Blood donor, component, and recipient‐specific factors associated with venous thromboembolism in transfused hospitalized adult patients: Data from the recipient epidemiology and donor evaluation Study‐III (REDS‐III)

Author:

Goel Ruchika12ORCID,Plimier Colleen3,Lee Catherine3,Tobian Aaron A. R.2ORCID,Josephson Cassandra D.45ORCID,Hod Eldad A.6ORCID,Roubinian Nareg H.378

Affiliation:

1. Department of Internal Medicine and Pediatrics Simmons Cancer Institute at SIU School of Medicine Springfield Illinois USA

2. Division of Transfusion Medicine, Department of Pathology Johns Hopkins University School of Medicine Baltimore Maryland USA

3. Kaiser Permanente Northern California Division of Research Oakland California USA

4. Department of Oncology and Cancer and Blood Disorders Institute Johns Hopkins University School of Medicine Baltimore Maryland USA

5. Johns Hopkins All Children's Hospital St. Petersburg Florida USA

6. Department of Pathology Columbia University Medical Center New York New York USA

7. Vitalant Research Institute San Francisco California USA

8. UCSF Department of Laboratory Medicine San Francisco California USA

Abstract

AbstractObjectiveGrowing evidence suggests multiple pathophysiological mechanisms linking red blood cells (RBC) transfusions to thrombosis. This study examined blood donor, component, and recipient factors which may be associated with thromboembolic outcomes following RBC transfusion.MethodsWe utilized the Recipient Epidemiology Donor Evaluation Study‐III (REDS‐III) database on patients transfused in 12 hospitals between 2013–2016. Stratified Cox proportional hazards regression models with time‐dependent exposures were used to examine associations of donor and component modification characteristics on venous thromboembolism (VTE) in patients transfused RBC units.Results59,603 patients were transfused 229,500 RBC units during 79,298 hospitalizations with post‐transfusion VTE occurring in 1869 (2.4%) of patients. In adjusted regression analyses, a per RBC‐unit risk of VTE was present for gamma irradiation (HR = 1.03; 95% CI: 1.02–1.03), female donor sex (HR = 1.01; 95% CI: 1.00–1.01), storage duration greater than 5 weeks (HR = 1.01; 95% CI: 1.01–1.02), AS‐1 storage solution (HR = 1.01; 95% CI: 1.00–1.01), and apheresis‐derived collections (HR = 1.01; 95% CI: 1.01–1.02). Among recipient factors, male sex (HR = 1.03; 95% CI: 1.02–1.04), pre‐transfusion hemoglobin level (HR = 0.94; 95% CI: 0.94–0.94), body mass index strata (HR = 1.11; 95% CI: 1.08–1.14), and principal diagnoses including malignancy (HR = 1.13; 95% CI: 1.10–1.16), cardiac arrest (HR = 1.38; 95% CI:1.07–1.77) and hip fracture (HR = 1.59; 95% CI:1.53–1.66) were associated with VTE in adjusted analyses.DiscussionWe identified several donor, component, and recipient‐specific factors associated with VTE in transfused hospitalized adult patients. In adjusted models, the dose‐dependent associations of donor and component‐specific factors with VTE were modest and unlikely to be clinically significant in the majority of transfused patients. Additional mechanistic and clinical studies linking blood donor and component factors with thrombotic outcomes are needed.

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Reference24 articles.

1. Epidemiology of venous thromboembolism

2. The epidemiology of venous thromboembolism

3. CDC.Centers for Disease Control and Prevention 2017.https://www.cdc.gov/ncbddd/dvt/ha-vte-data.html.

4. The sugeon general's Call to Action to Prevent Deep Venous thrombosis and Pulmonary Embolism.2008.http://www.surgeongeneral.gov/topics/deepvein/calltoaction/call-to-action-on-dvt-2008.pdf.

5. Trends in the Incidence of Deep Vein Thrombosis and Pulmonary Embolism

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