Y.S. JPSS KAKENHI, 18K15860 ], Grant-in-Aid for Clinical Research from the Japanese Circulation Society [Y.S. 2019 ], Grant-in-Aid from the Japanese Ministry of Health, Labor and Welfare [S.K. H29-Refractory Disease-034 ], Health Labour Science Research Grant [S.K. 14528506 ], and Sakakibara Clinical Research Grant for the Promotion of Science [T.Y. 2012-2021 ].
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Background: Patients with heart failure (HF) presenting with low blood pressure (BP) have been underrepresented in large-scale clinical trials. We investigated the characteristics and implementation of conventional guideline-directed medical therapy (GDMT; renin-angiotensin system inhibitors and β-blockers) in patients with low BP hospitalized for HF with systolic dysfunction. Methods: Conventional GDMT was evaluated by discharge BP among 2043 consecutive patients with HF and left ventricular ejection fraction (LVEF) < 50% in the WET-HF registry. Among the 708 (34.7%) patients with lower discharge BP (≤ 100 mmHg; the lower tertiles), exploratory subgroups included patients with previous HF hospitalization, inotrope use, New York Heart Association (NYHA) III–IV class, and lower estimated glomerular filtration rate (eGFR) and LVEF (lower than median value). We evaluated the risk-adjusted association between GDMT implementation and 2-year adverse events (all-cause mortality or HF rehospitalization). Results: Among the 2043 patients (age 74 [63–82] years), the median systolic BP was 108 (98–120) mmHg. Among patients with lower BP, GDMT prescription rate was 62.7%, and GDMT use was associated with decreased adverse events (HR:0.74, 95%CI:0.58–0.94). GDMT prescription rates were lower among higher-NYHA class and lower-eGFR subgroups compared with their reference subgroups, and directionally similar outcomes were noted in all subgroups (favoring GDMT use); however, this association was somewhat attenuated in the lower-eGFR group (HR:0.87, 95%CI:0.64–1.17). Conclusions: Conventional GDMT use was associated with decreased adverse outcomes in most patients with HF compounded by systolic dysfunction and low BP, albeit caution is warranted in patients with renal dysfunction.
AB - Background: Patients with heart failure (HF) presenting with low blood pressure (BP) have been underrepresented in large-scale clinical trials. We investigated the characteristics and implementation of conventional guideline-directed medical therapy (GDMT; renin-angiotensin system inhibitors and β-blockers) in patients with low BP hospitalized for HF with systolic dysfunction. Methods: Conventional GDMT was evaluated by discharge BP among 2043 consecutive patients with HF and left ventricular ejection fraction (LVEF) < 50% in the WET-HF registry. Among the 708 (34.7%) patients with lower discharge BP (≤ 100 mmHg; the lower tertiles), exploratory subgroups included patients with previous HF hospitalization, inotrope use, New York Heart Association (NYHA) III–IV class, and lower estimated glomerular filtration rate (eGFR) and LVEF (lower than median value). We evaluated the risk-adjusted association between GDMT implementation and 2-year adverse events (all-cause mortality or HF rehospitalization). Results: Among the 2043 patients (age 74 [63–82] years), the median systolic BP was 108 (98–120) mmHg. Among patients with lower BP, GDMT prescription rate was 62.7%, and GDMT use was associated with decreased adverse events (HR:0.74, 95%CI:0.58–0.94). GDMT prescription rates were lower among higher-NYHA class and lower-eGFR subgroups compared with their reference subgroups, and directionally similar outcomes were noted in all subgroups (favoring GDMT use); however, this association was somewhat attenuated in the lower-eGFR group (HR:0.87, 95%CI:0.64–1.17). Conclusions: Conventional GDMT use was associated with decreased adverse outcomes in most patients with HF compounded by systolic dysfunction and low BP, albeit caution is warranted in patients with renal dysfunction.
KW - Blood pressure
KW - Guideline-directed medical therapy
KW - Heart failure
KW - Outcome
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U2 - 10.1016/j.ijcard.2022.10.129
DO - 10.1016/j.ijcard.2022.10.129
M3 - Article
C2 - 36270494
AN - SCOPUS:85140631242
VL - 370
SP - 255
EP - 262
JO - International Journal of Cardiology
JF - International Journal of Cardiology
SN - 0167-5273
ER -