Prognostic Value of D-Dimer in Younger Patients with Pulmonary Embolism

Author:

Jovanović Ljiljana1,Subota Vesna1,Rajković Milena1,Subotić Bojana2,Džudović Boris2,Novčić Nataša2,Matijašević Jovan3,Mirić Milica3,Šalinger Sonja4,Nikolić Nataša Marković5,Nikolić Maja6,Miloradović Vladimir6,Kos Ljiljana7,Kovačevic-Preradović Tamara7,Obradović Slobodan28

Affiliation:

1. Institute of Biochemistry, Military Medical Academy , Belgrade , Serbia

2. Clinic of Cardiology and Emergency Internal Medicine, Military Medical Academy , Belgrade , Serbia

3. Institute for Pulmonary Diseases of Vojvodina, School of Medicine , University of Novi Sad , Sremska Kamenica , Serbia

4. Clinic of Cardiology, Clinical Center Nis , University of Nis , Serbia

5. University Clinical Center Zvezdara , School of Medicine , University of Belgrade , Serbia

6. Clinic of Cardiology, Clinical Center Kragujevac, School of Medicine , University of Kragujevac , Serbia

7. Clinic of Cardiology, Clinical Center Banja Luka, School of Medicine , University of Banja Luka , Bosnia and Herzegovina

8. School of Medicine , University of Defense , Belgrade , Serbia

Abstract

Abstract In patients with pulmonary embolism (PE), the D-Dimer assay is commonly utilized as part of the diagnostic workup, but data on D-Dimer for early risk stratification and short-term mortality prediction are limited. The purpose of this study was to determine D-Dimer levels as a predictive biomarker of PE outcomes in younger (<50 years of age) compared to older patients. We conducted retrospective analysis for 930 patients diagnosed with PE between 2015 and 2019 as part of the Serbian University Multicenter Pulmonary Embolism Registry (SUPER).All patients had D-Dimer levels measured within 24 hours of hospital admission. The primary outcome was mortality at 30 days or during hospitalization. Patients were categorized into two groups based on age (≤ 50 and >50 years of age). Younger patients constituted 20.5% of the study cohort. Regarding all-cause mortality, 5.2% (10/191)of patients died in group under the 50 years of age; the short-term all-causemortality was 12.4% (92/739) in older group.We have found that there was significant difference in plasma D-Dimer level between patients ≤ 50 years of age and older group (>50), p= 0.006.D-Dimer plasma level had good predictive value for the primary outcome in younger patients (c-statistics 0.710; 95% CI, 0.640-0.773; p<0.031). The optimal cutoff level for D-Dimer to predict PE-cause death in patients aged > 50 years was found to be 8.8 mg/l FEU(c-statistics 0,580; 95% CI 0.544-0.616; p=0.049). In younger PE patients, D-Dimer levels have good prognostic performance for 30-day all-cause mortalityand concentrations above 6.3 mg/l FEU are associated with increased risk of death. D-Dimer in patients aged over 50 years does not have predictive ability for all-caused short-term mortality. The relationship between D-Dimer and age in patients with PE may need further evaluation.

Publisher

Walter de Gruyter GmbH

Subject

General Medicine

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