Soluble endothelial protein C receptor is an independent predictor of venous thromboembolism after severe injury: Secondary analysis of a prospective cohort study.
Soluble endothelial protein C receptor is an independent predictor of venous thromboembolism after severe injury: Secondary analysis of a prospective cohort study.
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DOI:
10.1016/j.surg.2023.04.049
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发表时间:
2023-08
期刊:
影响因子:
3.8
通讯作者:
Cardenas, Jessica C.
中科院分区:
文献类型:
--
作者:
Sanders, Kelly E.;Holevinski, Sarah;Zhang, Xu;Cotton, Bryan A.;Cardenas, Jessica C.
Venous thromboembolism (VTE) is a leading cause of morbidity after trauma. Endothelial cells (ECs) are essential regulators of coagulation. While EC dysregulation is widely reported after trauma, the link between endothelial injury and VTE has not been reported. We conducted a secondary analysis of the Pragmatic Randomized Optimal Platelets and Plasma Ratios (PROPPR) study. Deaths from hemorrhage or within 24 hours were excluded. VTE was diagnosed by duplex ultrasound or chest computed tomography. Endothelial markers soluble endothelial protein c receptor (sEPCR), thrombomodulin (sTM), and syndecan-1 (Sdc1) were measured in plasma by enzyme-linked immunosorbent assay and compared over the first 72 hours from admission using Mann-Whitney test. Multivariable logistic regression assessed the adjusted effects of endothelial markers on VTE risk. Of 575 patients enrolled, 86 developed VTE (15%). Median time to VTE was 6 days ((Q1, Q3), (4, 13)). No differences were identified in demographics or injury severity. sEPCR, sTM, and Sdc1 showed significant increases over time among patients who developed VTE compared to those who did not. Using last available values, patients were stratified into high and low sEPCR, sTM, and Sdc1 groups. Multivariable analyses revealed an independent association between elevated sEPCR and VTE risk [Odds Ratio 1.63; 95% CI 1.01, 2.63; p=0.04]. Cox proportional hazards modeling demonstrated a strong yet non-significant trend between elevated sEPCR and time to VTE. Plasma markers of endothelial injury, in particular sEPCR are strongly associated with trauma-related VTE. Therapeutics targeting endothelial function could mitigate the incidence of VTE following trauma.
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影响因子:
3.1
作者:
Dillon, Gabrielle A.;Stanhewicz, Anna E.;Serviente, Corinna;Flores, Valerie A.;Stachenfeld, Nina;Alexander, Lacy M.
通讯作者:
Alexander, Lacy M.
DOI:
10.1161/atvbaha.118.310367
发表时间:
2018-06
期刊:
Arteriosclerosis, thrombosis, and vascular biology
影响因子:
--
作者:
Wang M;Hao H;Leeper NJ;Zhu L;Early Career Committee
通讯作者:
Early Career Committee
影响因子:
2.1
作者:
Yau JW;Teoh H;Verma S
通讯作者:
Verma S
影响因子:
20.3
作者:
Campbell, Robert A.;Overmyer, Katherine A.;Wolberg, Alisa S.
通讯作者:
Wolberg, Alisa S.
影响因子:
24
作者:
Chirinos, JA;Heresi, GA;Ahn, YS
通讯作者:
Ahn, YS