Clinical and Prognostic Values of ALBI Score in Patients With Acute Heart Failure.


Journal

Heart, lung & circulation
ISSN: 1444-2892
Titre abrégé: Heart Lung Circ
Pays: Australia
ID NLM: 100963739

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 20 03 2019
revised: 07 10 2019
accepted: 01 12 2019
pubmed: 14 3 2020
medline: 14 4 2021
entrez: 14 3 2020
Statut: ppublish

Résumé

Although liver dysfunction is one of the common complications in patients with acute heart failure (AHF), no integrated marker has been defined. The albumin-bilirubin (ALBI) score has recently been proposed as a novel, clinically-applicable scoring system for liver dysfunction. We investigated the utility of the ALBI score in patients with AHF compared to that for a preexisting liver dysfunction score, the Model of End-Stage Liver Disease Excluding prothrombin time (MELD XI) score. We evaluated ALBI and MELD XI scores in 1,190 AHF patients enrolled in the prospective, multicentre Registry Focused on Very Early Presentation and Treatment in Emergency Department of Acute Heart Failure study. The associations between the two scores and the clinical profile and prognostic predictive ability for 1-year mortality were evaluated. The mean MELD XI and ALBI scores were 13.4±4.8 and -2.25±0.48, respectively. A higher ALBI score, but not higher MELD XI score, was associated with findings of fluid overload. After adjusting for pre-existing prognostic factors, the ALBI score (HR 2.11, 95% CI: 1.60-2.79, p<0.001), but not the MELD XI score (HR 1.02, 95% CI: 0.99-1.06, p=0.242), was associated with 1-year mortality. Likewise, area under the receiver-operator-characteristic curves for 1-year mortality significantly increased when the ALBI score (0.71 vs. 0.74, p=0.020), but not the MELD XI score (0.71 vs. 0.72, p=0.448), was added to the pre-existing risk factors. The ALBI score is potentially a suitable liver dysfunction marker that incorporates information on fluid overload and prognosis in patients with AHF. These results provide new insights into heart-liver interactions in AHF patients.

Sections du résumé

BACKGROUND BACKGROUND
Although liver dysfunction is one of the common complications in patients with acute heart failure (AHF), no integrated marker has been defined. The albumin-bilirubin (ALBI) score has recently been proposed as a novel, clinically-applicable scoring system for liver dysfunction. We investigated the utility of the ALBI score in patients with AHF compared to that for a preexisting liver dysfunction score, the Model of End-Stage Liver Disease Excluding prothrombin time (MELD XI) score.
METHODS METHODS
We evaluated ALBI and MELD XI scores in 1,190 AHF patients enrolled in the prospective, multicentre Registry Focused on Very Early Presentation and Treatment in Emergency Department of Acute Heart Failure study. The associations between the two scores and the clinical profile and prognostic predictive ability for 1-year mortality were evaluated.
RESULTS RESULTS
The mean MELD XI and ALBI scores were 13.4±4.8 and -2.25±0.48, respectively. A higher ALBI score, but not higher MELD XI score, was associated with findings of fluid overload. After adjusting for pre-existing prognostic factors, the ALBI score (HR 2.11, 95% CI: 1.60-2.79, p<0.001), but not the MELD XI score (HR 1.02, 95% CI: 0.99-1.06, p=0.242), was associated with 1-year mortality. Likewise, area under the receiver-operator-characteristic curves for 1-year mortality significantly increased when the ALBI score (0.71 vs. 0.74, p=0.020), but not the MELD XI score (0.71 vs. 0.72, p=0.448), was added to the pre-existing risk factors.
CONCLUSIONS CONCLUSIONS
The ALBI score is potentially a suitable liver dysfunction marker that incorporates information on fluid overload and prognosis in patients with AHF. These results provide new insights into heart-liver interactions in AHF patients.

Identifiants

pubmed: 32165085
pii: S1443-9506(19)31553-7
doi: 10.1016/j.hlc.2019.12.003
pii:
doi:

Substances chimiques

Albumins 0
Biomarkers 0
Creatinine AYI8EX34EU
Bilirubin RFM9X3LJ49

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1328-1337

Informations de copyright

Copyright © 2019 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved.

Auteurs

Yuya Matsue (Y)

Department of Cardiology, Juntendo University and Cardiovascular, Tokyo, Japan; Respiratory Sleep Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.

Nobuyuki Kagiyama (N)

Department of Cardiology, The Sakakibara Heart Institute of Okayama, Okayama, Japan; Heart and Vascular Institute, West Virginia University, WV, USA. Electronic address: kgnb_27_hot@yahoo.co.jp.

Tetsuo Yamaguchi (T)

Department of Cardiology, Japanese Red Cross Musashino Hospital, Tokyo, Japan.

Shunsuke Kuroda (S)

Department of Cardiology, Kameda Medical Center, Chiba, Japan.

Takahiro Okumura (T)

Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Keisuke Kida (K)

Department of Cardiology, St. Marianna University School of Medicine, Kawasaki, Japan.

Atsushi Mizuno (A)

Department of Cardiology, St. Luke's International Hospital, Tokyo, Japan.

Shogo Oishi (S)

Department of Cardiology, Himeji Cardiovascular Center, Himeji, Japan.

Yasutaka Inuzuka (Y)

Department of Cardiology, Shiga Medical Center for Adults, Moriyama, Japan.

Eiichi Akiyama (E)

Division of Cardiology, Yokohama City University Medical Center, Yokohama, Japan.

Ryuichi Matsukawa (R)

Division of Cardiology, Cardiovascular and Aortic Center, Saiseikai Fukuoka General Hospital, Fukuoka, Japan.

Kota Kato (K)

Department of Cardiology, Tokyo Medical University, Tokyo, Japan.

Satoshi Suzuki (S)

Department of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.

Takashi Naruke (T)

Department of Cardiovascular Medicine, Kitasato University School of Medicine, Tokyo, Japan.

Kenji Yoshioka (K)

Department of Cardiology, Kameda Medical Center, Chiba, Japan.

Tatsuya Miyoshi (T)

Department of Cardiology, Ako City Hospital, Ako, Japan.

Yuichi Baba (Y)

Department of Cardiology and Geriatrics, Kochi Medical School, Kochi University, Kochi, Japan.

Masayoshi Yamamoto (M)

Cardiovascular Division, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.

Kazuo Mizutani (K)

Department of Cardiology, Kobe Century Memorial Hospital, Kobe, Japan.

Kazuki Yoshida (K)

Departments of Epidemiology & Biostatistics, Harvard T.H. Chan School of Public Health, Boston, USA.

Takeshi Kitai (T)

Department of Cardiovascular Medicine, Kobe City Medical Center General Hospital, Kobe, Japan; Department of Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic, Cleveland, Ohio, USA.

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Classifications MeSH