Evidence map›Paper›PMID 41257067›Full record

ArticleJournal of clinical practice and research2025

Prognostic Value of Modified Glasgow Prognostic Score in Acute Decompensated Heart Failure with Reduced Ejection Fraction.

Çağatay Tunca, Mehmet Taha Özkan, Alperen Taş, Ayşe Nur Özkaya İbiş, Ahmet Kıvrak, Veysel Ozan Tanık

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Article in Journal of clinical practice and research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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6citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Çağatay TuncaDepartment of Cardiology, Ankara Etlik City Hospital, Ankara, Türkiye.
Mehmet Taha ÖzkanDepartment of Cardiology, Ankara Etlik City Hospital, Ankara, Türkiye.
Alperen TaşDepartment of Cardiology, Ankara Etlik City Hospital, Ankara, Türkiye.
Ayşe Nur Özkaya İbişDepartment of Cardiology, Ankara Etlik City Hospital, Ankara, Türkiye.
Ahmet KıvrakDepartment of Cardiology, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
Veysel Ozan TanıkDepartment of Cardiology, Ankara Etlik City Hospital, Ankara, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Acute decompensated heart failure (ADHF) significantly contributes to hospital admissions and is associated with high morbidity and mortality. This study aimed to assess whether the Modified Glasgow Prognostic Score (mGPS) could predict long-term mortality in patients with heart failure with reduced ejection fraction (HFrEF) admitted for ADHF. Materials and Methods: HFrEF patients admitted for ADHF between January 2022 and March 2023 were retrospectively analyzed. Patients were stratified by mGPS into three groups: low risk (C-reactive protein [CRP] ≤10 mg/L, albumin ≥35 g/L), moderate risk (CRP >10 mg/L, albumin ≥35 g/L), and high risk (CRP >10 mg/L, albumin <35 g/L). The primary endpoint was all-cause mortality, determined from hospital records and telephone follow-up, and analyzed using Kaplan-Meier (KM) survival analysis. Results: Of 238 patients (predominantly male, 70%), those with high mGPS were significantly older and had a higher prevalence of hypertension, diabetes, and ischemic etiology. They also exhibited higher creatinine and white blood cell (WBC) counts, along with lower hemoglobin and albumin levels. Mortality was significantly higher in this group. Multiple Cox regression analysis identified high mGPS scores, older age, reduced left ventricular ejection fraction (LVEF), lower hemoglobin, and hypoalbuminemia as independent predictors of mortality. KM analysis demonstrated significantly reduced survival among patients with elevated mGPS. Conclusion: The mGPS, which incorporates both inflammatory and nutritional parameters, effectively predicts long-term mortality risk in HFrEF patients hospitalized for ADHF. Routine use of mGPS in clinical practice may improve patient stratification, guide therapeutic decisions, and potentially enhance patient outcomes.

Indexed as

Acute decompensated heart failure (ADHF)heart failure with reduced ejection fraction (HFrEF)Modified Glasgow Prognostic Score (mGPS)mortalityN-terminal pro-B-type natriuretic peptide (NT-proBNP)

Identifiers

PMID41257067
PMCPMC12478585

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.