Larissa Heart Failure Risk Score and Mode of Death in Acute Heart Failure: Insights from REALITY-AHF

Author:

Xanthopoulos Andrew1ORCID,Bourazana Angeliki1,Matsue Yuya2ORCID,Fujimoto Yudai2,Oishi Shogo3,Akiyama Eiichi4,Suzuki Satoshi5,Yamamoto Masayoshi6,Kida Keisuke7,Okumura Takahiro8,Giamouzis Grigorios1ORCID,Skoularigis John1ORCID,Triposkiadis Filippos1ORCID,Kitai Takeshi910ORCID

Affiliation:

1. Department of Cardiology, University Hospital of Larissa, 41110 Larissa, Greece

2. Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine, Tokyo 113-0033, Japan

3. Department of Cardiology, Himeji Cardiovascular Center, Himeji 670-8560, Japan

4. Division of Cardiology, Yokohama City University Medical Center, Yokohama 232-0024, Japan

5. Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima 960-1295, Japan

6. Cardiovascular Division, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8577, Japan

7. Department of Pharmacology, St. Marianna University School of Medicine, Kawasaki 216-8511, Japan

8. Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan

9. Department of Cardiovascular Medicine, Kobe City Medical Center General Hospital, Kobe 650-0047, Japan

10. Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Osaka 564-8565, Japan

Abstract

Patients with heart failure (HF) patients may die either suddenly (sudden cardiac death/SCD) or progressively from pump failure. The heightened risk of SCD in patients with HF may expedite important decisions about medications or devices. We used the Larissa Heart Failure Risk Score (LHFRS), a validated risk model for all-cause mortality and HF rehospitalization, to investigate the mode of death in 1363 patients enrolled in the Registry Focused on Very Early Presentation and Treatment in Emergency Department of Acute Heart Failure (REALITY-AHF). Cumulative incidence curves were generated using a Fine–Gray competing risk regression, with deaths that were not due to the cause of death of interest as a competing risk. Likewise, the Fine–Gray competing risk regression analysis was used to evaluate the association between each variable and the incidence of each cause of death. The AHEAD score, a well-validated HF risk score ranging from 0 to 5 (atrial fibrillation, anemia, age, renal dysfunction, and diabetes mellitus), was used for the risk adjustment. Patients with LHFRS 2–4 exhibited a significantly higher risk of SCD (HR hazard ratio adjusted for AHEAD score 3.15, 95% confidence interval (CI) (1.30–7.65), p = 0.011) and HF death (adjusted HR for AHEAD score 1.48, 95% CI (1.04–2.09), p = 0.03), compared to those with LHFRS 0,1. Regarding cardiovascular death, patients with higher LHFRS had significantly increased risk compared to those with lower LHFRS (HR 1.44 adjusted for AHEAD score, 95% CI (1.09–1.91), p = 0.01). Lastly, patients with higher LHFRS exhibited a similar risk of non-cardiovascular death compared to those with lower LHFRS (HR 1.44 adjusted for AHEAD score, 95% CI (0.95–2.19), p = 0.087). In conclusion, LHFRS was associated independently with the mode of death in a prospective cohort of hospitalized HF patients.

Publisher

MDPI AG

Subject

General Medicine

Reference34 articles.

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