Evidence map›Paper›PMID 40880284›Full record

SynthesisCardiology2025

Predictive Performance of HAS-BLED Score in Patients with Atrial Fibrillation and Cancer: A Meta-Analysis.

Alyaa M Ajabnoor, Reham M Baamer

Abstract readSystematic Review
In one paragraph

Synthesis in Cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Alyaa M AjabnoorDepartment of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
Reham M BaamerDepartment of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPatients with atrial fibrillation (AF) and history of cancer face unique bleeding risks, complicating the applicability of standard bleeding risk scores like HAS-BLED. This meta-analysis aimed to evaluate the performance of HAS-BLED in predicting bleeding events in this high-risk population.

methodsThe MEDLINE, PubMed, and EMBASE databases were searched from 1st of January 2010 to 30th of November 2024 for relevant studies using keywords, such as "AF" "cancer" "bleeding," and "HAS-BLED." Data on C-statistics were extracted to assess the predictive performance of HAS-BLED score.

resultsOur analysis included seven retrospective cohort studies, recruiting a total of 436,102 patients. The quality of the included studies was deemed acceptable for analysis. The reported C-statistics for HAS-BLED score varied widely across studies, ranging from 0.45 to 0.77. Subgroup analyses demonstrated moderate discrimination in patients with breast cancer (0.56-0.80), prostate cancer (0.58-0.72), and lung cancer (0.59-0.80), while poorer performance was observed in hematological malignancies (0.45-0.70) and in anticoagulated patients (pooled C-statistic = 0.55; 95% confidence interval: 0.54-0.56). Significant heterogeneity was observed in the overall analysis and most subgroups (I2 > 90%), except for the anticoagulated subgroup. A sensitivity analysis excluding the largest study reduced heterogeneity and improved funnel plot symmetry, indicating that study size contributed to variability in HAS-BLED performance.

conclusionThe HAS-BLED score has shown variable predictive abilities in AF patients with cancer ranging from poor to good, with notable heterogeneity across studies secondary to various contributing factors. This emphasizes the need for individualized risk assessment tailored to the unique characteristics of cancer patients to effectively guide clinical decision-making.

Indexed as

Atrial fibrillationBleeding and HAS-BLEDCancerStroke

Identifiers

PMID40880284
PMCPMC12503809

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