Association of D-dimer with short-term risk of venous thromboembolism in acutely ill medical patients: A systematic review and meta-analysis

Vasc Med. 2022 Oct;27(5):478-486. doi: 10.1177/1358863X221109855. Epub 2022 Aug 1.

Abstract

Background: D-dimer, a marker of ongoing procoagulant activity, has been widely used for the diagnosis of venous thromboembolism (VTE). The prognostic significance of D-dimer in stratifying VTE risk for acutely ill medical patients has not been well-established.

Methods: A literature search was performed to collect studies that compared the incidence of short-term VTE between acutely ill medical patients with elevated or nonelevated D-dimer levels. The cutoff of D-dimer was 0.5 μg/mL or otherwise defined by included studies. The study endpoint was any occurrence of VTE (inclusive of deep vein thrombosis [DVT], pulmonary embolism, or VTE-related death) within 90 days of hospital presentation. A meta-analytic approach was employed to estimate the odds ratio (OR) with 95% CI by fitting random-effects models using the generic inverse variance weighted approach.

Results: A total of 10 studies representing 31,119 acutely ill medical patients were included. Compared to those with nonelevated D-dimer levels, patients with elevated D-dimer had approximately threefold greater odds for short-term VTE within 90 days (OR, 3.28; 95% CI, 2.44 to 4.40; p < 0.0001). The association of elevated D-dimer with VTE composite (OR, 3.33; 95% CI, 2.20 to 5.02) and with DVT (OR, 3.26; 95% CI, 2.32 to 4.58) was comparable. The association was significant among patients who presented various acute medical illness (OR, 2.68; 95% CI, 2.01 to 3.58) and those who presented with acute stroke (OR, 3.25; 95% CI, 2.31 to 4.58).

Conclusion: Elevation of D-dimer was predictive of the occurrence of VTE within 90 days among acutely ill medical patients.

Keywords: D-dimer; biomarker; deep vein thrombosis (DVT); pulmonary embolism (PE); venous thromboembolism (VTE).

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Fibrin Fibrinogen Degradation Products / analysis
  • Humans
  • Incidence
  • Pulmonary Embolism* / complications
  • Pulmonary Embolism* / diagnosis
  • Venous Thromboembolism* / diagnosis
  • Venous Thromboembolism* / epidemiology
  • Venous Thromboembolism* / etiology

Substances

  • Fibrin Fibrinogen Degradation Products
  • fibrin fragment D