Background
The traditional paradigm is that deep venous thrombosis (DVT) and pulmonary embolus (PE) are different temporal phases of a single disease process, most often labeled as the composite endpoint venous thromboembolism (VTE). However, we theorize that after severe blunt injury, DVT and PE may represent independent thrombotic entities rather than different stages of a single pathophysiologic process and therefore exhibit different clinical risk factor profiles.
Methods
We examined a large, multi-center prospective cohort of severely injured blunt trauma patients to compare clinical risk factors for DVT and PE, including indicators of injury severity, shock, resuscitation parameters, comorbidities and VTE prophylaxis. Independent risk factors for each outcome were determined by cross-validated logistic regression modeling using advanced exhaustive model search procedures.
Results
The study cohort consisted of 1,822 severely injured blunt trauma patients (median ISS = 33, median base deficit = −9.5). Incidence of DVT and PE were 5.1% and 3.9% respectively. Only 9 of 73 (5.7%) patients with a PE were also diagnosed with DVT. Independent risk factors associated with DVT include prophylaxis initiation within 48 hours (OR 0.57, 95% CI 0.36–0.90) and thoracic AIS ≥ 3 (OR 1.82, 95% CI 1.12–2.95), while independent risk factors for PE were serum lactate >5 (OR 2.33, 95% CI 1.43–3.79) and male gender (OR 2.12, 95% CI 1.17–3.84). Both DVT and PE exhibited differing risk factor profiles from the classic composite endpoint of VTE.
Conclusion
Deep venous thrombosis and pulmonary embolus exhibit differing risk factor profiles following severe injury. Clinical risk factors for diagnosis of DVT after severe blunt trauma include the inability to initiate prompt pharmacologic prophylaxis and severe thoracic injury, which may represent overall injury burden. In contrast, risk factors for PE are male gender and physiologic evidence of severe shock. We hypothesize that post-injury DVT and PE may represent a broad spectrum of pathologic thrombotic processes as opposed to the current conventional wisdom of peripheral thrombosis and subsequent embolus.
Level of Evidence
Prognostic study, Level III