Evidence map›Paper›PMID 40842766›Full record

ArticleCureus2025

Can the Hemoglobin-Albumin-Lymphocyte-Platelet (HALP) Index Be Used as a Prognostic Marker in Patients Diagnosed With Idiopathic Pulmonary Fibrosis?

Esma Sevil Akkurt, Kerem Ensarioglu, Berna Akıncı Ozyurek, Tugce Sahin Ozdemirel, Ozlem Duvenci Birben, Tuhanan Dolmuş, Ozlem Ertan

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Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Esma Sevil AkkurtPulmonary Medicine, University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital, Ankara, TUR.
Kerem EnsariogluPulmonary Medicine, University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital, Ankara, TUR.
Berna Akıncı OzyurekPulmonary Medicine, University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital, Ankara, TUR.
Tugce Sahin OzdemirelPulmonary Medicine, University of Health Sciences Ankara Atatürk Sanatorium Training and Research Hospital, Ankara, TUR.
Ozlem Duvenci BirbenPulmonary Medicine, University of Health Sciences, Ankara Oncology Training and Research Hospital, Ankara, TUR.
Tuhanan DolmuşPulmonary Medicine, University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital, Ankara, TUR.
Ozlem ErtanPulmonary Medicine, University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital, Ankara, TUR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe hemoglobin-albumin-lymphocyte-platelet (HALP) score serves as an indicator of systemic inflammation and can be utilized as a prognostic marker. It has been previously associated with many cancers, but its relationship with prognosis in patients diagnosed with idiopathic pulmonary fibrosis (IPF) is unknown. In our study, we aimed to evaluate the usability of the HALP score as a prognostic marker in patients diagnosed with IPF.

methodsThe study evaluated patients with IPF who were diagnosed and had follow-up visits in the pulmonary medicine clinic of a tertiary hospital between January 2021 and March 2023. Patients' clinical information, comorbidities, laboratory values, pulmonary function test-diffusion capacity of the lung for carbon monoxide (PFT-DLCO) parameters at the time of diagnosis, six-minute walk tests, body mass indices, prognosis information, and death information were recorded.

resultsA total of 224 patients were included in the study, with a mean age of 66.27 (±8.83) years and a predominantly male population (84%). The mean HALP score was 53.27 (±27.73), and with a cut-off of 25 for HALP, survival duration of patients between groups were statistically; a median survival of 493 (40-945) days for patients with a score of 25 or below for HALP and 981 (752-1209) days for those above it (log-rank test result of 0.01 and X

conclusionThe HALP score is a reliable, simple, easily accessible, and inexpensive index for predicting the prognosis of IPF. Further studies are required to evaluate subgroup outcomes for IPF patients.

Indexed as

halp scoreidiopathic pulmonary fibrosisprognostic markersystemic inflammationusual interstitial pneumonia (uip)

Identifiers

PMID40842766
PMCPMC12366475

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