# Prognostic Value of Hemoglobin, Albumin, Lymphocyte, and Platelet Score in Predicting Mortality in Patients With Aortic Dissection: A Retrospective Single‐Center Study Based on ROC Curve Analysis

**Authors:** Canan Şahin, Yahya Şahin

PMC · DOI: 10.1155/emmi/6996031 · Emergency Medicine International · 2026-02-24

## TL;DR

This study explores the HALP score's ability to predict mortality in aortic dissection patients, finding it has moderate accuracy and high specificity.

## Contribution

The study is the first to evaluate the HALP score as a mortality predictor in aortic dissection.

## Key findings

- The HALP score showed an AUC of 0.715 for predicting mortality in aortic dissection patients.
- Classical parameters like RBC, hemoglobin, and hematocrit had higher AUCs than the HALP score.
- The HALP score demonstrated high specificity (82.4%) but moderate sensitivity (55.9%).

## Abstract

Aortic dissection (AD) is a life‐threatening cardiovascular emergency associated with high mortality. Early risk stratification through reliable biomarkers is critical for guiding clinical decisions. The hemoglobin, albumin, lymphocyte, and platelet (HALP) score is a novel composite index reflecting inflammation, nutritional status, and hematologic balance. Although it has shown prognostic relevance in several disease states, its utility in predicting mortality in AD remains unknown. This study aimed to investigate the prognostic value of the HALP score and other hematologic markers in patients with AD.

This retrospective study included 51 patients diagnosed with AD between January 2020 and December 2024 using contrast‐enhanced thoracoabdominal computed tomography. Patients were grouped as survivors or nonsurvivors. Hematologic parameters (hemoglobin, hematocrit, red blood cell, platelet count, and mean platelet volume) and inflammatory indices (neutrophil‐to‐lymphocyte ratio [NLR], platelet‐to‐lymphocyte ratio [PLR], systemic immune–inflammation index [SII], and HALP score) were recorded. The Shapiro–Wilk test assessed normality; Student′s t‐test or the Mann–Whitney U test was applied accordingly. ROC analysis was performed to evaluate the predictive power of each parameter. Statistical significance was defined as p < 0.05. The primary outcome was in‐hospital mortality.

Overall mortality was 33.3%. Nonsurvivors were older and had significantly lower levels of hemoglobin, hematocrit, RBC, and platelet count (p < 0.001). The HALP score was lower in the exitus group, though not statistically significant in direct comparison (p = 0.549). ROC analysis revealed that the HALP score had an AUC of 0.715 (95% CI: 0.572–0.857, p = 0.003), with 55.9% sensitivity and 82.4% specificity at a cutoff of 4.05. Classical parameters such as RBC (AUC = 0.824), Hgb (AUC = 0.802), and Htc (AUC = 0.811) demonstrated stronger predictive capacity. The in‐hospital mortality rate was 33.3%.

The HALP score demonstrated high specificity and moderate sensitivity in predicting mortality in AD, suggesting its potential as a complementary biomarker. Its ease of use and accessibility make it suitable for emergency clinical settings. Prospective multicenter studies are needed to confirm its prognostic validity and routine application in AD management.

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CYGB (cytoglobin) [NCBI Gene 114757] {aka HGB, NOD, STAP}
- **Diseases:** circulatory collapse (MESH:D012769), SII (MESH:D007249), hyperlipidemia (MESH:D006949), NLR (MESH:D015467), thrombosis (MESH:D013927), HT (MESH:D006973), malnutrition (MESH:D044342), Mortality (MESH:D003643), atherosclerosis (MESH:D050197), cardiovascular and systemic diseases (MESH:D002318), infection (MESH:D007239), endothelial dysfunction (MESH:D014652), immune dysfunction (MESH:D007154), AD (MESH:D000784), Lymphopenia (MESH:D008231), diabetes mellitus (MESH:D003920), cancer (MESH:D009369), vascular injury (MESH:D057772), cerebrovascular disease (MESH:D002561), NSTEMI (MESH:D000072658), organ malperfusion (MESH:D000092124), gastric cancer (MESH:D013274), emergencies (MESH:D004630), STEMI (MESH:D000072657), thromboinflammation (MESH:D000090882), chest pain (MESH:D002637), HALP (OMIM:194470), Hypoalbuminemia (MESH:D034141), renal or hepatic failure (MESH:D017093), immune dysregulation (OMIM:614878), sepsis (MESH:D018805), systemic diseases (MESH:D034721), hypoxia (MESH:D000860)
- **Chemicals:** oxygen (MESH:D010100), steroids (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12930098/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12930098/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12930098/full.md

---
Source: https://tomesphere.com/paper/PMC12930098