Clinical application of the Innovance D‑dimer assay in the diagnosis of acute pulmonary thromboembolism
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- Published online on: April 28, 2017 https://doi.org/10.3892/etm.2017.4400
- Pages: 3543-3548
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Abstract
Patients with acute pulmonary thromboembolism (APTE) have a high short‑term mortality rate. The current study aimed to investigate the use of D‑dimer in the diagnosis of APTE in suspected APTE patients. All suspected APTE patients were classified into diagnosis or control groups according to the results of a computed tomography pulmonary angiogram. Mann‑Whitney U and Kruskal‑Wallis H tests were used to evaluate the association between D‑dimer values and APTE. Area under the curve (AUC) values and the Youden Index were used to determine D‑dimer cut‑off levels for the prediction of APTE. The data of 112 suspected APTE patients (54.8% women; mean age, 70.5 years) were analyzed prospectively. There were no significant differences in age (74.5 vs. 73.5 years, P=0.538) or gender distribution (female ratio 56.5 vs. 53.0%, P=0.847) between the diagnosis and control groups. The incidence of symptoms including dyspnea (67.4 vs. 33.3%; P<0.01), chest distress (47.8 vs. 25.8%; P<0.05) and elevated D‑dimer (8.49 vs. 0.97 mg/l; P<0.001) were significantly higher in patients with APTE compared with the control group. D‑dimer values >3.32 mg/l fibrinogen equivalent units (FEU) were indicative of APTE and the Youden Index was 0.69. The maximum AUC was 0.87 (95% CI: 0.79‑0.92), the sensitivity and specificity were 89.13 and 80.30%, respectively, the positive and negative likelihood ratios were 4.53 and 0.14, respectively, and the positive and negative predictive values were 75.90 and 91.40%, respectively. A D‑dimer value <0.60 mg/l FEU was the optimal threshold for excluding APTE diagnosis, with a sensitivity of 100.0% and a specificity of 28.79%. The positive and negative likelihood ratios were 1.40 and 0.00, respectively, and the positive and negative predictive values were 49.50 and 100.00%, respectively. Thus, D‑dimer levels, combined with clinical assessment, yield high sensitivity and specificity in diagnosing APTE.