TY - JOUR
T1 - Multimorbidity, guideline-directed medical therapies, and associated outcomes among hospitalized heart failure patients
AU - West Tokyo Heart Failure Registry Investigators
AU - Takeuchi, Shinsuke
AU - Kohno, Takashi
AU - Goda, Ayumi
AU - Shiraishi, Yasuyuki
AU - Kawana, Masataka
AU - Saji, Mike
AU - Nagatomo, Yuji
AU - Nishihata, Yosuke
AU - Takei, Makoto
AU - Nakano, Shintaro
AU - Soejima, Kyoko
AU - Kohsaka, Shun
AU - Yoshikawa, Tsutomu
N1 - 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 and 26461088; T.K. 17K09526 and 20K08408; and A.G. 21K08087), a Grant‐in‐Aid for Young Scientists (Y.S. JPSS KAKENHI, 18K15860), a Grant‐in‐Aid for Clinical Research from the Japanese Circulation Society (Y.S. 2019), a Grant‐in‐Aid from the Japanese Ministry of Health, Labor and Welfare (S.K. H29‐Refractory Disease‐034), a Health Labour Science Research Grant (S.K. 14528506), and Sakakibara Clinical Research Grant for the Promotion of Science (T.Y. 2012–2019).
Funding Information:
Y.S. is affiliated with an endowed department that is supported by Nippon Shinyaku Co., Ltd., has received a research grant from the SECOM Science and Technology Foundation, and has received an honorarium from Otsuka Pharmaceutical Co., Ltd. S.K. has received an unrestricted research grant from the Department of Cardiology, Keio University School of Medicine, Bayer Pharmaceutical Co., Ltd., and Daiichi Sankyo Co., Ltd. S.T. has received a research grant from the Bayer Pharmaceutical Co., Ltd. The remaining authors have no conflicts of interest to disclose. There are no patents, products in development, or marketed products to declare.
Publisher Copyright:
© 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
PY - 2022/8
Y1 - 2022/8
N2 - Aims: Multimorbidity is common among heart failure (HF) patients and may attenuate guideline-directed medical therapy (GDMT). Multimorbid patients are under-represented in clinical trials; therefore, the effect of multimorbidity clustering on the prognosis of HF patients remains unknown. We evaluated the prevalence of multimorbidity clusters among consecutively registered hospitalized HF patients and assessed whether GDMT attenuated outcomes. Methods and results: We examined 1924 hospitalized HF patients with reduced left ventricular ejection fraction (<50%) in a multicentre registry (West Tokyo HF Registry: WET-HF). Ten comorbid conditions in the WET-HF were abstracted: coronary artery disease, atrial fibrillation, stroke, anaemia, chronic obstructive pulmonary disease, renal dysfunction, obesity, hypertension, dyslipidaemia, and diabetes. Patients were divided into three groups (0–2: n = 451; 3–4: n = 787; and ≥5: n = 686) based on the number of comorbid conditions. The primary composite endpoint was all-cause mortality and HF rehospitalization. The most prevalent comorbidities were renal dysfunction (67.9%), hypertension (66.0%), and anaemia (53.8%). Increased comorbidity was associated with increased adverse outcomes [3–4: hazard ratio (HR) 1.42, 95% confidence interval (CI) 1.13–1.77, P = 0.003; ≥5: HR 2.12, 95%CI 1.69–2.65, P < 0.001; and reference: 0–2] and lower GDMT prescription rate (0–2: 69.2%; 3–4: 57.7%; and ≥5: 57.6%). GDMT was associated with decreased adverse outcomes; this association was maintained even as the comorbidity burden increased but tended to weaken (0–2: HR 0.53, 95%CI 0.35–0.78; P = 0.001; 3–4: HR 0.82, 95%CI 0.65–1.04, P = 0.095; and ≥5: HR 0.81, 95%CI 0.65–1.00, P = 0.053; P for interaction = 0.156). Conclusions: Comorbidity clusters were prevalent and associated with poorer outcomes. GDMT remained beneficial regardless of the comorbidity burden but tended to weaken with increasing comorbidity burden. Further research is required to optimize medical care in these patients.
AB - Aims: Multimorbidity is common among heart failure (HF) patients and may attenuate guideline-directed medical therapy (GDMT). Multimorbid patients are under-represented in clinical trials; therefore, the effect of multimorbidity clustering on the prognosis of HF patients remains unknown. We evaluated the prevalence of multimorbidity clusters among consecutively registered hospitalized HF patients and assessed whether GDMT attenuated outcomes. Methods and results: We examined 1924 hospitalized HF patients with reduced left ventricular ejection fraction (<50%) in a multicentre registry (West Tokyo HF Registry: WET-HF). Ten comorbid conditions in the WET-HF were abstracted: coronary artery disease, atrial fibrillation, stroke, anaemia, chronic obstructive pulmonary disease, renal dysfunction, obesity, hypertension, dyslipidaemia, and diabetes. Patients were divided into three groups (0–2: n = 451; 3–4: n = 787; and ≥5: n = 686) based on the number of comorbid conditions. The primary composite endpoint was all-cause mortality and HF rehospitalization. The most prevalent comorbidities were renal dysfunction (67.9%), hypertension (66.0%), and anaemia (53.8%). Increased comorbidity was associated with increased adverse outcomes [3–4: hazard ratio (HR) 1.42, 95% confidence interval (CI) 1.13–1.77, P = 0.003; ≥5: HR 2.12, 95%CI 1.69–2.65, P < 0.001; and reference: 0–2] and lower GDMT prescription rate (0–2: 69.2%; 3–4: 57.7%; and ≥5: 57.6%). GDMT was associated with decreased adverse outcomes; this association was maintained even as the comorbidity burden increased but tended to weaken (0–2: HR 0.53, 95%CI 0.35–0.78; P = 0.001; 3–4: HR 0.82, 95%CI 0.65–1.04, P = 0.095; and ≥5: HR 0.81, 95%CI 0.65–1.00, P = 0.053; P for interaction = 0.156). Conclusions: Comorbidity clusters were prevalent and associated with poorer outcomes. GDMT remained beneficial regardless of the comorbidity burden but tended to weaken with increasing comorbidity burden. Further research is required to optimize medical care in these patients.
KW - Comorbidity
KW - Guideline-directed medical therapy
KW - Heart failure
KW - Multimorbidity
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U2 - 10.1002/ehf2.13954
DO - 10.1002/ehf2.13954
M3 - Article
C2 - 35561100
AN - SCOPUS:85131680893
SN - 2055-5822
VL - 9
SP - 2500
EP - 2510
JO - ESC heart failure
JF - ESC heart failure
IS - 4
ER -