Evidence map›Paper›PMID 42006493›Full record

ArticleEJIFCC2026

Correlation of D-dimer Measurement Values Using Quantum Dots Fluorescence Immunochromatographic Assay and Latex-Enhanced Immunoturbidimetric Assay.

Alif Ainudin, Ferdy Royland Marpaung, Paulus Budiono Notopuro

Abstract read
In one paragraph

Article in EJIFCC, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Alif AinudinClinical Pathology Specialization Programme, Faculty of Medicine - Universitas Airlangga, Surabaya, Indonesia.
Ferdy Royland MarpaungDepartment of Clinical Pathology, Faculty of Medicine - Universitas Airlangga, Surabaya, Indonesia.
Paulus Budiono NotopuroDepartment of Clinical Pathology, Faculty of Medicine - Universitas Airlangga, Surabaya, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: D-dimer, a fibrin degradation product, is widely used in the diagnosis of thrombotic disorders and in clinical decision-making. Quantum dots (QDs) fluorescence immunochromatography has emerged as a rapid method for detecting protein biomarkers; however, comparative data with the established latex-enhanced immunoturbidimetric assay remain limited. Methods: A laboratory-based method comparison study was conducted using 80 consecutively collected plasma samples from patients at Dr. Soetomo General Academic Hospital, Surabaya. D-dimer levels were measured using a QDs fluorescence immunochromatography assay (QD-S2000, Vazyme, China) and a latex-enhanced immunoturbidimetric assay (Sysmex CS-2500, Sysmex Corporation, Japan).Correlation and agreement between methods were assessed using Spearman correlation analysis and Bland-Altman plots. Results: Among the 80 samples (60% female, 40% male), a very strong correlation was observed between the two methods (Spearman r = 0.951, p < 0.001). Bland-Altman analysis demonstrated good agreement, with most data points falling within the 95% limits of agreement. Although the QDs fluorescence immunochromatography method consistently produced higher absolute D-dimer values, both assays showed comparable trends across the measurement range. Conclusion: QDs fluorescence immunochromatography and the latex-enhanced immunoturbidimetric assay demonstrated strong correlation and acceptable agreement in D-dimer measurement. Despite yielding higher absolute values, the QDs-based method showed consistent performance, supporting its potential as a reliable and rapid alternative for clinical D-dimer assessment.

Indexed as

D-dimerfluorescence immunochromatographylatex-enhanced immunoturbidimetric assay

Identifiers

PMID42006493
PMCPMC13088497

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